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儿童癌症的实验性治疗是否优于既定治疗方法?儿童肿瘤学组对随机对照试验的观察性研究。

Are experimental treatments for cancer in children superior to established treatments? Observational study of randomised controlled trials by the Children's Oncology Group.

作者信息

Kumar Ambuj, Soares Heloisa, Wells Robert, Clarke Mike, Hozo Iztok, Bleyer Archie, Reaman Gregory, Chalmers Iain, Djulbegovic Benjamin

机构信息

Department of Interdisciplinary Oncology, H Lee Moffitt Cancer Center and Research Institute, University of South Florida, Tampa, FL 33612, USA.

出版信息

BMJ. 2005 Dec 3;331(7528):1295. doi: 10.1136/bmj.38628.561123.7C. Epub 2005 Nov 18.

Abstract

OBJECTIVES

To assess how often new treatments for childhood cancer assessed in phase III randomised trials are superior or inferior to standard treatments and whether the pattern of successes and failures in new treatments is consistent with uncertainty being the ethical basis for enrolling patients in such trials.

DESIGN

Observational study.

SETTING

Phase III randomised controlled trials carried out under the aegis of the Children's Oncology Group between 1955 and 1997, regardless of whether they were published.

MAIN OUTCOME MEASURES

Overall survival, event free survival, and treatment related mortality.

RESULTS

126 trials were included, involving 152 comparisons and 36,567 patients. The odds ratio for overall survival with experimental treatments was 0.96 (99% confidence interval 0.89 to 1.03), indicating that new treatments are as likely to be inferior as they are to be superior to standard treatments. This result was not affected by publication bias, methodological quality, treatment type, disease, or comparator.

CONCLUSIONS

New treatments in childhood cancer tested in randomised controlled trials are, on average, as likely to be inferior as they are to be superior to standard treatments, confirming that the uncertainty principle has been operating.

摘要

目的

评估在III期随机试验中评估的儿童癌症新疗法优于或劣于标准疗法的频率,以及新疗法的成败模式是否与不确定性作为将患者纳入此类试验的伦理基础相一致。

设计

观察性研究。

背景

1955年至1997年在儿童肿瘤学组的支持下进行的III期随机对照试验,无论是否已发表。

主要观察指标

总生存期、无事件生存期和治疗相关死亡率。

结果

纳入126项试验,涉及152次比较和36567名患者。实验性治疗的总生存优势比为0.96(99%置信区间0.89至1.03),表明新疗法与标准疗法相比,劣于标准疗法的可能性与优于标准疗法的可能性相同。这一结果不受发表偏倚、方法学质量、治疗类型、疾病或对照的影响。

结论

在随机对照试验中测试的儿童癌症新疗法,平均而言,劣于标准疗法的可能性与优于标准疗法的可能性相同,证实了不确定性原则一直在起作用。

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