摘要
目的探讨UGT1A1*28基因多态性与CPT-11治疗晚期NSCLC的毒副反应与疗效的关系。方法外周血检测2015年6月至2016年6月在九江市第一人民医院所收治的50例晚期NSCLC患者UGTIA1*28 TATA盒基因序列,并对所有50例患者接受CPT-11为基础化疗方案的患者出现的不良反应和近期疗效随访记录,比较不同基因型之间的差别。结果 50例晚期NSCLC患者中UGTIA1*28位点突变型可以增加发生3级以上腹泻(P=0.007)和3级以上血小板减少(41.7%VS 10.5%,P=0.027)的风险。结论在CPT-11化疗的患者中,UGTl Al*28基因型TA6/7,或TA7/7基因型可增加晚期NSCLC患者发生Ⅲ度以上腹泻及血小板减少的风险,然而不影响化疗的近期疗效。
Objective To explore the realtionship UGT1A1 * 28 gene polymorphisms and irinotecan - associated toxicity and efficacy in treatment of non - small cell lung cancer. Methods The frequency of UGT1A1 *28 TATA box thymine - adenine (TA) was performed by direct sequencing. The influence of the UGT1A1 * 28 polymorphism on the short - term efficacy and toxicity of irinotecan was record. Results Among 50 patients with non - small lung cancer, marked increases in diarrhea ( 58.3% VS 15.8%, P = 0.007) and thrombocytopenia ( 41.7% VS 10.5%, P = 0.027) were observed in patients who had the TA6/7 or T7/7 genotype. Conclusion This study demonstated that UGT1A1 *28 polymorphism TA6/7 or T7/7 increased the risk the developing grade IH or more sever diarrhea and thrombocytopenia for patients after receiving irinotean treatment but no influence on short - term efficacy of chemotherapy.
作者
王璐
龚敏勇
熊超
曾灵芝
WANG Lu GONG Minyong XIONG Chao ZENG Lingzhi(THE Affiliated Jiujiang Hospital of Nanchang University, Jiujiang 332000, Chin)
出处
《广东微量元素科学》
CAS
2017年第5期27-29,共3页
Trace Elements Science
基金
2015年江西省九江市科技计划项目(编号20151001)
2015年中国医疗手牵手工程委员会、北京医学奖励基金会(编号326)