Optimal sequencing of docetaxel and abiraterone in men with metastatic castration-resistant prostate cancer

The Prostate ◽  
2015 ◽  
Vol 75 (15) ◽  
pp. 1814-1820 ◽  
Author(s):  
Benjamin L. Maughan ◽  
Xian C. Xhou ◽  
Daniel L. Suzman ◽  
Rosa Nadal ◽  
Sunakshi Bassi ◽  
...  
2016 ◽  
Vol 17 (11) ◽  
pp. 1301-1308 ◽  
Author(s):  
Orazio Caffo ◽  
Andrea Lunardi ◽  
Chiara Trentin ◽  
Francesca Maines ◽  
Antonello Veccia ◽  
...  

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. e16079-e16079
Author(s):  
Benjamin Louis Maughan ◽  
Daniel L. Suzman ◽  
Rosa Nadal ◽  
Sunakshi Bassi ◽  
Michael Thomas Schweizer ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 4522
Author(s):  
Carlo Cattrini ◽  
Rodrigo España ◽  
Alessia Mennitto ◽  
Melissa Bersanelli ◽  
Elena Castro ◽  
...  

The treatment landscape of advanced prostate cancer has completely changed during the last decades. Chemotherapy (docetaxel, cabazitaxel), androgen-receptor signaling inhibitors (ARSi) (abiraterone acetate, enzalutamide), and radium-223 have revolutionized the management of metastatic castration-resistant prostate cancer (mCRPC). Lutetium-177–PSMA-617 is also going to become another treatment option for these patients. In addition, docetaxel, abiraterone acetate, apalutamide, enzalutamide, and radiotherapy to primary tumor have demonstrated the ability to significantly prolong the survival of patients with metastatic hormone-sensitive prostate cancer (mHSPC). Finally, apalutamide, enzalutamide, and darolutamide have recently provided impactful data in patients with nonmetastatic castration-resistant disease (nmCRPC). However, which is the best treatment sequence for patients with advanced prostate cancer? This comprehensive review aims at discussing the available literature data to identify the optimal sequencing approaches in patients with prostate cancer at different disease stages. Our work also highlights the potential impact of predictive biomarkers in treatment sequencing and exploring the role of specific agents (i.e., olaparib, rucaparib, talazoparib, niraparib, and ipatasertib) in biomarker-selected populations of patients with prostate cancer (i.e., those harboring alterations in DNA damage and response genes or PTEN).


2018 ◽  
Author(s):  
Samer L Traboulsi ◽  
Fred Saad

Until 2010, the only approved life-prolonging treatment in patients with metastatic castration-resistant prostate cancer (mCRPC) was docetaxel. Since 2010, abiraterone acetate, enzalutamide, and cabazitaxel have demonstrated overall survival (OS) benefits in the postdocetaxel setting. The COU-AA-301 trial showed an OS advantage with abiraterone acetate plus prednisone compared with placebo plus prednisone. A superior OS was also seen in the AFFIRM trial that compared enzalutamide with placebo and in the TROPIC trial that compared cabazitaxel plus prednisone with mitoxantrone plus prednisone Radium-223 dichloride has also been approved based on the ALSYMPCA trial for symptomatic patients with castration-resistant prostate cancer (CRPC) metastatic to bone only. Optimal sequencing of approved therapies remains controversial. In this chapter, we will review the approved agents in second-line treatment of CRPC and discuss the sequencing options. This review contains 4 figures, 5 tables, and 57 references. Key Words: abiraterone acetate, cabazitaxel, castration-resistant, docetaxel, enzalutamide, MDV 3100, prostatic neoplasms, radium-223 dichloride, sequencing of therapy


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