4.4 Article

SEOM clinical guidelines for the treatment of advanced prostate cancer (2020)

Journal

CLINICAL & TRANSLATIONAL ONCOLOGY
Volume 23, Issue 5, Pages 969-979

Publisher

SPRINGER INT PUBL AG
DOI: 10.1007/s12094-021-02561-5

Keywords

Androgen; Castration; Molecular; Biomarkers; Research

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Recent advances in molecular research and new drug development have led to the evolution of advanced prostate cancer treatment. Individualized therapies can be selected based on dynamic aberrations in key pathways such as the androgen receptor, DNA repair genes, and PTEN-PI3K. Testing for specific genetic mutations like BRCA1 and BRCA2 is recommended, with a combination of treatments like castration, chemotherapy, and targeted therapies providing better outcomes for different patient populations.
The treatment of advanced prostate cancer has evolved due to recent advances in molecular research and new drug development. Dynamic aberrations in the androgen receptor, DNA repair genes, PTEN-PI3K, and other pathways drive the behavior of advanced prostate cancer allowing a better selection of therapies in each patient. Tumor testing for BRCA1 and BRCA2 is recommended for patients with metastatic prostate cancer, also considering a broad panel to guide decisions and genetic counseling. In symptomatic metastatic patients, castration should be stared to palliate symptoms and prolong survival. In high-risk or high-volume metastatic hormone-naive patients, castration should be combined with docetaxel, abiraterone, enzalutamide or apalutamide. Radiotherapy to the primary tumor combined with systemic therapy is recommended in low-volume mHNPC patients. In patients with non-metastatic castration-resistant tumors, risk stratification can define the frequency of imaging. Adding enzalutamide, darolutamide or apalutamide to these patients prolongs metastasis-free and overall survival, but potential adverse events need to be taken into consideration. The choice of docetaxel, abiraterone or enzalutamide for treating metastatic castration-resistant patients depends on previous therapies, with cabazitaxel being also recommended after docetaxel. Olaparib is recommended in BRCA1/BRCA2 mutated castration-resistant patients after progression on at least one new hormonal therapy. Aggressive variants of prostate cancer respond to platinum-based chemotherapy. To optimize treatment efficiency, oncologists should incorporate all of these advances into an overall therapeutic strategy.

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