Simon R
Biometric Research Branch, National Cancer Institute, Bethesda, MD 20892.
Cancer Treat Rep. 1987 Nov;71(11):1079-85.
A number of statistical designs for phase II trials have been published. These designs are critically reviewed. A new design is also introduced. Data are presented on the response rates observed for new chemotherapeutic agents introduced by the National Cancer Institute since 1975. Based upon this material, it is recommended that two-stage designs with a target sample size of 35-50 patients and substantial probability of early termination are usually appropriate. It is also recommended that for active drugs, two to three such trials are necessary to estimate the response rate with reasonable precision. Precise estimation of phase II response rates is not always important, however. For very rare diseases or situations where several dose levels of a biologic are to be evaluated, selection designs may be most appropriate. Such designs are described. Tables are presented to facilitate the design of new agent phase II clinical trials.
已发表了许多用于II期试验的统计设计。对这些设计进行了严格审查。还介绍了一种新设计。给出了自1975年以来美国国立癌症研究所引入的新化疗药物的观察缓解率数据。基于这些资料,建议采用目标样本量为35 - 50例患者且早期终止可能性较大的两阶段设计通常是合适的。还建议对于活性药物,需要进行两到三项此类试验才能合理精确地估计缓解率。然而,精确估计II期缓解率并非总是重要的。对于非常罕见的疾病或要评估生物制剂多个剂量水平的情况,选择设计可能最为合适。描述了此类设计。给出了表格以方便新药物II期临床试验的设计。