期刊文献+

阿帕替尼治疗晚期胃癌40例临床观察

Clinical observation of apapatinib in the treatment of advanced gastric cancer: a report of 40 cases
原文传递
导出
摘要 目的评估阿帕替尼治疗晚期胃癌的疗效与不良反应。方法选取40例应用阿替帕尼治疗的晚期胃癌患者,阿替帕尼用量:750 mg口服,1次/d,每4周为一疗程。评估患者的疗效,采用Kaplan-Meier方法分析无病生存期(DFS)与影响患者DFS的因素,记录并评估不良反应发生情况。结果40例全部为腺癌,疾病总缓解率为5.0%(2/40),疾病控制率为42.5%(17/40)。甲胎蛋白(AFP)阳性患者疾病控制率(71.4%)高于AFP阴性患者(30.3%),差异有统计学意义(P=0.025)。患者的DFS中位时间为3.87个月,采用Kaplan-Meier分析影响疗效的因素,结果表明美国东部协作组(ECOG)与AFP是患者DFS的影响因素(P=0.039、0.041)。最常见的不良反应为白细胞减少、高血压、血小板减少症。结论阿替帕尼治疗晚期胃癌疗效高,耐受性好,可以提高晚期胃癌患者的疾病控制率,延长患者的生存时间,值得推广应用。 Objective To evaluate the efficacy and adverse reaction of apatinib in the treatment of advanced gastric cancer.MethodsForty patients with advanced gastric cancer were selected and treated with alteplain of 850 mg once a day for one course of treatment. The efficacy on patients was evaluated, Kaplan-Meier method was used to analyze the disease-free survival (DFS), the influencing factors of DFS in patients and the adverse reactions were observed and evaluated.ResultsAll of the 40 patients were diagnosed with adenocarcinoma. The overall response rate was 5.0% (2/40) and the disease control rate was 42.5% (17/40). The control rate of alpha-fetoprotein-positive (AFP-positive) patients was significantly higher than that of AFP-negative patients (62.5% vs. 37.5%, P=0.025). The median value of DFS was 3.7 months. Kaplan-Meier analysis showed that ECOG and AFP were the influencing factors of DFS (P=0.039 and 0.041, respectively). The most common adverse reactions were leukopenia, hypertension and thrombocytopenia.ConclusionsThe treatment of advanced gastric cancer can get high efficacy and good tolerance and can improve the disease control rate of patients with advanced gastric cancer and prolong the survival time of patients. It is worth popularizing and applying.
出处 《中国实用医刊》 2017年第22期87-89,共3页 Chinese Journal of Practical Medicine
关键词 阿替帕尼 晚期胃癌 疗效 Etpenipine Advanced gastric cancer Efficacy
  • 相关文献

参考文献6

二级参考文献43

  • 1贺芳.美国FDA批准多西他赛用于治疗晚期胃癌[J].中华医学信息导报,2006,21(8):10-10. 被引量:3
  • 2阎家麒,童岩,王九一.紫杉醇脂质体的制备及其抑瘤作用的研究[J].药物生物技术,1996,3(3):154-157. 被引量:40
  • 3Daniel Drescher,Markus Moehler,Ines Gockel,Kirsten Frerichs,Annett Müller,Friedrich Dünschede,Thomas Borschitz,Stefan Biesterfeld,Martin Holtmann,Thomas Wehler,Andreas Teufel,Kerstin Herzer,Thomas Fischer,Martin R Berger,Theodor Junginger,Peter R Galle,Carl C Schimanski.Coexpression of receptor-tyrosine-kinases in gastric adenocarcinoma-a rationale for a molecular targeting strategy?[J].World Journal of Gastroenterology,2007,13(26):3605-3609. 被引量:4
  • 4Wagner AD,Grothe W,Haerting J,et al.Chemotherapy in ad-vanced gastric cancer:a systematic review and meta-analysisbased on aggregate data[ J].J Clin Oncol,2006,24(18):2903-2909.
  • 5Haller DG,Misset JL.Docetaxel in advanced gastric cancer [ J].Anticancer Drugs,2002,13(5):451-460.
  • 6Park KW,Ahn JS,Park YS,et al.Phase II study of docetaxeland cisplatin combination chemotherapy in metastatic gastriccancer [ J].Cancer Chemother Pharmacol,2007,59(1):17.
  • 7Thuss-Patience PC,Kretzschmar A,Repp M,et al.Docetaxeland continuous-infusion fluorouracil versus epirubicin,cisplatin,and fluorouracil for advanced gastric adenocarcinoma:a random-ized phase II study [ J].J Clin Oncol,2005,23(3):494-501.
  • 8Ajani JA,Fodor MB,Tjulandin SA,et al.Phase II multi-insti-tutional randomized trial of docetaxel plus cisplatin with or with-out fluorouracil in patients with untreated,advanced gastric,orgastroesophageal adenocarcinoma [ J].J Clin Oncol,2005,23(24):5660-5667.
  • 9Van Cutsem E,Moiseyenko VM,Tjulandin S,et al.Phase 瓜study of docetaxel and cisplatin plus fluorouracil compared withcisplatin and fluorouracil as first-line therapy for advanced gastriccancer:a report of the V325 Study Group [ J].J Clin Oncol,2006,24(31):4991-4997.
  • 10Tebbutt NC,Cummins MM,Sourjina T,et al.Randomised,non-comparative phase II study of weekly docetaxel with cisplatinand 5-fluorouracil or with capecitabine in oesophagogastric canc-er:the AGITG A1TAX trial[ J].Br J Cancer,2010,102(3):475-481.

共引文献39

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