摘要
Objective: Advanced epithelial ovarian cancer frequently recurs despite good response to first-line treatment, making maintenance therapy essential. Olaparib, a poly (ADP-ribose) polymerase (PARP) inhibitor, demonstrated significant benefit in BRCA-mutated disease in the SOLO-1 trial; however, real-world data from Taiwan remain limited. Materials and methods: We conducted a retrospective cohort study of patients with stage III/IV BRCA1/2-mutated epithelial ovarian cancer treated at Chang Gung Memorial Hospital, Linkou, between 2019 and 2025. Eligible patients achieved complete or partial response to first-line platinum-based chemotherapy and received olaparib. Primary endpoints were progression-free survival (PFS) and overall survival (OS), with adverse events (AEs) as the secondary endpoint. Results: Forty-one patients were analyzed, with a median follow-up of 30.4 months. The estimated mean PFS was 55.0 months, with 12-month, 24-month, and 36-month PFS rates of 90.0%, 78.1%, and 61.5%, respectively. Median OS was not reached (mean OS 62.2 months). Patients with partial response had higher recurrence rates than those with complete response. The most common hematologic AE was anemia (73.2%), predominantly grade 1–2. Frequently reported non-hematologic AEs included nausea, vomiting, and poor appetite. Dose adjustments occurred in 51.2% of patients, yet more than 80% maintained ≥75% of the recommended dose. No patient discontinued olaparib due to AEs. Conclusion: In Taiwanese patients with BRCA-mutated advanced stage epithelial ovarian cancer, real-world use of olaparib as first-line maintenance therapy demonstrated effectiveness comparable to the SOLO-1 trial, with manageable toxicity.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 926-931 |
| 頁數 | 6 |
| 期刊 | Taiwanese Journal of Obstetrics and Gynecology |
| 卷 | 65 |
| 發行號 | 5 |
| DOIs | |
| 出版狀態 | 已出版 - 09 2026 |
文獻附註
Publisher Copyright:© 2026 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V. This is an open access article under the CC BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0/
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