Evidence map›Paper›PMID 35501565›Full record

ArticleBone marrow transplantation2022

Impact of conditioning regimen intensity on outcomes of second allogeneic hematopoietic cell transplantation for secondary acute myelogenous leukemia.

Arnon Nagler, Christophe Peczynski, Bhagirathbhai Dholaria, Myriam Labopin, Thomas Valerius, Peter Dreger, Nicolaus Kröger, Hans Christian Reinhardt, Jürgen Finke, Georg-Nikolaus Franke and 11 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 16 institutions in 7 countries.

Arnon NaglerDivision of Hematology, Sheba Medical Center, Tel Hashomer, Israel.ORCID http://orcid.org/0000-0002-0763-1265
Christophe PeczynskiALWP of the EBMT Paris office, Paris, France.ORCID http://orcid.org/0000-0002-3829-0088
Bhagirathbhai DholariaVanderbilt University Medical Center, Nashville, TN, USA. Bhagirathbhai.r.dholaria@vumc.org.ORCID http://orcid.org/0000-0003-2371-3655
Myriam LabopinSorbonne University, Sevice d'hématologie Clinique et Thérapie Cellulaire, Hôpital Saint-Antoine, INSERM UMRs 938, Paris, France.ORCID http://orcid.org/0000-0003-4514-4748
Thomas ValeriusUniversity Medical Center Schleswig Holstein, Campus Kiel, Section for Stem Cell Transplantation and Immunotherapy, Kiel, Germany.
Peter DregerUniversity of Heidelberg, Medizinische Klinik u. Poliklinik V, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7429-8570
Nicolaus KrögerUniversity Hospital Eppendorf, Bone Marrow Transplantation Centre, Hamburg, Germany.
Hans Christian ReinhardtUniversity Duisburg-Essen, University Hospital Essen, Dept. of Bone Marrow Hematology and Stem Cell Transplantation, Essen, Germany.
Jürgen FinkeUniversity of Freiburg, Dept. of Medicine -Hematology, Oncology, Freiburg, Germany.
Georg-Nikolaus FrankeMedical Clinic and Policinic 1, Hematology and Cellular Therapy, University Hospital Leipzig, Leipzig, Germany.ORCID http://orcid.org/0000-0001-8239-002X
Fabio CiceriOspedale San Raffaele s.r.l., Haematology and BMT, Milano, Italy.ORCID http://orcid.org/0000-0003-0873-0123
Mareike VerbeekKlinikum Rechts der Isar, III Med Klinik der TU, Munich, Germany.
Igor Wolfgang BlauMedizinische Klinik m. S. Hämatologie, Onkologie und Tumorimmunologie, Charité Universitätsmedizin, Berlin, Germany.
Martin BornhäuserUniversitaetsklinikum Dresden, Medizinische Klinik und Poliklinik I, Dresden, Germany.
Alexandros SpyridonidisHematology Stem Cell Transplant Unit, School of Medicine, University of Patras, Patras, Greece.ORCID http://orcid.org/0000-0003-3097-2532
Gesine BugDepartment of Medicine 2, Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.ORCID http://orcid.org/0000-0003-2359-131X
Ali BazarbachiBone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.ORCID http://orcid.org/0000-0002-7171-4997
Christophe SchmidDepartment of Hematology and Oncology, University Hospital Augsburg, Augsburg, Germany.ORCID http://orcid.org/0000-0001-7070-487X
Ibrahim Yakoub-AghaCHU de Lille, Univ Lille, INSERM, U1285, Lille, France.
Bipin N SavaniVanderbilt University Medical Center, Nashville, TN, USA.
Mohamad MohtySorbonne University, Sevice d'hématologie Clinique et Thérapie Cellulaire, Hôpital Saint-Antoine, INSERM UMRs 938, Paris, France.ORCID http://orcid.org/0000-0002-7264-808X
Inserm · FRVanderbilt University Medical Center · USAmerican University of Beirut Medical Center · LBCharité - Universitätsmedizin Berlin · DEEssen University Hospital · DEEuropean Society for Blood and Marrow Transplantation · FRGoethe University Frankfurt · DEHeidelberg University · DEIRCCS Ospedale San Raffaele · ITSheba Medical Center · ILTUM Klinikum · DEUniversität Hamburg · DEUniversity Hospital Augsburg · DEUniversity Hospital Leipzig · DEUniversity of Freiburg · DEUniversity of Patras · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Limited data is available on factors impacting the outcomes of second hematopoietic cell transplantation (HCT2) in patients with secondary acute myeloid leukemia (sAML). This study aimed to assess HCT2 outcome for sAML comparing reduced-intensity (RIC) to myeloablative (MAC) conditioning. Two hundred and fifteen patients were included: RIC (n = 134), MAC (n = 81). The median follow-up was 41.1 (95% CI: 26.7-69.3) and 28.5 (95% CI: 23.9-75.4) months, respectively. At two years, the relapse incidence (RI) was 58.3% versus 51.1% in RIC and MAC, respectively. The 2-year leukemia free survival (LFS) was 26.6% versus 26%, and the graft-versus-host disease (GVHD)-free, relapse-free survival (GRFS) was 16.4% versus 12.1%, while OS was 31.4% and 39.7%, for RIC and MAC respectively. MVA showed a significantly lower RI [hazard ratio (HR) = 0.46 (95% CI, 0.26-0.8, p = 0.006)] and improved LFS [HR = 0.62 (95% CI, 0.39-0.98, p = 0.042)] with MAC versus RIC. The choice of conditioning regimen did not impact non-relapse mortality [HR = 1.14 (95% CI, 0.52-2.5, p = 0.74)], overall survival (OS) [HR = 0.72 (95% CI, 0.44-1.17, p = 0.18)] or GRFS [HR = 0.89 (95% CI, 0.59-1.36, p = 0.6)]. In conclusion, MAC was associated with a lower RI and superior LFS. These results support the use of MAC for eligible patients with sAML who are being considered for HCT2.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteNeoplasms, Second PrimaryHumansRecurrenceRetrospective StudiesTransplantation Conditioning

Identifiers

PMID35501565
OpenAlexW4225281025

What OpenQuestion 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 OpenQuestion graph.