| Literature DB >> 17971602 |
Boris Freidlin1, Edward L Korn, Stephen L George, Robert Gray.
Abstract
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.Entities:
Mesh:
Year: 2007 PMID: 17971602 DOI: 10.1200/JCO.2007.11.8711
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544