PMID- 32257208 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200928 IS - 2049-9450 (Print) IS - 2049-9469 (Electronic) IS - 2049-9450 (Linking) VI - 12 IP - 5 DP - 2020 May TI - Corticosteroids alleviate adverse events associated with enzalutamide in patients with metastatic castration-resistant prostate cancer. PG - 495-500 LID - 10.3892/mco.2020.2013 [doi] AB - The aim of the present study was to investigate the impact of the combined use of corticosteroid on adverse events (AEs) induced by enzalutamide (Enz) in patients with metastatic castration-resistant prostate cancer (mCRPC). The cohort of the present study included 121 consecutive patients with mCRPC who sequentially received androgen receptor-axis-targeted (ARAT) agents, abiraterone acetate (AA) and Enz, in any order, without prior docetaxel therapy. Detailed assessments of AEs during treatment with Enz were conducted according to whether or not corticosteroid was administered. Of these patients, 63 and 58 received ARAT therapy with the Enz-to-AA sequence (group 1) and the AA-to-Enz sequence (group 2), respectively. No patient in group 1 received corticosteroid during treatment with Enz, while corticosteroid was continuously administered in combination with Enz to all patients in group 2 following AA failure. When ARAT therapy was initiated, no significant differences in the major baseline characteristics were observed between the two groups. During Enz therapy, there were no significant differences in the incidence of any AEs or AEs >/= grade 3 between the two groups. However, the incidences of fatigue and appetite loss in group 1 were significantly higher when compared with those in group 2. Furthermore, the combined use of corticosteroid was revealed to be independently associated with the prevention of fatigue and appetite loss during Enz therapy. The results of the present study suggested that the combined use of corticosteroids could reduce the incidence of certain types of AE, particularly fatigue and appetite loss, in mCRPC patients treated with Enz. CI - Copyright (c) 2020, Spandidos Publications. FAU - Tamura, Keita AU - Tamura K AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. FAU - Matsushita, Yuto AU - Matsushita Y AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. FAU - Watanabe, Hiromitsu AU - Watanabe H AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. FAU - Motoyama, Daisuke AU - Motoyama D AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. FAU - Ito, Toshiki AU - Ito T AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. FAU - Sugiyama, Takayuki AU - Sugiyama T AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. FAU - Otsuka, Atsushi AU - Otsuka A AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. FAU - Miyake, Hideaki AU - Miyake H AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan. LA - eng PT - Journal Article DEP - 20200305 PL - England TA - Mol Clin Oncol JT - Molecular and clinical oncology JID - 101613422 PMC - PMC7087477 OTO - NOTNLM OT - abiraterone acetate OT - adverse event OT - corticosteroid OT - enzalutamide OT - metastatic castration-resistant prostate cancer EDAT- 2020/04/08 06:00 MHDA- 2020/04/08 06:01 PMCR- 2020/03/05 CRDT- 2020/04/08 06:00 PHST- 2019/08/20 00:00 [received] PHST- 2020/02/03 00:00 [accepted] PHST- 2020/04/08 06:00 [entrez] PHST- 2020/04/08 06:00 [pubmed] PHST- 2020/04/08 06:01 [medline] PHST- 2020/03/05 00:00 [pmc-release] AID - MCO-0-0-2013 [pii] AID - 10.3892/mco.2020.2013 [doi] PST - ppublish SO - Mol Clin Oncol. 2020 May;12(5):495-500. doi: 10.3892/mco.2020.2013. Epub 2020 Mar 5.