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2. Nonmetastatic Rhabdomyosarcoma in Children and Adolescents: Overall Results of the European Pediatric Soft Tissue Sarcoma Study Group RMS2005 Study

Author

Bisogno, Gianni, primary, Minard-Colin, Veronique, additional, Zanetti, Ilaria, additional, Ferrari, Andrea, additional, Gallego, Soledad, additional, Dávila Fajardo, Raquel, additional, Mandeville, Henry, additional, Kelsey, Anna, additional, Alaggio, Rita, additional, Orbach, Daniel, additional, Terwisscha van Scheltinga, Sheila, additional, Guillén Burrieza, Gabriela, additional, Ben-Arush, Myriam, additional, Glosli, Heidi, additional, Mudry, Peter, additional, Ferman, Sima, additional, Devalck, Christine, additional, Defachelles, Anne Sophie, additional, Merks, Johannes Hendrikus Maria, additional, and Jenney, Meriel, additional

Published
2023
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3. Developments in the Surgical Approach to Staging and Resection of Rhabdomyosarcoma

Author

Terwisscha van Scheltinga, Sheila, primary, Rogers, Timothy, additional, Smeulders, Naima, additional, deCorti, Federica, additional, Guerin, Florent, additional, Craigie, Ross, additional, Burrieza, Gabriela Guillén, additional, Smeele, Ludi, additional, Hol, Marinka, additional, van Rijn, Rick, additional, Fuchs, Joerg, additional, Seitz, Guido, additional, Schmidt, Andreas, additional, Timmermann, Beate, additional, Tunn, Per-Ulf, additional, Chargari, Cyrus, additional, Dávila Fajardo, Raquel, additional, Slater, Olga, additional, Gains, Jenny, additional, and Merks, Hans, additional

Published
2023
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4. Developments in the Surgical Approach to Staging and Resection of Rhabdomyosarcoma

Author

Terwisscha van Scheltinga, Sheila, Rogers, Timothy, Smeulders, Naima, deCorti, Federica, Guerin, Florent, Craigie, Ross, Burrieza, Gabriela Guillén, Smeele, Ludi, Hol, Marinka, van Rijn, Rick, Fuchs, Joerg, Seitz, Guido, Schmidt, Andreas, Timmermann, Beate, Tunn, Per-Ulf, Chargari, Cyrus, Dávila Fajardo, Raquel, Slater, Olga, Gains, Jenny, and Merks, Hans

Subjects
Medizin
Abstract

Although survival after rhabdosarcoma treatment has improved over the years, one third of patients still develop locoregional relapse. This review aims to highlight developments pertaining to staging and local treatment of specific RMS tumor sites, including head and neck, chest/trunk, bladder-prostate, female genito-urinary, perianal, and extremity sites. CA extern

Published
2023

6. Therapy and prognostic significance of regional lymph node involvement in embryonal rhabdomyosarcoma: a report from the European paediatric Soft tissue sarcoma Study Group

Author

Ben-Arush, Myriam, primary, Minard-Colin, Veronique, additional, Scarzello, Giovanni, additional, Fajardo, Raquel D., additional, Terwisscha Van Scheltinga, Sheila, additional, Bernier, Valérie, additional, Jenney, Meriel, additional, Gallego, Soledad, additional, Zanetti, Ilaria, additional, Cesen, Maja, additional, Merks, Johannes H.M., additional, and Bisogno, Gianni, additional

Published
2022
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7. Long-Term Oncological Outcomes of Papillary Thyroid Cancer and Follicular Thyroid Cancer in Children: A Nationwide Population-Based Study

Author

van de Berg, Daniël J., primary, Kuijpers, Anke M. J., additional, Engelsman, Anton F., additional, Drukker, Caroline A., additional, van Santen, Hanneke M., additional, Terwisscha van Scheltinga, Sheila C. E. J., additional, van Trotsenburg, A. S. Paul, additional, Mooij, Christiaan F., additional, Vriens, Menno R., additional, Nieveen van Dijkum, Els J. M., additional, and Derikx, Joep P. M., additional

Published
2022
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8. Perianal/perineal rhabdomyosarcoma: Results of the SIOP MMT 95, Italian RMS 96, and EpSSG RMS 2005 studies

Author

Rogers, Timothy, primary, Zanetti, Ilaria, additional, Coppadoro, Beatrice, additional, Martelli, Hélène, additional, Jenney, Meriel, additional, Minard‐Colin, Veronique, additional, Terwisscha van Scheltinga, Sheila E. J., additional, Skerritt, Clare, additional, Fajardo, Raquel Dávila, additional, Guérin, Florent, additional, Kelsey, Anna, additional, Merks, Johannes H. M., additional, Mandeville, Henry, additional, Guillén, Gabriela, additional, Glosli, Heidi, additional, De Corti, Federica, additional, and Bisogno, Gianni, additional

Published
2022
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9. Surgical management of extremity rhabdomyosarcoma: A consensus opinion from the Children's Oncology Group, the European Pediatric Soft‐Tissue Sarcoma Study Group, and the Cooperative Weichteilsarkom Studiengruppe.

Author

Morris, Carol D., Tunn, Per‐Ulf, Rodeberg, David A., Terwisscha van Scheltinga, Sheila, Binitie, Odion, Godzinski, Jan, Dall'Igna, Patrizia, Million, Lynn, Hawkins, Douglas S., Koscielniak, Ewa, Bisogno, Gianni, and Rogers, Timothy N.

Published
2023
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10. Local staging and treatment in extremity rhabdomyosarcoma. A report from the EpSSG‐RMS2005 study

Author

Terwisscha van Scheltinga, Sheila E. J., primary, Wijnen, Marc H. W. A., additional, Martelli, Hélène, additional, Rogers, Timothy, additional, Mandeville, Henry, additional, Gaze, Mark N., additional, McHugh, Keiran, additional, Corradini, Nadege, additional, Orbach, Daniel, additional, Jenney, Meriel, additional, Kelsey, Anna, additional, Chisholm, Julia, additional, Gallego, Soledad, additional, Glosli, Heidi, additional, Ferrari, Andrea, additional, Zanetti, Ilaria, additional, De Salvo, Gian Luca, additional, Minard‐Colin, Veronique, additional, Bisogno, Giani, additional, van Noesel, Max M., additional, and Merks, Hans H. M., additional

Published
2020
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11. Surgical management of extremity rhabdomyosarcoma: A consensus opinion from the Children's Oncology Group, the European Pediatric Soft‐Tissue Sarcoma Study Group, and the Cooperative Weichteilsarkom Studiengruppe

Author

Morris, Carol D., primary, Tunn, Per‐Ulf, additional, Rodeberg, David A., additional, Terwisscha van Scheltinga, Sheila, additional, Binitie, Odion, additional, Godzinski, Jan, additional, Dall'Igna, Patrizia, additional, Million, Lynn, additional, Hawkins, Douglas S., additional, Koscielniak, Ewa, additional, Bisogno, Gianni, additional, and Rogers, Timothy N., additional

Published
2020
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12. Paratesticular rhabdomyosarcoma—Impact of locoregional approach on patient outcome: A report from the European paediatric Soft tissue sarcoma Study Group (EpSSG)

Author

Rogers, Timothy N., primary, De Corti, Federica, additional, Burrieza, Gabriela Guillén, additional, Guérin, Florent, additional, Terwisscha van Scheltinga, Sheila, additional, Smeulders, Naima, additional, Craigie, Ross, additional, Jenney, Meriel, additional, Kelsey, Anna, additional, Zanetti, Ilaria, additional, Coppadoro, Beatrice, additional, De Salvo, Gian Luca, additional, Bisogno, Gianni, additional, and Martelli, Hélène, additional

Published
2020
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14. Long‐term oncological outcomes of follicular thyroid cancer in adolescents and young adults: A nationwide population‐based study.

Author

Berg, Daniël J., Mooij, Christiaan F., Trotsenburg, A. S. Paul, Santen, Hanneke M., Terwisscha van Scheltinga, Sheila C. E. J., Vriens, Menno R., Kruijff, Schelto, Nieveen van Dijkum, Els J. M., Engelsman, Anton F., and Derikx, Joep P. M.

Subjects
*THYROID cancer, *YOUNG adults, *PROPORTIONAL hazards models, *TEENAGERS, *OVERALL survival
Abstract

Background Methods Results Conclusions Follicular thyroid carcinoma (FTC) in adolescents and young adults (AYAs) is rare and data on long‐term oncological outcomes are scarce. This study aimed to describe the long‐term recurrence and survival rates of AYAs with FTC, and identify risk factors for recurrence.This is a retrospective cohort study combining two national databases, including all patients aged 15–39 years, diagnosed with FTC in The Netherlands between 2000 and 2016. Age, sex, tumor size, focality, positive margins, angioinvasion, pT‐stage, and pN‐stage were included in a Cox proportional hazard model to identify risk factors for recurrence.We included 192 patients. Median age was 31.0 years (IQR 24.7–36.3) and the male to female ratio was 1:4.1. Most patients presented with a minimally invasive FTC (MI‐FTC) (95%). Five patients presented with synchronous metastases (2.6%), including two with locoregional metastases (1%) and three with distant metastases (1.6%). During a median follow‐up of 12.0 years, three patients developed a recurrence (1.6%), of which one patient developed a local recurrence (33%), and two patients a distant recurrence (67%). Five patients died during follow‐up (2.6%). Cause of death was not captured. A Cox proportional hazard model could not be performed due to the low number of recurrences.FTC in AYAs is generally characterized as a low‐risk tumor, as it exhibits a very low recurrence rate, a high overall survival, and it typically presents as MI‐FTC without synchronous metastases. These findings underscore the favorable long‐term oncological prognosis of FTC in AYAs. [ABSTRACT FROM AUTHOR]

Published
2024
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15. Long-term oncological outcomes of follicular thyroid cancer in adolescents and young adults: A nationwide population-based study.

Author

van de Berg DJ, Mooij CF, van Trotsenburg ASP, van Santen HM, Terwisscha van Scheltinga SCEJ, Vriens MR, Kruijff S, Nieveen van Dijkum EJM, Engelsman AF, and Derikx JPM

Abstract

Background: Follicular thyroid carcinoma (FTC) in adolescents and young adults (AYAs) is rare and data on long-term oncological outcomes are scarce. This study aimed to describe the long-term recurrence and survival rates of AYAs with FTC, and identify risk factors for recurrence., Methods: This is a retrospective cohort study combining two national databases, including all patients aged 15-39 years, diagnosed with FTC in The Netherlands between 2000 and 2016. Age, sex, tumor size, focality, positive margins, angioinvasion, pT-stage, and pN-stage were included in a Cox proportional hazard model to identify risk factors for recurrence., Results: We included 192 patients. Median age was 31.0 years (IQR 24.7-36.3) and the male to female ratio was 1:4.1. Most patients presented with a minimally invasive FTC (MI-FTC) (95%). Five patients presented with synchronous metastases (2.6%), including two with locoregional metastases (1%) and three with distant metastases (1.6%). During a median follow-up of 12.0 years, three patients developed a recurrence (1.6%), of which one patient developed a local recurrence (33%), and two patients a distant recurrence (67%). Five patients died during follow-up (2.6%). Cause of death was not captured. A Cox proportional hazard model could not be performed due to the low number of recurrences., Conclusions: FTC in AYAs is generally characterized as a low-risk tumor, as it exhibits a very low recurrence rate, a high overall survival, and it typically presents as MI-FTC without synchronous metastases. These findings underscore the favorable long-term oncological prognosis of FTC in AYAs., (© 2024 The Author(s). World Journal of Surgery published by John Wiley & Sons Ltd on behalf of International Society of Surgery/Société Internationale de Chirurgie (ISS/SIC).)

Published
2024
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