Evidence map›Paper›PMID 34170480›Full record

ArticleInternational journal of hematology2021

Risk prediction for delayed clearance of high-dose methotrexate in pediatric hematological malignancies by machine learning.

Min Zhan, Zebin Chen, Changcai Ding, Qiang Qu, Guoqiang Wang, Sixi Liu, Feiqiu Wen

Abstract read
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In one paragraph

Article in International journal of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 11 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

7 authors at 2 institutions in 1 country.

Min Zhan *Department of Pharmacy, Shenzhen Children's Hospital, Shenzhen, 518036, People's Republic of China.
Zebin Chen *Department of Pharmacy, Shenzhen Children's Hospital, Shenzhen, 518036, People's Republic of China.
Changcai DingDepartment of Research and Development, Shenzhen Advanced Precision Medical CO., LTD, Shenzhen, 518000, People's Republic of China.
Qiang QuDepartment of Pharmacy, Xiangya Hospital Central South University, Changsha, 410008, People's Republic of China.
Guoqiang WangDepartment of Pharmacy, Shenzhen Children's Hospital, Shenzhen, 518036, People's Republic of China.
Sixi LiuDepartment of Hematology/Oncology, Shenzhen Children's Hospital, Shenzhen, 518036, People's Republic of China.
Feiqiu WenDepartment of Hematology/Oncology, Shenzhen Children's Hospital, Shenzhen, 518036, People's Republic of China. fwen62@126.com.
Shenzhen Children's Hospital · CNXiangya Hospital Central South University · CN

Funding

the National Natural Scientific Foundation of China 81503166the Natural Scientific Foundation of Hunan province in China 2018JJ3846
6 · The paper itself

Abstract

This study aimed to establish a predictive model to identify children with hematologic malignancy at high risk for delayed clearance of high-dose methotrexate (HD-MTX) based on machine learning. A total of 205 patients were recruited. Five variables (hematocrit, risk classification, dose, SLC19A1 rs2838958, sex) and three variables (SLC19A1 rs2838958, sex, dose) were statistically significant in univariable analysis and, separately, multivariate logistic regression. The data was randomly split into a "training cohort" and a "validation cohort". A nomogram for prediction of delayed HD-MTX clearance was constructed using the three variables in the training dataset and validated in the validation dataset. Five machine learning algorithms (cart classification and regression trees, naïve Bayes, support vector machine, random forest, C5.0 decision tree) combined with different resampling methods were used for model building with five or three variables. When developed machine learning models were evaluated in the validation dataset, the C5.0 decision tree combined with the synthetic minority oversampling technique (SMOTE) using five variables had the highest area under the receiver operating characteristic curve (AUC 0.807 [95% CI 0.724-0.889]), a better performance than the nomogram (AUC 0.69 [95% CI 0.594-0.787]). The results support potential clinical application of machine learning for patient risk classification.

Indexed as

Machine LearningAllelesAntimetabolites, AntineoplasticBiomarkersChildGenotypeHematologic NeoplasmsHumansMethotrexateNomogramsPharmacogenomic TestingPolymorphism, Single NucleotideReproducibility of ResultsRisk AssessmentROC CurveAntimetabolites, AntineoplasticBiomarkersMethotrexateMachine learningMethotrexate clearancePediatric hematological malignanciesPharmacogenomicsSNP genotyping

Identifiers

PMID34170480
OpenAlexW3174286854

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.