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  3. A Consensus Molecular Classification of Muscle-invasive Bladder Cancer.
 

A Consensus Molecular Classification of Muscle-invasive Bladder Cancer.

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BORIS DOI
10.7892/boris.134921
Date of Publication
April 2020
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Kamoun, Aurélie
de Reyniès, Aurélien
Allory, Yves
Sjödahl, Gottfrid
Robertson, A Gordon
Seiler-Blarer, Roland
Universitätsklinik für Urologie
Hoadley, Katherine A
Groeneveld, Clarice S
Al-Ahmadie, Hikmat
Choi, Woonyoung
Castro, Mauro A A
Fontugne, Jacqueline
Eriksson, Pontus
Mo, Qianxing
Kardos, Jordan
Zlotta, Alexandre
Hartmann, Arndt
Dinney, Colin P
Bellmunt, Joaquim
Powles, Thomas
Malats, Núria
Chan, Keith S
Kim, William Y
McConkey, David J
Black, Peter C
Dyrskjøt, Lars
Höglund, Mattias
Lerner, Seth P
Real, Francisco X
Radvanyi, François
Subject(s)

600 - Technology::610...

Series
European urology
ISSN or ISBN (if monograph)
0302-2838
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.eururo.2019.09.006
PubMed ID
31563503
Uncontrolled Keywords

Consensus Molecular t...

Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/183202
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1-s2.0-S0302283819306955-main.pdftextAdobe PDF3.15 MBAttribution-NonCommercial-NoDerivatives (CC BY-NC-ND 4.0)publishedOpen
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