首页|晚期胃癌患者血清miR-191、miR-425表达水平与XELOX化疗敏感性的关系

晚期胃癌患者血清miR-191、miR-425表达水平与XELOX化疗敏感性的关系

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目的 探讨晚期胃癌患者血清微小RNA-191(mi R-191)、微小RNA-425(mi R-425)表达水平与XELOX化疗敏感性的关系,以期为临床治疗决策的制定提供参考.方法 选择2021年1月—2023年12月在陕西某医院接受XELOX方案治疗的104例晚期胃癌患者为研究对象.所有患者接受XELOX方案治疗,根据疗效分为敏感组(36例)和耐药组(68例).化疗前检测患者血清mi R-191、mi R-425水平,同时收集所有患者的临床病理资料.采用受试者工作特征(ROC)曲线分析血清mi R-191、mi R-425预测晚期胃癌患者接受XELOX方案化疗敏感性的价值,采用多因素回归分析探讨晚期胃癌患者接受XELOX方案化疗敏感性的影响因素.结果 耐药组患者血清mi R-191、mi R-425水平均显著高于敏感组患者,差异均有统计学意义(P<0.05).血清mi R-191、mi R-425预测晚期胃癌患者XELOX化疗敏感性的曲线下面积(AUC)(95%CI)分别为0.787(0.742~0.832)、0.840(0.795~0.889),二者联合预测的AUC(95%CI)为0.901(0.856~0.956).敏感组与耐药组患者年龄、性别、美国东部肿瘤协作组体能状态评分(ECOG评分)、肿瘤部位、病理类型的差异均无统计学意义(P>0.05).耐药组低分化、Ⅳ期人数比例均高于敏感组患者,差异均有统计学意义(P<0.05).回归分析结果显示,TNM分期Ⅳ期(OR=2.050,95%CI:1.241~3.386),低分化程度(OR=2.838,95%CI:1.437~5.602),血清mi R-191≥2.27(OR=6.228,95%CI:2.234~17.358),血清mi R-425≥1.91(OR=5.078,95%CI:1.921~13.426)是晚期胃癌患者XELOX化疗敏感性的危险因素(P<0.05).结论 血清mi R-191、mi R-425表达水平与晚期胃癌患者XELOX化疗耐药有关,二者联合用于晚期胃癌患者XELOX化疗敏感性的预测价值较高.
Relationship between serum mi R-191,mi R-425 expression levels and XELOX chemotherapy sensitivity in patients with advanced gastric cancer
Objective To explore the relationship between the expression levels of serum micro RNA-191(mi R-191)and mi-cro RNA-425(mi R-425)and the sensitivity to XELOX chemotherapy in patients with advanced gastric cancer,aiming to provide a reference for clinical treatment decision-making.Methods A total of 104 patients with advanced gastric cancer who received XELOX regimen treatment at a hospital in Shaanxi from January 2021 to December 2023 were selected as the study participants.All patients received XELOX regimen treatment and were allocated to a sensitive group(36 cases)and a resistant group(68 cases)based on the therapeutic efficacy.The levels of serum mi R-191 and mi R-425 were detected before chemotherapy,and the clinical pathological data of all patients were collected.The receiver operating characteristic(ROC)curve was used to analyze the value of serum mi R-191 and mi R-425 in predicting the sensitivity of advanced gastric cancer patients to XELOX chemotherapy.Multivariate regression analysis was used to explore the influencing factors of XELOX chemotherapy sensitivity in these patients.Results The levels of serum mi R-191 and mi R-425 in the resistant group were significantly higher than those in the sensitive group(P<0.05).The area under the curve(AUC)(95%CI)for assessing the sensitivity of advanced gastric cancer patients to XELOX chemotherapy using serum mi R-191 and mi R-425 were 0.787(0.742-0.832)and 0.840(0.795-0.889),respectively,and the combined prediction AUC(95%CI)was 0.901(0.856-0.956).No significant differences were noted in age,gender,Eastern Cooperative Oncology Group performance status(ECOG score),tumor location,and pathological type between the sensitive and resistant groups(P>0.05).The propor-tion of poorly differentiated and stage Ⅳ patients in the resistant group was significantly higher than that in the sensitive group(P<0.05).regression analysis showed that TNM stage Ⅳ(OR=2.050,95%CI:1.241-3.386),low differentia-tion degree(OR=2.838,95%CI:1.437-5.602),serum mi R-191≥2.27(OR=6.228,95%CI:2.234-17.358),and serum mi R-425≥1.91(OR=5.078,95%CI:1.921-13.426)were risk factors for XELOX chemotherapy sensitivity in patients with advanced gastric cancer(P<0.05).Conclusion The expression levels of serum mi R-191 and mi R-425 are as-sociated with XELOX chemotherapy resistance in patients with advanced gastric cancer,and their combination has a high predictive value for the sensitivity of XELOX chemotherapy in these patients.

Advanced gastric cancermi R-191mi R-425XELOX regimenChemotherapy sensitivity

陈红男、张思若、段宝军、马晓颖、杨玉琮、刘文康、王雪

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陕西省人民医院检验科,西安 710068

陕西省人民医院肿瘤内科,西安 710068

陕西省人民医院病案室,西安 710068

西安交通大学第一附属医院检验科,西安 710061

陕西省人民医院消化内科,西安 710068

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晚期胃癌 miR-191 miR-425 XELOX方案 化疗敏感性

2024

保健医学研究与实践
西南大学

保健医学研究与实践

CSTPCD
影响因子:0.512
ISSN:1673-873X
年,卷(期):2024.21(10)