Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date

被引:43
作者
Chong, Julio T. [1 ]
Oh, William K. [2 ]
Liaw, Bobby C. [2 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Urol, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Med, Div Hematol & Med Oncol, New York, NY 10029 USA
关键词
antiandrogens; castration-resistant prostatic cancer; investigational new drugs; SIGNAL-TRANSDUCTION PATHWAYS; ANDROGEN-RECEPTOR; ANTITUMOR-ACTIVITY; PART; ENZALUTAMIDE; SAFETY; ABIRATERONE; ARN-509; ANTIANDROGEN; BICALUTAMIDE;
D O I
10.2147/OTT.S147168
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Advances in therapies have led to the approval of six therapeutic agents since 2004, each demonstrating overall survival benefit in randomized studies, and these have significantly improved the outlook for men facing metastatic castration-resistant prostate cancer (CRPC). More recently, efforts have been directed at trying to effect change at earlier phases of the disease. Apalutamide (ARN-509), a second-generation androgen receptor antagonist, recently received approval in the nonmetastatic (M0) CRPC space. Similar to enzalutamide, apalutamide inhibits the binding of androgen to androgen receptor (AR), nuclear translocation of the androgen-AR complex, and binding of AR transcription complex to DNA-binding sites and transcription elements. Phase I and II trial experience demonstrates the safety and tolerability of apalutamide, as well as its efficacy in effecting prostate-specific antigen response and radiographic-free survival in CRPC. US Food and Drug Administration approval in M0 CRPC was granted following positive results from the phase III SPARTAN study, where apalutamide demonstrated significant improvements in metastasis-free survival and time to symptomatic progression as compared to placebo.
引用
收藏
页码:2141 / 2147
页数:7
相关论文
共 32 条
[1]  
[Anonymous], N ENGL J MED
[2]  
[Anonymous], J CLIN ONCOL S
[3]  
[Anonymous], J CLIN ONCOL S
[4]   AR-V7 and Resistance to Enzalutamide and Abiraterone in Prostate Cancer [J].
Antonarakis, Emmanuel S. ;
Lu, Changxue ;
Wang, Hao ;
Luber, Brandon ;
Nakazawa, Mary ;
Roeser, Jeffrey C. ;
Chen, Yan ;
Mohammad, Tabrez A. ;
Chen, Yidong ;
Fedor, Helen L. ;
Lotan, Tamara L. ;
Zheng, Qizhi ;
De Marzo, Angelo M. ;
Isaacs, John T. ;
Isaacs, William B. ;
Nadal, Rosa ;
Paller, Channing J. ;
Denmeade, Samuel R. ;
Carducci, Michael A. ;
Eisenberger, Mario A. ;
Luo, Jun .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (11) :1028-1038
[5]  
Beer TM, 2014, NEW ENGL J MED, V371, P424, DOI 10.1056/NEJMoa1405095
[6]   Intratumoral De Novo Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors [J].
Cai, Changmeng ;
Chen, Sen ;
Ng, Patrick ;
Bubley, Glenn J. ;
Nelson, Peter S. ;
Mostaghel, Elahe A. ;
Marck, Brett ;
Matsumoto, Alvin M. ;
Simon, Nicholas I. ;
Wang, Hongyun ;
Chen, Shaoyong ;
Balk, Steven P. .
CANCER RESEARCH, 2011, 71 (20) :6503-6513
[7]   Abiraterone Treatment in Castration-Resistant Prostate Cancer Selects for Progesterone Responsive Mutant Androgen Receptors [J].
Chen, Eddy J. ;
Sowalsky, Adam G. ;
Gao, Shuai ;
Cai, Changmeng ;
Voznesensky, Olga ;
Schaefer, Rachel ;
Loda, Massimo ;
True, Lawrence D. ;
Ye, Huihui ;
Troncoso, Patricia ;
Lis, Rosina L. ;
Kantoff, Philip W. ;
Montgomery, Robert B. ;
Nelson, Peter S. ;
Bubley, Glenn J. ;
Balk, Steven P. ;
Taplin, Mary-Ellen .
CLINICAL CANCER RESEARCH, 2015, 21 (06) :1273-1280
[8]   Next-generation sequencing (NGS) of tissue and cell free DNA (cfDNA) to identify somatic and germline alterations in advanced prostate cancer. [J].
Cheng, Michael L. ;
Abida, Wassim ;
Rathkopf, Dana E. ;
Arcila, Maria E. ;
Barron, David ;
Autio, Karen A. ;
Zehir, Ahmet ;
Danila, Daniel Costin ;
Morris, Michael J. ;
Gopalan, Anuradha ;
Reuter, Victor E. ;
Kantoff, Philip W. ;
Slovin, Susan F. ;
Robson, Mark E. ;
Zhang, Liying ;
Mandelker, Diana ;
Tsui, Dana ;
Taylor, Barry S. ;
Solit, David B. ;
Scher, Howard I. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
[9]   ARN-509: A Novel Antiandrogen for Prostate Cancer Treatment [J].
Clegg, Nicola J. ;
Wongvipat, John ;
Joseph, James D. ;
Tran, Chris ;
Ouk, Samedy ;
Dilhas, Anna ;
Chen, Yu ;
Grillot, Kate ;
Bischoff, Eric D. ;
Cal, Ling ;
Aparicio, Anna ;
Dorow, Steven ;
Arora, Vivek ;
Shao, Gang ;
Qian, Jing ;
Zhao, Hong ;
Yang, Guangbin ;
Cao, Chunyan ;
Sensintaffar, John ;
Wasielewska, Teresa ;
Herbert, Mark R. ;
Bonnefous, Celine ;
Darimont, Beatrice ;
Scher, Howard I. ;
Smith-Jones, Peter ;
Klang, Mark ;
Smith, Nicholas D. ;
De Stanchina, Elisa ;
Wu, Nian ;
Ouerfelli, Ouathek ;
Rix, Peter J. ;
Heyman, Richard A. ;
Jung, Michael E. ;
Sawyers, Charles L. ;
Hager, Jeffrey H. .
CANCER RESEARCH, 2012, 72 (06) :1494-1503
[10]   The androgen receptor and signal-transduction pathways in hormone-refractory prostate cancer. Part 2: androgen-receptor cofactors and bypass pathways [J].
Edwards, J ;
Bartlett, JMS .
BJU INTERNATIONAL, 2005, 95 (09) :1327-1335