Miksad Rebecca A, Gönen Mithat, Lynch Thomas J, Roberts Thomas G
Department of Medicine, Division of Hematology and Oncology, Beth Israel Deaconess Hospital, Harvard Medical School, Boston, MA 02215, USA.
J Clin Oncol. 2009 May 1;27(13):2245-52. doi: 10.1200/JCO.2008.16.2586. Epub 2009 Mar 23.
When successive randomized trials contradict prior evidence, clinicians may be unsure how to evaluate them: Does accumulating evidence warrant changing practice? An increasingly popular solution, Bayesian statistics quantitatively evaluate new results in context. This study provides a clinically relevant example of Bayesian methods.
Three recent non-small-cell lung cancer adjuvant chemotherapy trials were evaluated in light of prior conflicting data. Results were used from International Adjuvant Lung Trial (IALT), JBR.10, and Adjuvant Navelbine International Trialist Association (ANITA). Prior evidence was sequentially updated to calculate the probability of each survival benefit level (overall and by stage) and variance. Sensitivity analysis was performed using expert opinion and uninformed estimates of survival benefit prior probability.
The probability of a 4% survival benefit increased from 33% before IALT to 64% after IALT. After sequential updating with JBR.10 and ANITA, this probability was 82% (hazard ratio = 0.84; 95% CI, 0.77 to 0.91). IALT produced the largest decrease in variance (61%) and decreased the chance of survival decrement to 0%. Sensitivity analysis did not support a survival benefit after IALT. However, sequential updating substantiated a 4% survival benefit and, for stage II and III, more than 90% probability of a 6% benefit and 50% probability of a 12% benefit.
When evaluated in context with prior data, IALT did not support a 4% survival benefit. However, sequential updating with JBR.10 and ANITA did. A model for future assessments, this study demonstrates the unique ability of Bayesian analysis to evaluate results that contradict prior evidence.
当连续的随机试验与先前的证据相矛盾时,临床医生可能不确定如何评估这些试验:积累的证据是否足以改变实践?一种越来越流行的解决方案是,贝叶斯统计在背景中定量评估新结果。本研究提供了一个贝叶斯方法在临床方面的相关示例。
根据先前相互矛盾的数据对最近三项非小细胞肺癌辅助化疗试验进行评估。结果来自国际辅助肺癌试验(IALT)、JBR.10和长春瑞滨国际辅助试验协作组(ANITA)。对先前的证据进行逐步更新,以计算每个生存获益水平(总体和按分期)的概率及方差。使用专家意见和对生存获益先验概率的无信息估计进行敏感性分析。
生存获益4%的概率从IALT之前的33%增加到IALT之后的64%。在用JBR.10和ANITA进行逐步更新后,该概率为82%(风险比=0.84;95%可信区间,0.77至0.91)。IALT使方差下降幅度最大(61%),并将生存降低的可能性降至0%。敏感性分析不支持IALT后的生存获益。然而,逐步更新证实了4%的生存获益,对于II期和III期,有超过90%的概率获得6%的获益,50%的概率获得12%的获益。
结合先前数据进行评估时,IALT不支持4%的生存获益。然而,用JBR.10和ANITA进行逐步更新则支持。作为未来评估的一个模型,本研究证明了贝叶斯分析评估与先前证据相矛盾结果的独特能力。