首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Comparison of continuous versus categorical tumor measurement-based metrics to predict overall survival in cancer treatment trials.
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Comparison of continuous versus categorical tumor measurement-based metrics to predict overall survival in cancer treatment trials.

机译:比较基于连续和分类肿瘤测量的指标来预测癌症治疗试验中的总体生存率。

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PURPOSE: The categorical definition of response assessed via the Response Evaluation Criteria in Solid Tumors has documented limitations. We sought to identify alternative metrics for tumor response that improve prediction of overall survival. EXPERIMENTAL DESIGN: Individual patient data from three North Central Cancer Treatment Group trials (N0026, n = 117; N9741, n = 1,109; and N9841, n = 332) were used. Continuous metrics of tumor size based on longitudinal tumor measurements were considered in addition to a trichotomized response [TriTR: response (complete or partial) vs. stable disease vs. progression). Cox proportional hazards models, adjusted for treatment arm and baseline tumor burden, were used to assess the impact of the metrics on subsequent overall survival, using a landmark analysis approach at 12, 16, and 24 weeks postbaseline. Model discrimination was evaluated by the concordance (c) index. RESULTS: The overall best response rates for the three trials were 26%, 45%, and 25%, respectively. Although nearly all metrics were statistically significantly associated with overall survival at the different landmark time points, the concordance indices (c-index) for the traditional response metrics ranged from 0.59 to 0.65; for the continuous metrics from 0.60 to 0.66; and for the TriTR metrics from 0.64 to 0.69. The c-indices for TriTR at 12 weeks were comparable with those at 16 and 24 weeks. CONCLUSIONS: Continuous tumor measurement-based metrics provided no predictive improvement over traditional response-based metrics or TriTR; TriTR had better predictive ability than best TriTR or confirmed response. If confirmed, TriTR represents a promising endpoint for future phase II trials.
机译:目的:通过实体瘤中的反应评估标准评估的反应分类定义具有局限性。我们试图确定替代肿瘤的指标,以改善整体存活率的预测。实验设计:使用来自北中部癌症治疗组三项试验的个体患者数据(N0026,n = 117; N9741,n = 1,109; N9841,n = 332)。除三分反应外,还考虑了基于纵向肿瘤测量的连续肿瘤大小指标(TriTR:反应(完全或部分)对稳定疾病对进展)。使用基线后12周,16周和24周的地标分析方法,对Cox比例风险模型进行了调整(针对治疗组和基线肿瘤负荷进行了调整),以评估这些指标对后续总体生存的影响。模型辨别力由一致性(c)指数评估。结果:这三项试验的总体最佳缓解率分别为26%,45%和25%。尽管几乎所有指标在不同的里程碑时间点上与总体生存率在统计学上都显着相关,但是传统响应指标的一致性指数(c-index)在0.59到0.65之间。连续指标从0.60到0.66;而TriTR指标从0.64到0.69。 TriTR在第12周时的c指数与第16和24周时的c指数相当。结论:连续的基于肿瘤测量的指标与传统的基于反应的指标或TriTR相比未提供预期的改善。 TriTR的预测能力优于最佳TriTR或已确认的反应。如果得到证实,TriTR将代表未来II期临床试验的有希望的终点。

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