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4. Correction: LiverScreen project: study protocol for screening for liver fibrosis in the general population in European countries

Author

Graupera, Isabel, Thiele, Maja, Ma, Ann T., Serra-Burriel, Miquel, Pich, Judit, Fabrellas, Núria, Caballeria, Llorenç, de Knegt, Robert J., Grgurevic, Ivica, Reichert, Mathias, Roulot, Dominique, Schattenberg, Jörn M., Pericas, Juan M., Angeli, Paolo, Tsochatzis, Emmanuel A., Guha, Indra Neil, Garcia-Retortillo, Montserrat, Morillas, Rosa M., Hernández, Rosario, Hoyo, Jordi, Fuentes, Matilde, Madir, Anita, Juanola, Adrià, Soria, Anna, Juan, Marta, Carol, Marta, Diaz, Alba, Detlefsen, Sönke, Toran, Pere, Pera, Guillem, Fournier, Céline, Llorca, Anne, Newsome, Phillip N., Manns, Michael, de Koning, Harry J., Serra-Burriel, Feliu, Cucchietti, Fernando, Arslanow, Anita, Korenjak, Marko, van Kleef, Laurens, Falcó, Josep Lluis, Kamath, Patrick S., Karlsen, Tom H., Castera, Laurent, Lammert, Frank, Krag, Aleksander, and Ginès, Pere

Published
2023
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6. Trade-Offs Between Harms and Benefits of Different Breast Cancer Screening Intervals Among Low-Risk Women

Author

van Ravesteyn, Nicolien T, Schechter, Clyde B, Hampton, John M, Alagoz, Oguzhan, van den Broek, Jeroen J, Kerlikowske, Karla, Mandelblatt, Jeanne S, Miglioretti, Diana L, Sprague, Brian L, Stout, Natasha K, de Koning, Harry J, Trentham-Dietz, Amy, Tosteson, Anna NA, and Network, from the Breast Cancer Surveillance Consortium and the Cancer Intervention and Surveillance Modeling

Subjects
Cancer, Breast Cancer, Health Services, Clinical Research, Prevention, Good Health and Well Being, Aged, Breast Neoplasms, Early Detection of Cancer, False Positive Reactions, Female, Humans, Mammography, Mass Screening, Middle Aged, Risk, Breast Cancer Surveillance Consortium and the Cancer Intervention and Surveillance Modeling Network, Oncology and Carcinogenesis, Oncology & Carcinogenesis
Abstract

BackgroundA paucity of research addresses breast cancer screening strategies for women at lower-than-average breast cancer risk. The aim of this study was to examine screening harms and benefits among women aged 50-74 years at lower-than-average breast cancer risk by breast density.MethodsThree well-established, validated Cancer Intervention and Surveillance Network models were used to estimate the lifetime benefits and harms of different screening scenarios, varying by screening interval (biennial, triennial). Breast cancer deaths averted, life-years and quality-adjusted life-years gained, false-positives, benign biopsies, and overdiagnosis were assessed by relative risk (RR) level (0.6, 0.7, 0.85, 1 [average risk]) and breast density category, for US women born in 1970.ResultsScreening benefits decreased proportionally with decreasing risk and with lower breast density. False-positives, unnecessary biopsies, and the percentage overdiagnosis also varied substantially by breast density category; false-positives and unnecessary biopsies were highest in the heterogeneously dense category. For women with fatty or scattered fibroglandular breast density and a relative risk of no more than 0.85, the additional deaths averted and life-years gained were small with biennial vs triennial screening. For these groups, undergoing 4 additional screens (screening biennially [13 screens] vs triennially [9 screens]) averted no more than 1 additional breast cancer death and gained no more than 16 life-years and no more than 10 quality-adjusted life-years per 1000 women but resulted in up to 232 more false-positives per 1000 women.ConclusionTriennial screening from age 50 to 74 years may be a reasonable screening strategy for women with lower-than-average breast cancer risk and fatty or scattered fibroglandular breast density.

Published
2021

7. Development, validation, and prognostic evaluation of a risk score for long-term liver-related outcomes in the general population: a multicohort study

Author

Alvarez, Marifé, Andersen, Peter, Angeli, Paolo, Ardèvol, Alba, Arslanow, Anita, Beggiato, Luca, Ben Abdesselam, Zahia, Bennett, Lucy, Boutouria, Bajiha, Brocca, Alessandra, Broquetas, M. Teresa, Caballeria, Llorenç, Calvino, Valeria, Camacho, Judith, Capdevila, Aura, Carol, Marta, Castera, Laurent, Cervera, Marta, Cucchietti, Fernando, de Fuentes, Anna, de Knegt, Rob, de Koning, Harry J, Detlefsen, Sonke, Diaz, Alba, Diéguez Bande, José, Esnault, Vanessa, Fabrellas, Núria, Falcó, Josep Lluis, Fernández, Rosa, Fournier, Céline, Fuentes, Matilde, Galle, Peter, García, Edgar, García-Retortillo, Montserrat, Garrido, Esther, Ginès, Pere, Gordillo Medina, Rosa, Gratacós-Ginès, Jordi, Graupera, Isabel, Grgurevic, Ivica, Guha, Indra Neil, Guix, Eva, Hansen, Johanne Kragh, Harris, Rebecca, Hernández Boluda, Elena, Hernández-Ibañez, Rosario, Hoyo, Jordi, Ikram, Arfan, Incicco, Simone, Israelsen, Mads, Juan, Marta, Juanola, Adrià, Kaiser, Ralf, Kamath, Patrick S, Karlsen, Tom H, Kjærgaard, Maria, Korenjak, Marko, Krag, Aleksander, Krawczyk, Marcin, Laboulaye, Philippe, Lambert, Irina, Lammert, Frank, Langkjær Sørensen, Simon, Laserna-Jiménez, Cristina, Lazaro Pi, Sonia, Ledain, Elsa, Levy, Vincent, Lindvig, Katrine Prier, Llorca, Anne, Londoño, Vanessa, Loyer, Guirec, Ma, Ann T., Madir, Anita, Manns, Michael, Marshall, Denise, Martí, M. Lluïsa, Martínez, Sara, Martínez Sala, Ricard, Masa-Font, Roser, Møller Jensen, Jane, Morillas, Rosa M, Muñoz, Laura, Nadal, Ruth, Napoleone, Laura, Navarrete, JM, Newsome, Phillip N, Nielsen, Vibeke, Pérez, Martina, Pericás-Pulido, Juan Manuel, Piano, Salvatore, Pich, Judit, Pose, Elisa, Presas Escobet, Judit, Reichert, Matthias, Riba, Carlota, Roulot, Dominique, Rubio, Ana Belén, Sánchez-Morata, Maria, Schattenberg, Jörn, Serra-Burriel, Miquel, Serra-Burriel, Feliu, Skovborg Just, Louise, Sonneveld, Milan, Soria, Anna, Stern, Christiane, Such, Patricia, Thiele, Maja, Tonon, Marta, Toran, Pere, Torrejón, Antoni, Tsochatzis, Emmanuel A, van Kleef, Laurens, van Wijngaarden, Paulien, Velázquez, Vanessa, Viu, Ana, Weber, Susanne Nicole, Wildsmith, Tracey, Pera, Guillem, Reichert, Mathias, Pericàs, Juan M, Schattenberg, Jörn M, Tsochatztis, Emmanuel A, Garcia-Retortillo, Montserrat, Hernández, Rosario, Expósito, Carmen, Martínez, Alba, Detlefsen, Sönke, Martini, Andrea, Ma, Ann T, Pich, Judith, Bonfill, Eva, Navarrete, J M, Hernáez, Rubén, Allen, Alina, de Knegt, Robert J, and Wong, Vincent Wai-Sun

Published
2023
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8. The Impact of Model Assumptions on Personalized Lung Cancer Screening Recommendations

Author

ten Haaf, Kevin, primary, de Nijs, Koen, additional, Simoni, Giulia, additional, Alban, Andres, additional, Cao, Pianpian, additional, Sun, Zhuolu, additional, Yong, Jean, additional, Jeon, Jihyoun, additional, Toumazis, Iakovos, additional, Han, Summer S., additional, Gazelle, G. Scott, additional, Kong, Chung Ying, additional, Plevritis, Sylvia K., additional, Meza, Rafael, additional, and de Koning, Harry J., additional

Published
2024
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10. Early detection of obstructive coronary artery disease in the asymptomatic high-risk population: objectives and study design of the EARLY-SYNERGY trial

Author

Ties, Daan, van Dorp, Paulien, Pundziute, Gabija, van der Aalst, Carlijn M., Gratama, Jan Willem C., Braam, Richard L., Kuijpers, Dirkjan, Lubbers, Daniël D., van der Bilt, Ivo A.C., Westenbrink, B. Daan, Wolcherink, Martijn J. Oude, Doggen, Carine J.M., Išgum, Ivana, Nijveldt, Robin, de Koning, Harry J., Vliegenthart, Rozemarijn, Oudkerk, Matthijs, and van der Harst, Pim

Published
2022
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12. LiverScreen project: study protocol for screening for liver fibrosis in the general population in European countries

Author

Graupera, Isabel, Thiele, Maja, Ma, Ann T., Serra-Burriel, Miquel, Pich, Judit, Fabrellas, Núria, Caballeria, Llorenç, de Knegt, Robert J., Grgurevic, Ivica, Reichert, Mathias, Roulot, Dominique, Schattenberg, Jörn M., Pericas, Juan M., Angeli, Paolo, Tsochatzis, Emmanuel A., Guha, Indra Neil, Garcia-Retortillo, Montserrat, Morillas, Rosa M., Hernández, Rosario, Hoyo, Jordi, Fuentes, Matilde, Madir, Anita, Juanola, Adrià, Soria, Anna, Juan, Marta, Carol, Marta, Diaz, Alba, Detlefsen, Sönke, Toran, Pere, Pera, Guillem, Fournier, Céline, Llorca, Anne, Newsome, Phillip N., Manns, Michael, de Koning, Harry J., Serra-Burriel, Feliu, Cucchietti, Fernando, Arslanow, Anita, Korenjak, Marko, van Kleef, Laurens, Falcó, Josep Lluis, Kamath, Patrick S., Karlsen, Tom H., Castera, Laurent, Lammert, Frank, Krag, Aleksander, and Ginès, Pere

Published
2022
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19. Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

Author

Hobbs, Brian D, de Jong, Kim, Lamontagne, Maxime, Bossé, Yohan, Shrine, Nick, Artigas, María Soler, Wain, Louise V, Hall, Ian P, Jackson, Victoria E, Wyss, Annah B, London, Stephanie J, North, Kari E, Franceschini, Nora, Strachan, David P, Beaty, Terri H, Hokanson, John E, Crapo, James D, Castaldi, Peter J, Chase, Robert P, Bartz, Traci M, Heckbert, Susan R, Psaty, Bruce M, Gharib, Sina A, Zanen, Pieter, Lammers, Jan W, Oudkerk, Matthijs, Groen, HJ, Locantore, Nicholas, Tal-Singer, Ruth, Rennard, Stephen I, Vestbo, Jørgen, Timens, Wim, Paré, Peter D, Latourelle, Jeanne C, Dupuis, Josée, O'Connor, George T, Wilk, Jemma B, Kim, Woo Jin, Lee, Mi Kyeong, Oh, Yeon-Mok, Vonk, Judith M, de Koning, Harry J, Leng, Shuguang, Belinsky, Steven A, Tesfaigzi, Yohannes, Manichaikul, Ani, Wang, Xin-Qun, Rich, Stephen S, Barr, R Graham, Sparrow, David, Litonjua, Augusto A, Bakke, Per, Gulsvik, Amund, Lahousse, Lies, Brusselle, Guy G, Stricker, Bruno H, Uitterlinden, André G, Ampleford, Elizabeth J, Bleecker, Eugene R, Woodruff, Prescott G, Meyers, Deborah A, Qiao, Dandi, Lomas, David A, Yim, Jae-Joon, Kim, Deog Kyeom, Hawrylkiewicz, Iwona, Sliwinski, Pawel, Hardin, Megan, Fingerlin, Tasha E, Schwartz, David A, Postma, Dirkje S, MacNee, William, Tobin, Martin D, Silverman, Edwin K, Boezen, H Marike, and Cho, Michael H

Subjects
Biological Sciences, Genetics, Chronic Obstructive Pulmonary Disease, Lung, Human Genome, Clinical Research, Aetiology, 2.1 Biological and endogenous factors, Respiratory, Adult, Aged, Aged, 80 and over, Alleles, Asthma, Female, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Middle Aged, Phenotype, Polymorphism, Single Nucleotide, Pulmonary Disease, Chronic Obstructive, Pulmonary Fibrosis, Risk Factors, Smoking, COPDGene Investigators, ECLIPSE Investigators, LifeLines Investigators, SPIROMICS Research Group, International COPD Genetics Network Investigators, UK BiLEVE Investigators, International COPD Genetics Consortium, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology
Abstract

Chronic obstructive pulmonary disease (COPD) is a leading cause of mortality worldwide. We performed a genetic association study in 15,256 cases and 47,936 controls, with replication of select top results (P < 5 × 10-6) in 9,498 cases and 9,748 controls. In the combined meta-analysis, we identified 22 loci associated at genome-wide significance, including 13 new associations with COPD. Nine of these 13 loci have been associated with lung function in general population samples, while 4 (EEFSEC, DSP, MTCL1, and SFTPD) are new. We noted two loci shared with pulmonary fibrosis (FAM13A and DSP) but that had opposite risk alleles for COPD. None of our loci overlapped with genome-wide associations for asthma, although one locus has been implicated in joint susceptibility to asthma and obesity. We also identified genetic correlation between COPD and asthma. Our findings highlight new loci associated with COPD, demonstrate the importance of specific loci associated with lung function to COPD, and identify potential regions of genetic overlap between COPD and other respiratory diseases.

Published
2017

20. Incidence of Interval Colorectal Cancer After Negative Results From First-Round Fecal Immunochemical Screening Tests, by Cutoff Value and Participant Sex and Age

Author

van der Beek, A., Otte, J.A., Wiersma, Tj., Masclee, A.A.M., van Bergeijk, J., Meijer, G., de Graaf, E.J.R., van Grevenstein, W.M.U., Frasa, M., Jacobs, L.H.J., Stoker, J., Vink, G., Elferink, M.A., Toes-Zoutendijk, Esther, Kooyker, Arthur I., Dekker, Evelien, Spaander, Manon C.W., Opstal-van Winden, Annemieke W.J., Ramakers, Christian, Buskermolen, Maaike, van Vuuren, Anneke J., Kuipers, Ernst J., van Kemenade, Folkert J., Velthuysen, Marie-Louise F., Thomeer, Maarten G.J., van Veldhuizen, Harriët, van Ballegooijen, Marjolein, Nagtegaal, Iris D., de Koning, Harry J., van Leerdam, Monique E., and Lansdorp-Vogelaar, Iris

Published
2020
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21. Radiation-Induced Breast Cancer Incidence and Mortality From Digital Mammography Screening: A Modeling Study.

Author

Miglioretti, Diana L, Lange, Jane, van den Broek, Jeroen J, Lee, Christoph I, van Ravesteyn, Nicolien T, Ritley, Dominique, Kerlikowske, Karla, Fenton, Joshua J, Melnikow, Joy, de Koning, Harry J, and Hubbard, Rebecca A

Subjects
Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Cancer, Prevention, Clinical Research, Health Services, Biomedical Imaging, Breast Cancer, Good Health and Well Being, Adult, Aged, Breast, Breast Neoplasms, Computer Simulation, Early Detection of Cancer, Female, Humans, Incidence, Mammography, Mass Screening, Middle Aged, Neoplasms, Radiation-Induced, Radiation Dosage, Risk Factors, United States, Clinical Sciences, Public Health and Health Services
Abstract

BackgroundEstimates of risk for radiation-induced breast cancer from mammography screening have not considered variation in dose exposure or diagnostic work-up after abnormal screening results.ObjectiveTo estimate distributions of radiation-induced breast cancer incidence and mortality from digital mammography screening while considering exposure from screening and diagnostic mammography and dose variation among women.Design2 simulation-modeling approaches.SettingU.S. population.PatientsWomen aged 40 to 74 years.InterventionAnnual or biennial digital mammography screening from age 40, 45, or 50 years until age 74 years.MeasurementsLifetime breast cancer deaths averted (benefits) and radiation-induced breast cancer incidence and mortality (harms) per 100,000 women screened.ResultsAnnual screening of 100,000 women aged 40 to 74 years was projected to induce 125 breast cancer cases (95% CI, 88 to 178) leading to 16 deaths (CI, 11 to 23), relative to 968 breast cancer deaths averted by early detection from screening. Women exposed at the 95th percentile were projected to develop 246 cases of radiation-induced breast cancer leading to 32 deaths per 100,000 women. Women with large breasts requiring extra views for complete examination (8% of population) were projected to have greater radiation-induced breast cancer risk (266 cancer cases and 35 deaths per 100,000 women) than other women (113 cancer cases and 15 deaths per 100,000 women). Biennial screening starting at age 50 years reduced risk for radiation-induced cancer 5-fold.LimitationLife-years lost from radiation-induced breast cancer could not be estimated.ConclusionRadiation-induced breast cancer incidence and mortality from digital mammography screening are affected by dose variability from screening, resultant diagnostic work-up, initiation age, and screening frequency. Women with large breasts may have a greater risk for radiation-induced breast cancer.Primary funding sourceAgency for Healthcare Research and Quality, U.S. Preventive Services Task Force, National Cancer Institute.

Published
2016

22. Collaborative Modeling of the Benefits and Harms Associated With Different U.S. Breast Cancer Screening Strategies.

Author

Mandelblatt, Jeanne S, Stout, Natasha K, Schechter, Clyde B, van den Broek, Jeroen J, Miglioretti, Diana L, Krapcho, Martin, Trentham-Dietz, Amy, Munoz, Diego, Lee, Sandra J, Berry, Donald A, van Ravesteyn, Nicolien T, Alagoz, Oguzhan, Kerlikowske, Karla, Tosteson, Anna NA, Near, Aimee M, Hoeffken, Amanda, Chang, Yaojen, Heijnsdijk, Eveline A, Chisholm, Gary, Huang, Xuelin, Huang, Hui, Ergun, Mehmet Ali, Gangnon, Ronald, Sprague, Brian L, Plevritis, Sylvia, Feuer, Eric, de Koning, Harry J, and Cronin, Kathleen A

Subjects
Breast, Humans, Breast Neoplasms, False Positive Reactions, Mammography, Mass Screening, Incidence, Risk Assessment, Age Factors, Comorbidity, Time Factors, Computer Simulation, Adult, Aged, Middle Aged, United States, Female, Early Detection of Cancer, Prevention, Health Services, Cancer, Clinical Research, Breast Cancer, Biomedical Imaging, Good Health and Well Being, Medical and Health Sciences, General & Internal Medicine
Abstract

BackgroundControversy persists about optimal mammography screening strategies.ObjectiveTo evaluate screening outcomes, taking into account advances in mammography and treatment of breast cancer.DesignCollaboration of 6 simulation models using national data on incidence, digital mammography performance, treatment effects, and other-cause mortality.SettingUnited States.PatientsAverage-risk U.S. female population and subgroups with varying risk, breast density, or comorbidity.InterventionEight strategies differing by age at which screening starts (40, 45, or 50 years) and screening interval (annual, biennial, and hybrid [annual for women in their 40s and biennial thereafter]). All strategies assumed 100% adherence and stopped at age 74 years.MeasurementsBenefits (breast cancer-specific mortality reduction, breast cancer deaths averted, life-years, and quality-adjusted life-years); number of mammograms used; harms (false-positive results, benign biopsies, and overdiagnosis); and ratios of harms (or use) and benefits (efficiency) per 1000 screens.ResultsBiennial strategies were consistently the most efficient for average-risk women. Biennial screening from age 50 to 74 years avoided a median of 7 breast cancer deaths versus no screening; annual screening from age 40 to 74 years avoided an additional 3 deaths, but yielded 1988 more false-positive results and 11 more overdiagnoses per 1000 women screened. Annual screening from age 50 to 74 years was inefficient (similar benefits, but more harms than other strategies). For groups with a 2- to 4-fold increased risk, annual screening from age 40 years had similar harms and benefits as screening average-risk women biennially from 50 to 74 years. For groups with moderate or severe comorbidity, screening could stop at age 66 to 68 years.LimitationOther imaging technologies, polygenic risk, and nonadherence were not considered.ConclusionBiennial screening for breast cancer is efficient for average-risk populations. Decisions about starting ages and intervals will depend on population characteristics and the decision makers' weight given to the harms and benefits of screening.Primary funding sourceNational Institutes of Health.

Published
2016

26. Benefits, harms, and cost-effectiveness of supplemental ultrasonography screening for women with dense breasts.

Author

Sprague, Brian L, Stout, Natasha K, Schechter, Clyde, van Ravesteyn, Nicolien T, Cevik, Mucahit, Alagoz, Oguzhan, Lee, Christoph I, van den Broek, Jeroen J, Miglioretti, Diana L, Mandelblatt, Jeanne S, de Koning, Harry J, Kerlikowske, Karla, Lehman, Constance D, and Tosteson, Anna NA

Subjects
Reproductive Medicine, Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Women's Health, Cancer, Health Services, Breast Cancer, Clinical Research, Biomedical Imaging, Cost Effectiveness Research, Prevention, Comparative Effectiveness Research, Good Health and Well Being, Aged, Biopsy, Breast, Breast Neoplasms, Computer Simulation, Cost-Benefit Analysis, Early Detection of Cancer, False Positive Reactions, Female, Humans, Mammography, Mass Screening, Middle Aged, Quality-Adjusted Life Years, Risk Factors, Sensitivity and Specificity, Ultrasonography, Mammary, United States, Clinical Sciences, Public Health and Health Services
Abstract

BackgroundMany states have laws requiring mammography facilities to tell women with dense breasts and negative results on screening mammography to discuss supplemental screening tests with their providers. The most readily available supplemental screening method is ultrasonography, but little is known about its effectiveness.ObjectiveTo evaluate the benefits, harms, and cost-effectiveness of supplemental ultrasonography screening for women with dense breasts.DesignComparative modeling with 3 validated simulation models.Data sourcesSurveillance, Epidemiology, and End Results Program; Breast Cancer Surveillance Consortium; and medical literature.Target populationContemporary cohort of women eligible for routine screening.Time horizonLifetime.PerspectivePayer.InterventionSupplemental ultrasonography screening for women with dense breasts after a negative screening mammography result.Outcome measuresBreast cancer deaths averted, quality-adjusted life-years (QALYs) gained, biopsies recommended after a false-positive ultrasonography result, and costs.Results of base-case analysisSupplemental ultrasonography screening after a negative mammography result for women aged 50 to 74 years with heterogeneously or extremely dense breasts averted 0.36 additional breast cancer deaths (range across models, 0.14 to 0.75), gained 1.7 QALYs (range, 0.9 to 4.7), and resulted in 354 biopsy recommendations after a false-positive ultrasonography result (range, 345 to 421) per 1000 women with dense breasts compared with biennial screening by mammography alone. The cost-effectiveness ratio was $325,000 per QALY gained (range, $112,000 to $766,000). Supplemental ultrasonography screening for only women with extremely dense breasts cost $246,000 per QALY gained (range, $74,000 to $535,000).Results of sensitivity analysisThe conclusions were not sensitive to ultrasonography performance characteristics, screening frequency, or starting age.LimitationProvider costs for coordinating supplemental ultrasonography were not considered.ConclusionSupplemental ultrasonography screening for women with dense breasts would substantially increase costs while producing relatively small benefits.Primary funding sourceNational Cancer Institute.

Published
2015

29. MRI versus mammography for breast cancer screening in women with familial risk (FaMRIsc): a multicentre, randomised, controlled trial

Author

van Deurzen, Carolien HM, Loo, Claudette E, Wesseling, Jelle, Schlooz-Vries, Margrethe, van der Meij, Suzan, Mesker, Wilma, Keymeulen, Kristien, Contant, Carolien, Madsen, Eva, Koppert, Linetta B, Rothbarth, Joost, Veldhuis, Wouter B, Witkamp, Arjen J, Tetteroo, Eric, de Monye, Cecile, van Rosmalen, Mandy M, Remmelzwaal, Jolanda, Gort, Huub B W, Roi-Antonides, Roelie, Wasser, Martin NJM, van Druten, Edith, Saadatmand, Sepideh, Geuzinge, H Amarens, Rutgers, Emiel J T, Mann, Ritse M, de Roy van Zuidewijn, Diderick B W, Zonderland, Harmien M, Tollenaar, Rob A E M, Lobbes, Marc B I, Ausems, Margreet G E M, van 't Riet, Martijne, Hooning, Maartje J, Mares-Engelberts, Ingeborg, Luiten, Ernest J T, Heijnsdijk, Eveline A M, Verhoef, Cees, Karssemeijer, Nico, Oosterwijk, Jan C, Obdeijn, Inge-Marie, de Koning, Harry J, and Tilanus-Linthorst, Madeleine M A

Published
2019
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33. Benefits, Harms, and Costs for Breast Cancer Screening After US Implementation of Digital Mammography

Author

Stout, Natasha K, Lee, Sandra J, Schechter, Clyde B, Kerlikowske, Karla, Alagoz, Oguzhan, Berry, Donald, Buist, Diana SM, Cevik, Mucahit, Chisholm, Gary, de Koning, Harry J, Huang, Hui, Hubbard, Rebecca A, Miglioretti, Diana L, Munsell, Mark F, Trentham-Dietz, Amy, van Ravesteyn, Nicolien T, Tosteson, Anna NA, and Mandelblatt, Jeanne S

Subjects
Cost Effectiveness Research, Clinical Research, Health Services, Cancer, Biomedical Imaging, Breast Cancer, Prevention, Good Health and Well Being, Adult, Aged, Breast Neoplasms, Cost-Benefit Analysis, Direct Service Costs, Early Detection of Cancer, False Positive Reactions, Female, Humans, Mammography, Mass Screening, Middle Aged, Predictive Value of Tests, Quality-Adjusted Life Years, Sensitivity and Specificity, Time Factors, United States, Oncology and Carcinogenesis, Oncology & Carcinogenesis
Abstract

BackgroundCompared with film, digital mammography has superior sensitivity but lower specificity for women aged 40 to 49 years and women with dense breasts. Digital has replaced film in virtually all US facilities, but overall population health and cost from use of this technology are unclear.MethodsUsing five independent models, we compared digital screening strategies starting at age 40 or 50 years applied annually, biennially, or based on density with biennial film screening from ages 50 to 74 years and with no screening. Common data elements included cancer incidence and test performance, both modified by breast density. Lifetime outcomes included mortality, quality-adjusted life-years, and screening and treatment costs.ResultsFor every 1000 women screened biennially from age 50 to 74 years, switching to digital from film yielded a median within-model improvement of 2 life-years, 0.27 additional deaths averted, 220 additional false-positive results, and $0.35 million more in costs. For an individual woman, this translates to a health gain of 0.73 days. Extending biennial digital screening to women ages 40 to 49 years was cost-effective, although results were sensitive to quality-of-life decrements related to screening and false positives. Targeting annual screening by density yielded similar outcomes to targeting by age. Annual screening approaches could increase costs to $5.26 million per 1000 women, in part because of higher numbers of screens and false positives, and were not efficient or cost-effective.ConclusionsThe transition to digital breast cancer screening in the United States increased total costs for small added health benefits. The value of digital mammography screening among women aged 40 to 49 years depends on women's preferences regarding false positives.

Published
2014

34. Development, validation, and prognostic evaluation of a risk score for long-term liver-related outcomes in the general population: a multicohort study

Author

Serra-Burriel, Miquel, primary, Juanola, Adrià, additional, Serra-Burriel, Feliu, additional, Thiele, Maja, additional, Graupera, Isabel, additional, Pose, Elisa, additional, Pera, Guillem, additional, Grgurevic, Ivica, additional, Caballeria, Llorenç, additional, Piano, Salvatore, additional, van Kleef, Laurens, additional, Reichert, Mathias, additional, Roulot, Dominique, additional, Pericàs, Juan M, additional, Schattenberg, Jörn M, additional, Tsochatztis, Emmanuel A, additional, Guha, Indra Neil, additional, Garcia-Retortillo, Montserrat, additional, Hernández, Rosario, additional, Hoyo, Jordi, additional, Fuentes, Matilde, additional, Expósito, Carmen, additional, Martínez, Alba, additional, Such, Patricia, additional, Madir, Anita, additional, Detlefsen, Sönke, additional, Tonon, Marta, additional, Martini, Andrea, additional, Ma, Ann T, additional, Pich, Judith, additional, Bonfill, Eva, additional, Juan, Marta, additional, Soria, Anna, additional, Carol, Marta, additional, Gratacós-Ginès, Jordi, additional, Morillas, Rosa M, additional, Toran, Pere, additional, Navarrete, J M, additional, Torrejón, Antoni, additional, Fournier, Céline, additional, Llorca, Anne, additional, Arslanow, Anita, additional, de Koning, Harry J, additional, Cucchietti, Fernando, additional, Manns, Michael, additional, Newsome, Phillip N, additional, Hernáez, Rubén, additional, Allen, Alina, additional, Angeli, Paolo, additional, de Knegt, Robert J, additional, Karlsen, Tom H, additional, Galle, Peter, additional, Wong, Vincent Wai-Sun, additional, Fabrellas, Núria, additional, Castera, Laurent, additional, Krag, Aleksander, additional, Lammert, Frank, additional, Kamath, Patrick S, additional, Ginès, Pere, additional, Alvarez, Marifé, additional, Andersen, Peter, additional, Ardèvol, Alba, additional, Beggiato, Luca, additional, Ben Abdesselam, Zahia, additional, Bennett, Lucy, additional, Boutouria, Bajiha, additional, Brocca, Alessandra, additional, Broquetas, M. Teresa, additional, Calvino, Valeria, additional, Camacho, Judith, additional, Capdevila, Aura, additional, Cervera, Marta, additional, de Fuentes, Anna, additional, de Knegt, Rob, additional, Detlefsen, Sonke, additional, Diaz, Alba, additional, Diéguez Bande, José, additional, Esnault, Vanessa, additional, Falcó, Josep Lluis, additional, Fernández, Rosa, additional, García, Edgar, additional, García-Retortillo, Montserrat, additional, Garrido, Esther, additional, Gordillo Medina, Rosa, additional, Guix, Eva, additional, Hansen, Johanne Kragh, additional, Harris, Rebecca, additional, Hernández Boluda, Elena, additional, Hernández-Ibañez, Rosario, additional, Ikram, Arfan, additional, Incicco, Simone, additional, Israelsen, Mads, additional, Kaiser, Ralf, additional, Kjærgaard, Maria, additional, Korenjak, Marko, additional, Krawczyk, Marcin, additional, Laboulaye, Philippe, additional, Lambert, Irina, additional, Langkjær Sørensen, Simon, additional, Laserna-Jiménez, Cristina, additional, Lazaro Pi, Sonia, additional, Ledain, Elsa, additional, Levy, Vincent, additional, Lindvig, Katrine Prier, additional, Londoño, Vanessa, additional, Loyer, Guirec, additional, Ma, Ann T., additional, Marshall, Denise, additional, Martí, M. Lluïsa, additional, Martínez, Sara, additional, Martínez Sala, Ricard, additional, Masa-Font, Roser, additional, Møller Jensen, Jane, additional, Muñoz, Laura, additional, Nadal, Ruth, additional, Napoleone, Laura, additional, Navarrete, JM, additional, Nielsen, Vibeke, additional, Pérez, Martina, additional, Pericás-Pulido, Juan Manuel, additional, Pich, Judit, additional, Presas Escobet, Judit, additional, Reichert, Matthias, additional, Riba, Carlota, additional, Rubio, Ana Belén, additional, Sánchez-Morata, Maria, additional, Schattenberg, Jörn, additional, Serra-Burriel, Miquel, additional, Skovborg Just, Louise, additional, Sonneveld, Milan, additional, Stern, Christiane, additional, Tsochatzis, Emmanuel A, additional, van Wijngaarden, Paulien, additional, Velázquez, Vanessa, additional, Viu, Ana, additional, Weber, Susanne Nicole, additional, and Wildsmith, Tracey, additional

Published
2023
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39. Accuracy of screening women at familial risk of breast cancer without a known gene mutation: Individual patient data meta-analysis

Author

Phi, Xuan-Anh, Houssami, Nehmat, Hooning, Maartje J., Riedl, Christopher C., Leach, Martin O., Sardanelli, Francesco, Warner, Ellen, Trop, Isabelle, Saadatmand, Sepideh, Tilanus-Linthorst, Madeleine M.A., Helbich, Thomas H., van den Heuvel, Edwin R., de Koning, Harry J., Obdeijn, Inge-Marie, and de Bock, Geertruida H.

Published
2017
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48. Data from Differences in Natural History between Breast Cancers in BRCA1 and BRCA2 Mutation Carriers and Effects of MRI Screening-MRISC, MARIBS, and Canadian Studies Combined

Author

Heijnsdijk, Eveline A.M., primary, Warner, Ellen, primary, Gilbert, Fiona J., primary, Tilanus-Linthorst, Madeleine M.A., primary, Evans, Gareth, primary, Causer, Petrina A., primary, Eeles, Rosalind A., primary, Kaas, Reinie, primary, Draisma, Gerrit, primary, Ramsay, Elizabeth A., primary, Warren, Ruth M.L., primary, Hill, Kimberly A., primary, Hoogerbrugge, Nicoline, primary, Wasser, Martin N.J.M., primary, Bergers, Elisabeth, primary, Oosterwijk, Jan C., primary, Hooning, Maartje J., primary, Rutgers, Emiel J.T., primary, Klijn, Jan G.M., primary, Plewes, Don B., primary, Leach, Martin O., primary, and de Koning, Harry J., primary

Published
2023
Full Text
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