Lübeck University Hospital, Lübeck, Germany.
Guy's Hospital, London, UK.
Eur Urol. 2021 Apr;79(4):519-529. doi: 10.1016/j.eururo.2020.12.039. Epub 2021 Jan 23.
Genomic testing is becoming increasingly important in patients with advanced prostate cancer (PC) and is being incorporated in clinical practice to guide treatment.
To review the current understanding of genomic alterations and the status of genomic testing in patients with metastatic castration-resistant PC (mCRPC), and the potential use of genomic tests in clinical practice.
We reviewed recent publications (past 15 yr) from PubMed, proceedings of scientific conferences, and published guidelines. Reports on mCRPC in the following areas were selected: development, testing, and validation of techniques for identifying genomic alterations; molecular characterization; and trials of genetically targeted therapies.
mCRPC tumors harbor molecular alterations that are possible targets for treatment, and a number of therapies are in development to exploit these alterations (eg, PD-1 inhibitors, PARP inhibitors, tyrosine kinase inhibitors). Next-generation sequencing of DNA from tumor tissue can identify somatic alterations that would not be identified by germline testing. Work is ongoing to evaluate the use of less invasive somatic testing methods (eg, sequencing of cell-free circulating tumor DNA). Current international guidelines recommend germline and/or somatic testing for men with advanced and/or high-risk PC regardless of family history to identify those with homologous recombination repair gene mutations or mismatch repair defects/microsatellite instability who may be eligible for treatment with a PARP inhibitor or pembrolizumab, respectively.
Genomic testing for mCRPC may provide information on prognostic, predictive, and resistance biomarkers. Although the incorporation of testing into clinical practice remains challenging, routine genomic testing of men with advanced PC is recommended to guide management and treatment decisions.
Similar to many cancers, prostate cancer is caused by defects in the cancer's DNA, which are called genetic or genomic defects. New treatments targeting these defects are approved for metastatic castration-resistant prostate cancer. Specific new tests are under development to detect these potentially treatable genetic defects.
基因组检测在晚期前列腺癌(PC)患者中变得越来越重要,并被纳入临床实践以指导治疗。
综述转移性去势抵抗性前列腺癌(mCRPC)患者中基因组改变的最新认识以及基因组检测的现状,以及基因组检测在临床实践中的潜在应用。
我们回顾了来自 PubMed 的最新出版物(过去 15 年)、科学会议的会议记录和已发布的指南。选择了以下领域的 mCRPC 报告:用于识别基因组改变的技术的开发、检测和验证;分子特征;以及基因靶向治疗的试验。
mCRPC 肿瘤存在可能成为治疗靶点的分子改变,并且有许多疗法正在开发中以利用这些改变(例如,PD-1 抑制剂、PARP 抑制剂、酪氨酸激酶抑制剂)。肿瘤组织的 DNA 下一代测序可以识别不会通过种系测试识别的体细胞改变。正在努力评估使用侵入性较小的体细胞测试方法(例如,循环肿瘤 DNA 测序)。当前的国际指南建议对晚期和/或高危 PC 的男性进行种系和/或体细胞检测,无论家族史如何,以确定那些具有同源重组修复基因突变或错配修复缺陷/微卫星不稳定性的男性,他们可能有资格分别接受 PARP 抑制剂或 pembrolizumab 治疗。
mCRPC 的基因组检测可能提供预后、预测和耐药生物标志物的信息。尽管将检测纳入临床实践仍然具有挑战性,但建议对晚期 PC 男性进行常规基因组检测,以指导管理和治疗决策。
与许多癌症一样,前列腺癌是由癌症 DNA 的缺陷引起的,这些缺陷称为遗传或基因组缺陷。针对这些缺陷的新治疗方法已被批准用于转移性去势抵抗性前列腺癌。正在开发特定的新测试来检测这些潜在可治疗的遗传缺陷。