血清膜联蛋白A3联合缺氧诱导因子-1α在结直肠癌铂类耐药预测中的应用研究

Application of serum annexin A3 combined with hypoxia-inducible factor-1α in the prediction of platinum resistance in colorectal cancer

  • 摘要:
    目的 探讨外周血膜联蛋白A3(ANXA3)、缺氧诱导因子-1α(HIF-1α)表达与结直肠癌铂类耐药的关系。
    方法 回顾性分析使用铂类药物化疗的122例结直肠癌患者的临床资料。化疗6个周期后进行耐药性评价,根据患者对铂类药物的敏感性分为耐药组(48例)和敏感组(74例)。比较2组患者的临床资料及外周血ANXA3、HIF-1α水平; 采用Logistic回归模型分析铂类耐药的影响因素; 绘制受试者工作特征(ROC)曲线分析外周血ANXA3、HIF-1α对铂类耐药的预测效能。
    结果 耐药组与敏感组的性别构成、年龄、TNM分期、组织学分级比较,差异均无统计学意义(P>0.05)。耐药组的外周血ANXA3、HIF-1α水平高于敏感组,差异有统计学意义(P<0.05)。耐药组患者的中位无进展生存期(PFS)为20.5个月(95%CI: 16.744~30.254), 敏感组患者中位PFS为30.4个月(95%CI: 23.617~34.569)。耐药组的中位PFS短于敏感组,差异有统计学意义(P<0.05)。ROC曲线显示, ANXA3以2.03 mg/L为截断值时,预测铂类耐药的曲线下面积(AUC)为0.847; HIF-1α以189.57 pg/mL为截断值时,预测铂类耐药的AUC为0.722。ANXA3预测铂类耐药的AUC大于HIF-1α, 差异有统计学意义(Z=2.201, P<0.05)。ANXA3联合HIF-1α的AUC为0.915, 大于ANXA3、HIF-1α单用,差异有统计学意义(Z=2.150、3.021, P<0.05)。与ANXA3相比, ANXA3联合HIF-1α预测铂类耐药的灵敏度更高; 与HIF-1α相比, ANXA3联合HIF-1α预测铂类耐药的特异度更高。
    结论 外周血ANXA3、HIF-1α高表达与结直肠癌铂类耐药密切相关。ANXA3、HIF-1α联合检测对结直肠癌铂类耐药的预测效能较高。

     

    Abstract:
    Objective To investigate the relationships between the expression of peripheral blood annexin A3 (ANXA3), hypoxia-inducible factor-1α (HIF-1α) and platinum resistance in colorectal cancer.
    Methods Clinical data of 122 patients with colorectal cancer treated with platinum-based chemotherapy were retrospectively analyzed. Drug resistance was evaluated after 6 cycles of chemotherapy, and patients were divided into drug resistant group (48 cases) and sensitive group (74 cases) according to their sensitivity to platinum drugs. the clinical data and the levels of ANXA3 and HIF-1α in peripheral blood of the two groups were compared; Logistic regression model was used to analyze the influencing factors of platinum resistance; the receiver operating characteristic (ROC) curve was drawn to analyze the predictive efficacy of ANXA3 and HIF-1α in peripheral blood on platinum-based drug resistance.
    Results There were no significant differences in sex composition, age, TNM stage and histological grade between the drug resistant group and sensitive group (P > 0.05). ANXA3 and HIF-1α levels in peripheral blood of the drug resistant group were significantly higher than those in the sensitive group (P < 0.05). The median progression free survival (PFS) of patients in the drug resistant group was 20.5 months (95%CI, 16.744 to 30.254), and the median PFS of patients in the sensitive group was 30.4 months (95%CI, 23.617 to 34.569). The median PFS of the drug resistant group was significantly shorter than that of the sensitive group (P < 0.05). ROC curve showed that the area under the curve (AUC) for predicting platinum resistance was 0.847 when 2.03 mg/L was the cut-off value; when HIF-1α was truncated at 189.57 pg/mL, the predicted AUC of platinum resistance was 0.722. The AUC of platinum resistance predicted by ANXA3 was significantly larger than that of HIF-1α(Z=2.201, P < 0.05). The AUC of ANXA3 combined with HIF-1α was 0.915, which was significantly larger than that of ANXA3 and HIF-1α alone (Z=2.150, 3.021, P < 0.05). Compared with ANXA3, ANXA3 combined with HIF-1α showed higher sensitivity in predicting platinum resistance; compared with HIF-1α, ANXA3 combined with HIF-1α had higher specificity in predicting platinum resistance.
    Conclusion High levels of ANXA3 and HIF-1α in peripheral blood are closely related to platinum-resistance in colorectal cancer. The combination of ANXA3 and HIF-1α shows high predictive efficacy in the determination of platinum-type drug resistance in colorectal cancer.

     

/

返回文章
返回