Evidence map›Paper›PMID 40781625›Full record

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.

Wentong Liu, Kaiyue Ji, Qianwen Tang, Weiqi Xia, Wei Zhang, Lina Shao, Jiana Shi, Yukun Li, Ping Huang, Xiaolan Ye

Abstract readValidation Study
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from 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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Wentong Liu *Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital(Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Kaiyue Ji *Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital(Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Qianwen TangSchool of Pharmaceutical Sciences, Hangzhou Medical College, Hangzhou, Zhejiang, 311399, China.
Weiqi XiaCenter for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital(Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Wei ZhangUrology & Nephrology Center, Department of Nephrology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Lina ShaoUrology & Nephrology Center, Department of Nephrology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Jiana ShiCenter for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital(Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Yukun LiPharmacy Department, The First People's Hospital of Aksu Prefecture, Aksu, Xinjiang, 843000, China.
Ping HuangCenter for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital(Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China. 28948379@qq.com.
Xiaolan YeCenter for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital(Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China. yexl1120@126.com.

Funding

Zhejiang Provincial Health Science and Technology Plan 2022KY063Zhejiang Provincial People's Hospital Seed Fund C-2022-YYQD26Zhejiang Yangtze River Delta Health Research Fund Project 2022CSJ-A002Zhejiang Yangtze River Delta Health Research Fund Project 2022CSJ-A003
6 · The paper itself

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

Acute Kidney InjuryImmune Checkpoint InhibitorsMachine LearningNeoplasmsAgedFemaleHumansMaleMiddle AgedProgrammed Cell Death 1 ReceptorRetrospective StudiesRisk AssessmentImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorAKIInterpretableMachine learningPD-1/PD-L1Predictive model

Identifiers

PMID40781625
PMCPMC12333227

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LicenceCC BY-NC-ND
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Registered trials

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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.