首页|结直肠癌MMR表达与微卫星病灶状态及预后水平的关联研究

结直肠癌MMR表达与微卫星病灶状态及预后水平的关联研究

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目的 分析结直肠癌错配修复(MMR)基因表达情况与微卫星病灶状态及预后水平的关联。方法 本次研究以2020年7月至2022年7月河南省濮阳惠民医院收治的102例结直肠癌患者为研究对象,根据免疫组化检测结果,将MMR表达缺失的42例患者列为dMMR组,将其余60例MMR完全表达的患者列为pMMR组,收集、对比两组患者的一般资料、临床资料,经统计学单因素分析、Logistic多因素回归分析归纳结直肠癌MMR表达缺失的危险因素;所有患者均行含奥沙利铂的一线化疗,并开展为期1年随访,比较两组治疗后的生存情况,应用Spearman相关性系数验证MMR表达与微卫星不稳定(MSI)及预后水平的关联。结果 统计学单因素分析结果显示,两组患者的年龄、病灶直径、肿瘤分化程度、肿瘤区域淋巴结受累情况、肿瘤远处转移情况及微卫星病灶状态均差异有统计学意义(P<0。05);Logistic多因素回归分析结果显示,年龄≥60岁、病灶直径≥5 cm、肿瘤低分化、区域淋巴结受累N0、肿瘤远处转移M0、微卫星病灶检测标志物<40%或≥40%(MSI-L或MSI-H)为导致结直肠癌MMR表达缺失的主要影响因素。经含奥沙利铂一线化疗治疗后,pMMR组的客观缓解率(ORR)为75。00%(45/60),疾病控制率(DCR)为80。00%(48/60),中位无进展生存期(PFS)为(10。24±3。35)个月,中位总生存期(OS)为(11。46±2。49)个月,均高于dMMR组[52。38%(22/42)、59。52%(25/42)、(8。28±3。14)个月、(10。33±2。02)个月],MSI 为(32。44±5。18)%,低于 dMMR组(35。45±5。26)%,差异有统计学意义(P<0。05)。经Spearman相关性系数验证,MMR表达与结直肠癌的O RR、DCR、中位PFS、中位OS负相关,与MSI表达正相关。结论 区域淋巴结未受累且无发生远处转移,及MSI为导致结直肠癌MMR表达缺失的主要影响因素,MMR表达缺失可导致结直肠癌患者MSI,若患者存在dMMR或MSI不宜应用含奥沙利铂一线化疗治疗。
Correlation study between MMR expression and microsatellite lesion status and prognosis level in colorectal cancer
[Objective]To analyze the correlation between the expression of mismatch repair(MMR)gene in colorectal cancer and the status and prognosis of microsatellite lesions.[Methods]This study focuses on 102 colorectal cancer patients admitted from July 2020 to July 2022.Based on immunohistochemical results,42 patients with MMR expression deficiency were classified as dMMR,and the remaining 60 patients with full MMR expression were classified as pMMR group.General and clinical data of the two groups of patients were collected and compared,and risk factors for MMR expression deficiency in colorectal cancer were summarized through statistical univariate analysis and logistic multiple regression analysis.All patients received first-line chemotherapy containing Oxaliplatin and were followed up for one year to compare the survival of the two groups after treatment.Spearman correlation coefficient was used to verify the correlation between MMR expression and microsatellite instability(MSI)and prognosis.[Results]The results of statistical univariate analysis showed that there were certain differences in age,lesion diameter,tumor differentiation,lymph node involvement in the tumor area,distant tumor metastasis,and microsatellite lesion status between the two groups of patients(P<0.05).The results of logistic multiple factor regression analysis showed that age ≥60 years old,lesion diameter ≥5 cm,poorly differentiated tumor,unaffected regional lymph nodes,no distant metastasis of the tumor,and microsatellite lesion detection biomarkers<40%or ≥40%(MSH-L or MSI-H)were the main influencing factors for the loss of MMR expression in colorectal cancer.After the first-line chemotherapy with Oxaliplatin,the objective response rate(ORR)of the pMMR group was 75.00%(45/60),the disease control rate(DCR)was 80.00%(48/60),the median progression-free survival(PFS)was 10.24±3.35 months,and the median overall survival(OS)was 11.46±2.49 months,which were higher than those of the dMMR group[52.38%(22/42),59.52%(25/42),8.28±3.14 months,and 10.33±2.02 months],and the MSI was 32.44%±5.18%,which was lower than that of the dMMR group 35.45%±5.26%(P<0.05).According to Spearman correlation coefficient validation,MMR expression is negatively correlated with ORR,DCR,median PFS,and median OS in colorectal cancer,and positively correlated with MSI expression.[Conclusion]The absence of involvement of regional lymph nodes and the absence of distant metastasis,as well as MSI,are the main influencing factors leading to the loss of MMR expression in colorectal cancer.The loss of MMR expression can lead to MSI in colorectal cancer patients.If patients have dMMR or MSI,they should not be treated with first-line chemotherapy containing Oxaliplatin.

colorectal cancermismatch repair genesunstable microsatellitesprognostic situationcorrelation analysis

韩金兰、张惠瑞

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河南省濮阳惠民医院病理科,河南濮阳 457000

结直肠癌 错配修复基因 微卫星不稳定 预后情况 相关性分析

河南省医学科技攻关计划

LHGJ202200131

2024

中国医学工程
中国医药生物技术协会 卫生部肝胆肠外科研究中心

中国医学工程

影响因子:0.504
ISSN:1672-2019
年,卷(期):2024.32(4)
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