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Chemotherapy with or without irinotecan in patients with advanced or recurrent gastric cancer: a meta-analysis of randomized controlled trials

Chemotherapy with or without irinotecan in patients with advanced or recurrent gastric cancer: a meta-analysis of randomized controlled trials
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摘要 Background Studies have shown that irinotecan can improve survival in patients with advanced or recurrent gastric cancer,but the overall benefit of irinotecan in the treatment of advanced or recurrent gastric cancer remains controversial.The aim of this study was to evaluate the benefits and risks of irinotecan for survival in patients with advanced or recurrent gastric cancer.Method We searched PubMed,EmBase,the Cochrane Central Register of Controlled Trials,reference lists of articles,and proceedings of major conferences for relevant clinical trials.We included randomized controlled trials that reported on the efficacy and safety of irinotecan in patients with advanced or recurrent gastric cancer.Outcomes were analyzed by survival rate,objective response rate (ORR),and toxicity.Furthermore,the analysis was further stratified by factors that could affect the treatment effects.Results Eight trials recruiting 1 546 patients with advanced or recurrent gastric cancer were included in the analysis.Overall,irinotecan therapy was associated with a 6% improvement in survival rate,but this difference was not statistically significant (odds ratio (OR) 0.94; 95% confidence interval (95% CI) 0.70-1.27; P=-0.69).However,irinotecan therapy had more frequent ORR than irinotecan-free arm (OR 1.70; 95% CI 1.34-2.17; P <0.001).Furthermore,irinotecan therapy was associated with a clinically and statistically significant increase in the risk for declined hemoglobin,hyponatremia,and diarrhea,but it also protected against thrombocytopenia risk when compared with irinotecan-free therapy.Conclusions There is no evidence to support the use of irinotecan therapy in patients with advanced or recurrent gastric cancer; however,given the significant advantage in ORR irinotecan therapy using combination regimens may be considered for further evaluation in subsets of patients who may benefit from this treatment. Background Studies have shown that irinotecan can improve survival in patients with advanced or recurrent gastric cancer,but the overall benefit of irinotecan in the treatment of advanced or recurrent gastric cancer remains controversial.The aim of this study was to evaluate the benefits and risks of irinotecan for survival in patients with advanced or recurrent gastric cancer.Method We searched PubMed,EmBase,the Cochrane Central Register of Controlled Trials,reference lists of articles,and proceedings of major conferences for relevant clinical trials.We included randomized controlled trials that reported on the efficacy and safety of irinotecan in patients with advanced or recurrent gastric cancer.Outcomes were analyzed by survival rate,objective response rate (ORR),and toxicity.Furthermore,the analysis was further stratified by factors that could affect the treatment effects.Results Eight trials recruiting 1 546 patients with advanced or recurrent gastric cancer were included in the analysis.Overall,irinotecan therapy was associated with a 6% improvement in survival rate,but this difference was not statistically significant (odds ratio (OR) 0.94; 95% confidence interval (95% CI) 0.70-1.27; P=-0.69).However,irinotecan therapy had more frequent ORR than irinotecan-free arm (OR 1.70; 95% CI 1.34-2.17; P <0.001).Furthermore,irinotecan therapy was associated with a clinically and statistically significant increase in the risk for declined hemoglobin,hyponatremia,and diarrhea,but it also protected against thrombocytopenia risk when compared with irinotecan-free therapy.Conclusions There is no evidence to support the use of irinotecan therapy in patients with advanced or recurrent gastric cancer; however,given the significant advantage in ORR irinotecan therapy using combination regimens may be considered for further evaluation in subsets of patients who may benefit from this treatment.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2014年第5期951-956,共6页 中华医学杂志(英文版)
关键词 IRINOTECAN gastric cancer META-ANALYSIS irinotecan gastric cancer meta-analysis
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  • 1A. N. Narovlyansky,M. Yu. Vershinina,A. M. Amchenkova,M. V. Mezentseva,F. I. Yershov.The Role of Cytokine mRNAs in Cell Sensitivity to α-Interferon[J]. Doklady Biological Sciences . 2002 (1-6)
  • 2B. Glimelius,K. Ekstr?m,K. Hoffman,W. Graf,P.-O. Sj?dén,U. Haglund,C. Svensson,L.-K. Enander,T. Linné,H. Sellstr?m,R. Heuman.Randomized comparison between chemotherapy plus best supportive care with best supportive care in advanced gastric cancer[J]. Annals of Oncology . 1997 (2)
  • 3González Barón M,Espinosa E,Feliu J,Ordóez A,Zamora P,de Castro J,García Girón C,García Alfonso P,Garrido P,Belón J,Lomas M.The UFT/leucovorin/etoposide regimen for the treatment of advanced gastric cancer.Oncopaz Co-operative Group. Oncology (Williston Park) . 1997
  • 4Khne CH,Wils JA,Wilke HJ.Developments in the treatment of gastric cancer in Europe. Oncology (Williston Park) . 2000
  • 5Kim JH,Lee KW,Kim YH,Lee KH,Oh do Y,Kim J,Yang SH,Im SA,Choi SH,Bang YJ.Individualized tumor response testing for prediction of response to Paclitaxel and Cisplatin chemotherapy in patients with advanced gastric cancer. Journal of Korean Medical Science . 2010
  • 6Chun JH,Kim HK,Lee JS,Choi JY,Lee HG,Yoon SM,Choi IJ,Ryu KW,Kim YW,Bae JM.Weekly irinotecan in patients with metastatic gastric cancer failing cisplatin-based chemotherapy. Japanese Journal of Clinical Oncology . 2004
  • 7Bouché O,Raoul JL,Bonnetain F,Giovannini M,Etienne PL,Lledo G,Arsène D,Paitel JF,Guérin-Meyer V,Mitry E,Buecher B,Kaminsky MC,Seitz JF,Rougier P,Bedenne L,Milan C.Randomized multicenter phase II trial of a bi-weekly regimen of fluorouracil and leucovorin (LV5FU2)LV5FU2plus cisplatin or LV5FU2plus irinotecan in patients with previously untreated metastatic gastric cancer:a Federation Francophone de Cancerologie Dige. Journal of Clinical Oncology . 2004
  • 8BouchéO,Raoul JL,Bonnetain F,Giovannini M,Etienne PL,Lledo G,Arsène D,Paitel JF,Guérin-Meyer V,Mitry E,Buecher B,Kaminsky MC,Seitz JF,Rougier P,Bedenne L,Milan C.Randomized multicenter phase Ⅱ trial of a biweekly regimen of fluorouracil and leucovorin (LV5FU2)LV5FU2 plus cisplatin or LV5FU2 plus irinotecan in patients with previously untreated metastatic gastric cancer:a Federation Francophone de Cancerologie Dig. Journal of Clinical Oncology . 2004
  • 9Dank M,Zaluski J,Barone C,Valvere V,Yalcin S,Peschel C,Wenczl M,Goker E,Cisar L,Wang K,Bugat R.Randomized phase Ⅲ study comparing irinotecan combined with 5-fluo-rouracil and folinic acid to cisplatin combined with 5-fluo-rouracil in chemotherapy naive patients with advanced adenocarcinoma of the stomach or esophagogastric junction. Annals of Oncology . 2008
  • 10Nakashima K,Hironaka S,Boku N,Onozawa Y,Fuku-tomi A,Yamazaki K,Yasui H,Taku K,Kojima T,Machida N.Irinotecan plus cisplatin therapy and S-1 plus cisplatin therapy for advanced or recurrent gastric cancer in a single institution. Japanese Journal of Clinical Oncology . 2008

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