Evidence map›Paper›PMID 33941226›Full record

ArticleJournal of hematology & oncology2021

Allogeneic hematopoietic cell transplantation with cord blood versus mismatched unrelated donor with post-transplant cyclophosphamide in acute myeloid leukemia.

Bhagirathbhai Dholaria, Myriam Labopin, Jaime Sanz, Annalisa Ruggeri, Jan Cornelissen, Hélène Labussière-Wallet, Didier Blaise, Edouard Forcade, Patrice Chevallier, Anna Grassi and 8 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal of hematology & oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it, 19 citations in OpenAlex.

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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

18 authors at 17 institutions in 9 countries.

Bhagirathbhai DholariaDepartment of Hematology-Oncology, Vanderbilt University Medical Center, 220 Pierce Ave, 777 Preston Research Building, Nashville, TN, 37232, USA. Bhagirathbhai.R.Dholaria@vumc.org.ORCID 0000-0003-2371-3655
Myriam LabopinEBMT ALWP Office, Hôpital Saint-Antoine, Paris, France.
Jaime SanzHematology Department, University Hospital La Fe, Valencia, Spain.
Annalisa RuggeriDepartment of Pediatric Hematology and Oncology IRCCS, Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Jan CornelissenDepartment of Hematology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Hélène Labussière-WalletHôpital Lyon Sud, Hospices Civils de Lyon, Pierre Bénite, France.
Didier BlaiseProgramme de Transplantation and Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.
Edouard ForcadeHôpital Haut-Leveque, CHU Bordeaux, Pessac, France.
Patrice ChevallierDepartment of D'Hematologie, CHU Nantes, Nantes, France.
Anna GrassiHematology and Bone Marrow Transplant Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
Ludmila ZubarovskayaRM Gorbacheva Research Institute, Pavlov University, St. Petersburg, Russian Federation.
Jürgen KuballDepartment of Haematology, University Medical Centre, Utrecht, The Netherlands.
Patrice CeballosDépartement d'Hématologie Clinique, CHU Lapeyronie, Montpellier, France.
Fabio CiceriOspedale San Raffaele S.R.L., Haematology and BMT, Milan, Italy.
Frederic BaronCHU and University of Liège, Liège, Belgium.
Bipin N SavaniDepartment of Hematology-Oncology, Vanderbilt University Medical Center, 220 Pierce Ave, 777 Preston Research Building, Nashville, TN, 37232, USA.
Arnon NaglerChaim Sheba Medical Center, Tel Hashomer, Israel.
Mohamad MohtyEBMT ALWP Office, Hôpital Saint-Antoine, Paris, France.
Vanderbilt University Medical Center · USBambino Gesù Children's Hospital · ITCentre de Recherche en Cancérologie de Marseille · FRCentre Hospitalier Universitaire de Nantes · FRErasmus MC · NLFirst Pavlov State Medical University of St. Petersburg · RUHeidelberg University · DEHôpital Cardiologique du Haut-Lévêque · FRHôpital Lapeyronie · FRHospices Civils de Lyon · FRHospital Universitari i Politècnic La Fe · ESInserm · FRIRCCS Ospedale San Raffaele · ITOspedale Papa Giovanni XXIII · ITSheba Medical Center · ILSorbonne Université · FRUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAllogeneic hematopoietic cell transplantation (allo-HCT) using a mismatched unrelated donor (MMUD) and cord blood transplantation (CBT) are valid alternatives for patients without a fully human leukocyte antigen (HLA)-matched donor. Here, we compared the allo-HCT outcomes of CBT versus single-allele-mismatched MMUD allo-HCT with post-transplant cyclophosphamide (PTCy) in acute myeloid leukemia.

methodsPatients who underwent a first CBT without PTCy (N = 902) or allo-HCT from a (HLA 9/10) MMUD with PTCy (N = 280) were included in the study. A multivariate regression analysis was performed for the whole population. A matched-pair analysis was carried out by propensity score-based 1:1 matching of patients (177 pairs) with known cytogenetic risk.

resultsThe incidence of grade II-IV and grade III-IV acute graft-versus-host disease (GVHD) at 6 months was 36% versus 32% (p = 0.07) and 15% versus 11% (p = 0.16) for CBT and MMUD cohorts, respectively. CBT was associated with a higher incidence of graft failure (11% vs. 4%, p < 0.01) and higher 2-year non-relapse mortality (NRM) (30% vs. 16%, p < 0.01) compared to MMUD. In the multivariate analysis, CBT was associated with a higher risk of, NRM (HR = 2.09, 95% CI 1.46-2.99, p < 0.0001), and relapse (HR = 1.35, 95% CI 1-1.83, p = 0.05), which resulted in worse leukemia-free survival (LFS) (HR = 1.68, 95% CI 1.34-2.12, p < 0.0001), overall survival (OS) (HR = 1.7, 95% CI 1.33-2.17, p < 0.0001), and GVHD-free, relapse-free survival (GRFS) (HR = 1.49, 95% CI 1.21-1.83, p < 0.0001) compared to MMUD. The risk of grade II-IV acute GVHD (p = 0.052) and chronic GVHD (p = 0.69) did not differ significantly between the cohorts. These results were confirmed in a matched-pair analysis.

conclusionsCBT was associated with lower LFS, OS, and GRFS due to higher NRM, compared to MMUD allo-HCT with PTCy. In the absence of a fully matched donor, 9/10 MMUD with PTCy may be preferred over CBT.

Indexed as

AdolescentAdultAgedCord Blood Stem Cell TransplantationCyclophosphamideFemaleHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedRetrospective StudiesTransplantation ConditioningUnrelated DonorsYoung AdultCyclophosphamideAcute leukemiaAcute myeloid leukemiaAllogeneic hematopoietic cell transplantationBone marrowCord blood transplantationCord blood unitDisease relapseGraft-versus-host diseaseHuman leukocyte antigenMismatched donorPeripheral blood stem cellPost-transplant cyclophosphamideToxicity

Identifiers

PMID33941226
PMCPMC8094558
OpenAlexW3158885412

What OpenQuestion holds

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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.