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Review
. 2015 Feb;7(1):9-21.
doi: 10.1177/1756287214555336.

An update on enzalutamide in the treatment of prostate cancer

Affiliations
Review

An update on enzalutamide in the treatment of prostate cancer

Axel S Merseburger et al. Ther Adv Urol. 2015 Feb.

Abstract

Enzalutamide is an oral androgen receptor inhibitor that targets multiple steps in the androgen receptor signaling pathway. In the randomized phase III AFFIRM study, significant improvements in survival versus placebo were observed when enzalutamide was used as a treatment for patients with metastatic castration-resistant prostate cancer (mCRPC) following prior treatment with docetaxel. Additional benefits included significant delay in time to first skeletal-related event, and improvement in several measures of pain and health-related quality of life. Treatment effects were consistent across all prespecified subgroups. The phase III PREVAIL study evaluated enzalutamide versus placebo in patients with mCRPC who had not received chemotherapy. Enzalutamide significantly decreased the risk of radiographic progression and death. There were also significant improvements in all secondary and prespecified exploratory endpoints, including delayed initiation of chemotherapy, reduction in risk of first skeletal-related event and a high percentage of patients with objective response compared with placebo. Enzalutamide was also studied in hormone naïve patients (as monotherapy) in a small, open-label phase II study in patients with prostate cancer who were eligible for androgen-deprivation therapy. A prostate-specific antigen (PSA) response, defined as ⩾80% decline in PSA level from baseline at week 25, was achieved in 92.5% of patients. Long-term follow up is ongoing. Despite differences between these three trials, enzalutamide displayed a favorable safety profile in all three patient populations. Similar rates of adverse events between the enzalutamide and placebo groups were observed in AFFIRM and PREVAIL, with fatigue, diarrhea, back pain and hot flashes being more common with enzalutamide than with placebo. Hypertension was reported at a higher rate in the enzalutamide group than in the placebo group in PREVAIL. Breast-related disorders associated with enzalutamide treatment were also reported in the Monotherapy trial. Few seizures were reported in any trial. Enzalutamide is being studied in several early disease state populations.

Keywords: AFFIRM trial; PREVAIL trial; efficacy; enzalutamide; prostate cancer; safety.

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Conflict of interest statement

Conflict of interest statement: A.S.M. has received consulting fees from Medivation, Astellas, Janssen-Cilag, Bayer, Roche, Ipsen, Novartis, and Amgen, and payment for speaker bureau from Novartis, Bayer, Janssen-Cilag, Astellas, Ipsen, GlaxoSmithKline, Hexal and Amgen. G.P.H. is an employee of Astellas. C.-A.vK. has received consulting fees from Janssen-Cilag, Teva and Astellas.

Figures

Figure 1.
Figure 1.
Overall survival, AFFIRM. CI, confidence interval. From Scher et al. (2012). Copyright © 2012 Massachusetts Medical Society. Reprinted with permission from Massachusetts Medical Society.
Figure 2.
Figure 2.
Radiographic progression-free survival, PREVAIL. CI, confidence interval. From Beer et al. (2014). Copyright © 2014 Massachusetts Medical Society. Reprinted with permission from Massachusetts Medical Society.
Figure 3.
Figure 3.
Overall PSA change from baseline to week 25 (Monotherapy study). Datapoints are means and whiskers depict standard deviations. PSA, prostate-specific antigen. From Tombal et al. (2014). Reprinted with permission from Elsevier.

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