甲磺酸阿帕替尼与多西他赛治疗晚期非小细胞肺癌的疗效比较
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  • 英文篇名:Mesylate apatinib versus docetaxel in treatment of advanced non-small cell lung cancer
  • 作者:王雅婕 ; 秦博宇 ; 胡毅
  • 英文作者:WANG Yajie;QIN Boyu;HU Yi;School of Medicine, Nankai University;No.1 Department of Medical Oncology, Chinese PLA General Hospital;
  • 关键词:非小细胞肺癌 ; 阿帕替尼 ; 多西他赛 ; 临床疗效
  • 英文关键词:non-small cell lung cancer;;apatinib;;docetaxel;;clinical efficacy
  • 中文刊名:JYJX
  • 英文刊名:Academic Journal of Chinese PLA Medical School
  • 机构:南开大学医学院;解放军总医院肿瘤内一科;
  • 出版日期:2018-03-20 17:18
  • 出版单位:解放军医学院学报
  • 年:2018
  • 期:v.39;No.229
  • 基金:国家自然科学基金项目(81672996)~~
  • 语种:中文;
  • 页:JYJX201805001
  • 页数:5
  • CN:05
  • ISSN:10-1117/R
  • 分类号:7-10+14
摘要
目的比较甲磺酸阿帕替尼与多西他赛用于三线及以上治疗晚期非小细胞肺癌(non-small-cell lung cancer,NSCLC)的临床疗效和安全性。方法回顾解放军总医院2016年3月-2017年6月收治的共128例三线及以上治疗使用阿帕替尼或多西他赛的晚期NSCLC患者的临床资料,观察组(n=60)接受口服阿帕替尼治疗,剂量为500 mg/d;对照组(n=68)使用多西他赛化疗,剂量为75 mg/m~2。两组均以21天为1个治疗周期,每2个周期复查评价两组患者的近期疗效及不良反应。结果 128例患者均可进行临床评价。阿帕替尼组中位无进展生存期(median progress-free survival,m PFS)显著长于多西他赛组(3.7个月vs 3.0个月,P=0.026),疾病控制率(disease control rate,DCR)显著高于多西他赛组(61.7%vs 8.6%,P=0.037);阿帕替尼组的客观缓解率(overall response rate,ORR)为20.0%(12/60),高于多西他赛组的19.1%(13/68),但差异无统计学意义(P>0.05)。阿帕替尼组生活质量明显优于多西他赛组(P<0.05)。阿帕替尼组Ⅲ~Ⅳ级不良反应发生率为18.3%(11/60),明显低于多西他赛的29.4%(20/68)(P<0.05)。两种药物不良反应多数为Ⅰ级或Ⅱ级,给予积极对症处理后患者大多可耐受。结论甲磺酸阿帕替尼可用于三线及以上治疗晚期NSCLC患者,其临床疗效优于多西他赛,且安全性较高,能够提高患者的生存时间和质量,可作为临床治疗的选择。
        Objective To observe the clinical efficacy and adverse reactions of mesylate apatinib versus docetaxel for advanced non-small cell lung cancer after failure of second-line treatment. Methods Clinical data about 128 patients with advanced NSCLC admittted to our hospital from March 2016 to June 2017 were analyzed. The observation group(n=60) was treated with apatinib(500 mg/d) and the control group(n=68) was treated with docetaxel(75 mg/m~2). Treatment cycle of the two groups was 21 d. The clinical efficacy and adverse reaction of two groups were evaluated in every 2 cycles. Results The clinical evaluation was performed in 128 patients. The m PFS and DCR in apatinib were significantly greater than those in docetaxel group(3.7 months vs 3 months, 61.7% vs 48.6%, P <0.05, respectively). The ORR of docetaxel group was lower than that of apatinib group, but the difference was not statistically significant(20.0% vs 19.1%, P >0.05). As for improving the quality of life, apatinib was superior to docetaxel with significant difference(P <0.05). The incidence rate of serious adverse reactions of apatinib was 18.3%(11/60), which was significantly lower than 29.4%(20/68) in docetaxel group(P <0.05). Most of the adverse effects of these two drugs were gradeⅠorⅡ, which could be tolerated by most of the patients after symptomatic treatment. Conclusion The mesylate apatinib can be used for the advanced NSCLC treatment, and the clinical efficacy is superior to docetaxel with higher safety and longer survival time.
引文
1 Chen W,Zheng R,Baade PD,et al.Cancer statistics in China,2015[J].CA Cancer J Clin,2016,66(2):115-132.
    2 Torre LA,Siegel RL,Jemal A.Lung Cancer Statistics[J].Adv Exp Med Biol,2016,893:1-19.
    3 Carnio S,Di Stefano RF,Novello S.Fatigue in lung cancer patients:symptom burden and management of challenges[J].Lung Cancer(Auckl),2016,7:73-82.
    4 Zhang K,Yuan Q.Current mechanism of acquired resistance to epidermal growth factor receptor-tyrosine kinase inhibitors and updated therapy strategies in human nonsmall cell lung cancer[J].J Cancer Res Ther,2016,12(Supplement):C131-C137.
    5 Howard SA,Rosenthal MH,Jagannathan JP,et al.Beyond the vascular endothelial growth factor axis:update on role of imaging in nonantiangiogenic molecular targeted therapies in oncology[J].AJR Am J Roentgenol,2015,204(5):919-932.
    6 Ding J,Chen X,Dai X,et al.Simultaneous determination of apatinib and its four major metabolites in human plasma using liquid chromatography-tandem mass spectrometry and its application to a pharmacokinetic study[J].J Chromatogr B Analyt Technol Biomed Life Sci,2012,895-896:108-115.
    7 Zhang H.Apatinib for molecular targeted therapy in tumor[J].Drug Des Devel Ther,2015,9:6075-6081.
    8 Treanor C,Donnelly M.A methodological review of the Short Form Health Survey 36(SF-36)and its derivatives among breast cancer survivors[J].Qual Life Res,2015,24(2):339-362.
    9 Fizazi K,Faivre L,Lesaunier F,et al.Androgen deprivation therapy plus docetaxel and estramustine versus androgen deprivation therapy alone for high-risk localised prostate cancer(GETUG 12):a phase 3 randomised controlled trial[J].Lancet Oncol,2015,16(7):787-794.
    10 Geng R,Li J.Apatinib for the treatment of gastric cancer[J].Expert Opin Pharmacother,2015,16(1):117-122.
    11 Li J,Qin S,Xu J,et al.Randomized,Double-Blind,PlaceboControlled Phase III Trial of Apatinib in Patients With ChemotherapyRefractory Advanced or Metastatic Adenocarcinoma of the Stomach or Gastroesophageal Junction[J].J Clin Oncol,2016,34(13):1448-1454.
    12 Roviello G,Polom K,Roviello F,et al.Targeting VEGFR-2 in Metastatic Gastric Cancer:Results From a Literature-Based MetaAnalysis[J].Cancer Invest,2017,35(3):187-194.
    13 Zhang Y,Han C,Li J,et al.Efficacy and safety for Apatinib treatment in advanced gastric cancer:a real world study[J].Sci Rep,2017,7(1):13208.
    14 Hu X,Zhang J,Xu B,et al.Multicenter phase II study of apatinib,a novel VEGFR inhibitor in heavily pretreated patients with metastatic triple-negative breast cancer[J].Int J Cancer,2014,135(8):1961-1969.
    15 Hu X,Cao J,Hu W,et al.Multicenter phase II study of apatinib in non-triple-negative metastatic breast cancer[J].BMC Cancer,2014,14:820.
    16 Lin Y,Wu Z,Zhang J,et al.Apatinib for metastatic breast cancer in non-clinical trial setting:Satisfying efficacy regardless of previous anti-angiogenic treatment[J].Tumour Biol,2017,39(6):1010428317711033.
    17 Li J,Wang L.Efficacy and safety of apatinib treatment for advanced esophageal squamous cell carcinoma[J].Onco Targets Ther,2017,10:3965-3969.
    18 Miao M,Deng G,Luo S,et al.A phase II study of apatinib in patients with recurrent epithelial ovarian cancer[J].Gynecol Oncol,2018,148(2):286-290.
    19 Kong Y,Sun L,Hou Z,et al.Apatinib is effective for treatment of advanced hepatocellular carcinoma[J].Oncotarget,2017,8(62):105596-105605.
    20 Kou P,Zhang Y,Shao W,et al.Significant efficacy and well safety of apatinib in an advanced liver cancer patient:a case report and literature review[J].Oncotarget,2017,8(12):20510-20515.
    21 Peng H,Zhang Q,Li J,et al.Apatinib inhibits VEGF signaling and promotes apoptosis in intrahepatic cholangiocarcinoma[J].Oncotarget,2016,7(13).
    22 Lu W,Ke H,Qianshan D,et al.Apatinib has anti-tumor effects and induces autophagy in colon cancer cells[J].Iran J Basic Med Sci,2017,20(9):990-995.
    23 张力,李凯,史美祺,等.甲磺酸阿帕替尼治疗晚期非鳞非小细胞肺癌随机、双盲、安慰剂对照、多中心Ⅱ期临床研究[C].第十五届全国临床肿瘤学大会暨2012年CSCO学术年会论文集,2012:24.
    24 Wu F,Zhang S,Gao G,et al.Successful treatment using apatinib with or without docetaxel in heavily pretreated advanced nonsquamous non-small cell lung cancer:A case report and literature review[J].Cancer Biol Ther,2018,19(3):141-144.
    25 Song Z,Yu X,Lou G,et al.Salvage treatment with apatinib for advanced non-small-cell lung cancer[J].Onco Targets Ther,2017,10:1821-1825.
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