Optimizing the treatment of metastatic castration-resistant prostate cancer: a Latin America perspective
- PMID: 29556815
- PMCID: PMC5859699
- DOI: 10.1007/s12032-018-1105-8
Optimizing the treatment of metastatic castration-resistant prostate cancer: a Latin America perspective
Abstract
Prostate cancer is a significant burden and cause of mortality in Latin America. This article reviews the treatment options for patients with metastatic castration-resistant prostate cancer (mCRPC) and provides consensus recommendations to assist Latin American prostate cancer specialists with clinical decision making. A multidisciplinary expert panel from Latin America reviewed the available data and their individual experience to develop clinical consensus opinions for the use of life-prolonging agents in mCRPC, with consideration given to factors influencing patient selection and treatment monitoring. There is a lack of level 1 evidence for the best treatment sequence or combinations in mCRPC. In this context, consensus recommendations were provided for the use of taxane-based chemotherapies, androgen receptor axis-targeted agents and targeted alpha therapy, for patients in Latin America. Prostate-specific antigen (PSA) changes alone, during treatment, should be treated with caution; PSA may not be a suitable biomarker for radium-223. Bone scans and computed tomography are the standard imaging modalities in Latin America. Imaging should be prompted during treatment where symptomatic decline and/or significant worsening of laboratory evaluations are reported, or where a course of therapy has been completed and another antineoplastic agent is under consideration. Recommendations and guidance for treatment options in Latin America are provided in the context of country-level variable access to approved agents and technologies for treatment monitoring. Patients should be treated with the purpose of prolonging overall survival and preserving quality of life through increasing the opportunity to administer all available life-prolonging therapies when appropriate.
Keywords: Chemotherapy; Hormonal therapy; Latin America; Radium-223; mCRPC.
Conflict of interest statement
P Bernal, Consultant for Bayer, is indirectly related to the work submitted; L Nogueira, Advisory board member for Bayer, Astellas and Janssen, is indirectly related to the work submitted; D Bastos plays Consultant and advisory roles for Janssen, Astellas, Bayer, Merck and Roche; Research funding to his institution is from Janssen Astellas and Pfizer; S Bella, Consultant for Bayer, is directly related to the work submitted; ND Shore is a Consultant for Astellas, Bayer, Ferring, Janssen, Medivation, Sanofi, Tolmar and Valeant. All other authors have no potential conflicts of interest to declare.
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