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作 者:季明华[1] 查文武[1] 恽文[2] 李建[3] 赵建华[4] 唐金海[3]
机构地区:[1]江苏省肿瘤医院放疗科,江苏南京210009 [2]徐州医学院外科系,江苏徐州221004 [3]江苏省肿瘤医院乳腺外科,江苏南京210009 [4]江苏省肿瘤医院江苏省临床检验中心,江苏南京210009
出 处:《中华肿瘤防治杂志》2012年第10期735-737,共3页Chinese Journal of Cancer Prevention and Treatment
基 金:国家自然科学基金(30840093)
摘 要:目的:探讨MDR1基因多态性与乳腺癌患者化疗疗效以及血液毒副反应的关系。方法:筛选70例新辅助化疗的女性患者,利用PCR-RFLP技术检测其外周血MDR1C3435T基因型,分析不同基因型患者化疗后的疗效及血液毒副反应。结果:70例新辅助化疗患者当中,3435TT基因型化疗有效率仅为23.1%,与3435CC和3435CT基因型相比差异有统计学意义(χ2=6.122,P=0.047,95%CI:0.043~0.051);血液毒性方面,3435CC型患者中性粒细胞Ⅲ~Ⅳ度减少的发生率为6.7%,较CT型(37.5%)和TT型(53.8%)发生率低(χ2=7.512,P=0.023,95%CI:0.016~0.021)。结论:携带MDR1 3435C等位基因的患者其化疗疗效可能较好;携带3435T等位基因的患者其中性粒细胞减少的风险可能较高。OBJECTIVE: To investigate whether MDR1 polymorphisms are associated with therapeutic outcome and hematologic toxicities of preoperative chemotherapy in breast cancer patients. METHODS: MDR1 variants were determined in the blood samples from 70 patients by using PCR-RFLP technique. An analysis was carried out among the genotypes and therapeutic outcome and hematologic toxicities. RESULTS: The efficient rate of patients carrying MDR1 3435TT was 23.1% ,significantly lower than those carrying CC or CT(Х^2 =6. 122,P:0. 047,95%CI:0. 043-0. 051). Patients carrying MDR1 3435CC showed a significantly lower toxicity response rate of Ⅲ- Ⅳ degree neutropenia (6.7 % ) than those with 3435 CT (37.5%),3435TT(53.8%,Х2=7. 512,P=0. 023,95%CI:0. 016-0. 021). CONCLUSION: Patients carrying MDR1 3435C allele may have better response to chemotherapy,and those with T allele may have an increased risk of developing neutropenia.
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