Correlation Engine 2.0
Clear Search sequence regions


  • asians (1)
  • diarrhea (5)
  • genotypes (4)
  • had (3)
  • irinotecan (6)
  • meta analysis (1)
  • neutropenia (6)
  • odds ratios (7)
  • patients (8)
  • TA7 (5)
  • UGT1A1 (5)
  • Sizes of these terms reflect their relevance to your search.

    The UGT1A1*28 polymorphism was suggested to be significantly connected with irinotecan-induced toxicity and response to chemotherapy. However, the results of previous studies are controversial. Hence we carried out a meta-analysis to investigate the effect of UGT1A1*28 polymorphism on severe diarrhea, neutropenia, and response of patients who had undergone irinotecan-based chemotherapy. The PubMed, Web of Science, Wanfang, and CNKI databases were searched for clinical trials assessing the association of UGT1A1*28 polymorphism with severe diarrhea, neutropenia, and response to irinotecan-based chemotherapy. The combined odds ratios (ORs) and 95% confidence intervals (CIs) were used to evaluate the relationship under a fixed- or random-effects model. Fifty-eight studies including 6087 patients with cancer were included. Our results showed that patients carrying the TA6/7 and TA7/7 genotypes had a greater prevalence of diarrhea and neutropenia than those with the TA6/6 genotype (TA6/7+TA7/7 vs. TA6/6: diarrhea, OR = 2.18, 95%CI = 1.68-2.83; neutropenia, OR = 2.15, 95%CI = 1.71-2.70), particularly patients with metastatic colorectal cancer. Stratified analysis showed that Asians with the TA6/7 and TA7/7 genotypes were more likely to have diarrhea and neutropenia, and Caucasians with the TA6/7 and TA7/7 genotypes were more likely to have neutropenia than other groups. However, patients with the TA6/7+TA7/7 genotypes showed a higher response than patients with TA6/6 genotype (OR = 1.20, 95%CI = 1.07-1.34), particularly Caucasians (OR = 1.23, 95%CI = 1.06-1.42) and patients with metastatic colorectal cancer (OR = 1.24, 95%CI = 1.05-1.48). Our data showed that the UGT1A1*28 polymorphism had a significant relationship with toxicity and response to irinotecan-based chemotherapy. This polymorphism may be useful as a monitoring index for cancer patients receiving irinotecan-based chemotherapy.

    Citation

    Xing-Han Liu, Jun Lu, Wei Duan, Zhi-Ming Dai, Meng Wang, Shuai Lin, Peng-Tao Yang, Tian Tian, Kang Liu, Yu-Yao Zhu, Yi Zheng, Qian-Wen Sheng, Zhi-Jun Dai. Predictive Value of UGT1A1*28 Polymorphism In Irinotecan-based Chemotherapy. Journal of Cancer. 2017;8(4):691-703


    PMID: 28367249

    View Full Text