Department of Statistics, University of Kentucky, Lexington, Kentucky, USA.
Biostatistics and Bioinformatics Shared Resource Facility Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA.
Pharm Stat. 2021 Jan;20(1):117-128. doi: 10.1002/pst.2060. Epub 2020 Sep 1.
Cancer immunotherapy often reflects the improvement in both short-term risk reduction and long-term survival. In this scenario, a mixture cure model can be used for the trial design. However, the hazard functions based on the mixture cure model between two groups will ultimately crossover. Thus, the conventional assumption of proportional hazards may be violated and study design using standard log-rank test (LRT) could lose power if the main interest is to detect the improvement of long-term survival. In this paper, we propose a change sign weighted LRT for the trial design. We derived a sample size formula for the weighted LRT, which can be used for designing cancer immunotherapy trials to detect both short-term risk reduction and long-term survival. Simulation studies are conducted to compare the efficiency between the standard LRT and the change sign weighted LRT.
癌症免疫疗法通常反映了短期风险降低和长期生存的改善。在这种情况下,可以使用混合治愈模型进行试验设计。然而,两组之间基于混合治愈模型的危险函数最终会交叉。因此,如果主要兴趣是检测长期生存的改善,那么基于比例风险的传统假设可能会被违反,使用标准对数秩检验(LRT)的研究设计可能会失去效力。在本文中,我们提出了一种用于试验设计的变号加权 LRT。我们推导出了加权 LRT 的样本量公式,可用于设计癌症免疫疗法试验,以检测短期风险降低和长期生存。进行了模拟研究,以比较标准 LRT 和变号加权 LRT 之间的效率。