The optimal upfront therapy in metastatic hormone-sensitive prostate cancer: A network meta-analysis

Hasan Mutlu1, Hakan Bozcuk2

  • 1Department of Oncology, School of Medicine, Istinye University, Istanbul, Turkey.

Abstract

Insights

For metastatic hormone-sensitive prostate cancer (mHSPC), abiraterone acetate (AA) is best for high-volume disease, while enzalutamide is preferred for low-volume or docetaxel-naive cases when combined with androgen-deprivation therapy (ADT).

Area of Science:

  • Oncology
  • Medical treatment efficacy
  • Prostate cancer research

Background:

  • Prostate cancer (PC) is a prevalent malignancy in men.
  • Androgen-deprivation therapy (ADT) is a standard treatment for metastatic hormone-sensitive PC (mHSPC).
  • Newer agents offer survival benefits for mHSPC patients.

Purpose of the Study:

  • To determine the most effective treatment strategy for mHSPC using network meta-analysis (NMA).
  • To compare the efficacy of different treatment modalities for mHSPC.
  • To identify optimal therapies based on disease volume and prior treatment.

Main Methods:

  • Network meta-analysis (NMA) of 10 clinical trials.
  • Analysis included all mHSPC cases, low-volume, high-volume, and docetaxel-naive subgroups.
  • Comparison of overall survival outcomes for various treatment combinations with ADT.

Main Results:

  • Abiraterone acetate (AA) combined with ADT showed the highest probability of efficacy in general and high-volume mHSPC subgroups.
  • Enzalutamide combined with ADT was most effective in docetaxel-naive and low-volume mHSPC subgroups.
  • Specific hazard ratios demonstrated superiority of enzalutamide in low-volume/docetaxel-naive settings and AA in high-volume/general settings compared to ADT alone.

Conclusions:

  • Disease volume, particularly based on the CHAARTED trial criteria, is crucial for selecting mHSPC treatment.
  • AA plus prednisone is recommended for high-volume mHSPC, while enzalutamide is favored for low-volume mHSPC, both in combination with ADT.
  • Alternative options include docetaxel or apalutamide for high-volume disease and local radiotherapy for low-volume disease, depending on patient factors.