Hua Yuan, Lin Xiu, Ning Li, Yifan Li, Lingying Wu, Hongwen Yao
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The majority of these patients were reported to be platinum sensitive (92.1%, 35/38). 21 patients (53.8%) received PARPis treatment with 16 patients (76.2%) for maintenance treatment and 5 patients (5/21, 23.8%) for salvage treatment. The median duration for PARPis maintenance and salvage treatment was 14.9 months (range=2.0-56.9) and 8.2 months (range=5.2-20.7), respectively. In the entire cohort, 5-year progression-free survival (PFS) and overall survival (OS) rate was 33.1% and 78.9%, respectively. Patients with BRCA1 mutation had a non-significantly worse 5-year PFS (28.6% vs. 45.8%, p=0.346) and 5-year OS (76.9% vs. 83.3%, p=0.426) than those with BRCA2 mutation. In patients with stage III-IV (n=31), first line PARPis maintenance treatment associated with a non-significantly better PFS (median PFS: NR vs. 22.4 months; 5-year PFS: 64.3% vs. 21.9%, p=0.096).</p><p><strong>Conclusion: </strong>The current study shows that these patients may have a good response to platinum-based chemotherapy and a favorable survival. And these patients can benefit from PARPis treatment and will likely be suitable candidates for PARPis.</p>","PeriodicalId":15868,"journal":{"name":"Journal of Gynecologic Oncology","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11262894/pdf/","citationCount":"0","resultStr":"{\"title\":\"PARPis response and outcome of ovarian cancer patients with BRCA1/2 germline mutation and a history of breast cancer.\",\"authors\":\"Hua Yuan, Lin Xiu, Ning Li, Yifan Li, Lingying Wu, Hongwen Yao\",\"doi\":\"10.3802/jgo.2024.35.e51\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>The aim of this study was to determine the poly (ADP-ribose) polymerase inhibitors (PARPis) response and outcome of ovarian cancer (OC) patients with BRCA1/2 germline mutation and a history of breast cancer (BC).</p><p><strong>Methods: </strong>Thirty-nine OC patients with BRCA1/2 germline mutation and a history of BC were included. The clinicopathological characteristics, PARPis response and prognosis were analyzed.</p><p><strong>Results: </strong>The median interval from BC to OC diagnosis was 115.3 months (range=6.4-310.1). A total of 38 patients (38/39, 97.4%) received platinum-based chemotherapy after surgical removal. The majority of these patients were reported to be platinum sensitive (92.1%, 35/38). 21 patients (53.8%) received PARPis treatment with 16 patients (76.2%) for maintenance treatment and 5 patients (5/21, 23.8%) for salvage treatment. The median duration for PARPis maintenance and salvage treatment was 14.9 months (range=2.0-56.9) and 8.2 months (range=5.2-20.7), respectively. In the entire cohort, 5-year progression-free survival (PFS) and overall survival (OS) rate was 33.1% and 78.9%, respectively. Patients with BRCA1 mutation had a non-significantly worse 5-year PFS (28.6% vs. 45.8%, p=0.346) and 5-year OS (76.9% vs. 83.3%, p=0.426) than those with BRCA2 mutation. In patients with stage III-IV (n=31), first line PARPis maintenance treatment associated with a non-significantly better PFS (median PFS: NR vs. 22.4 months; 5-year PFS: 64.3% vs. 21.9%, p=0.096).</p><p><strong>Conclusion: </strong>The current study shows that these patients may have a good response to platinum-based chemotherapy and a favorable survival. 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引用次数: 0
摘要
研究目的本研究旨在确定多聚(ADP-核糖)聚合酶抑制剂(PARPis)对 BRCA1/2 基因突变且有乳腺癌(BC)病史的卵巢癌(OC)患者的反应和预后:方法:纳入 39 例 BRCA1/2 基因突变且有 BC 病史的卵巢癌患者。方法:纳入 39 例 BRCA1/2 基因突变且有 BC 病史的 OC 患者,分析其临床病理特征、PARPis 反应和预后:从 BC 诊断到 OC 诊断的中位间隔为 115.3 个月(范围=6.4-310.1)。共有 38 名患者(38/39,97.4%)在手术切除后接受了铂类化疗。据报道,这些患者中的大多数对铂类药物敏感(92.1%,35/38)。21 名患者(53.8%)接受了 PARPis 治疗,其中 16 名患者(76.2%)接受了维持治疗,5 名患者(5/21,23.8%)接受了挽救治疗。PARPis维持治疗和挽救治疗的中位持续时间分别为14.9个月(范围=2.0-56.9)和8.2个月(范围=5.2-20.7)。在整个队列中,5年无进展生存率(PFS)和总生存率(OS)分别为33.1%和78.9%。与 BRCA2 基因突变患者相比,BRCA1 基因突变患者的 5 年无进展生存期(28.6% 对 45.8%,P=0.346)和 5 年总生存期(76.9% 对 83.3%,P=0.426)无显著性差异。在III-IV期患者(31人)中,一线PARPis维持治疗与无显著性改善的PFS相关(中位PFS:NR vs. 22.4个月;5年PFS:64.3% vs. 21.9%,p=0.096):结论:目前的研究表明,这些患者可能对铂类化疗有良好的反应,并有较好的生存期。结论:本研究表明,这些患者对以铂类为基础的化疗反应良好,生存期较长,可以从PARPis治疗中获益,并有可能成为PARPis的合适候选者。
PARPis response and outcome of ovarian cancer patients with BRCA1/2 germline mutation and a history of breast cancer.
Objective: The aim of this study was to determine the poly (ADP-ribose) polymerase inhibitors (PARPis) response and outcome of ovarian cancer (OC) patients with BRCA1/2 germline mutation and a history of breast cancer (BC).
Methods: Thirty-nine OC patients with BRCA1/2 germline mutation and a history of BC were included. The clinicopathological characteristics, PARPis response and prognosis were analyzed.
Results: The median interval from BC to OC diagnosis was 115.3 months (range=6.4-310.1). A total of 38 patients (38/39, 97.4%) received platinum-based chemotherapy after surgical removal. The majority of these patients were reported to be platinum sensitive (92.1%, 35/38). 21 patients (53.8%) received PARPis treatment with 16 patients (76.2%) for maintenance treatment and 5 patients (5/21, 23.8%) for salvage treatment. The median duration for PARPis maintenance and salvage treatment was 14.9 months (range=2.0-56.9) and 8.2 months (range=5.2-20.7), respectively. In the entire cohort, 5-year progression-free survival (PFS) and overall survival (OS) rate was 33.1% and 78.9%, respectively. Patients with BRCA1 mutation had a non-significantly worse 5-year PFS (28.6% vs. 45.8%, p=0.346) and 5-year OS (76.9% vs. 83.3%, p=0.426) than those with BRCA2 mutation. In patients with stage III-IV (n=31), first line PARPis maintenance treatment associated with a non-significantly better PFS (median PFS: NR vs. 22.4 months; 5-year PFS: 64.3% vs. 21.9%, p=0.096).
Conclusion: The current study shows that these patients may have a good response to platinum-based chemotherapy and a favorable survival. And these patients can benefit from PARPis treatment and will likely be suitable candidates for PARPis.
期刊介绍:
The Journal of Gynecologic Oncology (JGO) is an official publication of the Asian Society of Gynecologic Oncology. Abbreviated title is ''J Gynecol Oncol''. It was launched in 1990. The JGO''s aim is to publish the highest quality manuscripts dedicated to the advancement of care of the patients with gynecologic cancer. It is an international peer-reviewed periodical journal that is published bimonthly (January, March, May, July, September, and November). Supplement numbers are at times published. The journal publishes editorials, original and review articles, correspondence, book review, etc.