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奥拉帕利单药治疗铂敏感复发性卵巢癌患者的生存的临床和生物标志物因素:一项多中心回顾性研究。

Clinical and biomarker factors affecting survival in patients with platinum-sensitive relapsed ovarian cancer receiving olaparib monotherapy: a multicenter retrospective study.

机构信息

Department of Pharmacy, National Cancer Center Hospital, Tokyo, Japan.

Division of Pharmaceutical Care Sciences, Keio University Graduate School of Pharmaceutical Sciences, Tokyo, Japan.

出版信息

Sci Rep. 2023 Jul 24;13(1):11962. doi: 10.1038/s41598-023-39224-0.

DOI:10.1038/s41598-023-39224-0
PMID:37488223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10366208/
Abstract

The standard treatment for platinum-sensitive relapsed ovarian cancer (PSROC) is platinum-based chemotherapy followed by olaparib monotherapy. A retrospective study was conducted to identify factors affecting the survival of patients with PSROC undergoing olaparib monotherapy in real-world clinical settings. The study enrolled 122 patients who received olaparib monotherapy between April 2018 and December 2020 at three national centers in Japan. The study used the Kaplan-Meier method and univariable and multivariable Cox proportional hazards models to evaluate the associations between factors and progression-free survival (PFS). Patients with BRCA1/2 mutations had a significantly longer median PFS than those without these mutations. Both the BRCA1/2 mutation-positive and mutation-negative groups exhibited a prolonged PFS when the platinum-free interval (PFI) was ≥ 12 months. Cancer antigen 125 (CA-125) level within reference values was significantly linked to prolonged PFS, while a high platelet-to-lymphocyte ratio (≥ 210) was significantly associated with poor PFS in the BRCA1/2 mutation-negative group. The study suggests that a PFI of ≥ 12 months may predict survival after olaparib monotherapy in patients with PSROC, regardless of their BRCA1/2 mutation status. Additionally, a CA-125 level within reference values may be associated with extended survival in patients without BRCA1/2 mutations. A larger prospective study should confirm these findings.

摘要

铂敏感复发性卵巢癌(PSROC)的标准治疗是铂类化疗后奥拉帕利单药治疗。本回顾性研究旨在确定在真实临床环境中接受奥拉帕利单药治疗的 PSROC 患者的生存影响因素。该研究纳入了 2018 年 4 月至 2020 年 12 月在日本三个国家中心接受奥拉帕利单药治疗的 122 例患者。该研究采用 Kaplan-Meier 法和单变量及多变量 Cox 比例风险模型评估了各因素与无进展生存期(PFS)之间的相关性。BRCA1/2 突变患者的中位 PFS 明显长于无这些突变的患者。BRCA1/2 突变阳性和阴性组的铂无治疗间隔(PFI)≥12 个月时,PFS 均延长。CA-125 水平在参考值内与 PFS 延长显著相关,而在 BRCA1/2 突变阴性组中,血小板与淋巴细胞比值(≥210)较高与 PFS 不良显著相关。该研究表明,PFI≥12 个月可能预示着 PSROC 患者接受奥拉帕利单药治疗后的生存情况,无论其 BRCA1/2 突变状态如何。此外,CA-125 水平在参考值内可能与无 BRCA1/2 突变患者的生存延长有关。更大规模的前瞻性研究应证实这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2de/10366208/392b7707cf4c/41598_2023_39224_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2de/10366208/2482a089fb16/41598_2023_39224_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2de/10366208/392b7707cf4c/41598_2023_39224_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2de/10366208/2482a089fb16/41598_2023_39224_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2de/10366208/392b7707cf4c/41598_2023_39224_Fig2_HTML.jpg

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本文引用的文献

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Olaparib maintenance monotherapy in platinum-sensitive relapsed ovarian cancer patients without a germline BRCA1/BRCA2 mutation: OPINION primary analysis.
奥拉帕利维持单药治疗无胚系BRCA1/BRCA2突变的铂敏感复发性卵巢癌患者:OPINION初步分析
Gynecol Oncol. 2022 Mar;164(3):498-504. doi: 10.1016/j.ygyno.2021.12.025. Epub 2022 Jan 19.
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Cediranib suppresses homology-directed DNA repair through down-regulation of BRCA1/2 and RAD51.西地尼布通过下调 BRCA1/2 和 RAD51 来抑制同源定向 DNA 修复。
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