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Modified two‐dimensional response as surrogate marker of overall survival in patients with metastatic colorectal cancer

机译:改良的二维反应作为转移性结直肠癌患者总生存的替代指标

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摘要

The identification of surrogate markers for long‐term outcomes in patients with metastatic colorectal cancer (mCRC) may help in designing treatment regimens. The aim of this study was to assess whether two‐dimensional response (2‐DR) can serve as a new surrogate marker for overall survival (OS) in patients with mCRC. The study group consisted of 99 patients with mCRC from two independent cohorts who were treated with oxaliplatin‐based chemotherapy plus bevacizumab. Two‐dimensional response was defined as an area enclosed by coordinate points, including early tumor shrinkage at 8 weeks, depth of response at nadir, and 20% increase over nadir at progression. Each variable was weighted by its contribution rate to OS. The model was developed and internally validated in the learning cohort, and the performance of this model was externally verified in the validation cohort. Spearman correlation coefficients for 2‐DR and OS in the learning and validation cohorts were 0.593 and 0.661, respectively. The C‐indexes in predicting OS were 0.724 (95% confidence interval, 0.623–0.815) in the learning cohort and 0.762 (95% confidence interval, 0.651–0.873) in the validation cohort. Overall survival was significantly longer in patients with high 2‐DR values than in patients with low 2‐DR values in both the learning (37.0 vs. 24.1 months, P < 0.001) and validation (41.2 vs. 20.4 months, P < 0.001) cohorts. In contrast, differences in early tumor shrinkage and depth of response were not statistically significant. Multivariate analyses showed that 2‐DR was an independent prognostic factor for OS.
机译:确定转移性结直肠癌(mCRC)患者长期预后的替代指标可能有助于设计治疗方案。这项研究的目的是评估二维反应(2-DR)是否可以作为mCRC患者总体生存(OS)的新替代指标。该研究组由来自两个独立队列的99例mCRC患者组成,他们接受了以奥沙利铂为基础的化疗加贝伐单抗的治疗。二维反应定义为由坐标点包围的区域,包括8周时早期肿瘤缩小,最低点处的反应深度以及进展时比最低点增加20%。每个变量均按其对操作系统的贡献率加权。该模型已开发并在学习队列中进行了内部验证,并且该模型的性能在验证队列中进行了外部验证。在学习和验证队列中2-DR和OS的Spearman相关系数分别为0.593和0.661。在学习队列中,预测OS的C指数为0.724(95%置信区间,0.623-0.815),在验证队列中,C指数为0.762(95%置信区间,0.651-0.873)。在学习(37.0 vs. 24.1个月,P <0.001)和验证(21.2 vs. 20.4个月,P <0.001)方面,高2‐DR值的患者的总体生存期显着长于低2‐DR值的患者队列。相反,早期肿瘤缩小和反应深度的差异无统计学意义。多因素分析表明2-DR是OS的独立预后因素。

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