Evidence map›Paper›PMID 25310308›Full record

Trial reportBone marrow transplantation2015

A multicentre UK study of GVHD following DLI: rates of GVHD are high but mortality from GVHD is infrequent.

J J Scarisbrick, F L Dignan, S Tulpule, E D Gupta, S Kolade, B Shaw, F Evison, G Shah, E Tholouli, G Mufti and 3 more

Abstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Bone marrow transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
–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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Feasibility of Lenalidomide Therapy for Persistent Chronic Lymphocytic Leukemia after Allogeneic Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Trial
  3. Trial
  4. Article
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  7. Adoptive T-cell therapy for virus-associated diseases.Clinical microbiology reviews · 2025
    Review
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  12. Article
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  19. Observational
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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

13 authors.

J J ScarisbrickDepartment Dermatology, University Hospital Birmingham NHS Trust, Birmingham, UK.
F L DignanDepartment of Haematology, Manchester Royal Infirmary, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
S TulpuleDepartment of Haematology, Nottingham University Hospitals NSH Trust, Nottingham, UK.
E D GuptaDepartment of Haematology, Nottingham University Hospitals NSH Trust, Nottingham, UK.
S KoladeDepartment of Haematology, The Royal Marsden NHS Foundation Trust, Surrey, UK.
B ShawDepartment of Haematology, The Royal Marsden NHS Foundation Trust, Surrey, UK.
F EvisonDepartment of Statistics, University Hospital Birmingham NHS Trust, Birmingham, UK.
G ShahDepartment of Haematology, King's College Hospital, London, UK.
E TholouliDepartment of Haematology, Manchester Royal Infirmary, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
G MuftiDepartment of Haematology, King's College Hospital, London, UK.
A PagliucaDepartment of Haematology, King's College Hospital, London, UK.
R MalladiDepartment Haematology, University Hospital Birmingham NHS Trust, Birmingham, UK.
K RajDepartment of Haematology, King's College Hospital, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DLIs are frequently used following haematopoietic SCT (HSCT) in patients with risk of relapse but data on GVHD following DLI are scarce. We report on 68 patients who received DLI following HSCT. Most patients developed GVHD following DLI (71%), which was acute in 22 patients (32%) almost half of whom had grade III-IV acute GVHD (aGVHD). Thirty patients (44%) developed cGVHD which followed aGVHD in four patients and was graded severe in nine patients. Corticosteroids were the most common first-line therapy for both acute and chronic GVHD. A wide range of second/third-line agents included cyclosporin, mycophenolate, tacrolimus, imatinib, infliximab and ECP. Relapse of initial malignancy occurred in 37%. Relapse was significantly less frequent in those receiving pre-emptive DLI. Relapse rates were also lower in those with GVHD (31%) than those without GVHD (50%), but this did not reach statistical significance. At 55 months post DLI, 34% of patients had died most commonly from relapse and 22% had on-going GVHD. Although GVHD was an important cause of morbidity post DLI (71%), only 6% died from GVHD. Although most patients develop GVHD post DLI and may require consecutive therapies, mortality from GVHD is infrequent. DLI remains an important option for relapse post transplant and manipulation of the GVT effect needs to be optimised to induce remission without morbidity from GVHD.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLymphocyte TransfusionAdultAgedAllograftsDisease-Free SurvivalFemaleHematologic NeoplasmsHumansImmunosuppressive AgentsLiving DonorsMaleMiddle AgedSurvival RateUnited KingdomImmunosuppressive Agents

Identifiers

PMID25310308

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.