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A prognostic score for non-small cell lung cancer resected after neoadjuvant therapy in comparison with the tumor-node-metastases classification and major pathological response

机译:与肿瘤 - 节点转移分类和重大病理反应相比,Neoadjuvant治疗后切除非小细胞肺癌的预后分数

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Studies validating the prognostic accuracy of the tumor-node-metastases (TNM) classification in patients with lung cancer treated by neoadjuvant therapy are scarce. Tumor regression, particularly major pathological response (MPR), is an acknowledged prognostic factor in this setting. We aimed to validate a novel combined prognostic score. This retrospective single-center study was conducted on 117 consecutive patients with non-small cell lung cancer resected after neoadjuvant treatment at a Swiss University Cancer Center between 2000 and 2016. All cases were clinicopathologically re-evaluated. We assessed the prognostic performance of a novel prognostic score (PRSC) combining T-category, lymph node status, and MPR, in comparison with the eighth edition of the TNM classification (TNM8), the size adapted TNM8 as proposed by the International Association for the Study of Lung Cancer (IASLC) and MPR alone. The isolated ypT-category and the combined TNM8 stages accurately differentiated overall survival (OS, stage p = 0.004) and disease-free survival (DFS, stage p = 0.018). Tumor regression had a prognostic impact. Optimal cut-offs for MPR emerged as 65% for adenocarcinoma and 10% for non-adenocarcinoma and were statistically significant for survival (OS p = 0.006, DFS p < 0.001). The PRSC differentiated between three prognostic groups (OS and DFS p < 0.001), and was superior compared to the stratification using MPR alone or the TNM8 systems, visualized by lower Akaike (AIC) and Bayesian information criterion (BIC) values. In the multivariate analyses, stage III tumors (HR 4.956, p = 0.003), tumors without MPR (HR 2.432, p = 0.015), and PRSC high-risk tumors (HR 5.692, p < 0.001) had significantly increased risks of occurring death. In conclusion, we support 65% as the optimal cut-off for MPR in adenocarcinomas. TNM8 and MPR were comparable regarding their prognostic significance. The novel prognostic score performed distinctly better regarding OS and DFS.
机译:验证Neoadjuvant疗法治疗的肺癌患者肿瘤节点转移(TNM)分类的预后准确性的研究是稀缺的。肿瘤回归,特别是主要的病理反应(MPR),是该环境中的确认预后因素。我们旨在验证新的综合预后分数。该回顾性单中心研究是在2000年至2016年间在瑞士大学癌症中心的新辅助治疗后切除的117例非小细胞肺癌患者进行。临床病理学诊断。我们评估了新型预后评分(PRSC)的预后性能,与TNM分类(TNM8)的第八版本相比,组合T型类别,淋巴结状态和MPR,其尺寸适应了国际协会提出的TNM8单独研究肺癌(IASLC)和MPR。分离的YPT类别和组合的TNM8阶段精确分化的整体存活(OS,阶段P = 0.004)和无病生存(DFS,阶段P = 0.018)。肿瘤回归具有预后的影响。用于MPR的最佳截止截止为65%的腺癌,非腺癌10%,对存活有统计学意义(OS P = 0.006,DFS P <0.001)。 PRSC在三种预后基团(OS和DFS P <0.001)之间分化,与使用MPR单独的分层或TNM8系统相比,由下αk(AIC)和贝叶斯信息标准(BIC)值相比优越。在多变量分析中,III阶段肿瘤(HR 4.956,P = 0.003),没有MPR的肿瘤(HR 2.432,P = 0.015)和PRSC高风险肿瘤(HR 5.692,P <0.001)显着增加了发生的发生风险。总之,我们支持65%的腺癌MPR的最佳截止值。 TNM8和MPR对其预后意义相当。关于操作系统和DFS明显地表明新的预后分数。

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