Evidence map›Paper›PMID 32887941›Full record

ArticleBone marrow transplantation2021

Better leukemia-free survival with allogeneic than with autologous HCT in AML patients with isolated trisomy 8: a study from the ALWP of the EBMT.

Frédéric Baron, Myriam Labopin, Didier Blaise, Maija Itälä-Remes, Gérard Socié, Edouard Forcade, Ibrahim Yakoub-Agha, Norbert Claude Gorin, Jordi Esteve, Arnon Nagler and 1 more

Abstract read
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In one paragraph

Article in Bone marrow transplantation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Frédéric BaronLaboratory of Hematology, GIGA-I3, University of Liege and CHU of Liège, Liege, Belgium. f.baron@ulg.ac.be.ORCID http://orcid.org/0000-0002-2944-3812
Myriam LabopinEBMT Paris Study Office/CEREST-TC, Paris, France.ORCID http://orcid.org/0000-0003-4514-4748
Didier BlaiseDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.ORCID http://orcid.org/0000-0002-5684-9447
Maija Itälä-RemesStem Cell Transplantation Unit, HUCH Comprehensive Cancer Center, Helsinki, Finland.
Gérard SociéHématologie-Greffe AP-HP Hôpital Saint Louis et Inserm U976, Université de Paris, Paris, France.ORCID http://orcid.org/0000-0002-2114-7533
Edouard ForcadeService d'Hématologie Clinique et Thérapie Cellulaire, CHU Bordeaux, F-33000, Bordeaux, France.
Ibrahim Yakoub-AghaCHU de Lille, LIRIC, INSERM U995, Université de Lille, 59000, Lille, France.
Norbert Claude GorinDepartment of Haematology, Saint Antoine Hospital, Paris, France.
Jordi EsteveHematology Department, Hospital Clínic de Barcelona, Barcelona, Spain.
Arnon NaglerEBMT Paris Study Office/CEREST-TC, Paris, France.ORCID http://orcid.org/0000-0002-0763-1265
Mohamad MohtyEBMT Paris Study Office/CEREST-TC, Paris, France.

Funding

Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) Senior research associate mandate
6 · The paper itself

Abstract

The indication for performing an allogeneic hematopoietic stem cell transplantation (allo-HCT) in patients with isolated trisomy 8 AML in first complete remission (CR) is still debated. Here, we compared outcomes of such patients given either allo-HCT or autologous (auto)-HCT. Inclusion criteria consisted of adult patients with de novo AML, isolated trisomy 8, first HCT between 2000 and 2018, CR1 at transplantation, and either auto-HCT or allo-HCT with a HLA-identical sibling donor (MSD) or a 10/10 HLA-matched unrelated donor (UD 10/10). A total of 401 patients met the inclusion criteria. They underwent an auto-HCT (n = 81), allo-HCT with a MSD (n = 186) or allo-HCT with a 10/10 UD (n = 134). At 3 years, relapse incidence, nonrelapse mortality and leukemia-free survival (LFS) were 59%, 5%, and 37%, respectively, in auto-HCT recipients; 31% (P < 0.001), 14% (P = 0.04), and 55% (P = 0.033), respectively, in MSD recipients and 29% (P < 0.001), 13% (P = 0.15), and 59% (P = 0.03), respectively, in UD 10/10 recipients. In multivariate analysis, in comparison to auto-HCT, MSD and UD 10/10 were associated with a lower risk of relapse (HR = 0.47, P < 0.001 and HR = 0.40, P < 0.001, respectively) translating to better LFS (HR = 0.69, P = 0.04 and HR = 0.60, P = 0.03, respectively). There was also a similar trend for overall survival (HR = 0.73, P = 0.12 and HR = 0.65, P = 0.08).

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAdultChromosomes, Human, Pair 8HumansNeoplasm Recurrence, LocalRetrospective StudiesTransplantation ConditioningTrisomy

Identifiers

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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.