Department of Obstetrics and Gynecology, Chang Gung Memorial Hospital Linkou Branch and Chang Gung University College of Medicine, Taoyuan 333, Taiwan.
Gynecologic Cancer Research Center, Chang Gung Memorial Hospital Linkou Branch and Chang Gung University, Taoyuan 333, Taiwan.
Genes (Basel). 2021 Oct 9;12(10):1593. doi: 10.3390/genes12101593.
With the advent of next-generation sequencing (NGS), The Cancer Genome Atlas (TCGA) research network has given gynecologic cancers molecular classifications, which impacts clinical practice more and more. New cancer treatments that identify and target pathogenic abnormalities of genes have been in rapid development. The most prominent progress in gynecologic cancers is the clinical efficacy of poly(ADP-ribose) polymerase (PARP) inhibitors, which have shown breakthrough benefits in reducing hazard ratios (HRs) (HRs between 0.2 and 0.4) of progression or death from mutated ovarian cancer. Immune checkpoint inhibition is also promising in cancers that harbor mismatch repair deficiency (dMMR)/microsatellite instability (MSI). In this review, we focus on the druggable genetic alterations in gynecologic cancers by summarizing literature findings and completed and ongoing clinical trials.
随着下一代测序(NGS)的出现,癌症基因组图谱(TCGA)研究网络为妇科癌症提供了分子分类,这对临床实践的影响越来越大。越来越多的新癌症治疗方法正在识别和针对基因的致病性异常。妇科癌症最显著的进展是聚(ADP-核糖)聚合酶(PARP)抑制剂的临床疗效,它在降低突变卵巢癌的进展或死亡风险比(HR)(0.2 至 0.4 之间的 HR)方面显示出突破性的益处。在存在错配修复缺陷(dMMR)/微卫星不稳定(MSI)的癌症中,免疫检查点抑制也很有前景。在这篇综述中,我们通过总结文献发现和已完成及正在进行的临床试验,重点介绍妇科癌症中可用药的遗传改变。