ArticleBMC medical informatics and decision making2025
Development and validation of interpretable machine learning models for predicting AKI risk in patients treated with PD-1/PD-L1: a retrospective study.
Article in BMC medical informatics and decision making, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
4 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Impact of tumor immunotherapy on kidney injury and multi-organ outcomes: a mechanistic and clinical perspective.Frontiers in immunology · 2026Pooled it
- Prediction of Acute Kidney Injury in Oncology: From Clinical Risk Scores to AI-Enabled Precision Onco-Nephrology.Cancers · 2026Review
- Machine learning-based prediction of meniscal tears in ACL reconstruction using BMI, time to surgery, injury mechanism, and Tegner activity score: A temporally validated decision tool.Journal of experimental orthopaedics · 2026Article
- Leveraging ICT Tools to Improve Kidney Health: A Comprehensive Review of Innovations in Nephrology.Healthcare (Basel, Switzerland) · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
backgroundAnti-programmed cell death protein 1 (PD-1)/programmed cell death ligand 1 (PD-L1) immunotherapy has revolutionized cancer treatment. However, it can cause immune-related adverse events, including acute kidney injury (AKI). Such adverse events can interrupt treatment, affecting patient outcomes. Early prediction of AKI is essential for improved prognosis and personalized therapeutic strategies. Previous research has been constrained by significant limitations, underscoring the necessity for AKI risk prediction models for patients treated with PD-1/PD-L1 inhibitors. This study aimed to develop and validate an interpretable machine learning (ML) model for early AKI prediction in patients undergoing PD-1/PD-L1 inhibitor therapy using a retrospective cohort design.
methodsThis study collected data from patients treated with PD-1/PD-L1 inhibitors at Zhejiang Provincial People's Hospital between January 2018 and January 2024. Nine ML models were evaluated. SHapley Additive exPlanations (SHAP) were employed to rank feature importance and interpret the final model. Additionally, a web-based calculator based on the model was developed.
resultsAmong the nine ML models evaluated, the Grandient Boosting Machine (GBM) model achieved the best predictive performance. In the validation set, the GBM model achieved an AUC of 0.850 (95%CI: 0.830-0.870). In the test set, the AUC was 0.795(95% CI: 0.747-0.844), demonstrating accurate AKI risk prediction. Calibration curves demonstrated a strong concordance between predicted and observed risk probabilities. An interpretable final GBM model with 13 features was developed after feature reduction based on feature importance ranking. A web-based calculator accessible at https://predicatingaki.shinyapps.io/PDmodel/ has been developed to assist clinicians in AKI risk assessment.
conclusionThis study developed and validated an interpretable ML model using a large dataset to predict AKI risk in patients receiving PD-1/PD-L1 inhibitor therapy. This model can assist clinicians in the early identification of high-risk patients, facilitating personalized treatment plans.
trial registrationThe study was conducted following the Declaration of Helsinki and was approved by the Ethics Committee of Zhejiang Provincial People's Hospital (Approval No. KT2024116) in 3 Jan. 2025. As it was a retrospective study with anonymized data, informed consent was waived.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.