Biweekly cabazitaxel is a safe treatment option for metastatic castration-resistant prostate cancer (mCRPC) patients after docetaxel ⇓ a final analysis of the prosty II trial

2Citations
Citations of this article
31Readers
Mendeley users who have this article in their library.

Abstract

Background/Aim: Our phase III trial showed that biweekly docetaxel (D) is better tolerated than triweekly D in metastatic castration-resistant prostate cancer (mCRPC). The safety of biweekly cabazitaxel (CBZ) post-docetaxel was studied in mCRPC. Patients and Methods: Altogether, 60 patients received CBZ 16 mg/m2 i.v. on day 1 and day 14 of a 4-week cycle. The mean serum PSA levels were 305 ng/ml, and the mean age 67 years. The primary endpoint was safety according to CTCAEv4.0. Results: A total of 255 4-week cycles of CBZ were administered. The most common grade 3/4 adverse events were neutropenia (16.7%), pain (13.3%), fatigue (10.0%), anemia (5.0%) and non-neutropenic infection (10.0%). PSA responses occurred in 10 patients (16.7%). Clinical benefit rate was 38.3% and median survival 10 months. Conclusion: Biweekly CBZ is a well-tolerated treatment resulting in meaningful benefits for heavily pretreated mCRPC patients.

Cite

CITATION STYLE

APA

Kellokumpu-Lehtinen, P. L., Marttila, T., Jekunen, A., Hervonen, P., Klintrup, K., Kataja, V., … Huttunen, T. (2020). Biweekly cabazitaxel is a safe treatment option for metastatic castration-resistant prostate cancer (mCRPC) patients after docetaxel ⇓ a final analysis of the prosty II trial. Anticancer Research, 40(12), 6915–6921. https://doi.org/10.21873/anticanres.14715

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free