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苏州大学附属第二医院药学部,江苏 苏州 215004
Published:30 March 2024,
Received:19 September 2023,
Revised:28 February 2024,
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汤柳星,吕波,蒋文婷等.基因多态性对含奥沙利铂化疗方案治疗Ⅲ、Ⅳ期结直肠癌疗效及毒副作用的影响 Δ[J].中国药房,2024,35(06):734-738.
TANG Liuxing,LYU Bo,JIANG Wenting,et al.Effects of gene polymorphism on efficacy and toxic effect of chemotherapy regimen containing oxaliplatin in stage Ⅲ and Ⅳ colorectal cancer[J].ZHONGGUO YAOFANG,2024,35(06):734-738.
汤柳星,吕波,蒋文婷等.基因多态性对含奥沙利铂化疗方案治疗Ⅲ、Ⅳ期结直肠癌疗效及毒副作用的影响 Δ[J].中国药房,2024,35(06):734-738. DOI: 10.6039/j.issn.1001-0408.2024.06.17.
TANG Liuxing,LYU Bo,JIANG Wenting,et al.Effects of gene polymorphism on efficacy and toxic effect of chemotherapy regimen containing oxaliplatin in stage Ⅲ and Ⅳ colorectal cancer[J].ZHONGGUO YAOFANG,2024,35(06):734-738. DOI: 10.6039/j.issn.1001-0408.2024.06.17.
目的
2
探讨
GSTP1、XRCC1、ABCB1、MTHFR
基因多态性对接受含奥沙利铂化疗方案Ⅲ、Ⅳ期结直肠癌患者疗效及毒副作用的影响。
方法
2
回顾性收集2018年9月至2020年3月苏州大学附属第二医院接受含奥沙利铂化疗方案(XELOX、FOLFOX)的Ⅲ、Ⅳ期结直肠癌患者资料76例。采用单因素、多因素COX回归模型分析基因型与无进展生存期(PFS)、毒副作用的相关性。
结果
2
ABCB1
3435T>C位点C等位基因(TC/CC型)携带者的疾病进展风险显著高于TT基因型患者[HR=2.39,95%CI(1.05,5.50),
P
=0.038],Ⅳ期患者的疾病进展风险显著高于Ⅲ期患者[HR=8.11,95%CI(3.39,19.40),
P
<0.001];化疗方案、Karnofsky功能状态评分、肿瘤部位对疾病进展的影响不明显(
P
>0.05)。基因位点的突变与不良反应无相关性(
P
>0.05)。
结论
2
携带
ABCB1
TC/CC型且接受含奥沙利铂化疗方案患者的疾病进展风险较高,这可能与接受此类化疗方案的Ⅳ期结直肠癌患者(TT型)有更长的PFS相关,而
GSTP1、XRCC1、MTHFR
基因多态性无显著影响。
OBJECTIVE
2
To investigate the effects of
GSTP1, XRCC1, ABCB1, MTHFR
gene polymorphisms on efficacy and toxic effect of chemotherapy regimen containing oxaliplatin in patients with stage Ⅲ and Ⅳ colorectal cancer patients.
METHODS
2
Clinical data of 76 patients with stage Ⅲ and Ⅳ colorectal cancer who received chemotherapy regimen containing oxaliplatin (XELOX,FOLFOX) were collected from the Second Affiliated Hospital of Soochow University from September 2018 to March 2020. The correlation of genotypes with progression-free survival (PFS) and toxic effect was analyzed by using univariate and multivariate COX regression model.
RESULTS
2
Carriers of the
ABCB1
3435T>C locus C allele (TC/CC) had a significantly higher risk of progression compared to TT genotype patients [HR=2.39, 95%CI (1.05,5.50),
P
=0.038]. The risk of progression in patients at stage Ⅳ was significantly higher than those at stage Ⅲ [HR=8.11, 95%CI(3.39,19.40),
P
<0.001]. Chemotherapy regimen, Karnofsky performance status score and tumor site had no significant effect on disease progression (
P
>0.05). Mutations in gene loci were not correlated with adverse reactions (
P
>0.05).
CONCLUSIONS
2
Patients carrying
ABCB1
TC/CC and receiving chemotherapy regimen containing oxaliplatin have a higher risk of disease progression, which may be associated with longer PFS in patients (TT genotype) with stage Ⅳ colorectal cancer receiving the chemotherapy, while
GSTP1
,
XRCC1
, and
MTHFR
gene polymorphisms have no significant impact.
奥沙利铂基因多态性结直肠癌疗效毒副作用相关性
gene polymorphismcolorectal cancerefficacytoxic effectcorrelation
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