Evidence map›Paper›PMID 41954668›Full record

ArticleAnnals of hematology2026

A novel prognostic scoring system HATS for acute myeloid leukemia patients undergoing allogeneic hematopoietic stem cell transplantation.

Garret M K Leung, Yishan Ye, Yi Luo, Jimin Shi, Yanmin Zhao, Joycelyn P Y Sim, Yok-Lam Kwong, Huang He, Harinder Gill

Registry-linked trialAbstract read
In one paragraph

Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06702111 (Allogeneic Hematopoietic Stem Cell Transplant), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

NCT06702111 recruitingnot on this map

Allogeneic Hematopoietic Stem Cell Transplant (HSCT) in Adults: Clinical Outcome and Complications

Typeobservational_patient_registrySponsorThe University of Hong KongRan2024 to 2030Enrolled1,000ConditionsHematopoietic Stem Cell Transplant (HSCT)
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Garret M K Leung *Department of Medicine, School of Clinical Medicine, LKS Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Yishan Ye *Bone Marrow Transplantation Center, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yi LuoBone Marrow Transplantation Center, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jimin ShiBone Marrow Transplantation Center, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yanmin ZhaoBone Marrow Transplantation Center, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Joycelyn P Y SimDepartment of Medicine, School of Clinical Medicine, LKS Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Yok-Lam KwongDepartment of Medicine, School of Clinical Medicine, LKS Faculty of Medicine, University of Hong Kong, Hong Kong, China. ylkwong@hku.hk.
Huang HeBone Marrow Transplantation Center, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. hehuangyu@126.com.
Harinder GillDepartment of Medicine, School of Clinical Medicine, LKS Faculty of Medicine, University of Hong Kong, Hong Kong, China. gillhsh@hku.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal prognostication model for outcome following allogeneic hematopoietic stem cell transplantation (allo-HSCT) for acute myeloid leukemia (AML) remains undefined. To establish a prognostic scoring system, 466 consecutive AML patients undergoing allo-HSCT from 2014 to 2023 were analyzed as a training cohort. Six donor, leukemia and recipient related factors were identified as prognostically significant and assigned weighted scores, respectively 1 point each for donor cytomegalovirus seropositivity, Hemopoietic Cell Transplantation-specific Comorbidity Index ≥ 2, secondary AML, not in first complete remission, and low-intensity induction therapy; 3 points for inv(3)/t(3;3)(q21;q26) or KMT2A rearrangement; 4 points for − 5/del(5q) or TP53 mutation; 0 point for CEBPA bZIP in-frame mutation or core-binding factor AML; and 1 point for all other genetic risk groups. Scores were grouped into four risk categories: favorable (0–1), intermediate (2–3), poor (4–5), and very poor (≥ 6); constituting the HATS prognostication model. The corresponding 2-year overall survivals of favorable, intermediate, poor and very poor risk groups were 92%, 78%, 50%, and 7.4% (log-rank P < 0.001). An external validation cohort comprising 395 patients was similarly analyzed. With concordance statistics, HATS outperformed all six existing prognostication models. In conclusion, HATS represents a novel prognostication model devised for AML patients undergoing allo-HSCT.Clinicaltrials.gov identifier: NCT06702111.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAdolescentAdultAgedFemaleHumansMaleMiddle AgedPrognosisTransplantation, HomologousYoung Adultacute myeloid leukemiaallogeneic hematopoietic stem cell transplantationprognostic model

Identifiers

PMID41954668
PMCPMC13065535

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