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Efficacy and safety between temozolomide alone and temozolomide-based double therapy for malignant melanoma: A meta-analysis

机译:单独使用替莫唑胺和基于替莫唑胺的双重治疗恶性黑色素瘤的疗效和安全性:一项荟萃分析

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Temozolomide (TMZ) has received much attention, notably in the treatment of malignant glioma and malignant melanoma. The objective of this study was to compare the clinical efficacy and safety of TMZ alone and TMZ-based combination drug therapy in patients with melanoma. Using "temozolomide" as a keyword combined with "melanoma" and "randomized controlled trials" as Medical Subject Headings, the following electronic databases were searched: the Cochrane library, MEDLINE, EBSCO, EMBASE, Ovid, cNKI, and cBMDisc. The evaluating indicators were overall response rate (ORR), 1-year survival rate, and several of the most frequent adverse events. Five randomized controlled trials met our criteria and were included in the meta-analysis, with a total of 703 participants (309 patients received TMZ alone, and 394 patients received combined regimens). The meta-analysis showed that the ORR for TMZ-based drug therapy was higher than TMZ alone [relative risk (RR) = 1.44; 95 % confidence interval (CI), 1.06-1.95], but the 1-year survival rate was not significantly different between the two groups (RR = 1.13; 95 % CI, 0.92-1.40). These results suggested that the impact of these increased response rates was not translated into a survival benefit. Moreover, we found no difference in the incidence of adverse events analyzed. The currently available evidence showed that the TMZ-combination therapy may moderately improve the response rate, but there was no corresponding increased toxicity. Future large-scale, high-quality, placebo-controlled, double-blind trials are needed.
机译:替莫唑胺(TMZ)已引起广泛关注,尤其是在恶性神经胶质瘤和恶性黑色素瘤的治疗中。这项研究的目的是比较单独的TMZ和基于TMZ的联合药物治疗黑色素瘤患者的临床疗效和安全性。使用“替莫唑胺”作为关键字与“黑素瘤”和“随机对照试验”作为医学主题词的组合,搜索了以下电子数据库:Cochrane库,MEDLINE,EBSCO,EMBASE,Ovid,cNKI和cBMDisc。评估指标为总体缓解率(ORR),1年生存率以及一些最常见的不良事件。五项符合我们标准的随机对照试验包括在荟萃分析中,共有703名参与者(309名患者单独接受TMZ,394名患者接受联合治疗)。荟萃分析显示,基于TMZ的药物治疗的ORR高于单独的TMZ [相对风险(RR)= 1.44; 95%置信区间(CI),1.06-1.95],但两组的1年生存率无显着差异(RR = 1.13; 95%CI,0.92-1.40)。这些结果表明,这些增加的反应率的影响并未转化为生存益处。此外,我们发现所分析的不良事件发生率没有差异。目前可获得的证据表明,TMZ联合疗法可适度提高缓解率,但没有相应增加的毒性。需要未来的大规模,高质量,安慰剂对照,双盲试验。

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