| Literature DB >> 31986318 |
M C Cursano1, M Iuliani2, C Casadei3, M Stellato2, G Tonini2, G Paganelli4, D Santini2, U De Giorgi3.
Abstract
Chemotherapeutic agents (docetaxel, cabazitaxel), hormonal therapies (abiraterone, enzalutamide) and radium-223 improve survival in patients with bone metastatic castration-resistant prostate cancer (mCRPC). Combinations of radium-223 with these agents or novel drugs have been investigated in order to improve survival and decrease bone-related morbidity. In mCRPC, clinical and preclinical data indicate that radium-223, abiraterone and enzalutamide have a direct effect on prostate cancer cells and bone microenvironment when administered as single agents. Initial results from studies of radium-223 and abiraterone, enzalutamide or docetaxel demonstrated efficacy without any safety concern in pre-treated mCRPC; however, this safety profile changed when radium-based combination therapies were administered in un-pretreated mCRPC. This review underline the biological rationale for combining radium strategies, investigating their effects on bone in terms of control of skeletal-related events and bone disease progression. The aim is to understand the possible reasons why different radium-based combination treatments can led to different clinical outcomes.Entities:
Keywords: Abiraterone; Bone metastases; Bone protecting agents; Castration-resistant prostate cancer; Docetaxel; Enzalutamide; Radium-223; Skeletal-related events
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Year: 2020 PMID: 31986318 DOI: 10.1016/j.critrevonc.2020.102864
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312