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Updated: Feb 12, 2026

Using 22C3 Anti-PD-L1 Antibody Concentrate on Biopsy and Cytology Samples from Non-small Cell Lung Cancer Patients
Published on: September 25, 2018
Risk Factors and Prediction Model for Early-Onset Immune-Related Adverse Events in Pan-Cancer Patients Undergoing
Panpan Jiao1,2, Lijuan Xue1, Weijuan Tan1
1Department of Oncology, Zhongshan Hospital Affiliated to Xiamen University, Xiamen, Fujian, China.
Predicting immune-related adverse events (irAEs) from anti-PD-(L)1 immunotherapy is crucial. A new model using routine blood tests and clinical factors can identify high-risk patients for early intervention.
Area of Science:
- Oncology
- Immunology
- Medical Informatics
Background:
- Anti-programmed death 1 (PD-1) and anti-programmed death ligand 1 (PD-L1) immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment.
- Immune-related adverse events (irAEs) pose significant challenges to the clinical benefits of ICIs.
- Predicting irAEs is essential for timely detection and management.
Purpose of the Study:
- To develop and validate a predictive model for irAEs in patients receiving anti-PD-(L)1 immunotherapy.
- To identify key clinical and laboratory parameters associated with irAE development.
Main Methods:
- Logistic least absolute shrinkage and selection operator (LASSO) regression with 10-fold cross-validation was used to select relevant variables.
- Multivariate logistic regression analysis was employed to construct the prediction model.
- Patient data from January 2019 to May 2023 were retrospectively analyzed.
Main Results:
- A total of 680 patients were included, with 330 experiencing irAEs.
- Endocrinal toxicities were the most frequent irAEs (25.59%).
- The developed risk model, incorporating basophil percentage, hemoglobin, ALC, PLR, LMR, BUN, CCI, ECOG PS, and hepatitis B status, demonstrated good predictive performance (C-index = 0.727).
Conclusions:
- The established prediction model can effectively screen and monitor patients at high risk for irAEs.
- This tool has the potential to improve outcomes for pan-cancer patients undergoing anti-PD-(L)1 therapy.
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