Sumithra J. Mandrekar, Jeffrey Meyers, Axel Grothey, and Daniel J. Sargent, Mayo Clinic, Rochester, MN; Ming-Wen An, Vassar College, Poughkeepsie, NY; and Jan Bogaerts, European Organisation for Research and Treatment of Cancer, Brussels, Belgium.
J Clin Oncol. 2014 Mar 10;32(8):841-50. doi: 10.1200/JCO.2013.52.3019. Epub 2014 Feb 10.
We sought to test and validate the predictive utility of trichotomous tumor response (TriTR; complete response [CR] or partial response [PR] v stable disease [SD] v progressive disease [PD]), disease control rate (DCR; CR/PR/SD v PD), and dichotomous tumor response (DiTR; CR/PR v others) metrics using alternate cut points for PR and PD. The data warehouse assembled to guide the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 was used.
Data from 13 trials (5,480 patients with metastatic breast cancer, non-small-cell lung cancer, or colorectal cancer) were randomly split (60:40) into training and validation data sets. In all, 27 pairs of cut points for PR and PD were considered: PR (10% to 50% decrease by 5% increments) and PD (10% to 20% increase by 5% increments), for which 30% and 20% correspond to the RECIST categorization. Cox proportional hazards models with landmark analyses at 12 and 24 weeks stratified by study and number of lesions (fewer than three v three or more) and adjusted for average baseline tumor size were used to assess the impact of each metric on overall survival (OS). Model discrimination was assessed by using the concordance index (c-index).
Standard RECIST cut points demonstrated predictive ability similar to the alternate PR and PD cut points. Regardless of tumor type, the TriTR, DiTR, and DCR metrics had similar predictive performance. The 24-week metrics (albeit with higher c-index point estimate) were not meaningfully better than the 12-week metrics. None of the metrics did particularly well for breast cancer.
Alternative cut points to RECIST standards provided no meaningful improvement in OS prediction. Metrics assessed at 12 weeks have good predictive performance.
我们试图测试和验证三分类肿瘤反应(TriTR;完全缓解[CR]或部分缓解[PR]比稳定疾病[SD]比进展疾病[PD])、疾病控制率(DCR;CR/PR/SD 比 PD)和二分类肿瘤反应(DiTR;CR/PR 比其他)的预测效用,使用替代的 PR 和 PD 切点。使用为指导实体瘤反应评估标准(RECIST)1.1 版而组装的数据仓库。
来自 13 项试验(5480 例转移性乳腺癌、非小细胞肺癌或结直肠癌患者)的数据被随机分为训练集和验证数据集(60:40)。总共考虑了 27 对 PR 和 PD 的切点:PR(10%至 50%减少,每次减少 5%)和 PD(10%至 20%增加,每次增加 5%),其中 30%和 20%分别对应于 RECIST 分类。使用 Cox 比例风险模型,带有 12 周和 24 周的里程碑分析,按研究和病变数量分层(少于 3 个 v 3 个或更多个),并根据平均基线肿瘤大小进行调整,用于评估每个指标对总生存(OS)的影响。通过使用一致性指数(c-index)来评估模型的判别能力。
标准 RECIST 切点与替代的 PR 和 PD 切点表现出相似的预测能力。无论肿瘤类型如何,TriTR、DiTR 和 DCR 指标均具有相似的预测性能。24 周的指标(尽管 c-index 点估计值较高)并没有比 12 周的指标有明显的改善。这些指标对乳腺癌都没有特别好的效果。
替代 RECIST 标准的切点并没有在 OS 预测方面提供有意义的改进。在 12 周评估的指标具有良好的预测性能。