Department of Pharmacy, Cleveland Clinic, Cleveland, OH 44195, USA.
Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
Hum Mol Genet. 2020 Oct 20;29(R2):R177-R185. doi: 10.1093/hmg/ddaa134.
An individual's inherited genetic makeup and acquired genomic variants may account for a significant portion of observable variability in therapy efficacy and toxicity. Pharmacogenomics (PGx) is the concept that treatments can be modified to account for these differences to increase chances of therapeutic efficacy while minimizing risk of adverse effects. This is particularly applicable to oncology in which treatment may be multimodal. Each tumor type has a unique genomic signature that lends to inclusion of targeted therapy but may be associated with cumulative toxicity, such as cardiotoxicity, and can impact quality of life. A greater understanding of therapeutic agents impacted by PGx and subsequent implementation has the potential to improve outcomes and reduce risk of drug-induced adverse effects.
个体的遗传基因组成和后天获得的基因组变异可能是治疗效果和毒性可观察到的变异性的重要原因。药物基因组学(PGx)是指可以针对这些差异来调整治疗方法,以提高治疗效果的机会,同时最大限度地降低不良反应的风险。这在肿瘤学中尤其适用,因为治疗可能是多模式的。每种肿瘤类型都有独特的基因组特征,这使得靶向治疗成为可能,但也可能与累积毒性相关,如心脏毒性,并会影响生活质量。对受 PGx 影响的治疗药物的进一步了解及其后续实施,有可能改善治疗效果并降低药物不良反应的风险。