Open Access

ARTICLE

Practical guide to the use of enzalutamide

Jean Hoffman-Censits, Wm. Kevin Kelly

Department of Medical Oncology, Kimmel Cancer Center, Jefferson Medical College of Thomas Jefferson University, Philadelphia, Pennsylvania, USA
Address correspondence to Dr. Wm. Kevin Kelly, Department of Medical Oncology, Kimmel Cancer Center, Jefferson Medical College of Thomas Jefferson University, 1025 Walnut Street, Suite 700, Philadelphia, PA 19107 USA

Canadian Journal of Urology 2014, 21(Suppl.2), 64-69.

Abstract

instruction: Introduction: We summarize the development, definitive trials, and practical use of enzalutamide for practicing urologists and medical oncologists. The care paradigm for patients with metastatic castration-resistant prostate cancer (mCRPC) is a changing landscape, with the ongoing discovery of drivers of cancer progression yielding actionable targets for drug development. Since 2010, sipuleucel-T, cabazitaxel, abiraterone with prednisone, radium-223 and enzalutamide have been Food and Drug Administration (FDA) approved based upon improvement in overall survival in men with mCRPC.
instruction: Materials and methods: A MEDLINE search for "enzalutamide or MDV3100" yielded 258 results. Prospective trials were reviewed. Abstracts from ASCO (American Society of Clinical Oncology) meetings and press release information were included where applicable.
instruction: Results: Enzalutamide, an oral inhibitor of the androgen receptor pathway, was approved in 2012 based upon improvement in overall survival of 4.8 months in men with mCRPC following docetaxel versus placebo. Measures of prostate-specific antigen (PSA) and radiographic response, and clinically significant endpoints such as quality of life improvement and toxicity parameters favored enzalutamide. Toxicity is modest with asthenia and fatigue being most common, with a 1% incidence of seizure reported, though patients can be selected to decrease this risk.
instruction: Conclusion: Enzalutamide is an effective oral therapy for mCRPC, with an overall survival benefit before and following chemotherapy. Toxicity is mild, and seizure risk can be mitigated by careful patient selection. Ongoing studies will help determine the best sequence of novel agents for prostate cancer, along with safe and effective combinations of therapies. Better understanding of tumor characteristics, particularly reliance on the androgen receptor pathway, will lead to personalized approaches to prostate cancer therapy.

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