PREPARE ALL: An Artificial Intelligence Tool for Predicting Relapse in Children With Acute Lymphoblastic Leukemia.
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[PURPOSE] The Pediatric Relapse Prediction and Risk Evaluation for Acute Lymphoblastic Leukemia (PREPARE-ALL) tool aims to predict relapse in pediatric ALL by integrating clinical expertise with artif
- Sensitivity 68.5%
- Specificity 50.3%
APA
Saravanan S, Rengaswamy R, et al. (2026). PREPARE ALL: An Artificial Intelligence Tool for Predicting Relapse in Children With Acute Lymphoblastic Leukemia.. JCO clinical cancer informatics, 10, e2500222. https://doi.org/10.1200/CCI-25-00222
MLA
Saravanan S, et al.. "PREPARE ALL: An Artificial Intelligence Tool for Predicting Relapse in Children With Acute Lymphoblastic Leukemia.." JCO clinical cancer informatics, vol. 10, 2026, pp. e2500222.
PMID
41564371 ↗
Abstract 한글 요약
[PURPOSE] The Pediatric Relapse Prediction and Risk Evaluation for Acute Lymphoblastic Leukemia (PREPARE-ALL) tool aims to predict relapse in pediatric ALL by integrating clinical expertise with artificial intelligence and machine learning (ML), particularly Extreme Gradient Boosting (XGBoost). PREPARE-ALL demonstrates that multicenter, protocol-driven clinical and laboratory data can be used through ML to generate reproducible relapse predictions with greater sensitivity than individual clinician assessments.
[METHODS] PREPARE-ALL was developed using data from the ICiCLe ALL-14 pretrial cohort across five centers, incorporating 33 clinical and laboratory features.
[RESULTS] Among 2,252 patients enrolled in the study, 565 (25.1%) relapsed. Using an 80:20 train-test split, XGBoost achieved a sensitivity of 68.5% (245/447 relapses detected). Additional metrics included a positive predictive value of 31.3%, a negative predictive value of 82.8%, an accuracy of 54.8%, and a specificity of 50.3%. Key predictors of relapse included high hyperdiploidy and BCR-ABL1 fusion positive, positive measurable residual disease status at the end of induction, sex, age, highest presenting WBC, and final risk group. Three clinicians scored the validation data set; the developed model achieved a higher recall (68.5%) compared with clinical judgment (approximately 31%-36%).
[CONCLUSION] PREPARE-ALL identifies twice as many relapses as clinicians and serves as a practical decision-support tool for early relapse triage and treatment planning, enabling timely therapeutic adjustments and improved outcomes in pediatric ALL.
[METHODS] PREPARE-ALL was developed using data from the ICiCLe ALL-14 pretrial cohort across five centers, incorporating 33 clinical and laboratory features.
[RESULTS] Among 2,252 patients enrolled in the study, 565 (25.1%) relapsed. Using an 80:20 train-test split, XGBoost achieved a sensitivity of 68.5% (245/447 relapses detected). Additional metrics included a positive predictive value of 31.3%, a negative predictive value of 82.8%, an accuracy of 54.8%, and a specificity of 50.3%. Key predictors of relapse included high hyperdiploidy and BCR-ABL1 fusion positive, positive measurable residual disease status at the end of induction, sex, age, highest presenting WBC, and final risk group. Three clinicians scored the validation data set; the developed model achieved a higher recall (68.5%) compared with clinical judgment (approximately 31%-36%).
[CONCLUSION] PREPARE-ALL identifies twice as many relapses as clinicians and serves as a practical decision-support tool for early relapse triage and treatment planning, enabling timely therapeutic adjustments and improved outcomes in pediatric ALL.
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