Literature DB >> 29150561

Influence of Enzalutamide on Cabazitaxel Pharmacokinetics: a Drug-Drug Interaction Study in Metastatic Castration-resistant Prostate Cancer (mCRPC) Patients.

Bodine P S Belderbos1, Sander Bins1, Roelof W F van Leeuwen1,2, Esther Oomen-de Hoop1, Nelly van der Meer3, Peter de Bruijn1, Paul Hamberg4, Esther N M Overkleeft5, Wendy M van der Deure6, Martijn P Lolkema1, Ronald de Wit1, Ron H J Mathijssen7.   

Abstract

Purpose: In ongoing clinical research on metastatic castration-resistant prostate cancer (mCRPC) treatment, the potential enhanced efficacy of the combination of taxanes with AR-targeted agents, that is, enzalutamide and abiraterone, is currently being explored. Because enzalutamide induces the CYP3A4 enzyme and taxanes are metabolized by this enzyme, a potential drug-drug interaction needs to be investigated.Experimental Design: Therefore, we performed a pharmacokinetic cross-over study in mCRPC patients who were scheduled for treatment with cabazitaxel Q3W (25 mg/m2). Patients were studied for three consecutive cabazitaxel cycles. Enzalutamide (160 mg once daily) was administered concomitantly after the first cabazitaxel cycle, during 6 weeks. Primary endpoint was the difference in mean area under the curve (AUC) between the first (cabazitaxel monotherapy) and third cabazitaxel cycle, when enzalutamide was added.
Results: A potential clinically relevant 22% (95% CI, 9%-34%; P = 0.005) reduction in cabazitaxel exposure was found with concomitant enzalutamide use. The geometric mean AUC0-24h of cabazitaxel was 181 ng*h/mL (95% CI, 150-219 ng*h/mL) in cycle 3 and 234 ng*h/mL (95% CI, 209-261 ng*h/mL) in cycle 1. This combination did not result in excessive toxicity, whereas PSA response was promising.Conclusions: We found a significant decrease in cabazitaxel exposure when combined with enzalutamide. In an era of clinical trials on combination strategies for mCRPC, it is important to be aware of clinically relevant drug-drug interactions. Because recent study results support the use of a lower standard cabazitaxel dose of 20 mg/m2, the clinical relevance of this interaction may be substantial, because the addition of enzalutamide may result in subtherapeutic cabazitaxel exposure. Clin Cancer Res; 24(3); 541-6. ©2017 AACR. ©2017 American Association for Cancer Research.

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Year:  2017        PMID: 29150561     DOI: 10.1158/1078-0432.CCR-17-2336

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  4 in total

1.  Prostate cancer: Enzalutamide-cabazitaxel interactions.

Authors:  Rebecca Kelsey
Journal:  Nat Rev Urol       Date:  2017-12-12       Impact factor: 14.432

2.  Influence of Darolutamide on Cabazitaxel Systemic Exposure.

Authors:  Stefan A J Buck; Niels A D Guchelaar; Peter de Bruijn; Inge M Ghobadi Moghaddam-Helmantel; Esther Oomen-de Hoop; Hans M Westgeest; Paul Hamberg; Danielle Mathijssen-van Stein; Martijn P Lolkema; Stijn L W Koolen; Ronald de Wit; Ron H J Mathijssen
Journal:  Clin Pharmacokinet       Date:  2022-07-27       Impact factor: 5.577

3.  Effect of Gambogenic Acid on Cytochrome P450 1A2, 2B1 and 2E1, and Constitutive Androstane Receptor in Rats.

Authors:  Jing Sun; Xiaozhu Tang; Qianqian Xu; Tao Ge; Daiyin Peng; Weidong Chen
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2018-12       Impact factor: 2.441

4.  Dual Blockade of c-MET and the Androgen Receptor in Metastatic Castration-resistant Prostate Cancer: A Phase I Study of Concurrent Enzalutamide and Crizotinib.

Authors:  Abhishek Tripathi; Jeffrey G Supko; Kathryn P Gray; Zachary J Melnick; Meredith M Regan; Mary-Ellen Taplin; Atish D Choudhury; Mark M Pomerantz; Joaquim Bellmunt; Channing Yu; Zijie Sun; Sandy Srinivas; Philip W Kantoff; Christopher J Sweeney; Lauren C Harshman
Journal:  Clin Cancer Res       Date:  2020-09-17       Impact factor: 12.531

  4 in total

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