Emerging Categories of Disease in Advanced Prostate Cancer and Their Therapeutic Implications
- PMID: 28620903
Emerging Categories of Disease in Advanced Prostate Cancer and Their Therapeutic Implications
Abstract
The treatment of advanced prostate cancer has changed significantly in the last decade, as a result of the introduction of multiple new systemic therapies that have had a positive impact on treatment outcomes. The increasing number of therapies, along with new insights into the biological underpinnings of prostate cancer, have led to a growing appreciation for the heterogeneity of the disease and an awareness of emerging subcategories that have direct therapeutic implications for the practicing clinician. In the metastatic hormone-naive setting, the extent of metastatic disease visible on scans can serve as a useful measure to guide treatment decisions; the addition of docetaxel chemotherapy to hormonal therapy has significant benefit in patients whose scans show more extensive disease. In the castration-resistant setting, abiraterone and enzalutamide have both had a transformative impact; however, the emergence of resistance to these therapies often heralds a more aggressive phenotype. Emerging clinically relevant subcategories include disease that demonstrates treatment-emergent neuroendocrine differentiation, as well as tumors with somatic and/or germline alterations in the DNA repair pathway. Identification of these subtypes has direct clinical relevance with regard to the potential benefit of platinum-based chemotherapy, poly (ADP-ribose) polymerase inhibitors, and likely further therapies as new therapeutic targets are identified in these groups.
Similar articles
-
Sequencing Treatment for Castration-Resistant Prostate Cancer.Curr Treat Options Oncol. 2016 Dec;17(12):64. doi: 10.1007/s11864-016-0438-9. Curr Treat Options Oncol. 2016. PMID: 27822685 Review.
-
Drug therapies for metastatic castration-resistant prostate cancer.Future Oncol. 2015;11(17):2395-403. doi: 10.2217/fon.15.168. Epub 2015 Aug 14. Future Oncol. 2015. PMID: 26274603 Review.
-
Impact of bone-targeted therapies in chemotherapy-naïve metastatic castration-resistant prostate cancer patients treated with abiraterone acetate: post hoc analysis of study COU-AA-302.Eur Urol. 2015 Oct;68(4):570-7. doi: 10.1016/j.eururo.2015.04.032. Epub 2015 May 16. Eur Urol. 2015. PMID: 25985882 Free PMC article.
-
Advances in systemic therapies for metastatic castration-resistant prostate cancer.Future Oncol. 2014 Nov;10(14):2213-26. doi: 10.2217/fon.14.128. Future Oncol. 2014. PMID: 25471035
-
Castration-resistant prostate cancer: from new pathophysiology to new treatment.Eur Urol. 2014 Feb;65(2):289-99. doi: 10.1016/j.eururo.2013.08.008. Epub 2013 Aug 11. Eur Urol. 2014. PMID: 23957948 Review.
Cited by
-
Leveraging γ-Glutamyl Transferase To Direct Cytotoxicity of Copper Dithiocarbamates against Prostate Cancer Cells.Angew Chem Int Ed Engl. 2018 Sep 24;57(39):12780-12784. doi: 10.1002/anie.201807582. Epub 2018 Aug 29. Angew Chem Int Ed Engl. 2018. PMID: 30025197 Free PMC article.
-
Molecular Subtypes of Prostate Cancer.Curr Oncol Rep. 2018 Jun 1;20(8):58. doi: 10.1007/s11912-018-0707-9. Curr Oncol Rep. 2018. PMID: 29858674 Review.
-
Morphologic, Molecular and Clinical Features of Aggressive Variant Prostate Cancer.Cells. 2020 Apr 25;9(5):1073. doi: 10.3390/cells9051073. Cells. 2020. PMID: 32344931 Free PMC article. Review.
-
Enzalutamide and olaparib synergistically suppress castration-resistant prostate cancer progression by promoting apoptosis through inhibiting nonhomologous end joining pathway.Asian J Androl. 2023 Nov 1;25(6):687-694. doi: 10.4103/aja202316. Epub 2023 May 26. Asian J Androl. 2023. PMID: 37282383 Free PMC article.
-
Assessment of the Validity of Nuclear-Localized Androgen Receptor Splice Variant 7 in Circulating Tumor Cells as a Predictive Biomarker for Castration-Resistant Prostate Cancer.JAMA Oncol. 2018 Sep 1;4(9):1179-1186. doi: 10.1001/jamaoncol.2018.1621. JAMA Oncol. 2018. PMID: 29955787 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources