AI Article Synopsis

  • For decades, oncologists and urologists relied on androgen deprivation therapy (ADT) alone for treating metastatic hormone-sensitive prostate cancer (mHSPC), but recent trials show better survival with combination therapies.
  • Recent studies have demonstrated that combining ADT with docetaxel or second-generation oral androgen-receptor inhibitors (ARPIs) results in significant improvements in patient outcomes compared to ADT alone.
  • The analysis from the ARASENS trial suggests that triplet therapy (ADT plus docetaxel plus an ARPI) is beneficial for various patient subgroups, highlighting the importance of considering disease volume and risk when determining treatment plans.

Article Abstract

Journal of Clinical Oncology, For generations, oncologists and urologists have used androgen deprivation therapy (ADT) to manage metastatic hormone-sensitive prostate cancer (mHSPC). Until recently, ADT monotherapy was standard. Within the past decade, a series of trials have clearly demonstrated improved outcomes with a more aggressive up-front approach. Doublet intensification therapy, involving either ADT plus docetaxel or ADT plus any of several second-generation oral androgen-receptor pathway inhibitors (ARPIs), provide considerable survival advantages compared with ADT alone. In 2022, two trials, PEACE-1 and ARASENS, demonstrated the potential of triplet therapy, adding an ARPI to an ADT-docetaxel doublet. In the Original Report that accompanies this article, the authors provide a post hoc analysis of ARASENS (ADT plus docetaxel, with or without darolutamide), identifying the subpopulations of patients with mHSPC who might benefit most from a triplet regimen. They segment the ARASENS cohort by disease volume and disease risk profile, finding that triplet therapy is associated with improved outcomes regardless of category (although with limited power in the low-volume cohort). Meanwhile, trials are ongoing examining the role of radiotherapy (RT) in mHSPC, a modality previously reserved for localized disease or isolated, symptomatic metastases. Here, we present a mHSPC case and discuss our approach to mHSPC considering recent studies. We recommend triplet therapy for patients who are suitable candidates for chemotherapy, especially for patients with high-volume disease. We also favor aggressive use of RT, when feasible, for patients with low-volume mHSPC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325768PMC
http://dx.doi.org/10.1200/JCO.23.00723DOI Listing

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