Cura Yasmin, Pérez-Ramírez Cristina, Sánchez-Martín Almudena, Membrive-Jimenez Cristina, Valverde-Merino María Isabel, González-Flores Encarnación, Morales Alberto Jiménez
Pharmacy Service, Pharmacogenetics Unit, Hospital Universitario Virgen de las Nieves, Avda. de las Fuerzas Armadas 2, 18004 Granada, Spain.
Department of Biochemistry and Molecular Biology II, José Mataix Institute of Nutrition and Food Technology, Center for Biomedical Research, Universidad de Granada, Avda. del Conocimiento s/n, 18016 Granada, Spain.
Cancers (Basel). 2023 Mar 17;15(6):1821. doi: 10.3390/cancers15061821.
The aim of this systematic review was to provide a comprehensive overview of the literature published in the last decade on the association of single-nucleotide polymorphisms in genes involved in the pharmacodynamic and pharmacokinetic pathways of capecitabine with treatment outcomes among colorectal cancer patients. A systematic search of the literature published in the last 10 years was carried out in two databases (Medline and Scopus) using keywords related to the objective. Quality assessment of the studies included was performed using an assessment tool derived from the Strengthening the Reporting of Genetic Association (STREGA) statement. Thirteen studies were included in this systematic review. Genes involved in bioactivation, metabolism, transport, mechanism of action of capecitabine, DNA repair, and folate cycle were associated with toxicity. Meanwhile, genes related to DNA repair were associated with therapy effectiveness. This systematic review reveals that several SNPs other than the four variants that are screened in clinical practice could have an impact on treatment outcomes. These findings suggest the identification of future predictive biomarkers of effectiveness and toxicity in colorectal cancer patients treated with capecitabine. However, the evidence is sparse and requires further validation.
本系统评价的目的是全面综述过去十年发表的关于结直肠癌患者中,参与卡培他滨药效学和药代动力学途径的基因单核苷酸多态性与治疗结果之间关联的文献。使用与该目标相关的关键词,在两个数据库(Medline和Scopus)中对过去10年发表的文献进行了系统检索。对纳入研究的质量评估采用了源自加强遗传关联报告(STREGA)声明的评估工具。本系统评价纳入了13项研究。参与卡培他滨生物活化、代谢、转运、作用机制、DNA修复和叶酸循环的基因与毒性相关。同时,与DNA修复相关的基因与治疗效果相关。本系统评价表明,除了临床实践中筛查的四个变体之外,其他几个单核苷酸多态性可能会影响治疗结果。这些发现提示了在接受卡培他滨治疗的结直肠癌患者中,鉴定未来疗效和毒性预测生物标志物的可能性。然而,证据不足,需要进一步验证。