30 results on '"Vartolomei, M D"'
Search Results
2. Absolute basophil count is associated with time to recurrence in patients with high-grade T1 bladder cancer receiving bacillus Calmette–Guérin after transurethral resection of the bladder tumor
- Author
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Ferro, M., primary, Di Lorenzo, G., additional, Vartolomei, M. D., additional, Bruzzese, D., additional, Cantiello, F., additional, Lucarelli, G., additional, Musi, G., additional, Di Stasi, S., additional, Hurle, R., additional, Guazzoni, G., additional, Busetto, G. M., additional, Gabriele, A., additional, Del Giudice, F., additional, Damiano, R., additional, Perri, F., additional, Perdona, S., additional, Verze, P., additional, Borghesi, M., additional, Schiavina, R., additional, Almeida, G. L., additional, Bove, P., additional, Lima, E., additional, Autorino, R., additional, Crisan, N., additional, Farhan, A. R. Abu, additional, Battaglia, M., additional, Russo, G. I., additional, Ieluzzi, Vincenzo, additional, Morgia, G., additional, De Placido, P., additional, Terracciano, D., additional, Cimmino, A., additional, Scafuri, L., additional, Mirone, V., additional, De Cobelli, O., additional, Shariat, S., additional, Sonpavde, Guru, additional, and Buonerba, C., additional
- Published
- 2019
- Full Text
- View/download PDF
3. EAU–ESMO consensus statements on the management of advanced and variant bladder cancer - an international collaborative multi-stakeholder effort : under the auspices of the EAU and ESMO Guidelines Committees
- Author
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Horwich, A, Babjuk, M, Bellmunt, J, Bruins, H M, Reijke, T M De, Santis, M De, Gillessen, S, James, N, Maclennan, S, Palou, J, Powles, T, Ribal, M J, Shariat, S F, Kwast, T Van Der, Xylinas, E, Agarwal, N, Arends, T, Bamias, A, Birtle, A, Black, P C, Bochner, B H, Bolla, M, Boormans, J L, Bossi, A, Briganti, A, Brummelhuis, I, Burger, M, Castellano, D, Cathomas, R, Chiti, A, Choudhury, A, Compérat, E, Crabb, S, Culine, S, Bari, B De, Blok, W De, De Visschere, P J L, Decaestecker, K, Dimitropoulos, K, Dominguez-Escrig, J L, Fanti, S, Fonteyne, V, Frydenberg, M, Futterer, J J, Gakis, G, Geavlete, B, Gontero, P, Grubmüller, B, Hafeez, S, Hansel, D E, Hartmann, A, Hayne, D, Henry, A M, Hernandez, V, Herr, H, Herrmann, K, Hoskin, P, Huguet, J, Jereczek-Fossa, B A, Jones, R, Kamat, A M, Khoo, V, Kiltie, A E, Krege, S, Ladoire, S, Lara, P C, Leliveld, A, Linares-Espinós, E, Løgager, V, Lorch, A, Loriot, Y, Meijer, R, Mir, M Carmen, Moschini, M, Mostafid, H, Müller, A-C, Müller, C R, N'Dow, J, Necchi, A, Neuzillet, Y, Oddens, J R, Oldenburg, J, Osanto, S, Oyen, W J G, Pacheco-Figueiredo, L, Pappot, H, Patel, M I, Pieters, B R, Plass, K, Remzi, M, Retz, M, Richenberg, J, Rink, M, Roghmann, F, Rosenberg, J E, Rouprêt, M, Rouvière, O, Salembier, C, Salminen, A, Sargos, P, Sengupta, S, Sherif, Amir, Smeenk, R J, Smits, A, Stenzl, A, Thalmann, G N, Tombal, B, Turkbey, B, Lauridsen, S Vahr, Valdagni, R, Van Der Heijden, A G, Van Poppel, H, Vartolomei, M D, Veskimäe, E, Vilaseca, A, Rivera, F A Vives, Wiegel, T, Wiklund, P, Williams, A, Zigeuner, R, Witjes, J A, Horwich, A, Babjuk, M, Bellmunt, J, Bruins, H M, Reijke, T M De, Santis, M De, Gillessen, S, James, N, Maclennan, S, Palou, J, Powles, T, Ribal, M J, Shariat, S F, Kwast, T Van Der, Xylinas, E, Agarwal, N, Arends, T, Bamias, A, Birtle, A, Black, P C, Bochner, B H, Bolla, M, Boormans, J L, Bossi, A, Briganti, A, Brummelhuis, I, Burger, M, Castellano, D, Cathomas, R, Chiti, A, Choudhury, A, Compérat, E, Crabb, S, Culine, S, Bari, B De, Blok, W De, De Visschere, P J L, Decaestecker, K, Dimitropoulos, K, Dominguez-Escrig, J L, Fanti, S, Fonteyne, V, Frydenberg, M, Futterer, J J, Gakis, G, Geavlete, B, Gontero, P, Grubmüller, B, Hafeez, S, Hansel, D E, Hartmann, A, Hayne, D, Henry, A M, Hernandez, V, Herr, H, Herrmann, K, Hoskin, P, Huguet, J, Jereczek-Fossa, B A, Jones, R, Kamat, A M, Khoo, V, Kiltie, A E, Krege, S, Ladoire, S, Lara, P C, Leliveld, A, Linares-Espinós, E, Løgager, V, Lorch, A, Loriot, Y, Meijer, R, Mir, M Carmen, Moschini, M, Mostafid, H, Müller, A-C, Müller, C R, N'Dow, J, Necchi, A, Neuzillet, Y, Oddens, J R, Oldenburg, J, Osanto, S, Oyen, W J G, Pacheco-Figueiredo, L, Pappot, H, Patel, M I, Pieters, B R, Plass, K, Remzi, M, Retz, M, Richenberg, J, Rink, M, Roghmann, F, Rosenberg, J E, Rouprêt, M, Rouvière, O, Salembier, C, Salminen, A, Sargos, P, Sengupta, S, Sherif, Amir, Smeenk, R J, Smits, A, Stenzl, A, Thalmann, G N, Tombal, B, Turkbey, B, Lauridsen, S Vahr, Valdagni, R, Van Der Heijden, A G, Van Poppel, H, Vartolomei, M D, Veskimäe, E, Vilaseca, A, Rivera, F A Vives, Wiegel, T, Wiklund, P, Williams, A, Zigeuner, R, and Witjes, J A
- Abstract
BACKGROUND: Although guidelines exist for advanced and variant bladder cancer management, evidence is limited/conflicting in some areas and the optimal approach remains controversial. OBJECTIVE: To bring together a large multidisciplinary group of experts to develop consensus statements on controversial topics in bladder cancer management. DESIGN: A steering committee compiled proposed statements regarding advanced and variant bladder cancer management which were assessed by 113 experts in a Delphi survey. Statements not reaching consensus were reviewed; those prioritised were revised by a panel of 45 experts before voting during a consensus conference. SETTING: Online Delphi survey and consensus conference. PARTICIPANTS: The European Association of Urology (EAU), the European Society for Medical Oncology (ESMO), experts in bladder cancer management. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Statements were ranked by experts according to their level of agreement: 1-3 (disagree), 4-6 (equivocal), 7-9 (agree). A priori (level 1) consensus was defined as ≥70% agreement and ≤15% disagreement, or vice versa. In the Delphi survey, a second analysis was restricted to stakeholder group(s) considered to have adequate expertise relating to each statement (to achieve level 2 consensus). RESULTS AND LIMITATIONS: Overall, 116 statements were included in the Delphi survey. Of these, 33 (28%) statements achieved level 1 consensus and 49 (42%) statements achieved level 1 or 2 consensus. At the consensus conference, 22 of 27 (81%) statements achieved consensus. These consensus statements provide further guidance across a broad range of topics, including the management of variant histologies, the role/limitations of prognostic biomarkers in clinical decision making, bladder preservation strategies, modern radiotherapy techniques, the management of oligometastatic disease and the evolving role of checkpoint inhibitor therapy in metastatic disease. CONCLUSIONS: These consensus sta
- Published
- 2019
- Full Text
- View/download PDF
4. EAU-ESMO consensus statements on the management of advanced and variant bladder cancer-an international collaborative multi-stakeholder effort: under the auspices of the EAU and ESMO Guidelines Committees†.
- Author
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UCL - SSS/IREC/CHEX - Pôle de chirgurgie expérimentale et transplantation, UCL - (SLuc) Service d'urologie, Witjes, J A, Van Der Heijden, A G, Smits, A, Stenzl, A, Thalmann, G N, Tombal, Bertrand, Turkbey, B, Lauridsen, S Vahr, Valdagni, R, Van Poppel, H, Sherif, A, Vartolomei, M D, Veskimäe, E, Vilaseca, A, Rivera, F A Vives, Wiegel, T, Wiklund, P, Williams, A, Zigeuner, R, Smeenk, R J, Horwich, A, Babjuk, M, Bellmunt, J, Bruins, H M, Reijke, T M De, Santis, M De, Gillessen, S, James, N, Maclennan, S, Palou, J, Powles, T, Ribal, M J, Shariat, S F, Kwast, T Van Der, Xylinas, E, Agarwal, N, Arends, T, Bamias, A, Birtle, A, Black, P C, Bochner, B H, Bolla, M, Boormans, J L, Bossi, A, Briganti, A, Brummelhuis, I, Burger, M, Castellano, D, Cathomas, R, Chiti, A, Choudhury, A, Compérat, E, Crabb, S, Culine, S, Bari, B De, Blok, W De, De Visschere, P J L, Decaestecker, K, Dimitropoulos, K, Dominguez-Escrig, J L, Fanti, S, Fonteyne, V, Frydenberg, M, Futterer, J J, Gakis, G, Geavlete, B, Gontero, P, Grubmüller, B, Hafeez, S, Hansel, D E, Hartmann, A, Hayne, D, Henry, A M, Hernandez, V, Herr, H, Herrmann, K, Hoskin, P, Huguet, J, Jereczek-Fossa, B A, Jones, R, Kamat, A M, Khoo, V, Kiltie, A E, Krege, S, Ladoire, S, Lara, P C, Leliveld, A, Linares-Espinós, E, Løgager, V, Lorch, A, Loriot, Y, Meijer, R, Mir, M Carmen, Moschini, M, Mostafid, H, Müller, A-C, Müller, C R, N'Dow, J, Necchi, A, Neuzillet, Y, Oddens, J R, Oldenburg, J, Osanto, S, Oyen, W J G, Pacheco-Figueiredo, L, Pappot, H, Patel, M I, Pieters, B R, Plass, K, Remzi, M, Retz, M, Richenberg, J, Rink, M, Roghmann, F, Rosenberg, J E, Rouprêt, M, Rouvière, O, Salembier, C, Salminen, A, Sargos, P, Sengupta, S, UCL - SSS/IREC/CHEX - Pôle de chirgurgie expérimentale et transplantation, UCL - (SLuc) Service d'urologie, Witjes, J A, Van Der Heijden, A G, Smits, A, Stenzl, A, Thalmann, G N, Tombal, Bertrand, Turkbey, B, Lauridsen, S Vahr, Valdagni, R, Van Poppel, H, Sherif, A, Vartolomei, M D, Veskimäe, E, Vilaseca, A, Rivera, F A Vives, Wiegel, T, Wiklund, P, Williams, A, Zigeuner, R, Smeenk, R J, Horwich, A, Babjuk, M, Bellmunt, J, Bruins, H M, Reijke, T M De, Santis, M De, Gillessen, S, James, N, Maclennan, S, Palou, J, Powles, T, Ribal, M J, Shariat, S F, Kwast, T Van Der, Xylinas, E, Agarwal, N, Arends, T, Bamias, A, Birtle, A, Black, P C, Bochner, B H, Bolla, M, Boormans, J L, Bossi, A, Briganti, A, Brummelhuis, I, Burger, M, Castellano, D, Cathomas, R, Chiti, A, Choudhury, A, Compérat, E, Crabb, S, Culine, S, Bari, B De, Blok, W De, De Visschere, P J L, Decaestecker, K, Dimitropoulos, K, Dominguez-Escrig, J L, Fanti, S, Fonteyne, V, Frydenberg, M, Futterer, J J, Gakis, G, Geavlete, B, Gontero, P, Grubmüller, B, Hafeez, S, Hansel, D E, Hartmann, A, Hayne, D, Henry, A M, Hernandez, V, Herr, H, Herrmann, K, Hoskin, P, Huguet, J, Jereczek-Fossa, B A, Jones, R, Kamat, A M, Khoo, V, Kiltie, A E, Krege, S, Ladoire, S, Lara, P C, Leliveld, A, Linares-Espinós, E, Løgager, V, Lorch, A, Loriot, Y, Meijer, R, Mir, M Carmen, Moschini, M, Mostafid, H, Müller, A-C, Müller, C R, N'Dow, J, Necchi, A, Neuzillet, Y, Oddens, J R, Oldenburg, J, Osanto, S, Oyen, W J G, Pacheco-Figueiredo, L, Pappot, H, Patel, M I, Pieters, B R, Plass, K, Remzi, M, Retz, M, Richenberg, J, Rink, M, Roghmann, F, Rosenberg, J E, Rouprêt, M, Rouvière, O, Salembier, C, Salminen, A, Sargos, P, and Sengupta, S
- Abstract
BACKGROUND: Although guidelines exist for advanced and variant bladder cancer management, evidence is limited/conflicting in some areas and the optimal approach remains controversial. OBJECTIVE: To bring together a large multidisciplinary group of experts to develop consensus statements on controversial topics in bladder cancer management. DESIGN: A steering committee compiled proposed statements regarding advanced and variant bladder cancer management which were assessed by 113 experts in a Delphi survey. Statements not reaching consensus were reviewed; those prioritised were revised by a panel of 45 experts before voting during a consensus conference. SETTING: Online Delphi survey and consensus conference. PARTICIPANTS: The European Association of Urology (EAU), the European Society for Medical Oncology (ESMO), experts in bladder cancer management. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Statements were ranked by experts according to their level of agreement: 1-3 (disagree), 4-6 (equivocal), 7-9 (agree). A priori (level 1) consensus was defined as ≥70% agreement and ≤15% disagreement, or vice versa. In the Delphi survey, a second analysis was restricted to stakeholder group(s) considered to have adequate expertise relating to each statement (to achieve level 2 consensus). RESULTS AND LIMITATIONS: Overall, 116 statements were included in the Delphi survey. Of these, 33 (28%) statements achieved level 1 consensus and 49 (42%) statements achieved level 1 or 2 consensus. At the consensus conference, 22 of 27 (81%) statements achieved consensus. These consensus statements provide further guidance across a broad range of topics, including the management of variant histologies, the role/limitations of prognostic biomarkers in clinical decision making, bladder preservation strategies, modern radiotherapy techniques, the management of oligometastatic disease and the evolving role of checkpoint inhibitor therapy in metastatic disease. CONCLUSIONS: These consensus sta
- Published
- 2019
5. EAU-ESMO consensus statements on the management of advanced and variant bladder cancer-an international collaborative multi-stakeholder effort: under the auspices of the EAU and ESMO Guidelines Committees†
- Author
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Cancer, Verpleegkundig Specialisten, MS Urologische Oncologie, Horwich, A, Babjuk, M, Bellmunt, J, Bruins, H M, Reijke, T M De, Santis, M De, Gillessen, S, James, N, Maclennan, S, Palou, J, Powles, T, Ribal, M J, Shariat, S F, Kwast, T Van Der, Xylinas, E, Agarwal, N, Arends, T, Bamias, A, Birtle, A, Black, P C, Bochner, B H, Bolla, M, Boormans, J L, Bossi, A, Briganti, A, Brummelhuis, I, Burger, M, Castellano, D, Cathomas, R, Chiti, A, Choudhury, A, Compérat, E, Crabb, S, Culine, S, Bari, B De, Blok, W De, De Visschere, P J L, Decaestecker, K, Dimitropoulos, K, Dominguez-Escrig, J L, Fanti, S, Fonteyne, V, Frydenberg, M, Futterer, J J, Gakis, G, Geavlete, B, Gontero, P, Grubmüller, B, Hafeez, S, Hansel, D E, Hartmann, A, Hayne, D, Henry, A M, Hernandez, V, Herr, H, Herrmann, K, Hoskin, P, Huguet, J, Jereczek-Fossa, B A, Jones, R, Kamat, A M, Khoo, V, Kiltie, A E, Krege, S, Ladoire, S, Lara, P C, Leliveld, A, Linares-Espinós, E, Løgager, V, Lorch, A, Loriot, Y, Meijer, R, Mir, M Carmen, Moschini, M, Mostafid, H, Müller, A-C, Müller, C R, N'Dow, J, Necchi, A, Neuzillet, Y, Oddens, J R, Oldenburg, J, Osanto, S, Oyen, W J G, Pacheco-Figueiredo, L, Pappot, H, Patel, M I, Pieters, B R, Plass, K, Remzi, M, Retz, M, Richenberg, J, Rink, M, Roghmann, F, Rosenberg, J E, Rouprêt, M, Rouvière, O, Salembier, C, Salminen, A, Sargos, P, Sengupta, S, Sherif, A, Smeenk, R J, Smits, A, Stenzl, A, Thalmann, G N, Tombal, B, Turkbey, B, Lauridsen, S Vahr, Valdagni, R, Van Der Heijden, A G, Van Poppel, H, Vartolomei, M D, Veskimäe, E, Vilaseca, A, Rivera, F A Vives, Wiegel, T, Wiklund, P, Williams, A, Zigeuner, R, Witjes, J A, Cancer, Verpleegkundig Specialisten, MS Urologische Oncologie, Horwich, A, Babjuk, M, Bellmunt, J, Bruins, H M, Reijke, T M De, Santis, M De, Gillessen, S, James, N, Maclennan, S, Palou, J, Powles, T, Ribal, M J, Shariat, S F, Kwast, T Van Der, Xylinas, E, Agarwal, N, Arends, T, Bamias, A, Birtle, A, Black, P C, Bochner, B H, Bolla, M, Boormans, J L, Bossi, A, Briganti, A, Brummelhuis, I, Burger, M, Castellano, D, Cathomas, R, Chiti, A, Choudhury, A, Compérat, E, Crabb, S, Culine, S, Bari, B De, Blok, W De, De Visschere, P J L, Decaestecker, K, Dimitropoulos, K, Dominguez-Escrig, J L, Fanti, S, Fonteyne, V, Frydenberg, M, Futterer, J J, Gakis, G, Geavlete, B, Gontero, P, Grubmüller, B, Hafeez, S, Hansel, D E, Hartmann, A, Hayne, D, Henry, A M, Hernandez, V, Herr, H, Herrmann, K, Hoskin, P, Huguet, J, Jereczek-Fossa, B A, Jones, R, Kamat, A M, Khoo, V, Kiltie, A E, Krege, S, Ladoire, S, Lara, P C, Leliveld, A, Linares-Espinós, E, Løgager, V, Lorch, A, Loriot, Y, Meijer, R, Mir, M Carmen, Moschini, M, Mostafid, H, Müller, A-C, Müller, C R, N'Dow, J, Necchi, A, Neuzillet, Y, Oddens, J R, Oldenburg, J, Osanto, S, Oyen, W J G, Pacheco-Figueiredo, L, Pappot, H, Patel, M I, Pieters, B R, Plass, K, Remzi, M, Retz, M, Richenberg, J, Rink, M, Roghmann, F, Rosenberg, J E, Rouprêt, M, Rouvière, O, Salembier, C, Salminen, A, Sargos, P, Sengupta, S, Sherif, A, Smeenk, R J, Smits, A, Stenzl, A, Thalmann, G N, Tombal, B, Turkbey, B, Lauridsen, S Vahr, Valdagni, R, Van Der Heijden, A G, Van Poppel, H, Vartolomei, M D, Veskimäe, E, Vilaseca, A, Rivera, F A Vives, Wiegel, T, Wiklund, P, Williams, A, Zigeuner, R, and Witjes, J A
- Published
- 2019
6. EAU-ESMO consensus statements on the management of advanced and variant bladder cancer-an international collaborative multi-stakeholder effort:under the auspices of the EAU and ESMO Guidelines Committees†
- Author
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Horwich, A., Babjuk, M., Bellmunt, J., Bruins, H. M., Reijke, T. M.De, Santis, M. De, Gillessen, S., James, N., Maclennan, S., Palou, J., Powles, T., Ribal, M. J., Shariat, S. F., Kwast, T. Van Der, Xylinas, E., Agarwal, N., Arends, T., Bamias, A., Birtle, A., Black, P. C., Bochner, B. H., Bolla, M., Boormans, J. L., Bossi, A., Briganti, A., Brummelhuis, I., Burger, M., Castellano, D., Cathomas, R., Chiti, A., Choudhury, A., Compérat, E., Crabb, S., Culine, S., Bari, B. De, Blok, W. De, De Visschere, P. J.L., Decaestecker, K., Dimitropoulos, K., Dominguez-Escrig, J. L., Fanti, S., Fonteyne, V., Frydenberg, M., Futterer, J. J., Gakis, G., Geavlete, B., Gontero, P., Grubmüller, B., Hafeez, S., Hansel, D. E., Hartmann, A., Hayne, D., Henry, A. M., Hernandez, V., Herr, H., Herrmann, K., Hoskin, P., Huguet, J., Jereczek-Fossa, B. A., Jones, R., Kamat, A. M., Khoo, V., Kiltie, A. E., Krege, S., Ladoire, S., Lara, P. C., Leliveld, A., Linares-Espinós, E., Løgager, V., Lorch, A., Loriot, Y., Meijer, R., Mir, M. Carmen, Moschini, M., Mostafid, H., Müller, A. C., Müller, C. R., N'Dow, J., Necchi, A., Neuzillet, Y., Oddens, J. R., Oldenburg, J., Osanto, S., Oyen, W. J.G., Pacheco-Figueiredo, L., Pappot, H., Patel, M. I., Pieters, B. R., Plass, K., Remzi, M., Retz, M., Richenberg, J., Rink, M., Roghmann, F., Rosenberg, J. E., Rouprêt, M., Rouvière, O., Salembier, C., Salminen, A., Sargos, P., Sengupta, S., Sherif, A., Smeenk, R. J., Smits, A., Stenzl, A., Thalmann, G. N., Tombal, B., Turkbey, B., Lauridsen, S. Vahr, Valdagni, R., Van Der Heijden, A. G., Van Poppel, H., Vartolomei, M. D., Veskimäe, E., Vilaseca, A., Rivera, F. A.Vives, Wiegel, T., Wiklund, P., Williams, A., Zigeuner, R., Witjes, J. A., Horwich, A., Babjuk, M., Bellmunt, J., Bruins, H. M., Reijke, T. M.De, Santis, M. De, Gillessen, S., James, N., Maclennan, S., Palou, J., Powles, T., Ribal, M. J., Shariat, S. F., Kwast, T. Van Der, Xylinas, E., Agarwal, N., Arends, T., Bamias, A., Birtle, A., Black, P. C., Bochner, B. H., Bolla, M., Boormans, J. L., Bossi, A., Briganti, A., Brummelhuis, I., Burger, M., Castellano, D., Cathomas, R., Chiti, A., Choudhury, A., Compérat, E., Crabb, S., Culine, S., Bari, B. De, Blok, W. De, De Visschere, P. J.L., Decaestecker, K., Dimitropoulos, K., Dominguez-Escrig, J. L., Fanti, S., Fonteyne, V., Frydenberg, M., Futterer, J. J., Gakis, G., Geavlete, B., Gontero, P., Grubmüller, B., Hafeez, S., Hansel, D. E., Hartmann, A., Hayne, D., Henry, A. M., Hernandez, V., Herr, H., Herrmann, K., Hoskin, P., Huguet, J., Jereczek-Fossa, B. A., Jones, R., Kamat, A. M., Khoo, V., Kiltie, A. E., Krege, S., Ladoire, S., Lara, P. C., Leliveld, A., Linares-Espinós, E., Løgager, V., Lorch, A., Loriot, Y., Meijer, R., Mir, M. Carmen, Moschini, M., Mostafid, H., Müller, A. C., Müller, C. R., N'Dow, J., Necchi, A., Neuzillet, Y., Oddens, J. R., Oldenburg, J., Osanto, S., Oyen, W. J.G., Pacheco-Figueiredo, L., Pappot, H., Patel, M. I., Pieters, B. R., Plass, K., Remzi, M., Retz, M., Richenberg, J., Rink, M., Roghmann, F., Rosenberg, J. E., Rouprêt, M., Rouvière, O., Salembier, C., Salminen, A., Sargos, P., Sengupta, S., Sherif, A., Smeenk, R. J., Smits, A., Stenzl, A., Thalmann, G. N., Tombal, B., Turkbey, B., Lauridsen, S. Vahr, Valdagni, R., Van Der Heijden, A. G., Van Poppel, H., Vartolomei, M. D., Veskimäe, E., Vilaseca, A., Rivera, F. A.Vives, Wiegel, T., Wiklund, P., Williams, A., Zigeuner, R., and Witjes, J. A.
- Abstract
BACKGROUND: Although guidelines exist for advanced and variant bladder cancer management, evidence is limited/conflicting in some areas and the optimal approach remains controversial. OBJECTIVE: To bring together a large multidisciplinary group of experts to develop consensus statements on controversial topics in bladder cancer management. DESIGN: A steering committee compiled proposed statements regarding advanced and variant bladder cancer management which were assessed by 113 experts in a Delphi survey. Statements not reaching consensus were reviewed; those prioritised were revised by a panel of 45 experts before voting during a consensus conference. SETTING: Online Delphi survey and consensus conference. PARTICIPANTS: The European Association of Urology (EAU), the European Society for Medical Oncology (ESMO), experts in bladder cancer management. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Statements were ranked by experts according to their level of agreement: 1-3 (disagree), 4-6 (equivocal), 7-9 (agree). A priori (level 1) consensus was defined as ≥70% agreement and ≤15% disagreement, or vice versa. In the Delphi survey, a second analysis was restricted to stakeholder group(s) considered to have adequate expertise relating to each statement (to achieve level 2 consensus). RESULTS AND LIMITATIONS: Overall, 116 statements were included in the Delphi survey. Of these, 33 (28%) statements achieved level 1 consensus and 49 (42%) statements achieved level 1 or 2 consensus. At the consensus conference, 22 of 27 (81%) statements achieved consensus. These consensus statements provide further guidance across a broad range of topics, including the management of variant histologies, the role/limitations of prognostic biomarkers in clinical decision making, bladder preservation strategies, modern radiotherapy techniques, the management of oligometastatic disease and the evolving role of checkpoint inhibitor therapy in metastatic disease. CONCLUSIONS: These consensus
- Published
- 2019
7. The Place of Instilational Immunotherapy in the Treatment of Non-muscle Invasive Bladder tumors.
- Author
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Brad, A., Mateescu, Corina, Vida, A. O., Vartolomei, M. D., Balan, D., Catarig, C., Chibelean, C., Martha, Orsolya, and Porav, D.
- Subjects
IMMUNOTHERAPY ,URINARY organs ,GENDER ,CANCER invasiveness ,RURAL geography ,BLADDER cancer - Abstract
Introduction: Bladder tumors are the most common tumors of the urinary tract, accounting for about 5.5% of all cancers. In male it is on the 4th place, and in females it occupies the 7th place. TURBT is the gold standard for the initial treatment and diagnosis of bladder tumors. This intervention can be followed, in the case of non-muscle invasive tumors, by intravesical instillation, with a chemotherapeutic or with BCG. The aim of this work was to follow the evolution of patients with non-muscle invasive bladder tumors who have been treated with BCG (Bacillus Calmette-Guérin) immunotherapy. Matherial and methods: The study was a retrospective one, for a period of 5 years, between 2010 January 1 and 2014 December 31, including a number of 91 patients hospitalized in the Urology Clinic of Mureş County Clinical Hospital. Follow-up data at 24 months was present in 76 patients. Results: Of the 76 patients, 80.26% were male and 19.74% were female. The distribution of patients according to the environment of origin highlights the prevalence of the urban environment in the percentage of 72.36%, the rural area having a percentage of only 27.64%. The average age was 61.43 years. There was no statistically significant association between the gender of the patient and the rate of tumor recurrence. Of the 76 patients, 21 had tumor progression during the follow-up period. No patient was found to have progressed to invasive bladder tumor. Of the total number of 76 patients, at the end of the follow-up period, it was found that 8 discontinued treatment with BCG due to side effects such as: haematuria and tuberculous cystitis. In 3 patients, treatment with BCG failed and due to repeated recurrences required a total cystectomy. Conclusions: Instillational treatment with BCG immunotherapy remains the best option as an adjuvant in patients with non-muscle invasive bladder tumors to prevent recurrence and progression, in well-selected cases and with clear indication. [ABSTRACT FROM AUTHOR]
- Published
- 2019
8. Management of Penile Fractures.
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Porav-Hodade, D., Chibelean, C., Vartolomei, M. D., Chiujdea, A., Martha, O., Friedl, A., and Todea, C.
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PENIS curvatures ,PENILE induration ,SEXUAL abstinence ,IMPOTENCE ,TREATMENT of fractures ,PENILE transplantation ,PENILE prostheses - Abstract
Introduction and objectives. Penile fractures is rare medical condition and is a major urological emergency. Surgery is considered the standard therapy. In some cases it can be applied a conservative therapy. This study aims to assess the results of the two therapies in penile fractures. Material and Methods. Between January 2007 and October 2019 in Tirgu Mures Urology Clinic a total of 6 patients were admitted with penile fracture. At 4 of these patients we performed surgery intervention for treatment of penile fracture and at 2 of them conservative therapy because they refused surgery. We followed hospitalization period, the occurrence of penile angulation during erection and erectile function at more than 3 months post therapy using International Index of Erectile Function (IIEF). Results. Mean age was 37,35 years for patients with surgical therapy vs 22 years for patients with conservative treatment. Average days of hospitalization was 8,75 days vs 9 days. Average IIEF 1-5,15 at 3 months after surgery was 23,25 for the patients who undergone surgery and 27 for the patients with conservative treatment. Average IIEF 1-5,15 at 12 months after surgery was 22 for the patients who undergone surgery and 28 for the patients with conservative treatment. 2 patients with penile fracture were not subsequently presented to the control and we do not have data about erectile function at 12 months. In 1 patient with conservative treatment there was a slight angulation of about 10 degrees. The patient who had concomitant urethral involvement with the penile fracture had erectile dysfunction prior to trauma. For all patients with penile fracture we recommended a period of sexual abstinence for 8 weeks. Conclusions. Penile fracture although it is a rare pathological entity, it must be quickly diagnosed. The indicated treatment is the surgical one, the only one that ensures a reduced rate of complications. The conservative treatment being indicated only to the patients who refuse the surgery. Even though in our study erectile function was superior for patients treated conservatively, this is due to the presence in the group of patients treated surgicaly of a patient with middle/severe erectile dysfunction. [ABSTRACT FROM AUTHOR]
- Published
- 2019
9. Management of Colon Perforation Following Percutaneous Nephrolithotomy.
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Porav-Hodade, D., Balan, D., Ghirca, V. M., Vartolomei, M. D., Martha, O., and Todea, C.
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PERCUTANEOUS nephrolithotomy ,SURGICAL stents ,COMPUTED tomography ,COLON (Anatomy) ,COLECTOMY ,BRONCHIAL fistula ,TYMPANIC membrane perforation - Abstract
Introduction and Objectives. In the EAU guidelines the percutaneous nephrolithotomy (PCNL) is the main indication for kidney stones with dimensions over 2 cm. Early recognition of the colonic perforation an important step in limiting an infection that can lead to subsequent sequelae The objectives of this study is to evaluate the cases in which colonic perforation has occurred, both in terms of possible favoring factors and from the perspective of the treatment applied and of the subsequent evolution of the patient. Material and Methods. Between January 2009 and January 2019 we performed 1394 PCNL interventions. All patients were operated in prone position. We analyzed the cases in which the colonic perforation appeared. Positive diagnosis was made after computerized tomography. We took into account the patients' age, sex, previous surgical history, body mass index, time to diagnosis of colonic perforation, type of treatment applied in this complication, length of hospitalization as well as case evaluation at 6 weeks and 6 months, respectively. Results. Of the 1394 patients in whom we performed PCNL, colonic perforation appeared in 4 of them, all female patients. A conservative treatment was applied to all patients. In patients with colonic fistula on the left side, healing was done without complications. In the patient with colonic fistula on the right side at 4 days postoperatively, surgery was required which resulted in the right colectomy. The ureteral stent was suppressed in all patients 6 weeks after discharge. The control at 6 weeks and at 6 months revealed a kidney without lithiasis, sterile urine culture or sequelae of the colonic fistula. Conclusion. Colon perforation is a severe complication after PCNL. Factors favoring these complications should be recognized preoperatively and thus the risk of colonic perforation can be reduced. Conservative treatment can be applied especially in cases where colonic perforation occurs following a PCNL performed on the left side. [ABSTRACT FROM AUTHOR]
- Published
- 2019
10. Long-term Overall Survival of Patients with T1 Bladder Cancer following BCG Instillation.
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Tataru, O. S., Porav-Hodade, D., Martha, O., Balan, D., Vartolomei, M. D., and Chibelean, C. B.
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BLADDER cancer patients ,BLADDER cancer ,MULTIPLE tumors ,TRANSURETHRAL prostatectomy - Abstract
Introduction and Objectives. To evaluate long-term overall survival and predictive factors after TURBT and adjuvant intravesical Bacillus Calmette-Guérin (BCG) treatment, in patients with T1 bladder cancer. Materials and Methods. We retrospectively analyzed, 53 patients who underwent transurethral resection of bladder tumor (TURBT) for intermediate and high-grade T1 non-muscle invasive bladder cancer (NMIBC) followed by BCG instillations at our clinic between 2006 and 2008. Primary end-point was overall survival (OS). Data about survival were obtained from the National insurance registry. Survival analysis was performed using the Kaplan Meyer method, and the log-rank test was used for univariate comparisons. Univariable and multivariable Cox regression models addressed the association of prognostic factors with OS. Results. Median follow-up was 79 months (IQR 58-110 months), 33 (62.3%) patients died. In our study, males were 43 (81.13%) and females 10 (18.86%), 41 (77.35%) patients had tumors over 3 cm in diameter, 37 (69.81%) with multiple tumors at diagnosis and 43 (81.13%) patients with high risk tumors (G3). In univariable analysis, clinico-pathologic factors such as age (p=0.003) and recurrence of tumors (p=0.005) were associated with worse OS. In multivariable analysis, independent predictors of OS were gender (HR1.06, 95% CI 1.02-1.11, p=0.002), multifocality (HR 3.03, 95% CI 1.15-7.92, p=0.024) and tumor grade (HR3.59, 95% CI 1.23-10.14, p=0.019). Progression rate was 11.3%%. Recurrence rate was 30.2%. Five year overall survival was 72.2% (95%CI: 58.2-82.2) and at 10-yr 37% (95%CI: 24.4-49.6). Limitations include retrospective design, mono-center study and small sample size. Conclusions. Our study supports current evidence that BCG therapy with maintenance is an effective and safe therapy for T1 bladder cancer patients and it is a viable option for long-term use in such patients. We found that age and recurrence of tumors were associated with poor overall survival. Elderly patients should be strictly monitored and in recurrence patients alternative options may be offered. [ABSTRACT FROM AUTHOR]
- Published
- 2018
11. ESWL in Patients with Horseshoe Kidney - Single Center Experience.
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Brad, A., Mateescu, C., Bîță, R. G., Ghirca, V., Vartolomei, M. D., Porav, D., Simion, C., Chibelean, C., Oșan, V., and Martha, O.
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HEMATURIA ,RENAL colic ,URINARY tract infections ,TYPE 2 diabetes ,KIDNEYS ,HORSESHOES ,THERAPEUTICS - Abstract
Introduction and Objectives. Horseshoe kidney (HSK) is the most common renal fusion anomaly, affecting about 0.25% of the newborn. Sometimes this condition is associated with the obstruction of the ureteropelvic junction, lithiasis, is not uncommon for renal infections, abdominal masses and haematuria. For these patients, treatment of urolithiasis represents a particular challenge. ESWL is considered the first-line treatment for the majority of cases. Materials and Methods. We performed a retrospective review of all patients with horseshoe kidney treated and followed at the Urology Clinic of Targu Mures, from 23 July 1991 to 31 December 2017. All patients with stones within a horseshoe kidney that met the following inclusion criteria: a clear urinary path distal of the location of the stone, a functional kidney without stasis and the stone size ≤ 20 mm who underwent ESWL were included in the analysis. We performed a total of 158 ESWL treatments, with a mean of 1.95 ESWL procedures / stone. 3-months follow-up data were available for 60 patients. Results. From our patients 43 (53.08%) were men and 38 (46.92) were women. The average age was 46.32 years. The average size of the stone was 10.316 mm. Major complications after ESWL treatment were subcapsular renal hematoma in one case (1.23%) which only needed supportive care and observation, acute pyelonephritis in one case (1.23%), treated with appropriate antibiotics, hematuria with vesical globe in two cases (2.46%) which needed bladder washouts and catheterization with a three way catheter, with irrigation. Additional pathologies were present in 38 patients (46.91%), 16 had urinary tract infections (treated with the appropiate antibiotics before the ESWL), 12 patients had hypertension, 3 patients had type II diabetes and 16 suffered from obesity. Stone-free at 3 months was 70.31%. Conclusions. We can safely say that ESWL is a good and safe option of treatment in patients with horseshoe kidney if it is performed by a physician with extensive experience in this field. [ABSTRACT FROM AUTHOR]
- Published
- 2018
12. Endoscopic Treatment for Congenital and Acquired Hydronephrosis - The Role of Endopyelotomy.
- Author
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Boja, R., Tataru, O. S., Nedelcu, S., Vartolomei, M. D., Todea, C., and Mártha, Orsolya
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HYDRONEPHROSIS ,KIDNEY pelvis ,ENDOSCOPY ,SURGERY ,THERAPEUTICS - Abstract
Introduction and Objectives. The ureteropelvic junction (UPJ) dysfunction, having as consequence hydronephrosis, was traditionally treated surgically by pyeloplasty, the rate of success being 71-98%. Failure was followed by one of the following interventions: repeating pyeloplasty, replacement with ileum, ureterocalicostomy, renal autotransplantation and, lastly, nephrectomy. We evaluate the role of endopyelotomy in the management of ureteropelvic junction obstruction. Materials and Methods. In a period of 27 years (1987-2014), we performed a total of 833 endopyelotomies. In our study (1987-2002), we retrospectively identified 303 patients who underwent endopyelotomy for ureteropelvic junction obstruction, who came for regular check-ups. Patient demographics, operative information, complications and success rates were reviewed for 187 patients, who could be properly assessed, with a mean age of 51 years and mean follow-up of 44 months. Treatment success was defined as the absence of symptom recurrence and improved radiographic features on ultrasound, intravenous pyelography at most recent follow-up. Results. endopyelotomy data were analyzed in 187 patients. The success rate was 83.9%. Treatment failure occurred in 30 (16%) patients. There were 20 (10.69%) cases of ureteral hypoplasia with less favorable results. Four patients (2.13%) with renal-ureteral duplication had surgical failure at 6 to 12 months reevaluation. Four patients (2.13%) were found with renal ptosis and two patients (1.06%) with horseshoe kidney in which endopyelotomy failed. Conclusions. Antegrade endopyelotomy is a minimally aggressive surgical intervention in both children adults and the elderly. The endoscopic percutaneous approach of ureteropelvic junction allows solving of associated disorders, such as renal lithiasis. Laparoscopic and robotic assisted pyeloplasty are emerging as the gold standard of treatment for ureteropelvic junction obstruction, endopyelotomy it is the treatment of choice for failed open or laparoscopic pyeloplasty and concomitant renal calculi. [ABSTRACT FROM AUTHOR]
- Published
- 2017
13. The Place of ESWL in the Treatment of Urinary Stones in Patients with Renal Malformations.
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Brad, A., Simion, Alexandra, Moldovan, Veronica, Todea, C., Vartolomei, M. D., Porav, D., Simion, Carmen, Chibelean, C., Oşan, V., and Martha, Orsolya
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EXTRACORPOREAL shock wave therapy ,KIDNEY stones ,KIDNEY disease treatments - Abstract
Introduction and Objectives. Congenital anomalies occur more often in the kidney than in any other organ. The association of abnormalities with stones has important clinical relevance. Our goal was to determine the clinical success and stone-free rates for patients with renal anomalies treated with ESWL. Materials and Methods. We performed a retrospective review of patients with renal anomalies treated at the Urology Clinic of Targu Mures, since January 2004 to December 2014. The inclusion criteria were: a clear urinary path distal of the location of the stone, a functional kidney without stasis and the stone size ≤ 25 mm ( 118 patients). We performed a total of 184 ESWL treatments (a mean of 1.559 ESWL procedures/stone). 3-month follow-up data were available for 88 patients. Results. Of the total ESWL procedures performed, 35 (29%) were horseshoe kidneys, 48 (41%) duplex kidneys, 15 (13%) malrotated kidneys, 13 (11%) ectopic kidneys and 7 (6%) hypoplastic kidneys. From the total of patients, 57 were women and 61 men. The mean age was 43.26 years. The average size of the stone was 10.228 mm. The average pacient stay was 4.77 days. Complications were subcapsular renal hematoma in two (1.69%) cases, acute pyelonephritis in two (1.69%) pacients, hematuria with vesical globe in another two (1.69%) cases and stone-street formation in 10 (8.47%). In 3 cases (2.54%) the procedure was unsuccessful and retrograde ureteroscopy was needed. Associated pathology was pressent in 61 pacients (51.69%): 21 (17.79%) presented urinary tract infection, 17 (14.41%) pacients were diagnosed with hipertension, 2 (1.69%) with diabetes and 21 (17.79%) suffered by obesity. Stone-free rate was 71.77%. Conclusions. In our oppinion ESWL is the treatment of choice for reno-ureteral lithiasis in renal malformations because is a non invasive treatment, no need for anestesia, the pacient stay is short, complications occure rarely and stone free rate is high. [ABSTRACT FROM AUTHOR]
- Published
- 2016
14. CYTOMEGALOVIRUS ROLE IN INDUCING REJECTION REACTIONS IN HEART TRANSPLANTATION PATIENTS.
- Author
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HABOR, A., SIN, A., VARTOLOMEI, M. D., CIUCA, I., SUCIU, H., and TILINCA, M.
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CYTOMEGALOVIRUSES ,HEART transplant recipients ,ATHEROSCLEROSIS ,CELLULAR immunity ,T cells - Abstract
The study was performed on 45 patients with heart transplantation out of which 30 presented serologic cytomegalovirus infection. For histological study we used: hematoxylin eosin, van Gieson, Masson's trichrome, green methyl pironin stains. Immunohistochemistry was performed using ABC technique (avidin - biotin complexes or avidin - biotin) with the following monoclonal antibodies: CD8, CD4, CD20, CD68, CD31, CD45 RO, HLA-DR, and E13. In many of our cases cytomegalovirus infection was commonly associated with acute rejection. The presence of endothelial cells expressing HLA-DR antigens and subendothelial accumulation of activated T lymphocytes and macrophages, often in contact with endothelial cells, highlights the role of cellular immunity in the production of accelerated atherosclerosis lesions. [ABSTRACT FROM AUTHOR]
- Published
- 2016
15. KNOWLEDGE OF HUMAN PAPILLOMAVIRUS (HPV) INFECTION IN NON-MUSCLE INVASIVE BLADDER CANCER PATIENTS.
- Author
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VARTOLOMEI, M. D., GEAMBASU, S., COTOI, T., BADEA, M. A., CHIBELEAN, C. B., VOIDEZAN, S., ALBU, C., COTOI, O. S., DOGARU, G. A., BOJA, R. M., and MORARIU, S. H.
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PAPILLOMAVIRUSES , *CANCER patients , *BLADDER cancer patients , *CARCINOGENESIS , *QUESTIONNAIRES - Abstract
The etiological role of HPV infection in the pathogenesis of bladder tumors remains uncertain. Case-control study, NMIBC patients answered a 37 items questionnaire regarding knowledge of HPV, were compare with a healthy control group. Group A started earlier the sexual life than the group B (18 vs. 19 years), but the first cohabitation took place later (37 vs. 24 years, p = 0. 03).Group A had more sexual partners than group B (>10, 32% respectively 17.6%). 56% of patients with NMIBC heard about HPV infection and only 47% of controls and 32% of group A respectively 41% of group B didn't know if HPV infection represents a risk for their health. From this study results a lack of knowledge about HPV infection in NMIBC patients. [ABSTRACT FROM AUTHOR]
- Published
- 2015
16. PYODERMA GANGRENOSUM IN A PATIENT WITH PRIMARY SJÖGREN'S SYNDROME - CASE REPORT.
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BADEA, M. A., ŢILEA, A. M., COTOI, O. S., VARTOLOMEI, M. D., HODASZ, I., CHIOTOROIU, A. L., and MORARIU, S. H.
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PYODERMA gangrenosum ,SJOGREN'S syndrome ,BIOPSY ,LEG injuries ,DEBRIDEMENT ,PATIENTS ,DIAGNOSIS - Abstract
We will present the case study of a 61 years old Caucasian female patient who required a dermatological consult for two well defined painful ulcerations on her right leg, with overhanging borders, a geographical erythematous-purplish outline and a surface covered with adherent necrotic deposits. Ten years prior she was diagnosed with Sjögren's syndrome. After skin biopsy, pyoderma gangrenosum diagnostic was established, a rare finding in a Sjögren's syndrome patient. Systemic corticotherapy and chemical debridement of the lesions proved a successful treatment method. [ABSTRACT FROM AUTHOR]
- Published
- 2014
17. Multiple asymptomatic cutaneous pilar leiomyoma versus spontaneous eruptive keloids – A case report
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Morariu, S. H., Suciu, M., Badea, M. A., Vartolomei, M. D., Corneliu Florin Buicu, and Cotoi, O. S.
18. Impact of Age on Outcomes of Patients With Pure Carcinoma In Situ of the Bladder: Multi-Institutional Cohort Analysis
- Author
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Matteo Ferro, Sever Chiujdea, Gennaro Musi, Giuseppe Lucarelli, Francesco Del Giudice, Rodolfo Hurle, Rocco Damiano, Francesco Cantiello, Andrea Mari, Andrea Minervini, Gian Maria Busetto, Giuseppe Carrieri, Felice Crocetto, Biagio Barone, Vincenzo Francesco Caputo, Luigi Cormio, Pasquale Ditonno, Alessandro Sciarra, Daniela Terracciano, Antonio Cioffi, Stefano Luzzago, Mattia Piccinelli, Francesco Alessandro Mistretta, Mihai Dorin Vartolomei, Ottavio de Cobelli, Ferro, M., Chiujdea, S., Musi, G., Lucarelli, G., Giudice, F. D., Hurle, R., Damiano, R., Cantiello, F., Mari, A., Minervini, A., Busetto, G. M., Carrieri, G., Crocetto, F., Barone, B., Caputo, V. F., Cormio, L., Ditonno, P., Sciarra, A., Terracciano, D., Cioffi, A., Luzzago, S., Piccinelli, M., Mistretta, F. A., Vartolomei, M. D., and de Cobelli, O.
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Carcinoma, Transitional Cell ,Aging ,Bladder cancer ,Oncological outcomes ,Progression ,Recurrence ,Urology ,Urinary Bladder ,Settore MED/24 - Urologia ,Cohort Studies ,carcinoma in situ ,aging ,oncological outcomes ,recurrence ,progression ,bladder cancer ,Oncology ,Urinary Bladder Neoplasms ,BCG Vaccine ,Disease Progression ,Humans ,Neoplasm Recurrence, Local ,Carcinoma in Situ ,Aged ,Retrospective Studies ,Oncological outcome - Abstract
Introduction: The aim of this multicenter study was to investigate the role of age (cut-off 70 years) at diagnosis in predicting oncologic behavior of pure carcinoma in situ of the bladder. Material and Methods: Inclusion criteria were: patients with pure CIS confirmed and that followed intravesical BCG treatment. Pure CIS was defined at any CIS not associated with another urothelial cancer. Exclusion criteria were: any CIS associated with invasive urothelial carcinoma. A total of 172 with pure CIS treated between January 1, 2002 and December 31, 2012 at 8 academic institutions met the inclusion criteria. The maintenance schedule was generally according to the EAU guidelines at the time Results: A total of 99 (57.6%) patients had an age >70 years prior to TURBT. There was no difference between clinico-pathologic features among groups (group 1, age ≤ 70 years and group 2, age > 70 years), except that patients aged ≤ 70 years presented a larger size of CIS (35.6% vs. 21.2%), P =.02. In multivariable Cox regression analyses, the same clinico-pathologic factors (age, multifocality, and recurrent tumor state) were independently associated with worse RFS. Harrell's C-index was 65.75.In multivariable Cox regression analyses in addition to age (P =.006) and multifocality (P
- Published
- 2022
19. Modified Glasgow Prognostic Score as a Predictor of Recurrence in Patients with High Grade Non-Muscle Invasive Bladder Cancer Undergoing Intravesical Bacillus Calmette–Guerin Immunotherapy
- Author
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Matteo Ferro, Octavian Sabin Tătaru, Gennaro Musi, Giuseppe Lucarelli, Abdal Rahman Abu Farhan, Francesco Cantiello, Rocco Damiano, Rodolfo Hurle, Roberto Contieri, Gian Maria Busetto, Giuseppe Carrieri, Luigi Cormio, Francesco Del Giudice, Alessandro Sciarra, Sisto Perdonà, Marco Borghesi, Carlo Terrone, Evelina La Civita, Pierluigi Bove, Riccardo Autorino, Matteo Muto, Nicolae Crisan, Michele Marchioni, Luigi Schips, Francesco Soria, Daniela Terracciano, Rocco Papalia, Felice Crocetto, Biagio Barone, Giorgio Ivan Russo, Stefano Luzzago, Giuseppe Mario Ludovico, Mihai Dorin Vartolomei, Francesco Alessandro Mistretta, Vincenzo Mirone, Ottavio de Cobelli, Ferro, M., Tataru, O. S., Musi, G., Lucarelli, G., Abu Farhan, A. R., Cantiello, F., Damiano, R., Hurle, R., Contieri, R., Busetto, G. M., Carrieri, G., Cormio, L., Del Giudice, F., Sciarra, A., Perdona, S., Borghesi, M., Terrone, C., La Civita, E., Bove, P., Autorino, R., Muto, M., Crisan, N., Marchioni, M., Schips, L., Soria, F., Terracciano, D., Papalia, R., Crocetto, F., Barone, B., Russo, G. I., Luzzago, S., Ludovico, G. M., Vartolomei, M. D., Mistretta, F. A., Mirone, V., and de Cobelli, O.
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Clinical Biochemistry ,Modified Glasgow prognostic score ,Bacillus Calmette–Guérin ,modified Glasgow Prognostic Score ,non muscle invasive bladder cancer ,Non muscle invasive bladder cancer ,Settore MED/24 - Urologia ,modified Glasgow prognostic score - Abstract
Background: A systemic inflammatory marker, the modified Glasgow prognostic score (mGPS), could predict outcomes in non-muscle-invasive bladder cancer (NIMBC). We aimed to investigate the predictive power of mGPS in oncological outcomes in HG/G3 T1 NMIBC patients undergoing Bacillus Calmette–Guérin (BCG) therapy. Methods: We retrospectively reviewed patient’s medical data from multicenter institutions. A total of 1382 patients with HG/G3 T1 NMIBC have been administered adjuvant intravesical BCG therapy, every week for 3 weeks given at 3, 6, 12, 18, 24, 30 and 36 months. The analysis of mGPS for recurrence and progression was performed using multivariable and univariable Cox regression models. Results: During follow-up, 659 patients (47.68%) suffered recurrence, 441 (31.91%) suffered progression, 156 (11.28%) died of all causes, and 67 (4.84%) died of bladder cancer. At multivariable analysis, neutrophil to lymphocyte ratio [hazard ratio (HR): 7.471; p = 0.0001] and erythrocyte sedimentation rate (ESR) (HR: 0.706; p = 0.006 were significantly associated with recurrence. mGPS has no statistical significance for progression (p = 0.076). Kaplan–Meier survival analysis showed a significant difference in survival among patients from different mGPS subgroups. Five-year OS was 93% (CI 95% 92–94), in patients with mGPS 0, 82.2% (CI 95% 78.9–85.5) in patients with mGPS 1 and 78.1% (CI 95% 60.4–70) in mGPS 2 patients. Five-year CSS was 98% (CI 95% 97–99) in patients with mGPS 0, 90% (CI 95% 87–94) in patients with mGPS 1, and 100% in mGPS 2 patients. Limitations are applicable to a retrospective study. Conclusions: mGPS may have the potential to predict recurrence in HG/G3 T1 NMIBC patients, but more prospective, with large cohorts, studies are needed to study the influence of systemic inflammatory markers in prediction of outcomes in NMIBC for a definitive conclusion.
- Published
- 2022
20. Prostate Cancer Radiogenomics-From Imaging to Molecular Characterization
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Gian Maria Busetto, Alessandro Sciarra, Luigi Cormio, Martina Maggi, Biagio Barone, Francesco Del Giudice, Giuseppe Lucarelli, Ugo Falagario, Daniela Terracciano, Matteo Muto, Ottavio De Cobelli, Giuseppe Carrieri, Octavian Sabin Tătaru, Matteo Ferro, Felice Crocetto, Gennaro Musi, Mihai Dorin Vartolomei, Ferro, M., de Cobelli, O., Vartolomei, M. D., Lucarelli, G., Crocetto, F., Barone, B., Sciarra, A., Del Giudice, F., Muto, M., Maggi, M., Carrieri, G., Busetto, G. M., Falagario, U., Terracciano, D., Cormio, L., Musi, G., and Tataru, O. S.
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Diagnostic Imaging ,Male ,Computer science ,QH301-705.5 ,PET-CT ,radiogenomics ,Radiogenomics ,Genomics ,Review ,Computational biology ,Catalysis ,Settore MED/24 - Urologia ,Inorganic Chemistry ,molecular characterization ,Prostate cancer ,Radiomics ,Radiogenomic ,Risk Factors ,medicine ,genomics ,Humans ,MRI ,prostate cancer ,radiomics ,Physical and Theoretical Chemistry ,Medical diagnosis ,Biology (General) ,Molecular Biology ,QD1-999 ,Spectroscopy ,medicine.diagnostic_test ,Organic Chemistry ,Prostatic Neoplasms ,Magnetic resonance imaging ,General Medicine ,medicine.disease ,Molecular Imaging ,Computer Science Applications ,Chemistry ,Genomic ,Clinical value - Abstract
Radiomics and genomics represent two of the most promising fields of cancer research, designed to improve the risk stratification and disease management of patients with prostate cancer (PCa). Radiomics involves a conversion of imaging derivate quantitative features using manual or automated algorithms, enhancing existing data through mathematical analysis. This could increase the clinical value in PCa management. To extract features from imaging methods such as magnetic resonance imaging (MRI), the empiric nature of the analysis using machine learning and artificial intelligence could help make the best clinical decisions. Genomics information can be explained or decoded by radiomics. The development of methodologies can create more-efficient predictive models and can better characterize the molecular features of PCa. Additionally, the identification of new imaging biomarkers can overcome the known heterogeneity of PCa, by non-invasive radiological assessment of the whole specific organ. In the future, the validation of recent findings, in large, randomized cohorts of PCa patients, can establish the role of radiogenomics. Briefly, we aimed to review the current literature of highly quantitative and qualitative results from well-designed studies for the diagnoses, treatment, and follow-up of prostate cancer, based on radiomics, genomics and radiogenomics research.
- Published
- 2021
21. Fascin-1 and its role as a serological marker in prostate cancer: a prospective case–control study
- Author
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Călin Bogdan Chibelean, Liliana Vartolomei, Orsolya Martha, Ileana Sin, Septimiu Voidazan, Octavian Sabin Tătaru, Virgil Gheorghe Osan, Angela Borda, Daniel Porav-Hodade, Matteo Ferro, Biagio Barone, Andrada Loghin, Adina Hutanu, Carlo Buonerba, Giuseppe Lucarelli, Anca Sin, Felice Crocetto, Mihai Dorin Vartolomei, Tataru, O. S., Martha, O., Crocetto, F., Barone, B., Voidazan, S., Borda, A., Sin, A., Hutanu, A., Loghin, A., Sin, I., Porav-Hodade, D., Chibelean, C. B., Vartolomei, L., Lucarelli, G., Ferro, M., Osan, V. G., Buonerba, C., and Vartolomei, M. D.
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0301 basic medicine ,Oncology ,medicine.medical_specialty ,Serology ,03 medical and health sciences ,Prostate cancer ,0302 clinical medicine ,Internal medicine ,medicine ,fascin actin-bundling protein 1 ,Fascin-1 ,Fascin ,biology ,business.industry ,Case-control study ,medicine.disease ,prostate cancer ,030104 developmental biology ,030220 oncology & carcinogenesis ,biology.protein ,Biomarker (medicine) ,biomarker ,business ,serum ,Biotechnology ,Research Article - Abstract
Aim: This study aims to investigate any modification of serological FSCN1 in prostate cancer patients compared with patients without neoplasia. Material & methods: Clinical data and blood specimens from patients with and without prostate cancer were obtained. A quantitative sandwich ELISA method was used to determine serological values of FSCN1. Results: Although serum values of FSCN1 were dissimilar in the two cohorts of patients (6.90 vs 7.33 ng/ml), the difference was not statistically significant (p = 0.20). Serum values of FSCN1 stratified for Gleason score groups were not significantly distinguishable (p = 0.65). A negative correlation (rho = -0.331; p = 0.009) was reported between FSCN1 and age. Conclusion: Further studies are required to evaluate a possible diagnostic role of FSCN1 in prostate cancer., Lay abstract FSCN1 is a potential novel biomarker that we investigated in patients with prostate cancer and evaluated in serum through a quantitative assay. Although FSCN1 serum values were dissimilar between patients with and without prostate cancer (with lower values in the first group), data are currently inconclusive. A negative correlation between FSCN1 and age was instead reported. Further studies are required to investigate a possible diagnostic role of FSCN1.
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- 2021
22. The impact of sars-cov-2 pandemic on time to primary, secondary resection and adjuvant intravesical therapy in patients with high-risk non-muscle invasive bladder cancer: A retrospective multi-institutional cohort analysis
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Giovanni Liguori, F. Botticelli, Pierluigi Bove, Francesco Del Giudice, Michele Catellani, Savino M. Di Stasi, Alessandro Sciarra, Paolo Parma, Emanuele Montanari, Francesco Porpiglia, Luca Boeri, Davide Arcaniolo, Rodolfo Hurle, Felice Crocetto, Massimo Madonia, Gennaro Musi, Marco Borghesi, Matteo Manfredi, Luigi Cormio, Vincenzo Pagliarulo, Luca Carmignani, Mihai Dorin Vartolomei, Matteo Ferro, Giorgio Ivan Russo, Carlo Terrone, Riccardo Schiavina, Giuseppe Carrieri, Paolo Gontero, Michele Marchioni, Federico Deho, Eugenio Brunocilla, Giuseppe Lucarelli, Alessandro Antonelli, Marco Racioppi, Roberto Contieri, Pasquale Ditonno, A. Conti, Claudio Simeone, Alessandro Tedde, Alessandro Veccia, Roberto M Scarpa, Nicola Longo, Alessandro Tafuri, Elisabetta Costantini, Ester Iliano, Francesco Soria, Martina Maggi, Luigi Schips, Carlo Trombetta, Gian Maria Busetto, Lorenzo Spirito, Emanuele Zaffuto, Biagio Barone, Francesco Cantiello, Cristian Fiori, Rocco Papalia, Fabrizio Dal Moro, Rocco Damiano, Ottavio De Cobelli, Ferro, M., Del Giudice, F., Carrieri, G., Busetto, G. M., Cormio, L., Hurle, R., Contieri, R., Arcaniolo, D., Sciarra, A., Maggi, M., Porpiglia, F., Manfredi, M., Fiori, C., Antonelli, A., Tafuri, A., Bove, P., Terrone, C., Borghesi, M., Costantini, E., Iliano, E., Montanari, E., Boeri, L., Russo, G. I., Madonia, M., Tedde, A., Veccia, A., Simeone, C., Liguori, G., Trombetta, C., Brunocilla, E., Schiavina, R., Dal Moro, F., Racioppi, M., Vartolomei, M. D., Longo, N., Spirito, L., Crocetto, F., Cantiello, F., Damiano, R., Di Stasi, S. M., Marchioni, M., Schips, L., Parma, P., Carmignani, L., Conti, A., Soria, F., Gontero, P., Barone, B., Deho, F., Zaffuto, E., Papalia, R., Scarpa, R. M., Pagliarulo, V., Lucarelli, G., Ditonno, P., Botticelli, F. M. G., Musi, G., Catellani, M., de Cobelli, O., Ferro M., Del Giudice F., Carrieri G., Busetto G.M., Cormio L., Hurle R., Contieri R., Arcaniolo D., Sciarra A., Maggi M., Porpiglia F., Manfredi M., Fiori C., Antonelli A., Tafuri A., Bove P., Terrone C., Borghesi M., Costantini E., Iliano E., Montanari E., Boeri L., Russo G.I., Madonia M., Tedde A., Veccia A., Simeone C., Liguori G., Trombetta C., Brunocilla E., Schiavina R., Dal Moro F., Racioppi M., Vartolomei M.D., Longo N., Spirito L., Crocetto F., Cantiello F., Damiano R., Di Stasi S.M., Marchioni M., Schips L., Parma P., Carmignani L., Conti A., Soria F., Gontero P., Barone B., Deho F., Zaffuto E., Papalia R., Scarpa R.M., Pagliarulo V., Lucarelli G., Ditonno P., Botticelli F.M.G., Musi G., Catellani M., and de Cobelli O.
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Cancer Research ,medicine.medical_specialty ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,medicine.medical_treatment ,Article ,Resection ,Bladder cancer ,Intravesical BCG ,Re-TURBT ,SARS-CoV-2 ,Trans-urethral resection of bladder tumor ,COVID-19 ,pandemic ,residency ,residents ,urology ,Internal medicine ,Pandemic ,medicine ,RC254-282 ,business.industry ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Outbreak ,bladder cancer ,intravesical BCG ,trans-urethral resection of bladder tumor ,medicine.disease ,Settore MED/24 ,Oncology ,Intravesical bcg ,business ,Adjuvant ,Cohort study - Abstract
Background: To investigate the impact of COVID-19 outbreak on the diagnosis and treatment of non-muscle invasive bladder cancer (NMIBC). Methods: A retrospective analysis was performed using an Italian multi-institutional database of TURBT patients with high-risk urothelial NMIBC between January 2019 and February 2021, followed by Re-TURBT and/or adjuvant intravesical BCG. Results: A total of 2591 patients from 27 institutions with primary TURBT were included. Of these, 1534 (59.2%) and 1056 (40.8%) underwent TURBT before and during the COVID-19 outbreak, respectively. Time between diagnosis and TURBT was significantly longer during the COVID-19 period (65 vs. 52 days, p = 0.002). One thousand and sixty-six patients (41.1%) received Re-TURBT, 604 (56.7%) during the pre-COVID-19. The median time to secondary resection was significantly longer during the COVID-19 period (55 vs. 48 days, p <, 0.0001). A total of 977 patients underwent adjuvant intravesical therapy after primary or secondary resection, with a similar distribution across the two groups (n = 453, 86% vs. n = 388, 86.2%). However, the proportion of the patients who underwent maintenance significantly differed (79.5% vs. 60.4%, p <, 0.0001). Conclusions: The COVID-19 pandemic represented an unprecedented challenge to our health system. Our study did not show significant differences in TURBT quality. However, a delay in treatment schedule and disease management was observed. Investigation of the oncological impacts of those differences should be advocated.
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- 2021
23. Role of serum cholinesterase in patients treated with salvage radical prostatectomy
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Morgan Rouprêt, David D'Andrea, Romain Mathieu, Alberto Briganti, Mohammad Abufaraj, Francesco Soria, Pierre I. Karakiewicz, Marco Moschini, Mihai Dorin Vartolomei, Shahrokh F. Shariat, Shoji Kimura, Daher C. Chade, Beat Foerster, Vartolomei, M. D., D'Andrea, D., Chade, D. C., Soria, F., Kimura, S., Foerster, B., Abufaraj, M., Mathieu, R., Moschini, M., Roupret, M., Briganti, A., Karakiewicz, P. I., and Shariat, S. F.
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Male ,medicine.medical_treatment ,030232 urology & nephrology ,Salvage therapy ,Gastroenterology ,Metastasis ,Prostate cancer ,0302 clinical medicine ,Risk Factors ,Interquartile range ,Salvage radical prostatectomy ,Cholinesterases ,Prospective Studies ,Prospective cohort study ,Tumor ,integumentary system ,Prostatectomy ,Middle Aged ,Prognosis ,Survival Rate ,Local ,Oncology ,Lymphatic Metastasis ,030220 oncology & carcinogenesis ,Adenocarcinoma ,Female ,medicine.medical_specialty ,Biomarker ,Radiation-recurrent ,Serum cholinesterase ,Aged ,Biomarkers, Tumor ,Follow-Up Studies ,Humans ,Neoplasm Recurrence, Local ,Prostatic Neoplasms ,Salvage Therapy ,Urology ,03 medical and health sciences ,Internal medicine ,medicine ,Survival rate ,business.industry ,medicine.disease ,Neoplasm Recurrence ,business ,Biomarkers - Abstract
Background: Serum cholinesterase (ChE) a serine hydrolase that catalyses the hydrolysis of esters of choline, is involved in cellular proliferation and differentiation, therefore affecting carcinogenesis. The aim of this study was to understand the prognostic role of preoperative serum ChE in patients with radiation-recurrent prostate cancer (CaP) treated with salvage radical prostatectomy (SRP). Material and methods: This retrospective study included 214 patients with radiation-recurrent CaP treated with SRP from January 2007 to December 2015 at 5 academic centers. Patients were considered with abnormal/decreased ChE levels if
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- 2019
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24. Absolute basophil count is associated with time to recurrence in patients with high-grade T1 bladder cancer receiving bacillus Calmette-Guérin after transurethral resection of the bladder tumor
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O. De Cobelli, Francesco Perri, Riccardo Schiavina, Francesco Cantiello, P. De Placido, Vincenzo Mirone, S. M. Di Stasi, Carlo Buonerba, Riccardo Autorino, Giuseppe Morgia, Michele Battaglia, Rocco Damiano, Guru Sonpavde, Gennaro Musi, Vincenzo Ieluzzi, Giuseppe Lucarelli, Gian Maria Busetto, Mihai Dorin Vartolomei, A Gabriele, A.R. Abu Farhan, Pierluigi Bove, Giovanna Russo, S. Perdonà, Rodolfo Hurle, Amelia Cimmino, Giorgio Guazzoni, F. Del Giudice, G. Di Lorenzo, Estevão Lima, Luca Scafuri, Nicolae Crisan, Gilberto L. Almeida, Daniela Terracciano, Dario Bruzzese, Marco Borghesi, Paolo Verze, Matteo Ferro, S.F. Shariat, Ferro M, Di Lorenzo G, Vartolomei MD, Bruzzese D, Cantiello F, Lucarelli G, Musi G, Di Stasi S, Hurle R, Guazzoni G, Busetto GM, Gabriele A, Del Giudice F, Damiano R, Perri F, Perdona S, Verze P, Borghesi M, Schiavina R, Almeida GL, Bove P, Lima E, Autorino R, Crisan N, Farhan ARA, Battaglia M, Russo GI, Ieluzzi V, Morgia G, De Placido P, Terracciano D, Cimmino A, Scafuri L, Mirone V, De Cobelli O, Shariat S, Sonpavde G, Buonerba C, Ferro, M., Di Lorenzo, G., Vartolomei, M. D., Bruzzese, D., Cantiello, F., Lucarelli, G., Musi, G., Di Stasi, S., Hurle, R., Guazzoni, G., Busetto, G. M., Gabriele, A., Del Giudice, F., Damiano, R., Perri, F., Perdona, S., Verze, P., Borghesi, M., Schiavina, R., Almeida, G. L., Bove, P., Lima, E., Autorino, R., Crisan, N., Farhan, A. R. A., Battaglia, M., Russo, G. I., Ieluzzi, V., Morgia, G., De Placido, P., Terracciano, D., Cimmino, A., Scafuri, L., Mirone, V., De Cobelli, O., Shariat, S., Sonpavde, G., and Buonerba, C.
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Male ,Time Factors ,Neutrophils ,medicine.medical_treatment ,030232 urology & nephrology ,Leukocyte Count ,0302 clinical medicine ,Immunologic ,Retrospective Studie ,80 and over ,BCG ,Aged, 80 and over ,Univariate analysis ,Intravesical ,Neutrophil ,Bladder cancer ,basophils ,bladder cancer ,Middle Aged ,Basophils ,Administration, Intravesical ,Quartile ,Local ,030220 oncology & carcinogenesis ,Administration ,BCG Vaccine ,Disease Progression ,Female ,Human ,Adult ,medicine.medical_specialty ,Time Factor ,Urology ,Cystectomy ,Follow-Up Studie ,03 medical and health sciences ,Adjuvants, Immunologic ,Basophil ,medicine ,Humans ,Adjuvants ,Cancer staging ,Aged ,Neoplasm Staging ,Retrospective Studies ,Proportional hazards model ,business.industry ,Retrospective cohort study ,medicine.disease ,Follow-Up Studies ,Neoplasm Recurrence, Local ,Urinary Bladder Neoplasms ,Neoplasm Recurrence ,Settore MED/24 ,business ,BCG vaccine - Abstract
BACKGROUND: Basophils, eosinophils and monocytes may be involved in BCG-induced immune responses and be associated with outcomes of bladder cancer patients receiving intravesical BCG. Our objective was to explore the association of baseline counts of basophils, eosinophils and monocytes with outcomes of patients with high-grade T1 bladder cancer receiving a standard course of intravesical BCG. METHODS: We retrospectively reviewed medical records of patients with primary T1 HG/G3 bladder cancer. After re-TURBT, patients were treated with a 6-week course of intravesical BCG induction followed by intravesical BCG every week for 3 weeks given at 3, 6, 12, 18, 24, 30 and 36 months from initiation of therapy The analysis of potential risk factors for recurrence, muscle invasion and cancer-specific and overall survival was performed using univariable Cox regression models. Those factors that presented, at univariate analysis, an association with the event at a liberal p
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- 2020
25. Corrigendum to ‘EAU-ESMO Consensus Statements on the Management of Advanced and Variant Bladder Cancer—An International Collaborative Multistakeholder Effort Under the Auspices of the EAU-ESMO Guidelines Committees’ [European Urology 77 (2020) 223–250](S0302283819307638)(10.1016/j.eururo.2019.09.035)
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Bogdan Geavlete, Stefano Fanti, Susanne Krege, Alberto Briganti, Harry W. Herr, Shaista Hafeez, Mark Frydenberg, Marek Babjuk, Willem de Blok, Antti Salminen, Maria De Santis, Yann Neuzillet, Arnulf Stenzl, Joost L. Boormans, Hein Van Poppel, Karel Decaestecker, Vibeke Løgager, Jorg R. Oddens, Silke Gillessen, Pedro C. Lara, Berardino De Bari, Baris Turkbey, Andrew K. Williams, Thomas Wiegel, Mihai Dorin Vartolomei, Robert Jones, Riccardo Valdagni, Vincent Khoo, Ashish M. Kamat, Christoph R. Müller, Georgios Gakis, Neeraj Agarwal, Annemarie Leliveld, Franklin A. Vives Rivera, Robert Jan Smeenk, Luís Pacheco-Figueiredo, H. Maxim Bruins, Juan Palou, Jorge Huguet, Konstantinos Dimitropoulos, Jonathan E. Rosenberg, Carl Salembier, Ken Herrmann, Iris Brummelhuis, Morgan Rouprêt, Helle Pappot, Susanne Osanto, Shahrokh F. Shariat, Anita Smits, Susanne Vahr Lauridsen, Manish I. Patel, Theo H. van der Kwast, Paul Sargos, Michel Bolla, Karin Plass, Jurgen J. Fütterer, Hugh Mostafid, Olivier Rouvière, Valérie Fonteyne, Erik Veskimäe, Bradley R. Pieters, Richard P. Meijer, Anne E. Kiltie, Tom J.H. Arends, Arndt Hartmann, Amir Sherif, Antoni Vilaseca, Stéphane Culine, Wim J.G. Oyen, Evanguelos Xylinas, Daniel Castellano, Shomik Sengupta, James N'Dow, Maria J. Ribal, Mesut Remzi, Richard Zigeuner, A. Müller, Richard Cathomas, Joaquim Bellmunt, Nicholas D. James, Paolo Gontero, Pieter De Visschere, Eva Compérat, Alison Birtle, Margitta Retz, Dickon Hayne, Michael Rink, Virginia Hernández, J. Alfred Witjes, Marco Moschini, J. Domínguez-Escrig, Yohann Loriot, Estefania Linares-Espinós, Peter C. Black, Alberto Bossi, Bertrand Tombal, Sylvain Ladoire, Aristotle Bamias, Ananya Choudhury, Simon J. Crabb, Steven MacLennan, Peter Wiklund, Antoine G. van der Heijden, Arturo Chiti, Bernhard Grubmüller, Barbara Alicja Jereczek-Fossa, Alan Horwich, George N. Thalmann, Bernard H. Bochner, Florian Roghmann, Max Bürger, Jan Oldenburg, Peter Hoskin, Andrea Necchi, Jonathan Richenberg, Anja Lorch, Peter Paul M. Willemse, Donna E. Hansel, M. Carmen Mir, Thomas Powles, Theo M. de Reijke, Ann Henry, Witjes, J. A., Babjuk, M., Bellmunt, J., Bruins, H. M., De Reijke, T. M., De Santis, M., Gillessen, S., James, N., Maclennan, S., Palou, J., Powles, T., Ribal, M. J., Shariat, S. F., Van Der Kwast, T., Xylinas, E., Agarwal, N., Arends, T., Bamias, A., Birtle, A., Black, P. C., Bochner, B. H., Bolla, M., Boormans, J. L., Bossi, A., Briganti, A., Brummelhuis, I., Burger, M., Castellano, D., Cathomas, R., Chiti, A., Choudhury, A., Comperat, E., Crabb, S., Culine, S., De Bari, B., De Blok, W., De Visschere, P. J. L., Decaestecker, K., Dimitropoulos, K., Dominguez-Escrig, J. L., Fanti, S., Fonteyne, V., Frydenberg, M., Futterer, J. J., Gakis, G., Geavlete, B., Gontero, P., Grubmuller, B., Hafeez, S., Hansel, D. E., Hartmann, A., Hayne, D., Henry, A. M., Hernandez, V., Herr, H., Herrmann, K., Hoskin, P., Huguet, J., Jereczek-Fossa, B. A., Jones, R., Kamat, A. M., Khoo, V., Kiltie, A. E., Krege, S., Ladoire, S., Lara, P. C., Leliveld, A., Linares-Espinos, E., Logager, V., Lorch, A., Loriot, Y., Meijer, R., Mir, M. C., Moschini, M., Mostafid, H., Muller, A. -C., Muller, C. R., N'Dow, J., Necchi, A., Neuzillet, Y., Oddens, J. R., Oldenburg, J., Osanto, S., Oyen, W. J. G., Pacheco-Figueiredo, L., Pappot, H., Patel, M. I., Pieters, B. R., Plass, K., Remzi, M., Retz, M., Richenberg, J., Rink, M., Roghmann, F., Rosenberg, J. E., Roupret, M., Rouviere, O., Salembier, C., Salminen, A., Sargos, P., Sengupta, S., Sherif, A., Smeenk, R. J., Smits, A., Stenzl, A., Thalmann, G. N., Tombal, B., Turkbey, B., Lauridsen, S. V., Valdagni, R., Van Der Heijden, A. G., Van Poppel, H., Vartolomei, M. D., Veskimae, E., Vilaseca, A., Rivera, F. A. V., Wiegel, T., Wiklund, P., Willemse, P. -P. M., Williams, A., Zigeuner, R., Horwich, A., Urology, APH - Personalized Medicine, APH - Quality of Care, CCA - Cancer Treatment and Quality of Life, Radiotherapy, UCL - SSS/IREC/CHEX - Pôle de chirgurgie expérimentale et transplantation, and UCL - (SLuc) Service d'urologie
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medicine.medical_specialty ,Bladder cancer ,business.industry ,Urology ,030232 urology & nephrology ,MEDLINE ,Cancer ,Regret ,medicine.disease ,3. Good health ,03 medical and health sciences ,0302 clinical medicine ,030220 oncology & carcinogenesis ,Medicine ,Urologia ,University medical ,Bufeta -- Càncer ,Protocols clínics ,business - Abstract
The authors regret that a co-author was mistakenly missed from the authorship. The following co-author should have been included in the authorship: Peter-Paul M. Willemse Department of Oncological Urology, University Medical Center, Utrecht Cancer Center, Utrecht, The Netherlands
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- 2020
26. Beyond PSA: The Role of Prostate Health Index (phi)
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Daniela Terracciano, Matteo Muto, Angelo Porreca, Riccardo Autorino, Gian Maria Busetto, Mihai Dorin Vartolomei, Matteo Ferro, Giuseppe Lucarelli, Gennaro Musi, Rocco Damiano, Francesco Cantiello, Ottavio De Cobelli, Ferro, M., De Cobelli, O., Lucarelli, G., Porreca, A., Busetto, G. M., Cantiello, F., Damiano, R., Autorino, R., Musi, G., Vartolomei, M. D., Muto, M., and Terracciano, D.
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Oncology ,Male ,medicine.medical_specialty ,Biopsy ,clinical significance ,030232 urology & nephrology ,Context (language use) ,Review ,overdiagnosis ,Risk Assessment ,Catalysis ,Inorganic Chemistry ,lcsh:Chemistry ,03 medical and health sciences ,Prostate cancer ,0302 clinical medicine ,Prostate ,Internal medicine ,Biomarkers, Tumor ,Medicine ,Animals ,Humans ,Physical and Theoretical Chemistry ,Overdiagnosis ,Molecular Biology ,lcsh:QH301-705.5 ,Spectroscopy ,Screening procedures ,overdiagnosi ,business.industry ,Organic Chemistry ,Cancer ,Prostatic Neoplasms ,General Medicine ,Prostate-Specific Antigen ,medicine.disease ,prostate cancer ,Magnetic Resonance Imaging ,phi ,Computer Science Applications ,Prostate-specific antigen ,medicine.anatomical_structure ,lcsh:Biology (General) ,lcsh:QD1-999 ,030220 oncology & carcinogenesis ,Biomarker (medicine) ,Kallikreins ,business - Abstract
Background: Widespread use of prostate specific antigen (PSA) in screening procedures allowed early identification of an increasing number of prostate cancers (PCas), mainly including indolent cancer. Availability of different therapeutic strategies which have a very different impact on the patient’s quality of life suggested a strong need for tools able to identify clinically significant cancer at diagnosis. Multi-parametric magnetic resonance showed very good performance in pre-biopsy diagnosis. However, it is an expensive tool and requires an experienced radiologist. In this context, a simple blood-based test is worth investigating. In this context, researchers focused their attention on the development of a laboratory test able to minimize overdiagnosis without losing the identification of aggressive tumors. Results: Recent literature data on PCa biomarkers revealed a clear tendency towards the use of panels of biomarkers or a combination of biomarkers and clinical variables. Phi, the 4Kscore, and Stockholm3 as circulating biomarkers and the Mi-prostate score, Exo DX Prostate, and Select MD-X as urinary biomarker-based tests have been developed. In this scenario, phi is worthy of attention as a noninvasive test significantly associated with aggressive PCa. Conclusions: Literature data showed that phi had good diagnostic performance to identify clinically significant (cs) PCa, suggesting that it could be a useful tool for personalized treatment decision-making. In this review, phi potentialities, limitations, and comparisons with other blood- and urinary-based tests were explored.
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- 2020
27. Metabolomic profiling for the identification of novel diagnostic markers and therapeutic targets in prostate cancer: an update
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Michele Battaglia, Carlo Buonerba, Daniela Terracciano, Davide Loizzo, Mihai Dorin Vartolomei, Matteo Ferro, Monica Rutigliano, Pasquale Ditonno, Giuseppe Di Lorenzo, Carlo Bettocchi, Giuseppe Lucarelli, Francesco Cantiello, Ottavio De Cobelli, Lucarelli, G., Loizzo, D., Ferro, M., Rutigliano, M., Vartolomei, M. D., Cantiello, F., Buonerba, C., Di Lorenzo, G., Terracciano, D., De Cobelli, O., Bettocchi, C., Ditonno, P., and Battaglia, M.
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0301 basic medicine ,Biochemical recurrence ,Male ,Metabolomic ,SREBP ,Pathology and Forensic Medicine ,03 medical and health sciences ,Prostate cancer ,0302 clinical medicine ,Metabolomics ,Prostate ,Risk Factors ,lipid metabolism ,Genetics ,medicine ,Metabolome ,Biomarkers, Tumor ,Humans ,Obesity ,Risk factor ,Molecular Biology ,business.industry ,Fatty Acids ,Cancer ,Prostatic Neoplasms ,cholesterol ,medicine.disease ,prostate cancer ,Gene Expression Regulation, Neoplastic ,030104 developmental biology ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Lipogenesis ,Cancer research ,Molecular Medicine ,fatty acid ,business - Abstract
Introduction: An altered metabolic regulation is involved in the development and progression of different cancer types. As well as this, many genes associated with tumors are shown to have an important role in control of the metabolism. The incidence of prostate cancer (PCa) is increased in men with metabolic disorders. In particular, obesity is an established risk factor for PCa. An increased body mass index correlates with aggressive disease, and a higher risk of biochemical recurrence and prostate cancer-specific mortality. Increased lipogenesis is also one of the most significant events in PCa metabolism reprogramming. Areas covered: In this article, we provide an updated review of the current understanding of the PCa metabolome and evaluate the possibility of unveiling novel therapeutic targets. Expert opinion: Obesity is an established risk factor for PCa, and an increased BMI correlates with aggressive disease, and a higher risk of biochemical recurrence and prostate cancer-specific mortality. PCa metabolome is characterized by the accumulation of metabolic intermediates and an increased expression of genes in the tricarboxylic acid cycle, the induction of de novo lipogenesis and cholesterogenesis. PCa cells can induce different alterations in their microenvironment by modulating the crosstalk between cancer and stromal cells.
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- 2019
28. Systemic Inflammatory Markers and Oncologic Outcomes in Patients with High-risk Non-muscle-invasive Urothelial Bladder Cancer
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Francesco Cantiello, Vincenzo Serretta, Giuseppe Ucciero, Ottavio De Cobelli, Riccardo Autorino, Daniela Terracciano, Giorgio Guazzoni, Sisto Perdonà, Ettore De Berardinis, Paolo Verze, Antonio Cioffi, Giorgio Ivan Russo, Rocco Damiano, Vincenzo Mirone, Chiara Scafuro, Abdal Rahman Abu Farhan, Estevão Lima, Savino M. Di Stasi, Matteo Ferro, Gian Maria Busetto, Gilberto L. Almeida, Nicolae Crisan, Deliu Victor Matei, Rodolfo Hurle, Michele Battaglia, Riccardo Schiavina, Gennaro Musi, Giuseppe Morgia, Pierluigi Bove, Mihai Dorin Vartolomei, Shahrokh F. Shariat, Giuseppe Lucarelli, Marco Borghesi, Cantiello, Francesco, Russo, Giorgio I, Vartolomei, Mihai Dorin, Farhan, Abdal Rahman Abu, Terracciano, Daniela, Musi, Gennaro, Lucarelli, Giuseppe, Di Stasi, Savino M, Hurle, Rodolfo, Serretta, Vincenzo, Busetto, Gian Maria, Scafuro, Chiara, Perdonà, Sisto, Borghesi, Marco, Schiavina, Riccardo, Cioffi, Antonio, De Berardinis, Ettore, Almeida, Gilberto L, Bove, Pierluigi, Lima, Estevao, Ucciero, Giuseppe, Matei, Deliu Victor, Crisan, Nicolae, Verze, Paolo, Battaglia, Michele, Guazzoni, Giorgio, Autorino, Riccardo, Morgia, Giuseppe, Damiano, Rocco, de Cobelli, Ottavio, Mirone, Vincenzo, Shariat, Shahrokh F, Ferro, Matteo, Universidade do Minho, Cantiello F, Russo GI, Vartolomei MD, Farhan ARA, Terracciano D, Musi G, Lucarelli G, Di Stasi SM, Hurle R, Serretta V, Busetto GM, Scafuro C, Perdonà S, Borghesi M, Schiavina R, Cioffi A, De Berardinis E, Almeida GL, Bove P, Lima E, Ucciero G, Matei DV, Crisan N, Verze P, Battaglia M, Guazzoni G, Autorino R, Morgia G, Damiano R, de Cobelli O, Mirone V, Shariat SF, Ferro M, Cantiello, F., Russo, G. I., Vartolomei, M. D., Farhan, A. R. A., Terracciano, D., Musi, G., Lucarelli, G., Di Stasi, S. M., Hurle, R., Serretta, V., Busetto, G. M., Scafuro, C., Perdona, S., Borghesi, M., Schiavina, R., Cioffi, A., De Berardinis, E., Almeida, G. L., Bove, P., Lima, E., Ucciero, G., Matei, D. V., Crisan, N., Verze, P., Battaglia, M., Guazzoni, G., Autorino, R., Morgia, G., Damiano, R., de Cobelli, O., Mirone, V., Shariat, S. F., and Ferro, M.
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Oncology ,Male ,Bladder cancer ,Lymphocyte/monocyte ratio ,Neutrophil/lymphocyte ratio ,Platelet/lymphocyte ratio ,Prognosis ,Aged ,Biomarkers, Tumor ,Blood Platelets ,Carcinoma, Transitional Cell ,Cystectomy ,Disease Progression ,Female ,Follow-Up Studies ,Humans ,Inflammation ,Lymphocyte Count ,Lymphocytes ,Monocytes ,Neutrophils ,Risk Factors ,Urinary Bladder Neoplasms ,medicine.medical_treatment ,Lymphocyte ,Medicina Básica [Ciências Médicas] ,030232 urology & nephrology ,Monocyte ,Settore MED/24 - Urologia ,0302 clinical medicine ,Stage (cooking) ,Framingham Risk Score ,Tumor ,Neutrophil ,3. Good health ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Ciências Médicas::Medicina Básica ,medicine.symptom ,Human ,medicine.medical_specialty ,Prognosi ,Urology ,Follow-Up Studie ,03 medical and health sciences ,Internal medicine ,medicine ,Radiology, Nuclear Medicine and imaging ,Science & Technology ,business.industry ,Proportional hazards model ,Risk Factor ,Carcinoma ,Immunotherapy ,medicine.disease ,Blood Platelet ,Surgery ,Transitional Cell ,business ,Biomarkers - Abstract
Background: Serum levels of neutrophils, platelets, and lymphocytes have been recognized as factors related to poor prognosis for many solid tumors, including bladder cancer (BC). Objective: To evaluate the prognostic role of the combination of the neutrophil/lymphocyte ratio (NLR), platelet/lymphocyte ratio (PLR), and lymphocyte/monocyte ratio (LMR) in patients with high-risk non–muscle-invasive urothelial BC (NIMBC). Design, setting, and participants: A total of 1151 NMIBC patients who underwent first transurethral resection of the bladder tumor (TURBT) at 13 academic institutions between January 1, 2002 and December 31, 2012 were included in this analysis. The median follow-up was 48 mo. Intervention: TURBT with intravesical chemotherapy or immunotherapy. Outcome measurements and statistical analysis: Multivariable Cox regression analysis was performed to identify factors predictive of recurrence, progression, cancer-specific mortality, and overall mortality. A systemic inflammatory marker (SIM) score was calculated based on cutoffs for NLR, PLR, and LMR. Results and limitations: The 48-mo recurrence-free survival was 80.8%, 47.35%, 20.67%, and 17.06% for patients with an SIM score of 0, 1, 2, and 3, respectively (p < 0.01, log-rank test) while the corresponding 48-mo progression free-survival was 92.0%, 75.67%, 72.85%, and 63.1% (p < 0.01, log-rank test). SIM scores of 1, 2, and 3 were associated with recurrence (hazard ratio [HR] 3.73, 7.06, and 7.88) and progression (HR 3.15, 4.41, and 5.83). Limitations include the lack of external validation and comparison to other clinical risk models. Conclusions: Patients with high-grade T1 stage NMIBC with high SIM scores have worse oncologic outcomes in terms of recurrence and progression. Further studies should be conducted to stratify patients according to SIM scores to identify individuals who might benefit from early cystectomy. Patient summary: In this study, we defined a risk score (the SIM score) based on the measurement of routine systemic inflammatory markers. This score can identify patients with high-grade bladder cancer not invading the muscular layer who are more likely to suffer from tumor recurrence and progression. Therefore, the score could be used to select patients who might benefit from early bladder removal. Patients with high-risk non–muscle-invasive bladder cancer (BC) experienced greater recurrence and progression according to systemic inflammatory markers. This score could be used to select patients who might benefit from early cystectomy. The availability of these biomarkers in routine clinical practice gives further relevance to identification of the prognostic role of immune cells in patients with BC. These results could be translated into clinical practice to stratify patients who might benefit from early cystectomy.
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- 2018
29. Clinical value of cholinesterase in the prediction of biochemical recurrence after radical prostatectomy
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Beat Foerster, Mesut Remzi, Christian Seitz, David D'Andrea, Andrea Mari, Francesco Soria, Romain Mathieu, Shahrokh F. Shariat, Alberto Briganti, Pierre I. Karakiewicz, Mihai Dorin Vartolomei, Shoji Kimura, Kilian M. Gust, Mohammad Abufaraj, D'Andrea, D., Soria, F., Abufaraj, M., Gust, K., Foerster, B., Vartolomei, M. D., Kimura, S., Mari, A., Briganti, A., Remzi, M., Seitz, C. K., Mathieu, R., Karakiewicz, P. I., and Shariat, S. F.
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Male ,Oncology ,Lymphovascular invasion ,medicine.medical_treatment ,030232 urology & nephrology ,Prostate cancer ,Postoperative Complications ,0302 clinical medicine ,Cholinesterases ,Stage (cooking) ,Tumor ,biology ,Prostatectomy ,Incidence ,Middle Aged ,Prognosis ,Survival Rate ,Local ,Lymphatic Metastasis ,030220 oncology & carcinogenesis ,Biochemical recurrence ,Biomarker ,Cholinesterase ,Aged ,Biomarkers, Tumor ,Follow-Up Studies ,Humans ,Neoplasm Invasiveness ,Neoplasm Recurrence, Local ,Prostatic Neoplasms ,Retrospective Studies ,medicine.medical_specialty ,Urology ,03 medical and health sciences ,Internal medicine ,medicine ,Survival rate ,business.industry ,Perioperative ,Nomogram ,medicine.disease ,Neoplasm Recurrence ,Clinical value ,biology.protein ,business ,Biomarkers - Abstract
Purpose: To evaluate the predictive and prognostic role as well as the clinical impact on decision-making of serum cholinesterase (ChoE) levels in patients treated with radical prostatectomy for clinically nonmetastatic prostate cancer. Materials and methods: We conducted a retrospective analysis of our multi institutional database. Preoperative ChoE was evaluated as continuous and dichotomized variable using a visual assessment of the functional form of the association of ChoE with biochemical recurrence (BCR)-free survival. We assessed its association with perioperative clinicopathologic characteristics and outcomes. Multivariable models established its independent prognostic value for BCR. Cox proportional hazard coefficients were used to build nomograms for the prediction of early and late BCR. Decision curve analysis was used to assess the clinical impact on decision making of preoperative ChoE. Results: In all, 6,041 patients were available for the analysis. Decreased ChoE was associated with higher biopsy Gleason score, preoperative PSA levels, pathologic Gleason score, pathological stage, lymph node metastasis, positive surgical margin, and lymphovascular invasion at radical prostatectomy (all P < 0.01). Preoperative ChoE ≤ 6.52 U/ml was associated with higher probability of BCR (HR 1.72, 95% CI 1.48–1.99, P < 0.001). Preoperative and postoperative multivariable models that adjusted for the effects of established clinicopathologic features confirmed its independent association with BCR. In decision curve analysis inclusion of preoperative ChoE did not improve the net benefit of preoperative and postoperative models for the prediction of BCR. Conclusions: Despite independent association with clinicopathologic features and BCR, preoperative serum ChoE has no impact on clinical decision making. Future studies should investigate the possible relationship between ChoE activity and neoplastic cell transformation with a rational for targeting.
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- 2018
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30. EAU-ESMO consensus statements on the management of advanced and variant bladder cancer-an international collaborative multi-stakeholder effort: under the auspices of the EAU and ESMO Guidelines Committees†.
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Horwich A, Babjuk M, Bellmunt J, Bruins HM, De Reijke TM, De Santis M, Gillessen S, James N, Maclennan S, Palou J, Powles T, Ribal MJ, Shariat SF, Van Der Kwast T, Xylinas E, Agarwal N, Arends T, Bamias A, Birtle A, Black PC, Bochner BH, Bolla M, Boormans JL, Bossi A, Briganti A, Brummelhuis I, Burger M, Castellano D, Cathomas R, Chiti A, Choudhury A, Compérat E, Crabb S, Culine S, De Bari B, DeBlok W, De Visschere PJL, Decaestecker K, Dimitropoulos K, Dominguez-Escrig JL, Fanti S, Fonteyne V, Frydenberg M, Futterer JJ, Gakis G, Geavlete B, Gontero P, Grubmüller B, Hafeez S, Hansel DE, Hartmann A, Hayne D, Henry AM, Hernandez V, Herr H, Herrmann K, Hoskin P, Huguet J, Jereczek-Fossa BA, Jones R, Kamat AM, Khoo V, Kiltie AE, Krege S, Ladoire S, Lara PC, Leliveld A, Linares-Espinós E, Løgager V, Lorch A, Loriot Y, Meijer R, Carmen Mir M, Moschini M, Mostafid H, Müller AC, Müller CR, N'Dow J, Necchi A, Neuzillet Y, Oddens JR, Oldenburg J, Osanto S, Oyen WJG, Pacheco-Figueiredo L, Pappot H, Patel MI, Pieters BR, Plass K, Remzi M, Retz M, Richenberg J, Rink M, Roghmann F, Rosenberg JE, Rouprêt M, Rouvière O, Salembier C, Salminen A, Sargos P, Sengupta S, Sherif A, Smeenk RJ, Smits A, Stenzl A, Thalmann GN, Tombal B, Turkbey B, Vahr Lauridsen S, Valdagni R, Van Der Heijden AG, Van Poppel H, Vartolomei MD, Veskimäe E, Vilaseca A, Vives Rivera FA, Wiegel T, Wiklund P, Williams A, Zigeuner R, and Witjes JA
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- Delphi Technique, Europe, Humans, International Cooperation, Medical Oncology methods, Neoplasm Staging, Societies, Medical standards, Stakeholder Participation, Surveys and Questionnaires, Urinary Bladder pathology, Urinary Bladder Neoplasms pathology, Urology methods, Consensus, Medical Oncology standards, Practice Guidelines as Topic, Urinary Bladder Neoplasms therapy, Urology standards
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Background: Although guidelines exist for advanced and variant bladder cancer management, evidence is limited/conflicting in some areas and the optimal approach remains controversial., Objective: To bring together a large multidisciplinary group of experts to develop consensus statements on controversial topics in bladder cancer management., Design: A steering committee compiled proposed statements regarding advanced and variant bladder cancer management which were assessed by 113 experts in a Delphi survey. Statements not reaching consensus were reviewed; those prioritised were revised by a panel of 45 experts before voting during a consensus conference., Setting: Online Delphi survey and consensus conference., Participants: The European Association of Urology (EAU), the European Society for Medical Oncology (ESMO), experts in bladder cancer management., Outcome Measurements and Statistical Analysis: Statements were ranked by experts according to their level of agreement: 1-3 (disagree), 4-6 (equivocal), 7-9 (agree). A priori (level 1) consensus was defined as ≥70% agreement and ≤15% disagreement, or vice versa. In the Delphi survey, a second analysis was restricted to stakeholder group(s) considered to have adequate expertise relating to each statement (to achieve level 2 consensus)., Results and Limitations: Overall, 116 statements were included in the Delphi survey. Of these, 33 (28%) statements achieved level 1 consensus and 49 (42%) statements achieved level 1 or 2 consensus. At the consensus conference, 22 of 27 (81%) statements achieved consensus. These consensus statements provide further guidance across a broad range of topics, including the management of variant histologies, the role/limitations of prognostic biomarkers in clinical decision making, bladder preservation strategies, modern radiotherapy techniques, the management of oligometastatic disease and the evolving role of checkpoint inhibitor therapy in metastatic disease., Conclusions: These consensus statements provide further guidance on controversial topics in advanced and variant bladder cancer management until a time where further evidence is available to guide our approach., (© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
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- 2019
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