GlaxoSmithKline Research and Development, Stockley Park UB11 1BT, UK.
Stat Med. 2011 May 30;30(12):1329-38. doi: 10.1002/sim.4212. Epub 2011 Mar 22.
Large sample sizes in clinical trials increase the cost of clinical research and delay the availability of new treatments. Fewer patients could be recruited into clinical trials if historical data on the comparator could be used reliably in a trial's analysis. However, old trials may bias rather than augment data from a new trial if, for example, the standard of care has improved over time. A hierarchical model for the data from the current and historical trials decreases the weight given to the historical data in line with the discrepancy between the results from the different trials. This reduces the risk of substantial bias. This paper shows that this down-weighting is not sufficiently sensitive to differences in the response rates between trials. Motivated by recent trials in HIV, this paper proposes and examines a more conservative weighting of historical data. Simulation showed that both the standard hierarchical and the proposed weighting of historical data led to Type II error rates worse than those attained by ignoring the historical data completely. This underlines the risks of including historical data in the primary analysis of a trial for which strict control of error rates is paramount.
临床试验中的大样本量会增加临床研究的成本,并延迟新治疗方法的推出。如果可以在试验分析中可靠地使用比较器的历史数据,那么参与临床试验的患者人数可能会减少。然而,如果随着时间的推移,治疗标准有所改善,那么旧的试验可能会对新试验的数据产生偏差,而不是增强其数据。对当前和历史试验数据的分层模型会根据不同试验结果之间的差异,相应地降低历史数据的权重。这可以降低出现重大偏差的风险。本文表明,这种权重降低对试验之间的反应率差异不够敏感。受 HIV 近期试验的启发,本文提出并检验了对历史数据更保守的加权方法。模拟结果表明,标准分层模型和所提出的历史数据加权方法都导致了二类错误率高于完全忽略历史数据的情况。这突显了在对错误率要求严格的试验中,将历史数据纳入主要分析的风险。