Your browser doesn't support javascript.
loading
Role of Androgen Receptor Variants in Prostate Cancer: Report from the 2017 Mission Androgen Receptor Variants Meeting.
Luo, Jun; Attard, Gerhardt; Balk, Steven P; Bevan, Charlotte; Burnstein, Kerry; Cato, Laura; Cherkasov, Artem; De Bono, Johann S; Dong, Yan; Gao, Allen C; Gleave, Martin; Heemers, Hannelore; Kanayama, Mayuko; Kittler, Ralf; Lang, Joshua M; Lee, Richard J; Logothetis, Christopher J; Matusik, Robert; Plymate, Stephen; Sawyers, Charles L; Selth, Luke A; Soule, Howard; Tilley, Wayne; Weigel, Nancy L; Zoubeidi, Amina; Dehm, Scott M; Raj, Ganesh V.
Afiliação
  • Luo J; Department of Urology, James Buchanan Brady Urological Institute, Johns Hopkins University, Baltimore, MD, USA. Electronic address: jluo1@jhmi.edu.
  • Attard G; The Institute of Cancer Research, London, UK.
  • Balk SP; Hematology-Oncology Division, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Bevan C; Department of Surgery & Cancer, Imperial College London, Imperial Centre for Translational & Experimental Medicine (ICTEM), Hammersmith Hospital Campus, London, UK.
  • Burnstein K; Department of Molecular & Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Cato L; Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.
  • Cherkasov A; Department of Urologic Sciences, University of British Columbia, The Vancouver Prostate Centre, Vancouver, BC, Canada.
  • De Bono JS; Division of Clinical Studies, The Institute of Cancer Research, London, UK.
  • Dong Y; Department of Structural and Cellular Biology, Tulane University School of Medicine, New Orleans, LA, USA.
  • Gao AC; Department of Urology, University of California Davis, Sacramento, CA, USA.
  • Gleave M; Department of Urologic Sciences, University of British Columbia, The Vancouver Prostate Centre, Vancouver, BC, Canada.
  • Heemers H; Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA; Department of Urology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA; Department of Hematology/Medical Oncology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Kanayama M; Department of Urology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Kittler R; McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX, USA.
  • Lang JM; Department of Medicine, Carbone Cancer Center, University of Wisconsin, Madison, WI, USA.
  • Lee RJ; Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Logothetis CJ; Division of Cancer Medicine, Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Matusik R; Department of Urologic Surgery, Vanderbilt Prostate Cancer Center, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Plymate S; Department of Medicine, University of Washington and VAPSHCS GRECC, Seattle, WA, USA.
  • Sawyers CL; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Selth LA; Dame Roma Mitchell Cancer Research Laboratories and Freemasons Foundation Centre for Men's Health, Adelaide Medical School, The University of Adelaide, SA, Australia.
  • Soule H; Prostate Cancer Foundation, Santa Monica, CA, USA.
  • Tilley W; Dame Roma Mitchell Cancer Research Laboratories and Freemasons Foundation Centre for Men's Health, Adelaide Medical School, The University of Adelaide, SA, Australia.
  • Weigel NL; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA.
  • Zoubeidi A; Department of Urologic Sciences, University of British Columbia, The Vancouver Prostate Centre, Vancouver, BC, Canada.
  • Dehm SM; Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA; Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA; Department of Urology, University of Minnesota, Minneapolis, MN, USA. Electronic address: dehm@umn.edu.
  • Raj GV; Department of Urology, UT Southwestern Medical Center at Dallas, Dallas, TX, USA; Department of Urology and Pharmacology, UT Southwestern Medical Center at Dallas, Dallas, TX, USA. Electronic address: ganesh.raj@utsouthwestern.edu.
Eur Urol ; 73(5): 715-723, 2018 05.
Article em En | MEDLINE | ID: mdl-29258679
ABSTRACT
CONTEXT Although a number of studies have demonstrated the importance of constitutively active androgen receptor variants (AR-Vs) in prostate cancer, questions still remain about the precise role of AR-Vs in the progression of castration-resistant prostate cancer (CRPC).

OBJECTIVE:

Key stakeholders and opinion leaders in prostate cancer convened on May 11, 2017 in Boston to establish the current state of the field of AR-Vs. EVIDENCE ACQUISITION The meeting "Mission Androgen Receptor Variants" was the second of its kind sponsored by the Prostate Cancer Foundation (PCF). This invitation-only event was attended by international leaders in the field and representatives from sponsoring organizations (PCF and industry sponsors). Eighteen faculty members gave short presentations, which were followed by in-depth discussions. Discussions focused on three thematic topics (1) potential of AR-Vs as biomarkers of therapeutic resistance; (2) role of AR-Vs as functionally active CRPC progression drivers; and (3) utility of AR-Vs as therapeutic targets in CRPC. EVIDENCE

SYNTHESIS:

The three meeting organizers synthesized this meeting report, which is intended to summarize major data discussed at the meeting and identify key questions as well as strategies for addressing these questions. There was a critical consensus that further study of the AR-Vs is an important research focus in CRPC. Contrasting views and emphasis, each supported by data, were presented at the meeting, discussed among the participants, and synthesized in this report.

CONCLUSIONS:

This article highlights the state of knowledge and outlines the most pressing questions that need to be addressed to advance the AR-V field. PATIENT

SUMMARY:

Although further investigation is needed to delineate the role of androgen receptor (AR) variants in metastatic castration-resistant prostate cancer, advances in measurement science have enabled development of blood-based tests for treatment selection. Detection of AR variants (eg, AR-V7) identified a patient population with poor outcomes to existing AR-targeting therapies, highlighting the need for novel therapeutic agents currently under development.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Feniltioidantoína / Receptores Androgênicos / Neoplasias de Próstata Resistentes à Castração / Antagonistas de Androgênios Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Feniltioidantoína / Receptores Androgênicos / Neoplasias de Próstata Resistentes à Castração / Antagonistas de Androgênios Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article