Evidence map›Paper›PMID 32346079›Full record

SynthesisBone marrow transplantation2020

Haploidentical hematopoietic stem cell transplantation in aplastic anemia: a systematic review and meta-analysis of clinical outcome on behalf of the severe aplastic anemia working party of the European group for blood and marrow transplantation (SAAWP of EBMT).

Ghada ElGohary, Riad El Fakih, Regis de Latour, Antonio Risitano, Judith Marsh, Hubert Schrezenmeier, Eliane Gluckman, Britta Höchsmann, Filomena Pierri, Constantijn Halkes and 9 more

Open access · bronzeAbstract readMeta-AnalysisSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Bone marrow transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  3. Towards graft-Haematologica · 2025
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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

19 authors at 13 institutions in 9 countries.

Ghada ElGoharyKing Khalid University Hospital, Riyadh, Saudi Arabia. ghelgohary@gmail.com.ORCID http://orcid.org/0000-0002-9203-7446
Riad El FakihKing Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia. Relfakih1@kfshrc.edu.sa.
Regis de LatourSaint-Louis Hospital, Paris, France.
Antonio RisitanoFederico II University, Naples, Italy.ORCID http://orcid.org/0000-0002-4744-5109
Judith MarshKing's College Hospital/King's College London, London, UK.
Hubert SchrezenmeierUniversity Hospital Ulm, Ulm, Germany.
Eliane GluckmanEurocord, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France.
Britta HöchsmannUniversity Hospital Ulm, Ulm, Germany.
Filomena PierriHematology Unit, G Gaslini Children Research Hospital, Genova, Italy.
Constantijn HalkesLeiden University Medical Centre, Leiden, The Netherlands.
Hazzaa AlzahraniKing Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Josu De la FuenteImperial College Healthcare/Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-0974-1249
Simone CesaroPediatric Hematology Oncology, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Ali AlahmariKing Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Syed Osman AhmedKing Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Jakob PasswegUniversity Hospital Basel, Basel, Switzerland.
Carlo DufourHematology Unit, G Gaslini Children Research Hospital, Genova, Italy.
Andrea BacigalupoUniversita' Cattolica del Sacro Cuore, Roma, Italy.
Mahmoud AljurfKing Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
King Faisal Specialist Hospital & Research Centre · SAIstituto Giannina Gaslini · ITUniversity Hospital Ulm · DEAin Shams University · EGAzienda Ospedaliera Universitaria Integrata Verona · ITFederico II University Hospital · ITHôpital Saint-Louis · FRImperial College Healthcare NHS Trust · GBKing's College London · GBLeiden University Medical Center · NLUniversità Cattolica del Sacro Cuore · ITUniversité Paris Cité · FRUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aplastic anemia (AA) is a serious hematological disorder, which is solely cured by hematopoietic stem cell transplantation (HSCT). Haploidentical HSCT is an emerging modality with encouraging outcomes in several blood conditions. The present study aims to comprehensively assess the feasibility and safety of haploidentical HSCT in patients with severe and very severe AA. It is a systematic review and meta-analysis of studies related to haploidentical stem cell transplantation in idiopathic AA investigating rates of successful engraftment, acute graft-versus-host disease (aGvHD), chronic GvHD (cGvHD), transplant-related mortality (TRM), and posttransplantation viral infections (including cytomegalovirus [CMV]) in patients with AA. The effects of reduced-intensity conditioning (RIC) and nonmyeloablative conditioning (NMA), as well as various GvHD prophylaxis regimens on these outcomes were evaluated. In total 15 studies were identified, (577 patients, 58.9% males), successful engraftment was observed in 97.3% of patients (95% CI, 95.9-98.7) while grades II-IV aGvHD and cGvHD were reported in 26.6% and 25.0%, respectively. The pooled incidence of TRM was 6.7% per year (95% CI, 4.0-9.4). RIC regimens were associated with higher proportions of successful engraftment (97.7% vs 91.7%, P = 0.03) and aGvHD (29.5% vs 18.7%, P = 0.008) when compared with NMA regimens with no differences in cGvHD or mortality incidence. When compared with methotrexate-containing regimens and other regimens, posttransplant cyclophosphamide-containing regimens reduced the rates of aGvHD (28.6%, 27.8%, and 12.8%, respectively, P = 0.02), CMV viremia (55.7%, 38.6%, and 10.4%, respectively, P < 0.001), and CMV disease in initially viremic patients (2.1%, 33.0%, and 0%, respectively, P < 0.001). We have concluded that Haploidentical HSCT was associated with promising outcomes in terms of successful engraftment and reduced complications. Future prospective trials are needed to identify the preferred conditioning regimen, GvHD prophylaxis, and graft source in the setting of haploidentical transplant for AA.

Indexed as

Anemia, AplasticGraft vs Host DiseaseHematopoietic Stem Cell TransplantationBone MarrowFemaleHumansMaleTransplantation Conditioning

Identifiers

PMID32346079
OpenAlexW3017817564

What Socratic holds

Textmetadata
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.