TY - JOUR
T1 - Aggressive variants of castration-resistant prostate cancer
AU - Beltran, Himisha
AU - Tomlins, Scott
AU - Aparicio, Ana
AU - Arora, Vivek
AU - Rickman, David
AU - Ayala, Gustavo
AU - Huang, Jiaoti
AU - True, Lawrence
AU - Gleave, Martin E.
AU - Soule, Howard
AU - Logothetis, Christopher
AU - Rubin, Mark A.
PY - 2014/6/1
Y1 - 2014/6/1
N2 - A subset of patients with advanced castration-resistant prostate cancer may eventually evolve into an androgen receptor (AR)-independent phenotype, with a clinical picture associated with the development of rapidly progressive disease involving visceral sites and hormone refractoriness, often in the setting of a low or modestly rising serum prostate-specific antigen level. Biopsies performed in such patients may vary, ranging from poorly differentiated carcinomas to mixed adenocarcinoma-small cell carcinomas to pure small cell carcinomas. These aggressive tumors often demonstrate low or absent AR protein expression and, in some cases, express markers of neuroendocrine differentiation. Because tumor morphology is not always predicted by clinical behavior, the terms "anaplastic prostate cancer" or "neuroendocrine prostate cancer" have been used descriptively to describe these rapidly growing clinical features. Patients meeting clinical criteria of anaplastic prostate cancer have been shown to predict for poor prognosis, and these patients may be considered for platinum-based chemotherapy treatment regimens. Therefore, understanding variants within the spectrum of advanced prostate cancer has important diagnostic and treatment implications.
AB - A subset of patients with advanced castration-resistant prostate cancer may eventually evolve into an androgen receptor (AR)-independent phenotype, with a clinical picture associated with the development of rapidly progressive disease involving visceral sites and hormone refractoriness, often in the setting of a low or modestly rising serum prostate-specific antigen level. Biopsies performed in such patients may vary, ranging from poorly differentiated carcinomas to mixed adenocarcinoma-small cell carcinomas to pure small cell carcinomas. These aggressive tumors often demonstrate low or absent AR protein expression and, in some cases, express markers of neuroendocrine differentiation. Because tumor morphology is not always predicted by clinical behavior, the terms "anaplastic prostate cancer" or "neuroendocrine prostate cancer" have been used descriptively to describe these rapidly growing clinical features. Patients meeting clinical criteria of anaplastic prostate cancer have been shown to predict for poor prognosis, and these patients may be considered for platinum-based chemotherapy treatment regimens. Therefore, understanding variants within the spectrum of advanced prostate cancer has important diagnostic and treatment implications.
UR - http://www.scopus.com/inward/record.url?scp=84901818038&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-13-3309
DO - 10.1158/1078-0432.CCR-13-3309
M3 - Review article
C2 - 24727321
AN - SCOPUS:84901818038
SN - 1078-0432
VL - 20
SP - 2846
EP - 2850
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 11
ER -