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Prediction of pneumonia following neoadjuvant chemoradiotherapy in patients with oesophageal cancer

  • M L Frederiks
  • , M Berbéeb
  • , E Schuit
  • , H W M van Laarhoven
  • , P S N van Rossum
  • , Z van Kesteren
  • , M I van Berge Henegouwen
  • , G J Meijer
  • , S Mook
  • , J P Ruurda
  • , J J Nuyttens
  • , B Mostert
  • , H Rütten
  • , B Klarenbeek
  • , M D den Hartogh
  • , M Sosef
  • , R Canters
  • , R H A Verhoeven
  • , B van Etten
  • , J A Langendijk
  • B P L Wijnhoven, C T Muijsa,

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

BACKGROUND AND PURPOSE: Pneumonia is a frequent, severe complication following neoadjuvant chemoradiotherapy (nCRT) and esophagectomy for oesophageal cancer, adversely affecting outcomes. We aimed to develop a model to accurately predict this risk.

MATERIAL AND METHODS: This multicentre, retrospective study included oesophageal cancer patients (cT1-4N0-3M0) undergoing nCRT +/- esophagectomy (CROSS regimen) treated between 2015-2021. The endpoint was grade ≥2 pneumonia (CTCAE v5.0) within six months post-nCRT. To handle high dimensionality, principal component analysis (PCA) was used to condense lung and heart DVH patterns into interpretable dose patterns. A logistic regression model was developed and validated using internal-external cross-validation to assess discrimination, calibration, and heterogeneity across centres.

RESULTS: A total of 1,459 patients across five centers were included for the final model development; 314 (22%) of which developed pneumonia. The developed model included pre-existing lung disease, diabetes, esophagectomy, and three PCA-derived dose patterns (overall heart/lung dose, heart-versus-lung dose, and low-dose areas). The model showed low heterogeneity (I 2 = 0% for all measures), fair discrimination (pooled AUC 0.68; 95% CI, 0.63-0.72), and excellent calibration (slope 0.91; 95% CI, 0.56-1.26; calibration-in-the-large 0.02; 95% CI, -0.14-0.18).

CONCLUSION: We developed and validated a generalizable NTCP model for pneumonia prediction in oesophageal cancer patients. This multicentre pulmonary NTCP model showed good calibration and homogeneous performance between centres. It offers a promising tool to personalize treatment by facilitating radiotherapy plan optimization and treatment/technique selection.

Original languageEnglish
Article number111554
JournalRadiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
Volume220
Early online date2 May 2026
DOIs
Publication statusPublished - Jul 2026

Keywords

  • Dose-volume histogram
  • Internal external validation
  • Neoadjuvantchemoradiotherapy
  • Normal tissue complication probability (NTCP)
  • Oesophageal cancer
  • Pneumonia
  • Prediction model
  • Principal component analysis

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