...
首页> 外文期刊>BMC Cancer >Similar response rates and survival with PARP inhibitors for patients with solid tumors harboring somatic versus Germline BRCA mutations: a Meta-analysis and systematic review
【24h】

Similar response rates and survival with PARP inhibitors for patients with solid tumors harboring somatic versus Germline BRCA mutations: a Meta-analysis and systematic review

机译:与患有体细胞瘤的实体肿瘤患者的PARP抑制剂类似的响应率和生存率与种系BRCA突变:META分析和系统审查

获取原文
   

获取外文期刊封面封底 >>

       

摘要

PARP inhibitors (PARPi) have recently been approved for various malignancies based on the results of several clinical trials. However, these trials have mostly recruited patients with germline BRCA mutations, and it is unclear whether PARPi have similar efficacy in patients with somatic BRCA mutations. Our study aimed to determine the efficacy of PARPi in patients with somatic BRCA mutations. We performed a meta-analysis comparing overall response rate to PARPi in patients harboring somatic versus germline BRCA mutations. We looked at studies including somatic and germline mutations in BRCA patients that received PARPi. After screening and removing duplicates, 18 studies met our criteria for including both somatic and germline BRCA mutations. Only 8 studies reported response rates for both somatic and germline BRCA mutations. In those studies, 24 out of 43 patients with somatic BRCA mutations (55.8%), and 69 out of 157 (43.9%) patients with germline BRCA patients had a response to therapy to PARPi. This difference was not statistically significant (p?=?0.399). In all five studies that reported progression-free survival, there was no obvious difference in outcomes between somatic versus germline BRCA patients, however a precise statistical analysis could not be performed. Our meta-analysis and systematic review of the literature indicates similar response rates of PARPi therapy in patients with somatic and germline BRCA mutations. Investigation of use of PARPi therapy in a broader patient population, and the inclusion of somatic BRCA mutations in further clinical trials is paramount in improving therapeutic options for our patients.
机译:PARP抑制剂(PARPI)最近根据几种临床试验的结果批准了各种恶性肿瘤。然而,这些试验主要募集了种系BRCA突变患者,目前还不清楚Parpi是否对体细胞BRCA突变患者具有相似的疗效。我们的研究旨在确定Parpi在体细胞BRCA突变患者中的疗效。我们对患有细胞患者与种系BRCA突变的患者进行了荟萃分析比较患者对PARPI的荟萃分析。我们研究了在接受Parpi的BRCA患者中包括细胞和种系突变的研究。在筛选和去除重复后,18项研究达到了包括体细胞和种系BRCA突变的标准。只有8项研究报告了体细胞和种系BRCA突变的反应率。在这些研究中,43例中有44例体细胞BRCA突变(55.8%)和157例(43.9%)的种系BRCA患者的69例对Parpi进行了反应。这种差异没有统计学意义(p?= 0.399)。在报告无进展生存期的所有五项研究中,体细胞与种系BRCA患者的结果没有明显的差异,但不能进行精确的统计分析。我们对文献的荟萃分析和系统审查表明了对细胞和种系BRCA突变患者的PARPI治疗的类似反应率。在更广泛的患者群体中使用PARPI治疗的使用,以及在进一步的临床试验中包含体细胞BRCA突变至关重要的是改善患者治疗选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号