现代肿瘤医学
現代腫瘤醫學
현대종류의학
JOURNAL OF MODERN ONCOLOGY
2014年
9期
2142-2144
,共3页
XPG/ERCC5%单核苷酸多态性%奥沙利铂
XPG/ERCC5%單覈苷痠多態性%奧沙利鉑
XPG/ERCC5%단핵감산다태성%오사리박
XPG/ERCC5%polymorphism%oxaliplatin
目的:探讨Ⅲ期大肠癌患者外周血中XPG G3507C单核苷酸多态性与其对奥沙利铂化疗的临床疗效关系。方法:106例Ⅲ期大肠癌患者化疗前抽取静脉血并提取DNA,以TaqMan探针法对XPG G3507C位点进行SNP分型。患者接受奥沙利铂为基础的化疗方案治疗,比较不同基因型与临床特点及化疗疗效的关系。结果:106例患者的XPG G3507C位点G/G、G/C、C/C基因型分布频率分别为36.8%、47.2%和16.0%。针对性别、年龄、肿瘤部位、初诊时血清癌胚抗原水平、ECOG评分、肿瘤分化程度等因素的分层分析结果显示, XPG G3507C基因型分布无显著差异(P>0.05)。三种基因型患者的肿瘤复发或转移率、肿瘤相关死亡率、无疾病生存时间和总生存时间均无统计学差异(P>0.05)。结论:Ⅲ期大肠癌患者外周血中的XPG G3507C单核苷酸多态性与患者临床特征及接受奥沙利铂化疗后的临床疗效可能无相关性。
目的:探討Ⅲ期大腸癌患者外週血中XPG G3507C單覈苷痠多態性與其對奧沙利鉑化療的臨床療效關繫。方法:106例Ⅲ期大腸癌患者化療前抽取靜脈血併提取DNA,以TaqMan探針法對XPG G3507C位點進行SNP分型。患者接受奧沙利鉑為基礎的化療方案治療,比較不同基因型與臨床特點及化療療效的關繫。結果:106例患者的XPG G3507C位點G/G、G/C、C/C基因型分佈頻率分彆為36.8%、47.2%和16.0%。針對性彆、年齡、腫瘤部位、初診時血清癌胚抗原水平、ECOG評分、腫瘤分化程度等因素的分層分析結果顯示, XPG G3507C基因型分佈無顯著差異(P>0.05)。三種基因型患者的腫瘤複髮或轉移率、腫瘤相關死亡率、無疾病生存時間和總生存時間均無統計學差異(P>0.05)。結論:Ⅲ期大腸癌患者外週血中的XPG G3507C單覈苷痠多態性與患者臨床特徵及接受奧沙利鉑化療後的臨床療效可能無相關性。
목적:탐토Ⅲ기대장암환자외주혈중XPG G3507C단핵감산다태성여기대오사리박화료적림상료효관계。방법:106례Ⅲ기대장암환자화료전추취정맥혈병제취DNA,이TaqMan탐침법대XPG G3507C위점진행SNP분형。환자접수오사리박위기출적화료방안치료,비교불동기인형여림상특점급화료료효적관계。결과:106례환자적XPG G3507C위점G/G、G/C、C/C기인형분포빈솔분별위36.8%、47.2%화16.0%。침대성별、년령、종류부위、초진시혈청암배항원수평、ECOG평분、종류분화정도등인소적분층분석결과현시, XPG G3507C기인형분포무현저차이(P>0.05)。삼충기인형환자적종류복발혹전이솔、종류상관사망솔、무질병생존시간화총생존시간균무통계학차이(P>0.05)。결론:Ⅲ기대장암환자외주혈중적XPG G3507C단핵감산다태성여환자림상특정급접수오사리박화료후적림상료효가능무상관성。
Objective:To observe the relationship between XPG G3507C gene polymorphism and clinical outcome of patients with stage Ⅲcolorectal cancer treated by oxaliplatin chemotherapy.Methods:DNA was extracted from pe-ripheral venous blood before chemotherapy for 106 stage Ⅲ colorectal cancer patients.XPG G3507C genotypes were determined by TaqMan.All patients were treated with oxaliplatin based chemotherapy regimens.Results:The frequen-cy of G/G,G/C and C/C genotypes was 36.8%,47.2% and 16.0%,respectively(P>0.05).There was no signifi-cant difference between XPG G3507C genotypes and patients'gender,age,tumor location,serum carcinoembryonic an-tigen level,ECOG score and tumor differentiation.No significant difference between genotypes and disease recurrence and metastasis rates,mortality,disease-free survival time and overall survival time was found(P>0.05 ).Conclu-sion:There was no association between XPG G3507C gene polymorphism and clinical characteristic and clinical out-come of patients with stage Ⅲ colorectal cancer treated by oxaliplatin chemotherapy.