Evidence map›Paper›PMID 36815580›Full record

ArticlePediatric blood & cancer2023

Leveraging machine learning to identify acute myeloid leukemia patients and their chemotherapy regimens in an administrative database.

Lusha Cao, Yuan-Shung Huang, Chao Wu, Kelly Getz, Tamara P Miller, Jenny Ruiz, Brian T Fisher, Alix E Seif, Richard Aplenc, Yimei Li

Open access · greenAbstract read
In one paragraph

Article in Pediatric blood & cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 21% of its field
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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Lusha CaoDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-6157-6893
Yuan-Shung HuangDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-1942-6197
Chao WuDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Kelly GetzPerelman School of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Tamara P MillerDepartment of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0003-4250-5376
Jenny RuizPerelman School of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.ORCID 0000-0001-5319-3852
Brian T FisherPerelman School of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Alix E SeifPerelman School of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Richard AplencPerelman School of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Yimei LiPerelman School of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Children's Hospital of Philadelphia · USEmory University · US

Funding

Early Treatment-Related Cardiotoxicity and Subsequent Outcomes in Pediatric Acute Myeloid Leukemia: an Assessment of Development, Progression and MitigationK01HL143153 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI GETZ, KELLY DIRINGER · 2018 to 2022
$716k
NHLBI NIH HHS K01 HL143153
6 · The paper itself

Abstract

backgroundAdministrative datasets are useful for identifying rare disease cohorts such as pediatric acute myeloid leukemia (AML). Previously, cohorts were assembled using labor-intensive, manual reviews of patients' longitudinal chemotherapy data.

methodsWe utilized a two-step machine learning (ML) method to (i) identify pediatric patients with newly diagnosed AML, and (ii) among the identified AML patients, their chemotherapy courses, in an administrative/billing database. Using 2558 patients previously manually reviewed, multiple ML algorithms were derived from 75% of the study sample, and the selected model was tested in the remaining hold-out sample. The selected model was also applied to assemble a new pediatric AML cohort and further assessed in an external validation, using a standalone cohort established by manual chart abstraction.

resultsFor patient identification, the selected Support Vector Machine model yielded a sensitivity of 0.97 and a positive predictive value (PPV) of 0.97 in the hold-out test sample. For course-specific chemotherapy regimen and start date identification, the selected Random Forest model yielded overall PPV greater than or equal to 0.88 and sensitivity greater than or equal to 0.86 across all courses in the test sample. When applied to new cohort assembly, ML identified 3016 AML patients with 10,588 treatment courses. In the external validation subset, PPV was greater than or equal to 0.75 and sensitivity was greater than or equal to 0.82 for patient identification, and PPV was greater than or equal to 0.93 and sensitivity was greater than or equal to 0.94 for regimen identifications.

conclusionA carefully designed ML model can accurately identify pediatric AML patients and their chemotherapy courses from administrative databases. This approach may be generalizable to other diseases and databases.

Indexed as

Leukemia, Myeloid, AcuteAlgorithmsChildDatabases, FactualHumansMachine LearningPredictive Value of Testsacute myeloid leukemiaadministrative databasecase identification machine learning

Identifiers

PMID36815580
PMCPMC10402395
OpenAlexW4321611315

What OpenQuestion holds

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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.