Evidence map›Paper›PMID 41114809›Full record

ArticleAnnals of hematology2025

Transplantation strategy affects the risk of GvHD after prophylactic and preemptive donor lymphocyte infusion.

Eva A S Koster, Peter A von dem Borne, Joost G K van der Hem, Peter van Balen, Erik W A Marijt, Jennifer M L Tjon, Tjeerd J F Snijders, Daniëlle van Lammeren, Hendrik Veelken, J H Frederik Falkenburg and 2 more

Abstract read
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Eva A S KosterDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands. e.a.s.koster@lumc.nl.ORCID http://orcid.org/0000-0002-8446-5133
Peter A von dem BorneDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-7470-7346
Joost G K van der HemDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0003-3111-4249
Peter van BalenDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-9670-4664
Erik W A MarijtDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-7683-4560
Jennifer M L TjonDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-2393-715X
Tjeerd J F SnijdersDepartment of Hematology, Medical Spectrum Twente, Enschede, The Netherlands.
Daniëlle van LammerenDepartment of Hematology, HagaZiekenhuis, The Hague, The Netherlands.
Hendrik VeelkenDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-9108-3125
J H Frederik FalkenburgDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-9819-4813
Liesbeth C de WreedeDepartment of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-7667-9369
Constantijn J M HalkesDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-6573-0045

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Donor lymphocyte infusion (DLI) after allogeneic stem cell transplantation (alloSCT) can boost Graft-versus-Leukaemia (GvL) reactivity but may induce Graft-versus-Host-Disease (GvHD). It is essential to understand which factors besides timing, donor type, and dose influence DLI alloreactivity. We previously identified viral infections, ≥ 5% patient cells in bone marrow chimerism, and lymphopenia at the time of DLI as relevant factors for GvHD after DLI following alemtuzumab-based T-cell depletion. Here, we investigated these factors and the alloreactivity after DLI following alloSCT with posttransplant cyclophosphamide in 83 patients with acute leukaemia/myelodysplastic syndrome receiving a prophylactic or preemptive DLI. 5% had viral infections close to DLI, 6% had ≥ 5% mixed chimerism, and 17% had lymphopenia. 2-year cumulative incidence of GvHD requiring systemic treatment was low: 7% (95%-confidence interval 1-14%). 22 of the 28 patients with ≥ 1% mixed chimerism at the time of DLI (79%) converted to full-donor chimerism. None of these responders relapsed, indicating achievement of GvL despite the low incidence of GvHD. Our data show that DLI alloreactivity is determined by the conditions at the time of DLI which are influenced by the transplantation strategy. Adjusting the DLI dose based on these conditions may improve the balance between GvHD and GvL.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLymphocyte TransfusionAdolescentAdultAgedFemaleHumansMaleMiddle AgedMyelodysplastic SyndromesRisk FactorsTransplantation, HomologousYoung AdultAcute leukemiaAllogeneic stem cell transplantationChimerismDonor lymphocyte infusionGraft-versus-Host-DiseaseGraft-versus-Leukemia effect

Identifiers

PMID41114809
PMCPMC12619706

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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.