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Quantitation of Intra-peritoneal Ovarian Cancer Metastasis
Published on: July 18, 2016
Primary Tumour Burden Score: A Novel Staging Parameter for Oesophageal Squamous Cell Carcinoma after Neoadjuvant
Xu Huang1, Dongxian Jiang2, Tiantao Sun3
1Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Objectives:
This study aims to develop a prognostic predictor that substitutes the current ypT-category based on the hypothesis that posttreatment tumour status can be represented by pretreatment tumour status and its changes during neoadjuvant chemoradiotherapy (nCRT).
Methods:
This retrospective cohort study included oesophageal squamous cell carcinoma (ESCC) patients undergoing nCRT followed by surgery from 1 January 2010 to 2 February 2019. Eligible patients from the Department of Thoracic Surgery, Zhongshan Hospital of Fudan University, were enrolled in the training cohort (n = 187), and from the Department of Cardiothoracic Surgery, Lu'an Affiliated Hospital of Anhui Medical University, the validation cohort (n = 78). The primary tumour burden score (PTBS), calculated by multiplying the percentage of residual primary cancer cells and the pretreatment pathological T stage (prepT stage) after neoadjuvant therapy, was categorized into 3 groups using cutoff values of 0.20 and 2.80 (PTBS stage 1: ≤0.20; stage 2: 0.20-2.80; stage 3: >2.80).
Results:
Of the 187 patients included in the training cohort (158 men [84.5%]; median age at surgery, 62 [interquartile range, 56-67] years). The PTBS staging model outperformed the traditional parameters in terms of discriminatory power and goodness of fit (5-year area under the curve: PTBS vs ypT, prepT, cT, tumour regression grade (TRG), 0.720 vs 0.665, 0.623, 0.500, 0.664; Akaike's information criterion: PTBS vs ypT, prepT, cT, TRG, 736.03 vs 756.70, 762.72, 770.15, 756.34). Multivariable analysis indicated that PTBS independently predicted OS. Similar findings were observed in the validation cohort.
Conclusions:
The PTBS stage showed superior prognostic discriminatory ability compared with traditional primary lesion stage parameters, suggesting its potential to serve as a valuable supplement to the current ypT-category. However, validation in larger, multicenter cohorts is needed to confirm its clinical utility.
Clinical Registration Number:
NCT05839002.
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