We propose a multi-metric flexible Bayesian framework to support efficient interim decision-making in multi-arm multi-stage phase II clinical trials. Multi-arm multi-stage phase II studies increase the efficiency of drug development, but early decisions regarding the futility or desirability of a given arm carry considerable risk since sample sizes are often low and follow-up periods may be short. Further, since intermediate outcomes based on biomarkers of treatment response are rarely perfect surrogates for the primary outcome and different trial stakeholders may have different levels of risk tolerance, a single hypothesis test is insufficient for comprehensively summarizing the state of the collected evidence. We present a Bayesian framework comprised of multiple metrics based on point estimates, uncertainty, and evidence towards desired thresholds (a Target Product Profile, TPP) for 1) ranking of arms and 2) comparison of each arm against an internal control. Using a large public-private partnership targeting novel TB arms as a motivating example, we find via simulation study that our multi-metric framework provides sufficient confidence for decision-making with sample sizes as low as 30 patients per arm, even when intermediate outcomes have only moderate correlation with the primary outcome. Our reframing of trial design and the decision-making procedure has been well-received by research partners and is a practical approach to more efficient assessment of novel therapeutics.
翻译:此外,由于基于治疗反应生物标志的中期结果很少能完美地替代主要结果,不同的试验利益攸关方可能具有不同程度的风险容忍度,单一假设测试不足以全面总结所收集证据的状况。我们提出了一个基于点估计、不确定性和证据的多种衡量标准组成的巴伊西亚框架,这些衡量标准基于点估计、不确定性和达到预期阈值的证据(1个目标产品概况,TPP),1个武器等级,2个武器等级,2个武器比预期阈值(目标产品轮廓,TPP),2个武器比对内部控制。利用针对新型结核病新武器的大型公私伙伴关系作为激励因素,我们通过模拟研究发现,我们的多度框架为抽样规模小至每件30名患者的决策提供了足够的信心信任,即使中间结果仅与初步结果有适度的关联。我们通过更切合实际的治疗性研究设计和决策程序进行了新的研究评估。