Interpreting the results of noninferiority trials-a review

被引:23
|
作者
Cuzick, Jack [1 ]
Sasieni, Peter [2 ]
机构
[1] Queen Mary Univ London, Ctr Canc Prevent, Wolfson Inst Populat Hlth, Charterhouse Sq, London EC1M 6BQ, England
[2] Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London, England
关键词
EARLY BREAST-CANCER; ADJUVANT TREATMENT; TAMOXIFEN; ANASTROZOLE; WOMEN;
D O I
10.1038/s41416-022-01937-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Noninferiority trials are becoming increasing common, but are often poorly reported and misunderstood. A better understanding of the new components of a noninferiority trial and their interpretation is needed. Noninferiority trials are an extension of conventional superiority trials, which provide a basis for determining if a new treatment, which may have advantages other than efficacy, has sufficient efficacy to be useful in certain situations. A key feature is the need to specify a clinical noninferiority margin above which the lower boundary of the confidence interval for the difference between the new treatment and the conventional treatment must lie. In most cases a nontreated control arm is not included, and when the efficacy of the new treatment is less than that of the standard treatment, determining its efficacy versus no treatment can be a major challenge. Treatments meeting a clinical noninferiority requirement can be statistically significantly superior to standard treatment, of similar efficacy (i.e., no significant difference), or even significantly inferior in a conventional analysis. Noninferiority comparisons are an important addition to the reporting of clinical trials, but require prior consideration of several factors that conventional superiority analyses do not address.
引用
收藏
页码:1755 / 1759
页数:5
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