Freidlin Boris, Korn Edward L, George Stephen L, Gray Robert
Biometric Research Branch, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, MD 20892, USA.
J Clin Oncol. 2007 Nov 1;25(31):5019-23. doi: 10.1200/JCO.2007.11.8711.
The randomized clinical trial (RCT) is the gold standard for definitive evaluation of new therapies. RCTs designed to show that the therapeutic efficacy of a new therapy is not unacceptably inferior to that of standard therapy are called noninferiority trials. Traditionally, noninferiority trials have required very large sample sizes. Sometimes, a new treatment regimen with a favorable toxicity and/or tolerability profile is also expected to have some modest improvement in efficacy. In such specialized settings we describe a hybrid trial-design approach that requires a dramatically smaller sample size than that of a standard noninferiority design. This hybrid design can naturally incorporate a formal test of superiority as well as noninferiority.
随机临床试验(RCT)是对新疗法进行确定性评估的金标准。旨在表明新疗法的治疗效果不比标准疗法差到不可接受程度的RCT被称为非劣效性试验。传统上,非劣效性试验需要非常大的样本量。有时,具有良好毒性和/或耐受性特征的新治疗方案也有望在疗效上有一定程度的适度改善。在这种特殊情况下,我们描述了一种混合试验设计方法,该方法所需的样本量比标准非劣效性设计要小得多。这种混合设计可以自然地纳入优越性以及非劣效性的正式检验。