Evidence map›Paper›PMID 36823454›Full record

ArticleBone marrow transplantation2023

Allogeneic stem cell transplantation for patients with acute myeloid leukemia (AML) in second complete remission (CR2) transplanted from unrelated donors with post-transplant cyclophosphamide (PTCy). A study on behalf of the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation.

Arnon Nagler, Myriam Labopin, Ryszard Swoboda, Alexander Kulagin, Hélène Labussière-Wallet, Montserrat Rovira, Didier Blaise, Jan Vydra, Ibrahim Yakoub-Agha, Goda Choi and 5 more

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Article in Bone marrow transplantation, 2023. 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
0.9field-weighted citation impact, top 24% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

15 authors at 13 institutions in 10 countries.

Arnon NaglerDivision of Hematology, Sheba Medical Center, Tel Hashomer, Israel. arnon.nagler@sheba.health.gov.il.ORCID 0000-0002-0763-1265
Myriam LabopinALWP of the EBMT Paris office, Paris, France.
Ryszard SwobodaDepartment of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.ORCID 0000-0002-5897-3919
Alexander KulaginFirst State Pavlov Medical University of St. Petersburg, Raisa Gorbacheva Memorial Research Institute for Paediatric Oncology, Hematology, and Transplantation, St, Petersburg, Russia.ORCID 0000-0002-9589-4136
Hélène Labussière-WalletCentre Hospitalier Lyon Sud, Pavillon Marcel Bérard, Service Hematologie, Lyon, France.
Montserrat RoviraHospital Clinic, Department of Hematology, Institute of Hematology and Oncology, Barcelona, Spain.
Didier BlaiseProgramme de Transplantation & Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille; Institut Paoli Calmettes, Marseille, France.
Jan VydraInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.ORCID 0000-0002-4274-3895
Ibrahim Yakoub-AghaCHU de Lille, Univ Lille, INSERM U1286, Infinite, 59000, Lille, France.ORCID 0000-0003-4524-8782
Goda ChoiDeptartment of Hematology; University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Péter ReményiDél-pesti Centrumkórház -Országos Hematológiai és Infektológiai Intézet; Dept. Haematology and Stem Cell Transplant, Albert, Budapest, Hungary.
Yener KocMedicana International Hospital Istanbul; Bone Marrow Transplant Unit, Istanbul, Turkey.
Jaime SanzHospital Universitari i Politècnic La Fe, Valencia, Spain.ORCID 0000-0001-6934-4619
Fabio CiceriOspedale San Raffaele s.r.l. Haematology and BMT, Milano, Italy.ORCID 0000-0003-0873-0123
Mohamad MohtySorbonne University, Department of Clinical Hematology and Cellular Therapy, Hospital Saint Antoine, AP-HP, INSERM UMRs 938, Paris, France.
Inserm · FRCentre de Recherche en Cancérologie de Marseille · FRFirst Pavlov State Medical University of St. Petersburg · RUHôpital Lyon Sud · FRHospital Clínic de Barcelona · ESHospital Universitari i Politècnic La Fe · ESInstitute of Haematology and Blood Transfusion · CZIRCCS Ospedale San Raffaele · ITIstanbul Eye Hospital · TROrszágos Pszichiátriai és Neurológiai Intézet · HUSheba Medical Center · ILThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-transplant cyclophosphamide (PTCy) is being increasingly used as graft-versus-host disease (GVHD) prophylaxis post allogeneic hematopoietic stem cell transplantation (allo-HSCT) in patients with acute myeloid leukemia (AML) transplanted in first complete remission (CR1). However, results may differ in patients transplanted in CR2. We retrospectively evaluated transplant outcomes of adult AML patients transplanted between 2010-2019 from 9-10/10 human leukocyte antigen (HLA)-matched unrelated donor (UD) in CR2. In total, 127 patients were included (median age 45.5 years, 54% male). Median follow-up was 19.2 months. Conditioning was myeloablative (MAC) in 50.4% and the graft source was peripheral blood in 93.7% of the transplants. Incidence of acute (a)GVHD II-IV and III-IV was 26.2% and 9.2%. Two-year total and extensive chronic (c)GVHD were 34.3% and 13.8 %, respectively. Two-year non-relapse mortality (NRM), relapse incidence (RI), leukemia-free survival (LFS), overall survival (OS), and GVHD-free, relapse-free survival (GRFS) were 17.2%, 21.1%, 61.7, %, 65.2%, and 49.3%, respectively. Time from diagnosis to transplant (>18 months) was a favorable prognostic factor for RI, LFS, OS, and GRFS while favorable risk cytogenetics was a positive prognostic factor for OS. The patient's age was a poor prognostic factor for NRM and cGVHD. Finally, the female-to-male combination and reduced intensity conditioning (RIC) were poor and favorable prognostic factors for cGVHD, respectively. We conclude that PTCy is an effective method for GVHD prophylaxis in AML patients undergoing allo-HCT in CR2 from UD.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAcute DiseaseAdultBone MarrowCyclophosphamideFemaleHumansMaleMiddle AgedRecurrenceRetrospective StudiesTransplantation ConditioningUnrelated DonorsCyclophosphamide

Identifiers

PMID36823454
OpenAlexW4321617102

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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.