Nomogram for predicting pathological response to neoadjuvant treatment in patients with locally advanced gastric cancer: Data from a phase III clinical trial

Author:

Shao Han12,Li Nai12,Ling Yi‐hong13,Wang Ji‐jin124,Fang Yi12,Jing Ming12,Zhou Zhi‐wei15ORCID,Zhang Yu‐jing12ORCID

Affiliation:

1. State Key Laboratory of Oncology in South China Sun Yat‐sen University Cancer Center Guangzhou People's Republic of China

2. Department of Radiation Oncology Sun Yat‐sen University Cancer Center Guangzhou Guangdong People's Republic of China

3. Department of Pathology Sun Yat‐sen University Cancer Center Guangzhou Guangdong People's Republic of China

4. Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University Shandong Academy of Medical Science Jinan People's Republic of China

5. Department of Gastric Surgery Sun Yat‐sen University Cancer Center Guangzhou Guangdong People's Republic of China

Abstract

AbstractPurposeThis study aimed to establish a nomogram using routinely available clinicopathological parameters to predict the pathological response in patients with locally advanced gastric cancer (LAGC) undergoing neoadjuvant treatment.Materials and MethodsWe conducted this study based on the ongoing Neo‐CRAG trial, a prospective study focused on preoperative treatment in patients with LAGC. A total of 221 patients who underwent surgery following neoadjuvant chemotherapy (nCT) or neoadjuvant chemoradiotherapy (nCRT) at Sun Yat‐sen University Cancer Center between June 2013 and July 2022 were included in the analysis. We defined complete or near‐complete pathological regression and ypN0 as good response (GR), and determined the prognostic value of GR by Kaplan–Meier survival analysis. Eventually, a nomogram for predicting GR was developed based on statistically identified predictors through multivariate logistic regression analysis and internally validated by the bootstrap method.ResultsGR was confirmed in 54 patients (54/221, 24.4%). Patients who achieved GR had a longer progression‐free survival and overall survival. Then, five independent factors, including pretreatment tumor differentiation, clinical T stage, monocyte count, CA724 level, and the use of nCRT, were identified. Based on these predictors, the nomogram was established with an area under the curve (AUC) of 0.777 (95% CI, 0.705–0.850) and a bias‐corrected AUC of 0.752.ConclusionA good pathological response after neoadjuvant treatment was associated with an improved prognosis in LAGC patients. The nomogram we established exhibits a high predictive capability for GR, offering potential value in devising personalized and precise treatment strategies for LAGC patients.

Publisher

Wiley

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