Evidence map›Paper›PMID 36649566›Full record

ArticleBlood advances2023

T-cell replete cord transplants give superior outcomes in high-risk and relapsed/refractory pediatric myeloid malignancy.

Claire Horgan, Khushnuma Mullanfiroze, Archana Rauthan, Katharine Patrick, Naeem Akram Butt, Oana Mirci-Danicar, Olya O'Connor, Caroline Furness, Akshay Deshpande, Sarah Lawson and 14 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
10.8field-weighted citation impact, top 1% of its field
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

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

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 13 institutions in 2 countries.

Claire HorganRoyal Manchester Children's Hospital, Manchester, United Kingdom.
Khushnuma MullanfirozeGreat Ormond Street Hospital for Children, London, United Kingdom.
Archana RauthanGreat Ormond Street Hospital for Children, London, United Kingdom.ORCID 0000-0002-4745-7628
Katharine PatrickSheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.
Naeem Akram ButtBristol Royal Hospital for Children, Bristol, United Kingdom.
Oana Mirci-DanicarBristol Royal Hospital for Children, Bristol, United Kingdom.
Olya O'ConnorThe Royal Marsden NHS Foundation Trust, London, United Kingdom.
Caroline FurnessThe Royal Marsden NHS Foundation Trust, London, United Kingdom.
Akshay DeshpandeBirmingham Children's Hospital, Birmingham, United Kingdom.
Sarah LawsonBirmingham Children's Hospital, Birmingham, United Kingdom.
Valerie BroderickChildren's Health Ireland at Crumlin, Dublin, Ireland.
Pamela EvansChildren's Health Ireland at Crumlin, Dublin, Ireland.
Brenda GibsonRoyal Hospital for Children, Glasgow, United Kingdom.
Wing RobertsGreat North Children's Hospital, Victoria Wing, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
Salah AliLeeds Children's Hospital, Clarendon Wing, Leeds General Infirmary, Leeds, United Kingdom.
Sevasti GalaniCR UK & UCL Cancer Trials Centre, UCL Cancer Institute, University College London, London, United Kingdom.
Amy A KirkwoodCR UK & UCL Cancer Trials Centre, UCL Cancer Institute, University College London, London, United Kingdom.
Jelena JovanovicDepartment of Medical and Molecular Genetics, King's College London, Strand, London, United Kingdom.
Richard DillonDepartment of Medical and Molecular Genetics, King's College London, Strand, London, United Kingdom.
Paul VirgoDepartment of Immunology and Immunogenetics, North Bristol NHS Trust, Bristol, United Kingdom.
Beki JamesLeeds Children's Hospital, Clarendon Wing, Leeds General Infirmary, Leeds, United Kingdom.
Kanchan RaoGreat Ormond Street Hospital for Children, London, United Kingdom.
Persis J AmroliaGreat Ormond Street Hospital for Children, London, United Kingdom.ORCID 0000-0003-0480-3911
Robert F WynnRoyal Manchester Children's Hospital, Manchester, United Kingdom.
Great Ormond Street Hospital · GBBirmingham Children's Hospital · GBBristol Royal Hospital for Children · GBChildren's Health Ireland at Crumlin · IECRUK Lung Cancer Centre of Excellence · GBKing's College London · GBLeeds General Infirmary · GBRoyal Manchester Children's Hospital · GBRoyal Marsden NHS Foundation Trust · GBNorth Bristol NHS Trust · GBRoyal Hospital for Children · GBRoyal Victoria Infirmary · GBSheffield Children's NHS Foundation Trust · GB

Funding

Cancer Research UK 29806
6 · The paper itself

Abstract

Stem cell transplant (SCT) outcomes in high-risk and relapsed/refractory (R/R) pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) have been historically poor. Cord blood (CB) allows T-cell replete CB transplant (TRCB), enabling enhanced graft-versus-leukemia. We consecutively collected data from 367 patients undergoing TRCB (112 patients) or other cell source (255 patients) SCT for pediatric AML/MDS in the United Kingdom and Ireland between January 2014 and December 2021. Data were collected about the patient's demographics, disease, and its treatment; including previous transplant, measurable residual disease (MRD) status at transplant, human leukocyte antigen-match, relapse, death, graft versus host disease (GvHD), and transplant-related mortality (TRM). Univariable and multivariable analyses were undertaken. There was a higher incidence of poor prognosis features in the TRCB cohort: 51.4% patients were MRD positive at transplant, 46.4% had refractory disease, and 21.4% had relapsed after a previous SCT, compared with 26.1%, 8.6%, and 5.1%, respectively, in the comparator group. Event free survival was 64.1% within the TRCB cohort, 50% in MRD-positive patients, and 79% in MRD-negative patients. To allow for the imbalance in baseline characteristics, a multivariable analysis was performed where the TRCB cohort had significantly improved event free survival, time to relapse, and reduced chronic GvHD, with some evidence of improved overall survival. The effect appeared similar regardless of the MRD status. CB transplant without serotherapy may be the optimal transplant option for children with myeloid malignancy.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteMyelodysplastic SyndromesMyeloproliferative DisordersChildHumansRecurrenceStem Cell Transplantation

Identifiers

PMID36649566
PMCPMC10206437
OpenAlexW4317037753

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.