Laboratory of Pharmacogenetics & Pharmacogenomics, Pharmacy Department, Hospital General Universitario Gregorio Marañón, Doctor Esquerdo 46, Madrid, Spain.
Pharmacogenomics. 2012 Jul;13(10):1173-91. doi: 10.2217/pgs.12.95.
Chemotherapeutic agents used in colorectal cancer are frequently associated with severe adverse reactions that compromise the efficacy of treatment. Predicting toxicity could enable therapy to be tailored. Genetic variations have been associated with toxicity in patients treated with fluoropyrimidines (5-fluorouracil, capecitabine and tegafur), oxaliplatin, irinotecan and cetuximab. Complexity of treatment and variability in toxicity classifications make it difficult to compare studies. This article analyzes the association between toxicity and polymorphisms in DPYD, TYMS, MTHFR, ABCB1, UGT1A1, ERCC1, ERCC2, XRCC1, GSTT1 and GSTM1. In addition, the state-of-the-art and future perspectives are discussed.
结直肠癌化疗药物常伴有严重不良反应,影响治疗效果。预测毒性可使治疗个体化。氟嘧啶类(5-氟尿嘧啶、卡培他滨和替加氟)、奥沙利铂、伊立替康和西妥昔单抗治疗的患者中,遗传变异与毒性相关。治疗的复杂性和毒性分类的变异性使得难以比较研究。本文分析了 DPYD、TYMS、MTHFR、ABCB1、UGT1A1、ERCC1、ERCC2、XRCC1、GSTT1 和 GSTM1 多态性与毒性之间的关系。此外,还讨论了最新进展和未来展望。