ArticleAnnals of hematology2026
Prediction of avatrombopag-induced thrombocytosis in pediatric immune thrombocytopenia: an AI-based real-world study.
Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
16 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Avatrombopag (AVA), an oral thrombopoietin receptor agonist (TPO-RA), has demonstrated favorable efficacy in the treatment of pediatric immune thrombocytopenia (ITP). However, treatment-related thrombocytosis represents a clinically relevant adverse event that may compromise treatment safety and continuity. Currently, no validated tools are available to predict the risk of AVA-induced thrombocytosis before treatment initiation. In this real-world study, we aimed to develop and validate a predictive model for AVA-associated thrombocytosis in children with ITP. A total of 74 pediatric patients treated with AVA at the Hematology-Oncology Center of Beijing Children's Hospital between July 2021 and January 2024 were included. We compared the proposed model with established classical machine learning baselines, including Logistic Regression (LR), Support Vector Machine (SVM), Multilayer Perceptron (MLP), Random Forest (RF), and XGBoost, as well as state-of-the-art deep learning models for tabular data, including TabPFN, FT-Transformer, and HyperTab. Among the evaluated models, the FT-Transformer achieved the best performance, with an accuracy of 0.785 ± 0.023 and an area under the receiver operating characteristic curve (AUC) of 0.851 ± 0.021. Model interpretability was enhanced using Shapley Additive Explanations (SHAP), enabling visualization of individual feature contributions to thrombocytosis risk. This AI-driven prediction model, grounded in real-world clinical data, demonstrates robust predictive performance and offers clinically interpretable insights. It provides a reliable reference for individualized risk assessment and supports safer, more precise use of AVA in pediatric ITP management.
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.