中药对伊立替康致腹泻的预防作用及其与UGT1A1*28基因多态性的关系

Z. Pan, Zhansheng Jiang, Y. Ba, Jianzhong Liu, Yumei Feng, G. Xie
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引用次数: 1

摘要

目的:本研究旨在通过UGT1A1*28基因多态性分析中药对伊立替康化疗后腹泻的预防作用。方法:选取2011年10月至2013年5月天津医科大学肿瘤研究所附属医院中西医结合科收治的200例患者,随机分为对照组(单纯化疗组)和中草药组(化疗联合中草药组)。所有患者同意化疗前进行UGT1A1*28基因多态性检测。从化疗前2天至化疗后5天给予草药,有或没有氟尿嘧啶、亚叶酸和伊立替康方案。记录不良反应,定期评价近期疗效。结果:TA6/6野生基因型144例,非野生基因型56例(其中TA7/7纯合12例,TA6/7杂交44例)。共有58名患者出现2至4级腹泻。与对照组相比,中药组腹泻发生率降低14%(22%对36%,P=0.029)。除腹泻外,中药组2至4级呕吐明显低于对照组(15%比27%,P=0.037)。总有效率为37.5%。两组间无显著差异(40% vs. 35%, P=0.465)。UGT1A1*28野生基因型患者2 ~ 4级腹泻发生率(22.9%比44.6%,P=0.002)和2 ~ 4级呕吐发生率(23.2%比16.7%,P=0.016)低于非野生基因型患者。然而,在草药组中,2至4级腹泻(22.2%比21.9%,P=0.974)和呕吐(18.5%比13.7%,P=0.777)的发生率在非野生型组和野生型组之间无显著性差异。结论:中药能有效预作者单位:1天津医科大学肿瘤医院中西医结合科,国家肿瘤临床医学研究中心,天津市肿瘤防治重点实验室(天津市300060);2消化肿瘤内科;3结直肠肿瘤科;4生化及分子生物学研究室􀆽本文课题受天津市中医药管理局中医中西医结合科研项目(编号:11107)资助通信作者:谢广茹xieguangru@126.com 1441中国肿瘤临床2013年第40卷第23期下巴J肿瘤防治杂志2013 40卷,23号www.cjco.cn发泄腹泻伊立替康所致,也适用于UGT1A1 * 28 non-wild基因型患者。UGT1A1*28非野生型腹泻发生率明显高于野生型。因此,在伊立替康化疗前应检测UGT1A1*28基因型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of herbs on preventing diarrhea caused by irinotecan and its correlation with gene polymorphism of UGT1A1*28
Objective: This study aimed to determine the function of herbs in preventing diarrhea after irinotecan chemotherapy and analyze the efficacy of the herbs based on UGT1A1*28 gene polymorphism. Methods: A total of 200 patients admitted to the Department of Synergistic Chinese and Western Medicine, Tianjin Medical University Cancer Institute and Hospital between October 2011 and May 2013 were randomly divided into the control (chemotherapy alone) and herb (chemotherapy combined with herbs) groups. All patients consented to UGT1A1*28 gene polymorphism detection prior to chemotherapy. Herbs were administered from 2 d prior to chemotherapy to 5 d post chemotherapy, with or without the regimen of fluorouracil, folinic acid, and irinotecan. Adverse reactions were recorded, and short-term effect was evaluated regularly. Results: A total of 144 patients had TA6/6 wild genotype, and another 56 patients had non-wild genotype (12 of the 56 cases were TA7/7 homozygous, and the other 44 cases were TA6/7 hybrid). A total of 58 patients experienced grades 2 to 4 diarrhea. A 14% decrease in the incidence of diarrhea was observed in the herb group compared with that of the control group (22% vs. 36%, P=0.029). In addition to diarrhea, grades 2 to 4 vomiting was significantly lower in the herb group than in the control group (15% vs. 27%, P=0.037). The overall response rate was 37.5%. No significant difference was found between the two groups (40% vs. 35%, P=0.465). The incidences of grades 2 to 4 diarrhea (22.9% vs. 44.6%, P=0.002) and grades 2 to 4 vomiting (23.2% vs. 16.7%, P=0.016) were lower in patients with the UGT1A1*28 wild genotype than in those with the non-wild genotype. However, in the herb group, the incidences of grades 2 to 4 diarrhea (22.2% vs. 21.9%, P=0.974) and vomiting (18.5% vs. 13.7%, P=0.777) were not significant between the non-wildand wild-type groups. Conclusion: Herbs can effectively pre作者单位:1天津医科大学肿瘤医院中西医结合科,国家肿瘤临床医学研究中心,天津市肿瘤防治重点实验室(天津市300060);2消化肿瘤内科; 3结直肠肿瘤科;4生化及分子生物学研究室 􀆽本文课题受天津市中医药管理局中医中西医结合科研项目(编号:11107)资助 通信作者:谢广茹 xieguangru@126.com 1441 中国肿瘤临床 2013年第40卷第23期 Chin J Clin Oncol 2013, Vol. 40, No. 23 www.cjco.cn vent the late diarrhea caused by irinotecan, which is also applicable in UGT1A1*28 non-wild genotype patients. Incidence of diarrhea was obviously higher in the cases with UGT1A1*28 non-wild type than in those with wild genotype. Hence, the UGT1A1*28 gene type should be detected prior to chemotherapy with irinotecan.
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