# Docetaxel Rechallenge vs Cabazitaxel in Patients With Metastatic Castration-Resistant Prostate Cancer

## TL;DR

Docetaxel rechallenge improves survival more than cabazitaxel in prostate cancer patients who previously responded to docetaxel.

## Contribution

This study provides evidence that docetaxel rechallenge is more effective than cabazitaxel for certain prostate cancer patients.

## Key findings

- Docetaxel rechallenge was associated with longer overall survival (12.3 months) compared to cabazitaxel (9.6 months).
- Patients on docetaxel rechallenge had higher PSA response rates (9.8%) than those on cabazitaxel (3.0%).
- Time to next treatment or death was longer with docetaxel rechallenge (10.7 months) than with cabazitaxel (8.9 months).

## Abstract

Are there different outcomes associated with docetaxel rechallenge and cabazitaxel in patients who received prior docetaxel for metastatic castration-resistant prostate cancer (mCRPC) and did not experience disease progression?

In this cohort study of 669 patients in the nationwide Veterans Affairs health care system, docetaxel rechallenge was associated with longer overall survival compared with cabazitaxel.

Given that randomized clinical trials are unlikely to be conducted for this scenario, these findings support docetaxel rechallenge for patients with mCRPC who did not experience disease progression during prior docetaxel treatment.

This cohort study compares overall survival in patients with metastatic castration-resistant prostate cancer (mCRPC) receiving cabazitaxel or docetaxel rechallenge after initial treatment with docetaxel.

Docetaxel has been a standard treatment for metastatic castration-resistant prostate cancer (mCRPC) since 2004. Cabazitaxel, a related taxane, was approved in 2010 for patients with mCRPC who had been previously treated with docetaxel. The comparative effectiveness of docetaxel rechallenge vs switching to cabazitaxel after prior docetaxel for mCRPC remains unclear.

To compare the clinical outcomes associated with docetaxel rechallenge vs cabazitaxel in patients with mCRPC who did not experience disease progression during prior administration of docetaxel in the mCRPC setting.

This retrospective cohort study was conducted in the nationwide Veterans Affairs health care system, using inverse probability of treatment weighting to control for potential confounders. Patients who were diagnosed with chemonaive mCRPC between January 1, 2010, and December 31, 2023, received initial docetaxel treatment, and did not experience disease progression were eligible to participate.

Treatment with docetaxel rechallenge or cabazitaxel.

The primary outcome was overall survival (OS) from the initiation of the second course of taxane, which was compared in patients treated with docetaxel rechallenge vs cabazitaxel using weighted Kaplan-Meier analysis and Cox proportional hazards regression models. Secondary outcomes included prostate-specific antigen response, time to next systemic treatment or death, and subsequent treatments received.

A total of 669 patients (407 receiving cabazitaxel and 262 receiving docetaxel rechallenge) with a median age of 72 (IQR, 67-77) years were included. Patients treated with docetaxel rechallenge had a significantly longer OS (median, 12.3 [IQR, 10.5-13.8] months) compared with those treated with cabazitaxel (median, 9.6 [IQR, 8.6-11.1] months), with a hazard ratio of 0.81 (95% CI, 0.55-0.99; P = .04). Descriptive analysis of secondary outcomes was consistent with this finding, including prostate-specific antigen response (weighted 9.8% achieving reduction of 90% or more in the docetaxel rechallenge group vs 3.0% in the cabazitaxel group) and time to next treatment or death (median, 10.7 [IQR, 7.8-12.7] months in the docetaxel rechallenge group vs 8.9 [IQR, 7.1-10.5 months] in the cabazitaxel group). Use of platinum, immunotherapy, or poly (ADP-ribose) polymerase inhibitors was similar between patients treated with cabazitaxel and docetaxel rechallenge.

In this cohort study of patients with mCRPC, docetaxel rechallenge was associated with improved OS compared with cabazitaxel among patients who did not experience disease progression during prior docetaxel for mCRPC. These findings support docetaxel rechallenge as a treatment option for patients in this scenario.