Oral relugolix for androgen deprivation therapy in advanced prostate cancer: pooled safety analyses from randomized controlled studies

You have accessJournal of UrologyCME1 May 2022PD35-08 ORAL RELUGOLIX FOR ANDROGEN DEPRIVATION THERAPY IN ADVANCED PROSTATE CANCER: POOLED SAFETY ANALYSES FROM RANDOMIZED CONTROLLED STUDIES James L. Bailen, Fred Saad, Daniel J. George, Bryan Mehlhaff, Michael S. Cookson, Daniel R. Saltzstein, Ronald Tutrone, Bruce Brown, Andria G. M. Langenberg, Sophia Lu, Jina Lee, Sarah Hanson, Bertrand Tombal, and Neal D. Shore James L. BailenJames L. Bailen More articles by this author , Fred SaadFred Saad More articles by this author , Daniel J. GeorgeDaniel J. George More articles by this author , Bryan MehlhaffBryan Mehlhaff More articles by this author , Michael S. CooksonMichael S. Cookson More articles by this author , Daniel R. SaltzsteinDaniel R. Saltzstein More articles by this author , Ronald TutroneRonald Tutrone More articles by this author , Bruce BrownBruce Brown More articles by this author , Andria G. M. LangenbergAndria G. M. Langenberg More articles by this author , Sophia LuSophia Lu More articles by this author , Jina LeeJina Lee More articles by this author , Sarah HansonSarah Hanson More articles by this author , Bertrand TombalBertrand Tombal More articles by this author , and Neal D. ShoreNeal D. Shore More articles by this author View All Author Informationhttps://doi.org/10.1097/JU.0000000000002593.08AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract INTRODUCTION AND OBJECTIVE: Relugolix is a highly selective, orally active, nonpeptide GnRH receptor antagonist approved for the treatment of men with advanced prostate cancer. In the phase 3 HERO study, relugolix demonstrated sustained testosterone suppression superior to that of leuprolide, a safety profile consistent with its mechanism of action, and a 54% decrease in risk of major adverse cardiovascular events relative to leuprolide. In order to provide a detailed summary of the relugolix safety profile, we analyzed pooled data from 2 randomized relugolix clinical trials. METHODS: The pooled safety analyses include data from 1012 men with advanced prostate cancer: 934 men (relugolix:622; leuprolide:308) from the phase 3 HERO study and 78 men (relugolix:54; leuprolide: 24) from the C27002 randomized phase 2 study. Only men who received either relugolix 120 mg orally once daily (360 mg day 1 loading dose) or leuprolide injections every 12 weeks for 24-48 weeks were included in the analyses. Safety assessments included clinical laboratory tests, reporting of adverse events (AE) (assessed according to the National Cancer Institute Common Terminology Criteria for AEs, version 4.03), and major adverse cardiovascular events (MACE; defined as nonfatal myocardial infarction, non-fatal stroke, and death from any cause). Individual patient data were pooled and results of all analyses were summarized descriptively. RESULTS: The overall incidence of AEs was 93.0% and 93.7% in the relugolix and leuprolide groups, respectively (table). Hot flash was the most common AE in both groups (55.2% in the relugolix group and 52.4% in the leuprolide group). Grade ≥ 3 AEs occurred in 17.2% and 19.6% in the relugolix and leuprolide groups, respectively. The most common grade ≥ 3 AEs were hypertension (1.6% vs 0.6%) and syncope (1.0% vs 0.9%). Fatal events were reported for 1.0% of men in the relugolix group and 3.0% in the leuprolide group. MACE incidence in this pooled analysis was 2.8% in the relugolix group and 6.3% in the leuprolide group. CONCLUSIONS: In the pooled safety analyses of 2 randomized clinical studies in advanced prostate cancer, relugolix was generally well tolerated, with a lesser incidence of MACE relative to leuprolide. Source of Funding: Myovant Sciences GmBH, in collaboration with Pfizer © 2022 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 207Issue Supplement 5May 2022Page: e630 Advertisement Copyright & Permissions© 2022 by American Urological Association Education and Research, Inc.MetricsAuthor Information James L. Bailen More articles by this author Fred Saad More articles by this author Daniel J. George More articles by this author Bryan Mehlhaff More articles by this author Michael S. Cookson More articles by this author Daniel R. Saltzstein More articles by this author Ronald Tutrone More articles by this author Bruce Brown More articles by this author Andria G. M. Langenberg More articles by this author Sophia Lu More articles by this author Jina Lee More articles by this author Sarah Hanson More articles by this author Bertrand Tombal More articles by this author Neal D. Shore More articles by this author Expand All Advertisement PDF downloadLoading ...