Department of Primary Health Care, University of Pécs, Rákóczi u 2, H-7623 Pécs, Hungary.
Faculty of Health Sciences, Doctoral School of Health Sciences, University of Pécs, Vörösmarty u 4, H-7621 Pécs, Hungary.
Genes (Basel). 2019 Aug 8;10(8):599. doi: 10.3390/genes10080599.
Prostate cancer is the fifth leading cause of male cancer death worldwide. Although docetaxel chemotherapy has been used for more than fifteen years to treat metastatic castration resistant prostate cancer, the high inter-individual variability of treatment efficacy and toxicity is still not well understood. Since prostate cancer has a high heritability, inherited biomarkers of the genomic signature may be appropriate tools to guide treatment. In this review, we provide an extensive overview and discuss the current state of the art of pharmacogenomic biomarkers modulating docetaxel treatment of prostate cancer. This includes (1) research studies with a focus on germline genomic biomarkers, (2) clinical trials including a range of genetic signatures, and (3) their implementation in treatment guidelines. Based on this work, we suggest that one of the most promising approaches to improve clinical predictive capacity of pharmacogenomic biomarkers in docetaxel treatment of prostate cancer is the use of compound, multigene pharmacogenomic panels defined by specific clinical outcome measures. In conclusion, we discuss the challenges of integrating prostate cancer pharmacogenomic biomarkers into the clinic and the strategies that can be employed to allow a more comprehensive, evidence-based approach to facilitate their clinical integration. Expanding the integration of pharmacogenetic markers in prostate cancer treatment procedures will enhance precision medicine and ultimately improve patient outcomes.
前列腺癌是全球男性癌症死亡的第五大主要原因。虽然多西他赛化疗已经被用于治疗转移性去势抵抗性前列腺癌超过十五年,但治疗效果和毒性的个体间高度差异仍未得到很好的理解。由于前列腺癌具有高度遗传性,基因组特征的遗传生物标志物可能是指导治疗的合适工具。在这篇综述中,我们提供了一个广泛的概述,并讨论了目前调节多西他赛治疗前列腺癌的药物基因组生物标志物的最新进展。这包括(1)专注于种系基因组生物标志物的研究,(2)包含多种遗传特征的临床试验,以及(3)它们在治疗指南中的实施。基于这些工作,我们认为,改善多西他赛治疗前列腺癌中药物基因组生物标志物临床预测能力的最有前途的方法之一是使用特定临床结果衡量标准定义的复合、多基因药物基因组面板。总之,我们讨论了将前列腺癌药物基因组生物标志物整合到临床中的挑战,以及可以采用的策略,以允许更全面、基于证据的方法来促进其临床整合。扩大药物遗传学标记在前列腺癌治疗方案中的整合将增强精准医疗,并最终改善患者的预后。