中国癌症防治杂志
中國癌癥防治雜誌
중국암증방치잡지
CHINESE JOURNAL OF ONCOLOGY PREVENTION AND TREATMENT
2014年
1期
35-38
,共4页
董翠梅%康马飞%赵燕仪%林静%陶利英
董翠梅%康馬飛%趙燕儀%林靜%陶利英
동취매%강마비%조연의%림정%도리영
肺肿瘤%非小细胞肺癌%亚甲基四氢叶酸还原酶%基因多态性%化疗疗效
肺腫瘤%非小細胞肺癌%亞甲基四氫葉痠還原酶%基因多態性%化療療效
폐종류%비소세포폐암%아갑기사경협산환원매%기인다태성%화료료효
Lung neoplasms%Non-small cell lung cancer%Methylenetetrahydrofolate reductase%Gene polymorphism%Chemotherapy
目的:观察肺腺癌患者亚甲基四氢叶酸还原酶(MTHFR)基因C677T多态性与化疗疗效的关系。方法化疗前抽取92例肺腺癌患者外周血液,用聚合酶链式反应-限制性片断长度多态性(PCR-RFLP)方法检测MTHFR基因C677T多态性,并分析其与化疗的疗效关系。结果92例肺腺癌患者中,MTHFR基因C677T野生型(CC)的分布为60.9%(56/92),纯合突变型(TT)为14.1%(13/92),杂合突变型(CT)为25.0%(23/92)。一线化疗方案使用培美曲塞/卡铂的疗效:野生型(CC)PR 20例,SD 19例,PD 17例,总有效率(ORR)为35.7%;纯合突变型(TT)PR 2例,SD 7例, PD 4例,ORR为15.4%;杂合突变型(CT)SD 13例,PD 10例,ORR为0。CC型患者化疗ORR显著高于TT型和CT型者(P=0.001)。CC型与TT型/CT型患者的肿瘤进展时间(TTP)分别为6.2个月和4.7个月,差异有统计学意义(P=0.023)。二线化疗方案使用吉西他滨/奈达铂或多西紫杉醇/奈达铂的疗效:CC型PR 2例,SD 5例,PD 10例;TT型SD 3例;CT型PR 1例,SD 2例,PD 7例,CC型与TT型/CT型患者的ORR比较,差异无统计学意义(P=1.000)。结论 MTHFR基因C677T野生型(CC)肺腺癌患者可能是使用培美曲塞联合卡铂化疗有效的人群。MTHFR基因C677T CC型患者的TTP显著长于TT型患者和CT型患者。MTHFR基因C677T多态性与吉西他滨/奈达铂或多西紫杉醇/奈达铂化疗疗效无关。
目的:觀察肺腺癌患者亞甲基四氫葉痠還原酶(MTHFR)基因C677T多態性與化療療效的關繫。方法化療前抽取92例肺腺癌患者外週血液,用聚閤酶鏈式反應-限製性片斷長度多態性(PCR-RFLP)方法檢測MTHFR基因C677T多態性,併分析其與化療的療效關繫。結果92例肺腺癌患者中,MTHFR基因C677T野生型(CC)的分佈為60.9%(56/92),純閤突變型(TT)為14.1%(13/92),雜閤突變型(CT)為25.0%(23/92)。一線化療方案使用培美麯塞/卡鉑的療效:野生型(CC)PR 20例,SD 19例,PD 17例,總有效率(ORR)為35.7%;純閤突變型(TT)PR 2例,SD 7例, PD 4例,ORR為15.4%;雜閤突變型(CT)SD 13例,PD 10例,ORR為0。CC型患者化療ORR顯著高于TT型和CT型者(P=0.001)。CC型與TT型/CT型患者的腫瘤進展時間(TTP)分彆為6.2箇月和4.7箇月,差異有統計學意義(P=0.023)。二線化療方案使用吉西他濱/奈達鉑或多西紫杉醇/奈達鉑的療效:CC型PR 2例,SD 5例,PD 10例;TT型SD 3例;CT型PR 1例,SD 2例,PD 7例,CC型與TT型/CT型患者的ORR比較,差異無統計學意義(P=1.000)。結論 MTHFR基因C677T野生型(CC)肺腺癌患者可能是使用培美麯塞聯閤卡鉑化療有效的人群。MTHFR基因C677T CC型患者的TTP顯著長于TT型患者和CT型患者。MTHFR基因C677T多態性與吉西他濱/奈達鉑或多西紫杉醇/奈達鉑化療療效無關。
목적:관찰폐선암환자아갑기사경협산환원매(MTHFR)기인C677T다태성여화료료효적관계。방법화료전추취92례폐선암환자외주혈액,용취합매련식반응-한제성편단장도다태성(PCR-RFLP)방법검측MTHFR기인C677T다태성,병분석기여화료적료효관계。결과92례폐선암환자중,MTHFR기인C677T야생형(CC)적분포위60.9%(56/92),순합돌변형(TT)위14.1%(13/92),잡합돌변형(CT)위25.0%(23/92)。일선화료방안사용배미곡새/잡박적료효:야생형(CC)PR 20례,SD 19례,PD 17례,총유효솔(ORR)위35.7%;순합돌변형(TT)PR 2례,SD 7례, PD 4례,ORR위15.4%;잡합돌변형(CT)SD 13례,PD 10례,ORR위0。CC형환자화료ORR현저고우TT형화CT형자(P=0.001)。CC형여TT형/CT형환자적종류진전시간(TTP)분별위6.2개월화4.7개월,차이유통계학의의(P=0.023)。이선화료방안사용길서타빈/내체박혹다서자삼순/내체박적료효:CC형PR 2례,SD 5례,PD 10례;TT형SD 3례;CT형PR 1례,SD 2례,PD 7례,CC형여TT형/CT형환자적ORR비교,차이무통계학의의(P=1.000)。결론 MTHFR기인C677T야생형(CC)폐선암환자가능시사용배미곡새연합잡박화료유효적인군。MTHFR기인C677T CC형환자적TTP현저장우TT형환자화CT형환자。MTHFR기인C677T다태성여길서타빈/내체박혹다서자삼순/내체박화료료효무관。
Objective To investigate a possible correlation between C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR)gene and chemotherapy efficacy in patients with pulmonary adenocarcinoma. Methods Peripheral blood samples from 92 p atients with pulmonary adenocarcinoma were collected before chemotherapy,and the C677T polymorphism was genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).We examined whether genotype correlated with whether the patients showed partial response(PR),stable disease(SD)or progressive disease(PD)following chemotherapy. Results Of the 92 patients,56 (60.9%) had wild-type genotype (CC),13(14.1%) were homozygous mutant(TT),and 23(25.0%) were heterozygous mutant(CT).Among the patients treated with pemetrexed/carpoplatin as first-line regimen,CC patients showed an overall response rate (ORR)of 35.7%,with 20 CC patients achieving PR;19,SD;and 17,PD.Among TT patients,ORR was 15.4%,with 2 patients achieving PR;7,SD;and 4,PD.Among CT patients,ORR was 0,with 13 achieving SD and 10,PD.ORR was significantly higher in CC patients than in TT or CT patients (P=0.001).In addition,CC patients showed significantly longer time to progression (6.2 months)than did TT or CT patients (4.7 months;P=0.023).Among the patients treated with gemcitabine/nedaplatin or docetaxel/nedaplatin as second-line regimen,2 CC patients showed PR;5,SD;and 10,PD.3 TT patients achieved SD;among CT patients, 1 achieved PR,2 SD and 7,PD.ORR was similar between CC and TT/CT patients (P=1.000). Conclusions Pemetrexed in combination with carboplatin may be associated with greater therapeutic efficacy and longer time to progression in CC patients than in TT/C T patients.However,genotype at the MTHFR C677T polymorphism does not appear to influence the therapeutic efficacy of gemcitabine/nedaplatin or docetaxel/nedaplatin.