A prospective, multicenter study on the clinical effectiveness of abiraterone in metastatic castration-resistant prostate cancer in Korea: Pre- vs. post-chemotherapyopen access
- Authors
- Jeong, Seung-Hwan; Yeon, Sang Eun; Kim, Su Youn; Kwon, Tae Gyun; Jeon, Seong Soo; Choi, Young Deuk; Kwon, Dongdeuk; Chung, Byung Ha; Hong, Sung-Hoo; Kim, Byung Hoon; Lee, Hyo Jin; Shin, Sang Joon; Choi, Woo Suk; Park, Sung Woo; Kang, Taek Won; Yun, Seok Joong; Cho, Jin Seon; Choi, See Min; Lee, Na-Ri; Kwak, Cheol
- Issue Date
- Sep-2023
- Publisher
- NLM (Medline)
- Keywords
- Abiraterone; Prostate cancer; Prostate-specific antigen; Real-world data
- Citation
- Investigative and clinical urology, v.64, no.5, pp 466 - 473
- Pages
- 8
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- Investigative and clinical urology
- Volume
- 64
- Number
- 5
- Start Page
- 466
- End Page
- 473
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/67951
- DOI
- 10.4111/icu.20230128
- ISSN
- 2466-0493
2466-054X
- Abstract
- PURPOSE: The proper treatment sequence for administering abiraterone acetate plus prednisolone (AAP) and chemotherapeutic agents has not yet been elucidated for metastatic castration-resistant prostate cancer (mCRPC). Hence, this study evaluated the effectiveness and safety of AAP in pre- and post-chemotherapy settings using real-world data. MATERIALS AND METHODS: This prospective, multicenter, open-label, observational study included 506 patients with mCRPC. Patients were classified according to the timing of chemotherapy into pre- and post-chemotherapy groups. The effectiveness and safety of AAP were compared between the groups; the prostate-specific antigen (PSA) response, PSA progression-free survival, and radiologic progression-free survival were assessed; and adverse drug reactions were recorded. RESULTS: Among the included patients, 319 and 187 belonged to the pre- and post-chemotherapy groups, respectively. Risk classification was similar between the two groups. The PSA response was 61.8% in the pre-chemotherapy group and 39.0% in the post-chemotherapy group (p<0.001). The median time to PSA progression (5.00 vs. 2.93 mo, p=0.001) and radiologic progression-free survival (11.84 vs. 9.17 mo, p=0.002) were significantly longer in the pre-chemotherapy group. Chemotherapy status was associated with PSA (hazard ratio [HR] 1.39, 95% confidence interval [CI] 1.09-1.77) and radiologic progression (HR 1.66, 95% CI 1.18-2.33) during AAP treatment. Adverse drug reactions were reported at similar frequencies in both groups. CONCLUSIONS: In this postmarketing surveillance, AAP benefited patients with mCRPC, especially in settings before chemotherapy was administered, resulting in a high PSA response and longer PSA and radiologic progression-free survival with tolerable adverse drug reactions. © The Korean Urological Association.
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