[Development of a nomogram for predicting pathological complete response after neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer].

R X Tian, X H Hu, H C Liu, P Cheng, J Y Li, M D L Bao, L M Zhao, Z X Zheng
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Abstract

Objective: To construct and validate a predictive model for pathological complete response (pCR) in patients with locally advanced rectal cancer (LARC) after neoadjuvant chemoradiotherapy. Methods: This retrospective observational study included 595 patients with stage T2-4 and (or) N+M0 LARC diagnosed in the Cancer Hospital of Chinese Academy of Medical Sciences and the Fourth Hospital of Hebei Medical University who had no metastases, tolerated neoadjuvant therapy, completed neoadjuvant therapy, and had undergone radical surgery after neoadjuvant therapy. The training set comprised 299 patients admitted to the Cancer Hospital of Chinese Academy of Medical Sciences from 2013 to 2018, the internal validation set 155 patients admitted from 2019 to 2023, and the external validation set 141 patients admitted to the Fourth Hospital of Hebei Medical University from 2013 to 2021. They were divided into pCR group and non-pCR groups according to postoperative pathology. Among the 299 patients in the training set, 247 were in the non-PCR and 52 in the pCR group; among the 155 patients verified internally, 113 were in the non-PCR and 42 in the pCR group; and among the 141 patients validated externally, 132 were in the non-pCR and nine in the pCR group. Logistic regression was used for univariate and multifactorial analysis to explore the factors associated with pCR and construct a nomogram prediction model. Receiver operating characteristic curves, calibration curves, and decision curve analysis (DCA) were used to validate the performance of the predictive model. Results: Univariate and multivariate logistic regression analysis showed that carbohydrate antigen 19-9 (P=0.040, OR=0.97, 95%CI: 0.93-0.99), neutrophil count (P<0.001, OR=0.66, 95%CI: 0.52-0.84), tumor T stage: Stage IV (P=0.011, OR=0.22, 95%CI: 0.07-0.70), tumor N stage: Stage I (P=0.003, OR=0.22,95%CI:0.08-0.60), Stage II (P<0.001, OR=0.03, 95%CI: 0.01-0.09) and involvement of mesorectal fascia (P=0.004, OR=0.09, 95%CI: 0.02-0.47) were independent predictors of pCR. In the training set, the area under the receiver operating characteristic curve of the model was 0.92 (95%CI: 0.87-0.96), whereas in the internal and external validation sets, the AUCs were 0.78 and 0.81, respectively. The calibration curve showed that the prediction model had good prediction efficiency in both the training and verification sets. Decision curve analysis showed that the net benefit of the model was largest when the threshold probability was in the range of 5.2% to 89.7% (in the internal and external validation sets, the threshold probabilities were in the range of 15.7% to 92.3% and 2.2% to 84.1%, respectively). Conclusion: The nomogram model constructed in this study showed efficacy in predicting whether patients with LARC will achieve pCR after receiving neoadjuvant chemoradiotherapy.

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[预测局部晚期直肠癌患者新辅助放化疗后病理完全缓解的nomogram]。
目的:建立并验证局部晚期直肠癌(LARC)患者新辅助放化疗后病理完全缓解(pCR)的预测模型。方法:本回顾性观察研究纳入595例在中国医学科学院肿瘤医院和河北医科大学第四医院确诊的T2-4期和(或)N+M0期LARC患者,患者无转移,新辅助治疗耐受,新辅助治疗完成,新辅助治疗后行根治性手术。训练集包括2013 - 2018年中国医学科学院肿瘤医院收治的299例患者,内部验证集包括2019 - 2023年收治的155例患者,外部验证集包括2013 - 2021年河北医科大学第四医院收治的141例患者。根据术后病理情况分为pCR组和非pCR组。训练集299例患者中,非pCR组247例,pCR组52例;155例内部验证患者中,非pCR组113例,pCR组42例;外部验证的141例患者中,非pCR组132例,pCR组9例。采用Logistic回归进行单因素和多因素分析,探讨与pCR相关的因素,并构建nomogram预测模型。采用受试者工作特征曲线、校准曲线和决策曲线分析(DCA)验证预测模型的性能。结果:单因素和多因素logistic回归分析显示,碳水化合物抗原19-9 (P=0.040, OR=0.97, 95%CI: 0.93-0.99)、中性粒细胞计数(PP=0.011, OR=0.22,95%CI: 0.07-0.70)、肿瘤N分期:I期(P=0.003, OR=0.22,95%CI:0.08-0.60)、II期(PP=0.004, OR=0.09, 95%CI: 0.02-0.47)是pCR的独立预测因子。在训练集中,模型的受试者工作特征曲线下面积为0.92 (95%CI: 0.87-0.96),而在内部和外部验证集中,auc分别为0.78和0.81。校正曲线表明,该预测模型在训练集和验证集上都具有良好的预测效率。决策曲线分析表明,当阈值概率在5.2% ~ 89.7%范围内时,模型的净效益最大(在内部和外部验证集中,阈值概率分别在15.7% ~ 92.3%和2.2% ~ 84.1%范围内)。结论:本研究构建的nomogram模型能够有效预测LARC患者接受新辅助放化疗后是否达到pCR。
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中华胃肠外科杂志
中华胃肠外科杂志 Medicine-Medicine (all)
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发文量
6776
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