Evidence map›Paper›PMID 40926330›Full record

GuidelineBritish journal of haematology2025

UK recommendations for chimerism testing and monitoring following allogeneic haematopoietic stem cell transplantation (HSCT): Best practice consensus guidelines from the British Society for Blood and Marrow Transplant and Cellular Therapies (BSBMTCT), NHS England Genomic Laboratory Hub (GLH) Haematological Malignancies Working Group, UK Cancer Genetics Group (UKCGG) and the UK National External Quality Assessment Service for Leucocyte Immunophenotyping (UK NEQAS LI).

Andrew Clark, Hazel Clouston, Kanchan Rao, Najeem Folarin, Josu De la Fuente, Angela Hamblin, Eduardo Olavarria, Debbie Richardson, Polly Talley, Victoria Potter and 3 more

Abstract readPractice Guideline
In one paragraph

Guideline in British journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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.

Andrew ClarkDepartment of Haematology, Queen Elizabeth University Hospital, Glasgow, UK.ORCID https://orcid.org/0000-0001-9593-9528
Hazel CloustonUK NEQAS for Leucocyte Immunophenotyping, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Kanchan RaoDepartment of Haematology, Great Ormond Street Hospital, London, UK.
Najeem FolarinSynnovis Molecular Biology Laboratory, Guys and St Thomas' Hospitals NHS Trust, London, UK.
Josu De la FuenteDepartment of Paediatric Haematolgy, Imperial College, London, UK.
Angela HamblinCentral and South Genomic Laboratory Hub, Oxford University Hospitals NHS Foundation, Oxford, UK.
Eduardo OlavarriaDepartment of Haematology, Imperial College, London, UK.
Debbie RichardsonDepartment of Haematology, Southampton University Hospitals Trust, Southampton, UK.
Polly TalleyLeeds Cancer Institute, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Victoria PotterDepartment of Haematology, Kings College Hospital NHS Foundation Trust, London, UK.
Justin LokeCentre for Haematology, University Hospital Birmingham NHS Foundation Trust, Birmingham, UK.
Terri McVeighThe Institute of Cancer Research, London, UK.
John SnowdenDepartment of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.ORCID https://orcid.org/0000-0001-6819-3476

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In allogeneic haematopoietic stem cell transplantation (HSCT), important clinical decisions depend upon assessment of chimerism, including immunosuppressant dosing and donor lymphocyte infusions (DLI), which in turn can have major impacts on disease control, graft-versus-host disease (GVHD), immunity and ultimately patient survival. There is a complex range of clinical and laboratory procedural considerations including methodology of testing, types of cell subset selection, frequency of testing, urgency of turnaround times (TATs), interplay with measurable residual disease (MRD) monitoring and duration of testing post-transplant. These aspects are routinely adapted according to disease indication, patient characteristics, donor source and intensity of transplant technique. To encourage the harmonisation of clinical and laboratory practice in the United Kingdom, we held a national workshop meeting to bring together key stakeholders to review the current literature with a view to producing a state-of-the-art position paper. Here, we present best practice consensus recommendations and identify key areas for future audit and research from the UK Cancer Genetics Group (UKCGG), NHS England Genomic Laboratory Hub (GLH) Haematological Oncology Malignancies Working Group, UK National External Quality Assessment Service for Leucocyte Immunophenotyping (UK NEQAS LI) and the British Society of Blood and Marrow Transplantation and Cellular Therapy (BSBMTCT).

Indexed as

ChimerismHematologic NeoplasmsHematopoietic Stem Cell TransplantationTransplantation ChimeraGraft vs Host DiseaseHumansImmunophenotypingNeoplasm, ResidualReview Literature as TopicTransplantation, HomologousUnited Kingdomallogeneic stem cell transplantBMTchimerismDLIPBSCT

Identifiers

PMID40926330
PMCPMC12624179

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.