Navigating therapeutic sequencing in the metastatic castration-resistant prostate cancer patient journey

Hannah D McManus1, Tanya Dorff2, Alicia K Morgans3

  • 1Duke Cancer Institute Center for Prostate and Urologic Cancer, Duke University, Durham, NC, USA.

Abstract

Insights

Selecting optimal treatments for metastatic castration-resistant prostate cancer (mCRPC) requires considering patient history, clinical factors, and utilizing genetic testing. Newer therapies like PARP inhibitors and [177Lu]Lu-PSMA-617 offer improved outcomes.

Area of Science:

  • Oncology
  • Urology
  • Medical Therapeutics

Background:

  • Metastatic castration-resistant prostate cancer (mCRPC) presents treatment selection challenges despite novel therapies.
  • Optimal sequencing of therapeutic agents for mCRPC remains an area of clinical uncertainty.

Purpose of the Study:

  • To provide an overview of the evolving mCRPC treatment landscape.
  • To discuss guideline-recommended options and clinical trial data for mCRPC.
  • To offer recommendations for optimal treatment sequencing based on individual patient factors.

Main Methods:

  • Comprehensive literature review of pivotal clinical trials and treatment guidelines for mCRPC.
  • Identification of knowledge gaps and future research directions in mCRPC therapy.

Main Results:

  • Treatment selection for mCRPC hinges on patient history, clinical characteristics, symptoms, prognosis, and trial availability.
  • Genetic testing and PSMA-targeted imaging are crucial for evaluating eligibility for novel agents.
  • Emerging therapies include PARP inhibitors, AR pathway inhibitors, and [177Lu]Lu-PSMA-617.

Conclusions:

  • The mCRPC treatment landscape is dynamic, with ongoing trials influencing future strategies.
  • Personalized treatment sequencing, guided by patient-specific factors, is essential for optimal mCRPC management.
  • Guideline-recommended options and emerging therapies are discussed in the context of clinical trial evidence.