Evidence map›Paper›PMID 42686993›Full record

ArticleBone marrow transplantation2026

Allogeneic stem cell transplantation with post-transplantation cyclophosphamide in patients with acute myeloid leukemia achieving first complete remission after one versus two inductions: a study from the ALWP/EBMT.

Arnon Nagler, Ryszard Swoboda, Allain Thibeault Ferhat, Didier Blaise, Jurjen Versluis, Gwendolyn Van Gorkom, Maija Itala-Remes, Mercedes Colorado Araujo, Helene Labussiere-Wallet, Ibrahim Yakoub-Agha and 13 more

Abstract read
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In one paragraph

Article in Bone marrow transplantation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Arnon Nagler *Division of Hematology, Sheba Medical Center, Tel Hashomer, Israel. arnon.nagler@sheba.health.gov.il.ORCID http://orcid.org/0000-0002-0763-1265
Ryszard Swoboda *Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.ORCID http://orcid.org/0000-0002-5897-3919
Allain Thibeault FerhatEBMT Paris study office; Department of Haematology, Saint Antoine Hospital, INSERM UMR 938, Sorbonne University, Paris, France.
Didier BlaiseProgramme de Transplantation & Therapie Cellulaire, Marseille, France.ORCID http://orcid.org/0000-0002-5684-9447
Jurjen VersluisErasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-2372-1663
Gwendolyn Van GorkomUniversity Hospital Maastricht, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0001-7327-7834
Maija Itala-RemesTurku University Hospital, Turku, Finland.
Mercedes Colorado AraujoMarqués de Valdecilla University Hospital, Santander, Spain.
Helene Labussiere-WalletHopital Lyon Sud, Hospices Civils de Lyon, Pierre Benite, France.ORCID http://orcid.org/0000-0003-0543-9592
Ibrahim Yakoub-AghaCHU de Lille, Université de Lille, INSERM U1286, Infinite, Lille, France.ORCID http://orcid.org/0000-0003-4524-8782
Regis Peffault de LatourSaint-Louis Hospital, BMT Unit, Paris, France.
Tobias Gedde-DahlOslo University Hospital, Rikshospitalet, Oslo, Norway.
Mieke W H RoevenRadboud University Medical Center, Nijmegen, The Netherlands.
Edouard ForcadeCHU Bordeaux, Hôpital Haut-Leveque, Pessac, France.ORCID http://orcid.org/0000-0002-8873-2868
Martin CarréCHU Grenoble Alpes - Universite Grenoble Alpes, Grenoble, France.
Patrice ChevallierCHU Nantes, Nantes, France.ORCID http://orcid.org/0000-0003-3142-5581
Deborah DesmierCHU de Poitiers, Poitiers, France.
Maurizio MussoOspedale La Maddalena - Dipartimento Oncologico, Palermo, Italy.
Jaime SanzUniversity Hospital La Fe, Departament de Medicina Universitat de Valencia, Valencia, Spain.ORCID http://orcid.org/0000-0001-6934-4619
Eolia BrissotService d'Hématologie clinique et Thérapie cellulaire, Hôpital Saint-Antoine, APHP, Paris, France.ORCID http://orcid.org/0000-0003-4471-418X
Ali BazarbachiBone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.ORCID http://orcid.org/0000-0002-7171-4997
Mohamad MohtySorbonne University, Department of Haematology, Saint Antoine Hospital, INSERM UMR 938, Paris, France.ORCID http://orcid.org/0000-0002-7264-808X
Fabio CiceriIRCCS Osspedale San Raffaele, Vita-Salute San Raffaele University Haematology and BMT, Milano, Italy.ORCID http://orcid.org/0000-0003-0873-0123

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation (alloHSCT) is a potentially curative treatment for high-risk acute myeloid leukemia (AML), and outcomes are strongly influenced by disease status at transplantation. In transplants using conventional graft-versus-host disease (GVHD) prophylaxis, outcomes also depend on the number of induction courses required to achieve first complete remission (CR1); however, this has not been evaluated in patients receiving post-transplant cyclophosphamide (PTCy). We retrospectively analyzed 677 adult AML patients transplanted in CR1 between 2012 and 2022 using PTCy-based GVHD prophylaxis. Outcomes were compared between patients achieving CR1 after one induction course (n = 518) and those requiring two courses (n = 159). Baseline characteristics, donor type, conditioning intensity, graft source, engraftment, and rates of acute and chronic GVHD were comparable between groups. Patients requiring two inductions had a higher 2-year cumulative incidence of relapse (27% vs. 19.3%; HR 1.75, p = 0.003). However, no significant differences were observed in 2-year overall survival (62.8% vs. 69%), leukemia-free survival (61.1% vs. 65%), GVHD-free/relapse-free survival (46.3% vs. 50.4%), or non-relapse mortality (11.9% vs. 15.7%). In AML patients receiving alloHSCT with PTCy, outcomes were largely similar regardless of whether CR1 was achieved after one or two-induction courses, with relapse incidence being higher in patients requiring 2 inductions.

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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.