Evidence map›Paper›PMID 34506688›Full record

ArticleThe oncologist2021

Validation of a Post-Transplant Lymphoproliferative Disorder Risk Prediction Score and Derivation of a New Prediction Score Using a National Bone Marrow Transplant Registry Database.

Chien-Chang Lee, Tzu-Chun Hsu, Chia-Chih Kuo, Michael A Liu, Ahmed M Abdelfattah, Chia-Na Chang, Ming Yao, Chi-Cheng Li, Kang-Hsi Wu, Tsung-Chih Chen and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The oncologist, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 13 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

19 authors at 13 institutions in 2 countries.

Chien-Chang LeeDepartment of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Tzu-Chun HsuDepartment of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Chia-Chih KuoDepartment of Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Michael A LiuDepartment of Medicine, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Ahmed M AbdelfattahInformation Services Department, Boston Children's Hospital, Boston, Massachusetts, USA.
Chia-Na ChangDepartment of Radiation Oncology, Taipei Municipal Wanfang Hospital, Taipei, Taiwan.
Ming YaoDivision of Hematology and Oncology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Chi-Cheng LiDivision of Pediatric Hematology and Oncology, China Medical University Children's Hospital, Taichung, Taiwan.
Kang-Hsi WuDivision of Pediatric Hematology and Oncology, China Medical University Children's Hospital, Taichung, Taiwan.
Tsung-Chih ChenDivision of Hematology and Oncology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Jyh-Pyng GauDivision of Hematology and Oncology, Department of Internal Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Po-Nan WangDivision of Hematology and Oncology, Department of Internal Medicine, Chang Gung Medical Foundation, Linkou Branch, Taoyuan, Taiwan.
Yi-Chang LiuDivision of Hematology and Oncology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Lun-Wei ChiouDepartment of Hematology and Medical Oncology, Koo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan.
Ming-Yang LeeDivision of Hematology and Oncology, Department of Internal Medicine, Ditmanson Medical Foundation Chiayi Christian Hospital, Chiayi, Taiwan.
Sin-Syue LiDivision of Hematology and Oncology, Department of Internal Medicine, National Cheng Kung University Hospital, Tainan, Taiwan.
Tsu-Yi ChaoDivision of Hemato-Oncology, Department of Internal Medicine, Taipei Medical University-Shuang Ho Hospital, Taipei, Taiwan.
Shiann-Tarng JouDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Hsiu-Hao ChangDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.ORCID 0000-0003-1832-8509
National Taiwan University Hospital · TWChina Medical University · TWBoston Children's Hospital · USBrown University · USChang Gung Memorial Hospital · TWChia-Yi Christian Hospital · TWKaohsiung Medical University · TWKoo Foundation Sun Yat-Sen Cancer Center · TWNational Cheng Kung University Hospital · TWTaichung Veterans General Hospital · TWTaipei Medical University-Shuang Ho Hospital · TWTaipei Municipal YangMing Hospital · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe externally validated Fujimoto's post-transplant lymphoproliferative disorder (PTLD) scoring system for risk prediction by using the Taiwan Blood and Marrow Transplant Registry Database (TBMTRD) and aimed to create a superior scoring system using machine learning methods. MATERIALS AND

methodsConsecutive allogeneic hematopoietic cell transplant (HCT) recipients registered in the TBMTRD from 2009 to 2018 were included in this study. The Fujimoto PTLD score was calculated for each patient. The machine learning algorithm, least absolute shrinkage and selection operator (LASSO), was used to construct a new score system, which was validated using the fivefold cross-validation method.

resultsWe identified 2,148 allogeneic HCT recipients, of which 57 (2.65%) developed PTLD in the TBMTRD. In this population, the probabilities for PTLD development by Fujimoto score at 5 years for patients in the low-, intermediate-, high-, and very-high-risk groups were 1.15%, 3.06%, 4.09%, and 8.97%, respectively. The score model had acceptable discrimination with a C-statistic of 0.65 and a near-perfect moderate calibration curve (HL test p = .81). Using LASSO regression analysis, a four-risk group model was constructed, and the new model showed better discrimination in the validation cohort when compared with The Fujimoto PTLD score (C-statistic: 0.75 vs. 0.65).

conclusionOur study demonstrated a more comprehensive model when compared with Fujimoto's PTLD scoring system, which included additional predictors identified through machine learning that may have enhanced discrimination. The widespread use of this promising tool for risk stratification of patients receiving HCT allows identification of high-risk patients that may benefit from preemptive treatment for PTLD. IMPLICATIONS FOR PRACTICE: This study validated the Fujimoto score for the prediction of post-transplant lymphoproliferative disorder (PTLD) development following hematopoietic cell transplant (HCT) in an external, independent, and nationally representative population. This study also developed a more comprehensive model with enhanced discrimination for better risk stratification of patients receiving HCT, potentially changing clinical managements in certain risk groups. Previously unreported risk factors associated with the development of PTLD after HCT were identified using the machine learning algorithm, least absolute shrinkage and selection operator, including pre-HCT medical history of mechanical ventilation and the chemotherapy agents used in conditioning regimen.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoproliferative DisordersHumansRegistriesResearch DesignRisk FactorsHematopoietic cell transplantLeast absolute shrinkage and selection operatorPost-transplant lymphoproliferative disorderPredictive scoring system

Identifiers

PMID34506688
PMCPMC8571765
OpenAlexW3196771371

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.