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Establishing a Competing Risk Regression Nomogram Model for Survival Data
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Comprehensive nomogram models for predicting checkpoint inhibitor pneumonitis.

Xiaohui Jia1, Yajuan Zhang1, Ting Liang2

  • 1Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University Xi'an 710061, Shaanxi, P. R. China.

American Journal of Cancer Research
|July 10, 2023
PubMed
Summary

Checkpoint inhibitor pneumonitis (CIP), a severe immune-related adverse event, lacks predictive tools. This study developed two nomograms to accurately predict CIP risk in patients receiving immunotherapy, aiding clinical decision-making.

Keywords:
Immunotherapybiomarkerscancerscheckpoint inhibitor pneumonitisnomogram

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Area of Science:

  • Oncology
  • Pulmonology
  • Immunology

Background:

  • Checkpoint inhibitor pneumonitis (CIP) is a frequent immune-related adverse event (irAE) associated with poor prognosis.
  • Effective biomarkers and predictive models for CIP occurrence are currently lacking.

Purpose of the Study:

  • To develop and validate predictive models for checkpoint inhibitor pneumonitis (CIP).
  • To identify independent risk factors for predicting CIP in patients undergoing immunotherapy.

Main Methods:

  • Retrospective enrollment of 547 patients receiving immunotherapy.
  • Development of two nomograms (Nomogram A and Nomogram B) using multivariate logistic regression.
  • Internal and external validation of the nomograms' predictive performance.

Main Results:

  • Nomogram A for any grade CIP showed C-indexes of 0.827 (training) and 0.860 (validation).
  • Nomogram B for grade ≥2 CIP demonstrated C-indexes of 0.873 (training) and 0.904 (validation).
  • Both nomograms exhibited satisfactory predictive power and clinical utility.

Conclusions:

  • Nomograms A and B are promising, personalized clinical tools for assessing CIP risk.
  • These visual and convenient tools can aid in the early identification and management of CIP.
  • Further clinical application of these nomograms may improve patient outcomes in immunotherapy.