London Hub for Trials Methodology Research, MRC Clinical Trials Unit, Aviation House, 125 Kingsway, WC2B 6NH, London.
Trials. 2013 Jan 23;14:23. doi: 10.1186/1745-6215-14-23.
In 2011, Royston et al. described technical details of a two-arm, multi-stage (TAMS) design. The design enables a trial to be stopped part-way through recruitment if the accumulating data suggests a lack of benefit of the experimental arm. Such interim decisions can be made using data on an available 'intermediate' outcome. At the conclusion of the trial, the definitive outcome is analyzed. Typical intermediate and definitive outcomes in cancer might be progression-free and overall survival, respectively. In TAMS designs, the stopping rule applied at the interim stage(s) affects the sampling distribution of the treatment effect estimator, potentially inducing bias that needs addressing.
We quantified the bias in the treatment effect estimator in TAMS trials according to the size of the treatment effect and for different designs. We also retrospectively 'redesigned' completed cancer trials as TAMS trials and used the bootstrap to quantify bias.
In trials in which the experimental treatment is better than the control and which continue to their planned end, the bias in the estimate of treatment effect is small and of no practical importance. In trials stopped for lack of benefit at an interim stage, the treatment effect estimate is biased at the time of interim assessment. This bias is markedly reduced by further patient follow-up and reanalysis at the planned 'end' of the trial.
Provided that all patients in a TAMS trial are followed up to the planned end of the trial, the bias in the estimated treatment effect is of no practical importance. Bias correction is then unnecessary.
2011 年,Royston 等人描述了两臂、多阶段(TAMS)设计的技术细节。如果累积数据表明实验臂没有获益,该设计可在招募过程中途停止试验。可以使用可用的“中间”结果数据做出这种中期决策。在试验结束时,对最终结果进行分析。癌症的典型中间和最终结果可能分别为无进展生存期和总生存期。在 TAMS 设计中,中期阶段应用的停止规则会影响治疗效果估计量的抽样分布,可能会产生需要解决的偏差。
根据治疗效果的大小和不同的设计,我们量化了 TAMS 试验中治疗效果估计量的偏差。我们还回顾性地将已完成的癌症试验重新设计为 TAMS 试验,并使用自举法来量化偏差。
在试验中,如果实验组治疗效果优于对照组,且试验继续进行到计划终点,则治疗效果估计量的偏差较小,并无实际意义。在因缺乏益处而在中期阶段停止的试验中,治疗效果的估计在中期评估时存在偏差。通过进一步的患者随访和计划试验“结束”时的重新分析,可以显著减少这种偏差。
只要 TAMS 试验中的所有患者都随访到计划的试验终点,估计治疗效果的偏差就没有实际意义。因此,不需要进行偏差校正。