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Impact of Molecular Subtypes in Muscle-invasive Bladder Cancer on Predicting Response and Survival after Neoadjuvant Chemotherapy.
Seiler, Roland; Ashab, Hussam Al Deen; Erho, Nicholas; van Rhijn, Bas W G; Winters, Brian; Douglas, James; Van Kessel, Kim E; Fransen van de Putte, Elisabeth E; Sommerlad, Matthew; Wang, Natalie Q; Choeurng, Voleak; Gibb, Ewan A; Palmer-Aronsten, Beatrix; Lam, Lucia L; Buerki, Christine; Davicioni, Elai; Sjödahl, Gottfrid; Kardos, Jordan; Hoadley, Katherine A; Lerner, Seth P; McConkey, David J; Choi, Woonyoung; Kim, William Y; Kiss, Bernhard; Thalmann, George N; Todenhöfer, Tilman; Crabb, Simon J; North, Scott; Zwarthoff, Ellen C; Boormans, Joost L; Wright, Jonathan; Dall'Era, Marc; van der Heijden, Michiel S; Black, Peter C.
Afiliación
  • Seiler R; Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada; Department of Urology, University of Bern, Bern, Switzerland.
  • Ashab HAD; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Erho N; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • van Rhijn BWG; Department of Surgical Oncology, Division of Urology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
  • Winters B; Department of Urology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Douglas J; Department of Urology, University Hospital of Southampton, Hampshire, UK.
  • Van Kessel KE; Department of Pathology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Fransen van de Putte EE; Department of Surgical Oncology, Division of Urology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
  • Sommerlad M; Department of Urology, University Hospital of Southampton, Hampshire, UK.
  • Wang NQ; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Choeurng V; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Gibb EA; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Palmer-Aronsten B; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Lam LL; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Buerki C; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Davicioni E; GenomeDx Biosciences, Inc., Vancouver, British Columbia, Canada.
  • Sjödahl G; Division of Urological Research, Department of Translational Medicine, Lund University, Malmö, Sweden.
  • Kardos J; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Hoadley KA; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Lerner SP; Scott Department of Urologic Oncology, Baylor College of Medicine, Houston, Texas, USA.
  • McConkey DJ; Department of Urology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Choi W; Department of Urology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Kim WY; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Kiss B; Department of Urology, University of Bern, Bern, Switzerland.
  • Thalmann GN; Department of Urology, University of Bern, Bern, Switzerland.
  • Todenhöfer T; Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Crabb SJ; Department of Medical Oncology, University Hospital of Southampton, Hampshire, UK.
  • North S; Cross Cancer Institute, Department of Oncology, University of Alberta Edmonton, Alberta, Canada.
  • Zwarthoff EC; Department of Pathology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Boormans JL; Department of Urology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Wright J; Department of Urology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Dall'Era M; UC Davis Comprehensive Cancer Center, Sacramento, California, USA.
  • van der Heijden MS; Department of Surgical Oncology, Division of Urology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
  • Black PC; Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada. Electronic address: pblack@mail.ubc.ca.
Eur Urol ; 72(4): 544-554, 2017 10.
Article en En | MEDLINE | ID: mdl-28390739
ABSTRACT

BACKGROUND:

An early report on the molecular subtyping of muscle-invasive bladder cancer (MIBC) by gene expression suggested that response to neoadjuvant chemotherapy (NAC) varies by subtype.

OBJECTIVE:

To investigate the ability of molecular subtypes to predict pathological downstaging and survival after NAC. DESIGN, SETTING, AND

PARTICIPANTS:

Whole transcriptome profiling was performed on pre-NAC transurethral resection specimens from 343 patients with MIBC. Samples were classified according to four published molecular subtyping methods. We developed a single-sample genomic subtyping classifier (GSC) to predict consensus subtypes (claudin-low, basal, luminal-infiltrated and luminal) with highest clinical impact in the context of NAC. Overall survival (OS) according to subtype was analyzed and compared with OS in 476 non-NAC cases (published datasets). INTERVENTION Gene expression analysis was used to assign subtypes. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

Receiver-operating characteristics were used to determine the accuracy of GSC. The effect of GSC on survival was estimated by Cox proportional hazard regression models. RESULTS AND

LIMITATIONS:

The models generated subtype calls in expected ratios with high concordance across subtyping methods. GSC was able to predict four consensus molecular subtypes with high accuracy (73%), and clinical significance of the predicted consensus subtypes could be validated in independent NAC and non-NAC datasets. Luminal tumors had the best OS with and without NAC. Claudin-low tumors were associated with poor OS irrespective of treatment regimen. Basal tumors showed the most improvement in OS with NAC compared with surgery alone. The main limitations of our study are its retrospective design and comparison across datasets.

CONCLUSIONS:

Molecular subtyping may have an impact on patient benefit to NAC. If validated in additional studies, our results suggest that patients with basal tumors should be prioritized for NAC. We discovered the first single-sample classifier to subtype MIBC, which may be suitable for integration into routine clinical practice. PATIENT

SUMMARY:

Different molecular subtypes can be identified in muscle-invasive bladder cancer. Although cisplatin-based neoadjuvant chemotherapy improves patient outcomes, we identified that the benefit is highest in patients with basal tumors. Our newly discovered classifier can identify these molecular subtypes in a single patient and could be integrated into routine clinical practice after further validation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Vejiga Urinaria / Biomarcadores de Tumor / Terapia Neoadyuvante / Transcriptoma Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur Urol Año: 2017 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Vejiga Urinaria / Biomarcadores de Tumor / Terapia Neoadyuvante / Transcriptoma Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur Urol Año: 2017 Tipo del documento: Article País de afiliación: Suiza