期刊文献+

卡瑞利珠单抗联合阿帕替尼治疗中晚期非小细胞肺癌的疗效 被引量:12

Clinical efficacy of camrelizumab combined with apatinib in the treatment of advanced non-small cell lung cancer
下载PDF
导出
摘要 目的探讨卡瑞利珠单抗联合阿帕替尼对中晚期非小细胞肺癌(non-small cell lung cancer,NSCLC)患者基质金属蛋白酶-9(matrix metalloproteinase-9,MMP-9)、角质蛋白21-1(cytokeratins 21-1,CYERA21-1)的影响,并分析其检测价值。方法选取NSCLC患者60例,记录患者的年龄、性别、吸烟史和体质量指数(body mass index,BMI)等一般临床资料。采用静脉滴注卡瑞利珠单抗联合口服甲磺酸阿帕替尼片的治疗方式,共治疗9周。采用酶联免疫吸附法(enzyme linked immunosorbent assay,ELISA)检测血清MMP-9水平,化学发光法检测血清CYERA21-1水平;受试者工作特征(receiver operating characteristic,ROC)曲线分析血清MMP-9及CYERA21-1对联合治疗疗效的诊断价值;Kaplan-Meier(K-M)分析绘制生存曲线,Log Rankχ^(2)检验比较生存率。结果治疗后,缓解组患者血清MMP-9和血清CYERA21-1水平均明显低于未缓解组(P<0.05);肿瘤直径大、病理分级高和肿瘤转移的NSCLC患者血清MMP-9及CYERA21-1表达水平明显高于肿瘤直径小、病理分级低和肿瘤未转移的患者(P<0.05);血清MMP-9、CYERA21-1及联合鉴别诊断联合治疗疗效的AUC分别为0.769、0.804、0.916;MMP-9、CYERA21-1低水平患者1、2年生存率和1、2年无病生存率均明显高于MMP-9、CYERA21-1高水平患者,MMP-9、CYERA21-1低水平患者中位生存时间明显长于MMP-9、CYERA21-1高水平患者(P<0.05)。结论血清MMP-9及CYERA21-1水平对卡瑞利珠单抗联合阿帕替尼治疗中晚期NSCLC的临床疗效具有较高的检测价值,其水平高低可客观反映患者的治疗缓解情况。 Objective To explore the effects of camrelizumab combined with apatinib on matrix metalloproteinase-9(MMP-9)and cytokeratins 21-1(CYERA21-1)in advanced non-small cell lung cancer(NSCLC),and analyze their detection value.Methods A retrospective analysis was performed on 60 patients confirmed with NSCLC.The general clinical data[age,gender,smoking history,body mass index(BMI)]were recorded.The patients were treated with intravenous injection of camrelizumaband oral Apatinib Mesylate Tablets for 9 weeks.The level of serum MMP-9 was detected by enzyme-linked immuno sorbent assay(ELISA).The level of serum CYERA21-1 was detected by chemiluminescence method.The detection value of MMP-9 and CYERA21-1 for curative effect of combined therapy was analyzed by receiver operating characteristic curves(ROC).The survival curves were drawn by Kaplan-Meier analysis(K-M),and the survival rate was compared by Log Rankχ^(2) test.Results After treatment,the levels of serum MMP-9 and CYERA21-1 in remission group were significantly lower than those in non-remission group(P<0.05).The levels of serum MMP-9 and CYERA21-1 in NSCLC patients with long tumor diameter,high pathological grading and tumor metastasis were significantly higher than those with short tumor diameter,low pathological grading and non-metastasis(P<0.05).AUC values of serum MMP-9,CYERA21-1 and their combination in detection curative effect of combined therapy were 0.769,0.804 and 0.916,respectively.The 1,2-year survival rate and 1,2-year disease-free survival rate in patients with low levels of MMP-9 and CYERA21-1 were significantly higher than those with high levels,and the median survival time was significantly longer than that with high levels(P<0.05).Conclusion The levels of serum MMP-9 and CYERA21-1 are of high detection value for clinical curative effect of camrelizumab combined with apatinib on advanced NSCLC.And their levels can objectively reflect treatment remission in patients.
作者 卢伟 马西淼 李礼 林巍 LU Wei;MA Ximiao;LI Li;LIN Wei(Department of Thoracic Surgery,Haikou People's Hospital,Haikou 570208,China)
出处 《西北药学杂志》 CAS 2023年第1期188-192,共5页 Northwest Pharmaceutical Journal
基金 海南省卫生计生行业科研项目(编号:20A200113)。
关键词 卡瑞利珠单抗 阿帕替尼 中晚期非小细胞肺癌(NSCLC) 基质金属蛋白酶-9(MMP-9) 角质蛋白21-1(CYERA21-1) camrelizumab apatinib advanced non-small cell lung cancer(NSCLC) matrix metalloproteinase-9(MMP-9) cytokeratin 21-1(CYERA21-1)
  • 相关文献

参考文献8

二级参考文献89

  • 1Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015[J]. CA Cancer J Clin, 2015, 65 (1):5-29.
  • 2ReckM, Popat S, Reinmuth N, et al. Metastatic non-small- cell lung cancer (NSCLC).. ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up[J]. Ann Oneol, 2014, 25 Suppl 3..iii27-39.
  • 3Shiono S, Katahira M, Abiko M, et al. Smoking is a perioperative risk factor and prognostic factor for lung cancer surgery[J]. Gen Thorac Cardiovasc Surg, 2015, 63 (2) :93-98.
  • 4Sun S, Schiller JH, Gazdar AF. Lung cancer in never smokers--a different disease[J]. Nat Rev Cancer, 2007, 7 (10) :778-790.
  • 5Balkwill F, Mantovani A. Inflammation and cancer: back to Virchow? [J]. Lancet, 2001, 357 (9255):539- 545.
  • 6Hussain SP, Harris CC. Inflammation and cancer: an ancient link with novel potentials[J].Int J Cancer, 2007, 121 (11) 2373-2380.
  • 7Schwartsburd PM. Chronic inflammation as inductor of pro- cancer microenvironment: pathogenesis of dysregulated feedback control[J].Cancer Metastasis Rev, 2003, 22 (1) 95-102.
  • 8Kundu JK, Surh YJ. Inflammation~ gearing the journey to cancer[J]. Murat Res, 2008, 659 (1-2):15-30.
  • 9Chaturvedi AK, Caporaso NE, Katki HA, et al. C-reactive protein and risk of lung cancer[J]. J Clin Oncol, 2010, 28 (16)l 2719-2726.
  • 10Jing X, Huang C, Zhou H, et al. Association between serum C-reactive protein value and prognosis of patients with non- small cell lung cancer: a meta-analysis[J]. Int J Clin Exp Med, 2015, 8(7): 10633-10639.

共引文献156

同被引文献125

引证文献12

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部