Evidence map›Paper›PMID 28100265›Full record

ArticleJournal of hematology & oncology2017

Allogeneic stem cell transplantation in adult patients with acute myeloid leukaemia and 17p abnormalities in first complete remission: a study from the Acute Leukemia Working Party (ALWP) of the European Society for Blood and Marrow Transplantation (EBMT).

Xavier Poiré, Myriam Labopin, Johan Maertens, Ibrahim Yakoub-Agha, Didier Blaise, Norbert Ifrah, Gérard Socié, Tobias Gedde-Dhal, Nicolaas Schaap, Jan J Cornelissen and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of hematology & oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06337331 (A Phase II Trial of Venetoclax-Enhanced Reduced Intensity HLA-Mismatched Allogeneic Transplant for Ultra-High-Risk Acute Myeloid Leukemia), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 6% 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.

NCT06337331 phase2withdrawnnot on this mapstarted 2024, after this paper: background citation

A Phase II Trial of Venetoclax-Enhanced Reduced Intensity HLA-Mismatched Allogeneic Transplant for Ultra-High-Risk Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS)

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2024 to 2027Enrolled0ConditionsAcute Myeloid Leukemia, Myelodysplastic SyndromesArmsVenetoclax, Decitabine, Fludarabine, Busulfan, Total Body Irradiation
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Novel immunotherapies in the treatment of AML: is there hope?Hematology. American Society of Hematology. Education Program · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Transplant for TP53-mutated MDS and AML: because we can or because we should?Hematology. American Society of Hematology. Education Program · 2022
    Article
  15. Novel investigational approaches for high-risk genetic subsets of AML: TP53, KMT2A, FLT3.Hematology. American Society of Hematology. Education Program · 2022
    Article
  16. Review
  17. How I TreatCancers · 2022
    Review
  18. Review
  19. TargetingOncoTargets and therapy · 2022
    Review
  20. 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

16 authors at 13 institutions in 5 countries.

Xavier PoiréSection of Hematology, Department of Medicine, Cliniques Universitaires Saint-Luc, 10, avenue Hippocrate, 1200, Brussels, Belgium. Xavier.Poire@uclouvain.be.
Myriam LabopinAcute Leukemia Working Party of the EBMT office, Paris, France.
Johan MaertensDepartment of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
Ibrahim Yakoub-AghaUAM allo-CSH, Hôpital HURIEZ, Lille, France.
Didier BlaiseProgramme de Transplantation et Thérapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.
Norbert IfrahService des Maladies du Sang, CHRU, Angers, France.
Gérard SociéDepartment of Hematology, Hôpital Saint-Louis, Paris, France.
Tobias Gedde-DhalDepartment of Medicine, Rikshospitalet, Oslo, Norway.
Nicolaas SchaapDepartment of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.
Jan J CornelissenDaniel den Hoed Cancer Centre, Erasmus Medical Center, Rotterdam, The Netherlands.
Stéphane VigourouxService d'Hématologie, CHU Bordeaux, Pessac, France.
Jaime SanzServicio de Hematologia, Hospital Universitario La Fe, Valencia, Spain.
Lucienne MichauxCenter for Human Genetics, KU Leuven and University Hospitals, Leuven, Belgium.
Jordi EsteveHematology department, IDIBAPS, Hospital Clinic, Barcelona, Spain.
Mohamad MohtyAcute Leukemia Working Party of the EBMT office, Paris, France.
Arnon NaglerAcute Leukemia Working Party of the EBMT office, Paris, France.
Centre de Recherche en Cancérologie de Marseille · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Bordeaux · FRCliniques Universitaires Saint-Luc · BEHôpital Claude Huriez · FRHôpital Saint-Louis · FRHospital Clínic de Barcelona · ESHospital Universitari i Politècnic La Fe · ESInserm · FRKU Leuven · BERadboud University Nijmegen · NLSheba Medical Center · ILUniversitair Ziekenhuis Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute myeloid leukaemia (AML) with 17p abnormalities (abn(17p)) carries a very poor prognosis due to high refractoriness to conventional chemotherapy, and allogeneic stem cell transplantation (allo-SCT) appears as the only potential curative option.

methodsTo address outcomes after allo-SCT in patients with abn(17p), we retrospectively analysed de novo or secondary AML undergoing SCT between 2000 and 2013 from the EBMT registry.

resultsOne hundred thirty-nine patients with confirmed abn(17p) have been selected. At the time of transplant, one hundred twenty-five were in first remission (CR1). Median age was 54 years old. Abn(17p) was associated with a monosomal karyotype in 83% of patients, complex karyotype in 91%, monosomy 5 or 5q deletion (-5/5q-) in 55%, monosomy 7 (-7) in 39% and both -5/5q and -7 in 27%. Seventy-three patients (59%) had a reduced-intensity conditioning regimen. The 2-year overall survival (OS) and leukaemia-free survival (LFS) were 28 and 24%, respectively. The 2-year non-relapse mortality (NRM) was 15%, and 2-year relapse incidence (RI) was 61%. The cumulative incidence of grade II to IV acute graft-versus-host disease (GvHD) was 24% and that of chronic GvHD was 21%. In multivariate analysis, the presence of a -5/5q- in addition to abn(17p) was significantly and independently associated with worse OS, LFS and higher RI. Age and donor types did not correlate with outcome. Conditioning intensity was not statistically associated with OS, LFS and NRM when adjusted for patients' age.

conclusionsIn contrast to the dismal prognosis reported for AML patients harbouring abn(17p) undergoing conventional chemotherapy, allogeneic SCT provides responses in about 25% of those patients transplanted in CR1.

Indexed as

AdultAllograftsChromosome AberrationsChromosomes, Human, Pair 17Disease-Free SurvivalEuropeFemaleFollow-Up StudiesGraft SurvivalGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedPrognosis17p abnormalitiesAcute myeloid leukaemiaFirst remissionStem cell transplantationSurvival

Identifiers

PMID28100265
PMCPMC5241968
OpenAlexW2576017084

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.