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Single-Arm Phase II Trials of Combination Therapies: A Review of the CTEP Experience 2008–2017

机译:联合疗法的单臂II期试验:2008-2017年CTEP经验回顾

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摘要

Designing and interpreting single-arm phase II trials of combinations of agents is challenging because it can be difficult, based on historical data, to identify levels of activity for which the combination would be worth pursuing. We identified Cancer Therapy Evaluation Program single-arm combination trials that were activated in 2008–2017 and tabulated their design characteristics and results. Positive trials were evaluated as to whether they provided credible evidence that the combination was better than its constituents. A total of 125 trials were identified, and 120 trials had results available. Twelve had designs where eligible patients were required to be resistant or refractory to all but one element of the combination. Only 17.8% of the 45 positive trials were deemed to provide credible evidence that the combination was better than its constituents. Of the 10 positive trials with observed rates 10 percentage points higher than their upper (alternative hypothesis) targets, only five were deemed to provide such credible evidence. Many trials were definitively negative, with observed clinical activity at or below their lower (null hypothesis) targets. Ideally, use of single-arm combination trials should be restricted to settings where each agent is known to have minimal monotherapy activity (and a randomized trial is infeasible). In these settings, an observed signal is attributable to synergy and thus could be used to decide whether the combination is worth pursuing. In other settings, credible evidence can still be obtained if the observed activity is much higher than expected, but experience suggests that this is a rare occurrence.
机译:设计和解释试剂组合的单臂II期临床试验具有挑战性,因为根据历史数据很难确定组合值得追求的活动水平。我们确定了于2008–2017年启动的癌症治疗评估计划单臂联合试验,并将其设计特征和结果制成表格。对阳性试验进行了评估,以确定它们是否提供可靠的证据表明该组合优于其组成。总共确定了125个试验,并且有120个试验可用。十二项设计中,要求合格的患者对除组合以外的所有要素均具有抵抗力或抵抗力。在45例阳性试验中,只有17.8%被认为提供了可靠的证据,表明该组合优于其组成。在10项阳性试验中,观察到的比率比其上限(替代假设)目标高出10个百分点,只有5项被视为提供了可靠的证据。许多试验最终都是阴性的,观察到的临床活动达到或低于其较低(无效假设)目标。理想情况下,应将单臂联合试验的使用限制在已知每种药物单药治疗活性最低的情况下(并且随机试验是不可行的)。在这些情况下,观察到的信号可归因于协同作用,因此可用于确定该组合是否值得追求。在其他情况下,如果观察到的活动比预期的高得多,仍然可以获得可靠的证据,但是经验表明,这种情况很少发生。

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