In a retrospective study presented at the Society for Urologic Oncology 2020 meeting, researchers from the Mayo Clinic reported a small 112 patient cohort with metastatic castration-resistant prostate cancer (mCRPC). The study included two different groups:
Group A (80 men) were given docetaxel chemotherapy (Taxotere) followed by one of the second-line hormonal therapies: either abiraterone (Zytiga) or enzalutamide (Xtandi)
Group B (32 men) were given a second-line hormonal therapy then followed by Taxotere. It was noted that bone metastases were more common in Group B (87%) than Group A (58%)
Three-year survival was:
· cancer-specific survival: 87% Group A vs. 64% Group B
· overall survival: 82% Group A vs. 61% Group B
· these results were similar for men who had a high-volume of metastases, excluding those with lymph node-only disease
This study was not a prospective randomized clinical trial; it was a retrospective trial. However, it comes to a different conclusion than from a couple of earlier retrospective analyses.
Sonpavde et al. reported from an analysis of 1445 men at VA hospitals that there was no difference in overall survival among those who started with taxanes vs. those that began with second-line hormonal therapy.
In a study at Johns Hopkins, Maughan et al. reported no statistically significant differences in total progression-free survival related to the order in which Taxotere or Zytiga were given. Both studies adjusted for disease characteristics.
In the STAMPEDE trial of newly diagnosed men with metastatic hormone-sensitive prostate cancer (mHSPC), there was no difference in survival among men who were randomized to get Taxotere or Zytiga first (see this link). The Mayo study's difference may be due to "selection bias" in the retrospective study - Group A may have received Taxotere first because they were healthier and more likely to survive.
But even if the survival difference is an artifact of the study methodology, there are other reasons to do Taxotere first:
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Joel T Nowak