期刊文献+

阿瑞吡坦防治化疗致恶心呕吐的Meta分析 被引量:19

A meta-analysis of aprepitant for prevention of chemotherapy-induced nausea and vomiting
下载PDF
导出
摘要 目的:系统评价阿瑞吡坦防治中、高度致吐风险化疗致恶心呕吐的有效性及安全性。方法:全面检索PubMed(1980年至2010年3月)、EMbase(1980年至2010年3月)、Cochrane Libraries(2010年第2期)、CNKI(1980年至2010年3月)、CBMdisc(1980年至2010年3月)、万方电子期刊(1982年至2010年3月)中纳入的阿瑞吡坦用于防治化疗致恶心呕吐的随机对照试验,并进行文献质量评价和资料提取,对同质研究作Meta分析。结果:共纳入10项研究(n=4376),均为高质量研究。Meta分析结果表明:(1)急性症状:"阿瑞吡坦+昂丹司琼+地塞米松"与"昂丹司琼+地塞米松"比较,呕吐的完全控制率提高了14.21%(分别为83.33%和72.96%,P<0.001),亚组分析显示接受顺铂化疗的患者获益高于AC方案化疗的患者,控制率分别提高了18.04%和10.85%;恶心的控制率仅提高3.92%(P=0.04),临床意义不大。(2)延迟性症状:"阿瑞吡坦"与"昂丹司琼"比较,呕吐的完全控制率提高了14.98%(P=0.004);"阿瑞吡坦+地塞米松"与"地塞米松"比较,呕吐的完全控制率提高了37.72%(P<0.001),恶心的控制率提高了11.24%(P=0.008)。(3)不良反应:阿瑞吡坦组疲劳/虚弱的发生率较高(P=0.001),便秘的发生率较低(P=0.002),其余发生率相似。结论:阿瑞吡坦可以改善肿瘤患者呕吐症状,对恶心作用不明显。接受顺铂化疗的患者获益高于AC方案。由于阿瑞吡坦价格昂贵,临床治疗需综合考虑化疗方案及患者的治疗意愿。此外,尚需进行药物经济学研究以考察其真实的临床价值。 Objective:To assess the efficacy and safety of aprepitant for the prevention of chemotherapy-induced nausea and vomiting (CINV) after moderately or highly emetogenic chemotherapy. Methods: Studies were identified by searching PubMed (1980 to March,2010),EMbase (1980 to March,2010),Cochrane Libraries (Issue 2,2010),CNKI (1980 to March,2010),CBMdisc (1980 to March,2010),and WanFang Data (1982 to March,2010). Randomized controlled trials of aprepitant for the prevention of CINV were included. The quality of included studies was assessed and meta-analysis was performed for the results of homogeneous studies by RevMan 5.0.23 software. Results: Ten studies involving 4 376 oncology patients were included. They were all high quality studies,with Jadad scores more than 5. The results of meta-analysis were as follows: (1) Acute CINV: The overall complete response rate was improved by 14.21% when aprepitant was combined with ondansetron and dexamethasone (83.33% vs 72.96%; P〈0.001). Subgroup analysis showed the patients receiving AC (anthracycline/cyclophosphamide) regimen benefited less than the patients receiving cisplatin chemotherapy. The rate of no significant nausea was only improved by 3.92% (P=0.04). (2) Delayed CINV: Compared with ondansetron,aprepitant could improve vomiting by 14.98% (P=0.004). When aprepitant was added with dexamethasone,the response rate of vomiting and nausea was improved by 37.72% (P〈0.001) and 11.24% (P=0.008) respectively. (3) Adverse reactions:The incidence of fatigue/asthenia was higher in the aprepitant regimen (P=0.001),while the incidence of constipation was lower (P=0.002).Conclusion:Aprepitant can improve the control of vomiting,but has slight effect on nausea. Patients receiving AC regimen benefit less than patients receiving cisplatin chemotherapy. In view of its high cost,pharmacoeconomics researches of aprepitant should be considered.
出处 《北京大学学报(医学版)》 CAS CSCD 北大核心 2010年第6期756-763,共8页 Journal of Peking University:Health Sciences
关键词 阿瑞吡坦 恶心 呕吐 抗肿瘤药 META分析 Aprepitant; Nausea; Vomiting; Antineoplastic agents; Meta-analysis;
  • 相关文献

参考文献20

  • 1Hiekok JT,Roscoe JA,Morrow GR,et al.Nausea and emesis remain significant problems of chemotherapy despite prophylaxis with 5-hydroxytryptamine-3 antiemetics:a University of Rochester James P.Wilmot Cancer Center Community Clinical Oneology Program Study of 360 cancer patients treated in the community[J].Cancer,2003,97(11):2880-2886.
  • 2Jordan K,Schmoll HJ,Aapro MS.Compamtive activity ofantiemetic drugs[J].Crit Rev oncol Hematol,2007,61(2):162-175.
  • 3张晓静,张频.肿瘤化疗所致恶心呕吐的发生机制和药物治疗的研究进展[J].癌症进展,2006,4(4):348-354. 被引量:128
  • 4Grunberg SM,Deuson RR,Mavros P.et al.Incidence of chemotherapy-induced nausea and emesis after modern antiemetics[J].Cancer,2004,100(10):2261-2268.
  • 5Massaro AM,Lenz KL.Aprepitant:A novel antiemetic for chemotherapy-induced nausea and vomiting[J].Ann Pharmacother,2005.39(1):77-85.
  • 6Warr DG,Hesketh PJ,Gralla RJ.et al.Efficacy and tolerability of aprepitant for the prevention of chemotherapy-induced nausea and vomiting in patients with breast cancer after moderately emetogenie chemotherapy[J].J Clin Oneol,2005,23(12):2822-2830.
  • 7National Comprehensive Cancer Network.NCCN Clinical Practice Guidelines in Oncology:Antiemesis,2nd,2010[M/OL].(2010-07-04)[2010-08-10].http://www.nccn.org/professionals/physician_gls/PDF/antiemesis.pdf.
  • 8Roila F,Hesketh PJ,Herrstedt J.Prevention of chemotherapyand radiotherapy-induced emesis:results of the 2004 Perugia International Antiemetic Consemus Conference[J].Ann Oncol,2006,17(1):20-28.
  • 9Kris MG,Hesketh PJ,Somerfield MR,et al.American Society of Clinical Oneology guideline for antiemetics in oncology:update 2006[J].J Clin Oncol,2006,24(18):2932-2947.
  • 10Yeo W,Mo FK,Suen JJ,et al.A randomized study of aprepirant,ondansetron and dexamethasone for chemotherapy-induced naugea and vomiting in Chinese breast cancer patients receiving moderately emetogenic chemotherapy[J].Breast Cancer Res Treat,2009,113(3):529-535.

二级参考文献24

  • 1[1]Wiser W,Berger A.Practical management of chemotherapy-induced nausea and vomiting.Oncology Williston Park),2005,19:637
  • 2[2]Aapro M,et al.Palonosetron is effective in preventing acute and delayed chemotherapy-induced nausea and vomiting in patients recieving highly emetogenic chemotherapy (HEC)[Abstract].Support Care Cancer,2003,11:A17
  • 3[3]Jordan K,Kasper C,Schmoll HJ.Chemotherapy-induced nausea and vomiting:Current and new standards in the antiemetic prophylaxis and treatment.Eur J Cancer,2005,41:199
  • 4[4]Roila F,Donati D,Tamberi S,et al.Delayed emesis:Incidence,pattern,prognostic factors and optimal treatment.Support Care Cancer,2002,10:88
  • 5[5]website:http//www.mascc.org.Multinational association for supportive care in cancer.Consensus Conference on antiemitic therapy Perugia,2004,March 29-31
  • 6[6]Hesketh PJ,Kris MG,Grunberg SM,et al.Proposal for classifying the acute emetogenicity of cancer chemotherapy.J Clin Oncol,1997,15:103
  • 7[7]Morrow GR.The effect of a susceptibility to motion sickness on the side effects of cancer chemotherapy.Cancer,1985,55:2766
  • 8[8]Osoba D,Zee B,Pater J,et al.Determinants of postchemotherapy nausea and vomiting in patients with cancer.Quality of Life and Symptom Control Committees of the National Cancer Institute of Canada Clinical Trials Group.J Clin Oncol,1997,15:116
  • 9[9]Doherty KM.Closing the gap in prophylactic antiemetic therapy:Patient factors in calculating the emetogenic potential of chemotherapy.Clin J Oncol Nurs,1999,3:113
  • 10[11]Antiemisis from NCCN clinical practice guidelines in oncology-version 1.2005.

共引文献127

同被引文献230

引证文献19

二级引证文献82

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