Department of Gynaecology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Department of Neurosurgery, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
BJOG. 2021 Feb;128(3):485-493. doi: 10.1111/1471-0528.16411. Epub 2020 Aug 2.
Up to 70% of patients with advanced ovarian cancer have a relapse after primary therapy. New agents and approaches are urgently needed to avoid or slow down this recurrence.
To investigate the efficacy of PARP inhibitors (PARPis) as maintenance treatment in patients with newly diagnosed advanced ovarian cancer.
PubMed, MEDLINE, EMBASE, Cochrane Library and Web of Science databases.
All randomised clinical trials (RCTs) that compared PARPis with placebo as first-line maintenance therapy in ovarian cancer.
Two reviewers extracted data. Pooled hazard ratio (HR) and risk ratio (RR) with 95% confidence interval (CI) were calculated.
PARPis were associated with significant improvement of progression-free survival (PFS) in advanced epithelial ovarian cancer (AeOC) (HR = 0.53, 95% CI 0.40-0.71; P < 0.0001). The benefit was not only in women with BRCA mutations (HR = 0.35, 95% CI 0.29-0.42; P < 0.00001) and homologous recombination deficiency (HRD) (HR = 0.43, 95% CI 0.32-0.60; P < 0.00001), but also in those with nonmutated BRCA (HR = 0.72, 95% CI 0.63-0.82; P < 0.00001) and even non-HRD (HR = 0.83, 95% CI 0.70-0.99; P = 0.04).
PARP inhibitors are effective as maintenance therapy among patients with newly diagnosed advanced ovarian cancer after platinum-based chemotherapy, regardless of BRCA mutation or HRD status.
PARPis provide a significant PFS benefit as first-line maintenance therapy in patients with newly diagnosed advanced ovarian cancer.
多达 70%的晚期卵巢癌患者在初次治疗后会复发。迫切需要新的药物和方法来避免或减缓这种复发。
研究聚腺苷二磷酸核糖聚合酶(PARP)抑制剂(PARPi)作为新诊断的晚期卵巢癌患者维持治疗的疗效。
PubMed、MEDLINE、EMBASE、Cochrane 图书馆和 Web of Science 数据库。
所有比较 PARPi 与安慰剂作为卵巢癌一线维持治疗的随机临床试验(RCT)。
两名评审员提取数据。计算合并的风险比(HR)和风险比(RR)及 95%置信区间(CI)。
PARPi 可显著改善晚期上皮性卵巢癌(AeOC)的无进展生存期(PFS)(HR=0.53,95%CI 0.40-0.71;P<0.0001)。这种益处不仅存在于携带 BRCA 突变(HR=0.35,95%CI 0.29-0.42;P<0.00001)和同源重组缺陷(HRD)(HR=0.43,95%CI 0.32-0.60;P<0.00001)的女性中,也存在于未突变 BRCA 的女性(HR=0.72,95%CI 0.63-0.82;P<0.00001)中,甚至存在于非 HRD 女性(HR=0.83,95%CI 0.70-0.99;P=0.04)中。
PARPi 作为铂类化疗后新诊断的晚期卵巢癌患者的维持治疗是有效的,无论 BRCA 突变或 HRD 状态如何。
研究结果表明,PARPi 作为铂类化疗后新诊断的晚期卵巢癌患者的维持治疗,可显著改善患者的无进展生存期,无论 BRCA 突变状态或 HRD 状态如何。