A Consensus Molecular Classification of Muscle-invasive Bladder Cancer

Aurélie Kamoun(La Ligue Contre le Cancer), Aurélien de Reyniès(La Ligue Contre le Cancer), Yves Allory(Centre National de la Recherche Scientifique), Gottfrid Sjödahl(Lund University), A. Gordon Robertson(BC Cancer Agency), Roland Seiler(University Hospital of Bern), Katherine A. Hoadley(University of North Carolina at Chapel Hill), Clarice S. Groeneveld(Centre National de la Recherche Scientifique), Hikmat Al-Ahmadie(Memorial Sloan Kettering Cancer Center), Woonyoung Choi(Johns Hopkins University), Mauro A.A. Castro(Universidade Federal do Paraná), Jacqueline Fontugne(Centre National de la Recherche Scientifique), Pontus Eriksson(Lund University), Qianxing Mo(Moffitt Cancer Center), Jordan Kardos(University of North Carolina at Chapel Hill), Alexandre Zlotta(Mount Sinai Hospital), Arndt Hartmann(Friedrich-Alexander-Universität Erlangen-Nürnberg), Colin P. Dinney(The University of Texas MD Anderson Cancer Center), Joaquim Bellmunt(Harvard University), Thomas Powles(Queen Mary University of London), Núria Malats(BC Cancer Agency), Keith Syson Chan(Cedars-Sinai Medical Center), William Y. Kim(University of North Carolina at Chapel Hill), David J. McConkey(Johns Hopkins University), Peter C. Black(University of British Columbia), Lars Dyrskjøt(Aarhus University Hospital), Mattias Höglund(Lund University), Seth P. Lerner(Baylor College of Medicine), Francisco X. Real(Spanish National Cancer Research Centre), François Radvanyi(Centre National de la Recherche Scientifique), Mattias Aine, Hikmat Al-Ahmadie(Memorial Sloan Kettering Cancer Center), Yves Allory(Centre National de la Recherche Scientifique), Joaquim Bellmunt(Harvard University), Isabelle Bernard-Pierrot(Laboratoire de Biologie et Modélisation de la Cellule), Peter C. Black(University of British Columbia), Mauro A.A. Castro(Universidade Federal do Paraná), Keith Syson Chan(Cedars-Sinai Medical Center), Woonyoung Choi(Johns Hopkins University), Bogdan Czerniak, Colin P. Dinney(The University of Texas MD Anderson Cancer Center), Lars Dyrskjøt(Aarhus University Hospital), Pontus Eriksson(Lund University), Jacqueline Fontugne(Centre National de la Recherche Scientifique), Ewan A. Gibb, Clarice S. Groeneveld(Centre National de la Recherche Scientifique), Arndt Hartmann(Friedrich-Alexander-Universität Erlangen-Nürnberg), Katherine A. Hoadley(University of North Carolina at Chapel Hill), Mattias Höglund(Lund University), Aurélie Kamoun(La Ligue Contre le Cancer), Jordan Kardos(University of North Carolina at Chapel Hill), Jaegil Kim(University of North Carolina at Chapel Hill), William Y. Kim(University of North Carolina at Chapel Hill), David J. Kwiatkowski, Thierry Lebrét(Université de Versailles Saint-Quentin-en-Yvelines), Seth P. Lerner(Baylor College of Medicine), Fredrik Liedberg, Núria Malats(BC Cancer Agency), David J. McConkey(Johns Hopkins University), Qianxing Mo(Moffitt Cancer Center), Thomas Powles(Queen Mary University of London), François Radvanyi(Centre National de la Recherche Scientifique), Francisco X. Real(Spanish National Cancer Research Centre), Aurélien de Reyniès(La Ligue Contre le Cancer), A. Gordon Robertson(BC Cancer Agency), Arlene O. Siefker‐Radtke, Nanor Sirab(Hôpital René Huguenin), Roland Seiler(University Hospital of Bern), Gottfrid Sjödahl(Lund University), Ann Taber(Friedrich-Alexander-Universität Erlangen-Nürnberg), John N. Weinstein, Alexandre Zlotta(Mount Sinai Hospital)
European Urology
September 26, 2019
Cited by 1,352Open Access
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Abstract

BACKGROUND: Muscle-invasive bladder cancer (MIBC) is a molecularly diverse disease with heterogeneous clinical outcomes. Several molecular classifications have been proposed, but the diversity of their subtype sets impedes their clinical application. OBJECTIVE: To achieve an international consensus on MIBC molecular subtypes that reconciles the published classification schemes. DESIGN, SETTING, AND PARTICIPANTS: We used 1750 MIBC transcriptomic profiles from 16 published datasets and two additional cohorts. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: We performed a network-based analysis of six independent MIBC classification systems to identify a consensus set of molecular classes. Association with survival was assessed using multivariable Cox models. RESULTS AND LIMITATIONS: We report the results of an international effort to reach a consensus on MIBC molecular subtypes. We identified a consensus set of six molecular classes: luminal papillary (24%), luminal nonspecified (8%), luminal unstable (15%), stroma-rich (15%), basal/squamous (35%), and neuroendocrine-like (3%). These consensus classes differ regarding underlying oncogenic mechanisms, infiltration by immune and stromal cells, and histological and clinical characteristics, including outcomes. We provide a single-sample classifier that assigns a consensus class label to a tumor sample's transcriptome. Limitations of the work are retrospective clinical data collection and a lack of complete information regarding patient treatment. CONCLUSIONS: This consensus system offers a robust framework that will enable testing and validation of predictive biomarkers in future prospective clinical trials. PATIENT SUMMARY: Bladder cancers are heterogeneous at the molecular level, and scientists have proposed several classifications into sets of molecular classes. While these classifications may be useful to stratify patients for prognosis or response to treatment, a consensus classification would facilitate the clinical use of molecular classes. Conducted by multidisciplinary expert teams in the field, this study proposes such a consensus and provides a tool for applying the consensus classification in the clinical setting.


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