Mechanisms, Challenges, and Opportunities in Combined Radiation and Hormonal Therapies

被引:3
|
作者
Coulter, Jonathan B. [1 ,2 ,3 ,4 ]
Song, Daniel Y. [2 ,3 ,4 ]
DeWeese, Theodore L. [1 ,2 ,3 ,4 ]
Yegnasubramanian, Srinivasan [2 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Sch Med, James Buchanan Brady Urol Inst, Dept Urol, 1550 Orleans St,154 JHUSOM Canc Res Bldg 2, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Radiat Oncol & Mol Radiat Sci, Baltimore, MD USA
[5] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
关键词
PROSTATE-CANCER; ANDROGEN RECEPTOR; DNA-REPAIR; RADIOTHERAPY; CASTRATION; CARCINOMA; DEPRIVATION; SUPPRESSION; SURVIVAL; DURATION;
D O I
10.1016/j.semradonc.2021.09.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Androgen receptor signaling blockade is perhaps the first example of targeted therapy in the treatment of cancer. Since the initial observations that prostate cancers depend on hormone signaling, hormonal therapies remain a cornerstone in the treatment of metastatic prostate cancer. Androgen deprivation therapy has been shown to improve outcomes involving treatment of prostate cancers with radiotherapy, though a mechanistic understanding into the optimal sequencing of androgen deprivation therapy and radiotherapy remains incomplete. In this review we highlight key clinical trials designed to study combinations of hormonal and radiotherapies and introduce recent discoveries into the complex biology of androgen receptor signaling and DNA damage and repair. These emerging mechanistic and translational studies may have profound implications on both our understanding of hormonal therapy and radiotherapy combinations and the development of novel treatment strategies for locally-advanced and metastatic castrate resistant prostate cancer. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:76 / 81
页数:6
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