Evidence map›Paper›PMID 42712399›Full record

ArticleFrontiers in immunology2026

Development of a stacked ensemble model for risk stratification of chronic GVHD after allogeneic HSCT: Japanese nation-wide cohort study.

Makoto Iwasaki, Junya Kanda, Fumihiko Kimura, Sachiko Seo, Yoshiko Atsuta, Naoyuki Uchida, Noriko Doki, Takahiro Fukuda, Tetsuya Nishida, Yuta Katayama and 10 more

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

20 authors.

Makoto IwasakiDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Junya KandaDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Fumihiko KimuraDivision of Hematology, Department of Internal Medicine, National Defense Medical College, Tokorozawa, Japan.
Sachiko SeoDepartment of Hematology and Oncology, Dokkyo Medical University School of Medicine, Tochigi, Japan.
Yoshiko AtsutaJapanese Data Center for Hematopoietic Cell Transplantation, Nagakute, Japan.
Naoyuki UchidaDepartment of Hematology, Federation of National Public Service Personnel Mutual Aid Associations TORANOMON HOSPITAL, Tokyo, Japan.
Noriko DokiHematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
Takahiro FukudaDepartment of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Tetsuya NishidaDepartment of Hematology, Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital, Nagoya, Japan.
Yuta KatayamaDepartment of Hematology, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima, Japan.
Masatsugu TanakaDepartment of Hematology, Kanagawa Cancer Center, Yokohama, Japan.
Taro TochigiDepartment of Hematology, Hamanomachi Hospital, Fukuoka, Japan.
Satoshi YoshiharaDepartment of Hematology, Hyogo Medical University Hospital, Nishinomiya, Japan.
Yoshinobu KandaDivision of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
Masashi SawaDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Makoto OnizukaDepartment of Hematology/Oncology, Tokai University School of Medicine, Isehara, Japan.
Moeko HinoDepartment of Pediatrics, School of Medicine, Chiba University, Chiba, Japan.
Koji KawamuraDivision of Hematology and Clinical Laboratory Medicine, Tottori University, Yonago, Japan.
Ken TabuchiJapanese Data Center for Hematopoietic Cell Transplantation, Nagakute, Japan.
Akifumi Takaori-KondoDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective risk stratification is vital for donor selection and treatment strategies in allogeneic hematopoietic stem cell transplantation (HSCT). We developed a prediction model for mid- to long-term outcomes after HSCT using a stacked ensemble model (SEM). Using data from the Japanese Transplant Registry Unified Management Program, we analyzed 14,430 patients alive without chronic GVHD (cGVHD) or relapse on day 100 after their first HSCT for hematologic malignancies between 2010 and 2018, predicting 24-month outcomes from pretransplant variables and posttransplant acute GVHD (aGVHD) information, including its treatment, accrued by days 30, 60, and 100. Data were randomly divided into training (80%) and validation (20%) sets, with 14 pretransplant risk factors as input variables. SEM achieved the highest C-index across evaluated endpoints, cGVHD, non-relapse mortality (NRM), and all-cause mortality (ACM), significantly exceeding the weaker learners for all endpoints and, using pretransplant factors, the strongest learner for NRM and ACM as well (both p=0.01), with a smaller, non-significant margin for cGVHD (C-index for cGVHD/NRM/ACM-SEM: 0.574/0.652/0.642, Cox-PH: 0.553/0.635/0.615, Random Survival Forest: 0.564/0.638/0.613, XGBoost: 0.556/0.633/0.627, Dynamic-DeepHit: 0.508/0.607/0.564). The C-index increased as posttransplant aGVHD information accrued (day 30: 0.581/0.655/0.649; day 60: 0.602/0.688/0.656; day 100: 0.606/0.696/0.664). Grade III to IV aGVHD showed predictive contribution to NRM, ultimately impacting ACM. Our SEM-based model offers a useful framework for predicting post-HSCT outcomes and highlights the critical impact of early aGVHD events on long-term prognosis.

Indexed as

Graft vs Host DiseaseHematologic NeoplasmsHematopoietic Stem Cell TransplantationAdolescentAdultChronic DiseaseCohort StudiesEast Asian PeopleFemaleHumansJapanMaleMiddle AgedRegistriesRisk AssessmentRisk Factorsacute graft-versus-host diseaseallogeneic hematopoietic stem cell transplantationchronic graft-versus-host diseasemachine learningrisk stratificationstacked ensemble model

Identifiers

PMID42712399
PMCPMC13549910

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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.