Evidence map›Paper›PMID 34861680›Full record

ArticleBlood advances2022

Outcome of allogeneic transplantation for mature T-cell lymphomas: impact of donor source and disease characteristics.

Mehdi Hamadani, Maud Ngoya, Anna Sureda, Qaiser Bashir, Carlos Alejandro Litovich, Hervé Finel, Yue Chen, Ariane Boumendil, Jasmine Zain, Luca Castagna and 16 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 4 pooled it
2.1field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 4 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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  19. The role of stem cell transplant (auto and allo) in PTCL and CTCL.Hematology. American Society of Hematology. Education Program · 2024
    Review
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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

26 authors at 20 institutions in 7 countries.

Mehdi HamadaniBMT and Cellular Therapy Program, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0001-5372-510X
Maud NgoyaEuropean Society for Blood and Marrow Transplantation, Paris, France.ORCID 0000-0002-7810-6900
Anna SuredaClinical Hematology Department, Catalan Institute of Oncology, Institut d'Investigació Biomèdica de Bellvitge IDIBELL, Universitat de Barcelona, Barcelona, Spain.
Qaiser BashirDepartment of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-4086-6453
Carlos Alejandro LitovichCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Hervé FinelEuropean Society for Blood and Marrow Transplantation, Paris, France.ORCID 0000-0002-0432-9765
Yue ChenCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Ariane BoumendilEuropean Society for Blood and Marrow Transplantation, Paris, France.ORCID 0000-0002-2552-0542
Jasmine ZainDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
Luca CastagnaBMT Unit, Humanitas Clinical and Research Center-IRCCS, Humanitas Cancer Center, Milan, Italy.
Amanda F CashenDivision of Oncology, Section of Stem Cell Transplantation, Washington University School of Medicine, St. Louis, MO.
Didier BlaiseTransplant and Cellular Immunotherapy Program, Department of Hematology, Institut Paoli-Calmettes, Aix Marseille University, CNRS, INSERM, CRCM, Marseille, France.ORCID 0000-0002-5684-9447
Mazyar ShadmanDepartment of Medicine, University of Washington, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0002-3365-6562
Rocco PastanoOnco-Hematology Division, Bone Marrow Transplant Unit, European Institute of Oncology, IRCCS, Milan, Italy.ORCID 0000-0003-3301-3628
Farhad KhimaniDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL.
Mutlu AratIstanbul Florence Nightingale Hospital, Hematology and HSCT Unit, Istanbul, Turkey.ORCID 0000-0003-2039-8557
Sascha DietrichDepartment of Medicine V, University of Heidelberg, Heidelberg, Germany.ORCID 0000-0002-0648-1832
Norbert SchmitzDepartment of Medicine A, Haematology, and Oncology, University Hospital Münster, Münster, Germany.
Bertram GlassEuropean Society for Blood and Marrow Transplantation, Paris, France.
Mohamed A Kharfan-DabajaDivision of Hematology-Oncology and Blood and Marrow Transplantation and Cellular Therapies Program, Mayo Clinic, Jacksonville, FL.ORCID 0000-0001-7394-5185
Paolo CorradiniDepartment of Oncology and Hematology, Fonzazione Istituto Nazionale dei Tumori, University of Milano, Milano, Italy.
Craig S SauterDepartment of Medicine, Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY.
Silvia MontotoDepartment of Haemato-oncology, St. Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom; and.ORCID 0000-0002-3006-9725
Mi KwonDepartment of Hematology, Gregorio Marañón General University Hospital, Institute of Health Research Gregorio Marañon, Madrid, Spain.
Alex F HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.ORCID 0000-0002-9665-7415
Peter DregerDepartment of Medicine V, University of Heidelberg, Heidelberg, Germany.
European Society for Blood and Marrow Transplantation · FRMedical College of Wisconsin · USCity of Hope · USHeidelberg University · DECentre National de la Recherche Scientifique · FREuropean Institute of Oncology · ITHelios Hospital Berlin-Buch · DEHospital General Universitario Gregorio Marañón · ESHumanitas University · ITInstitut d'Investigació Biomédica de Bellvitge · ESIstanbul Florence Nightingale Hospital · TRMayo Clinic in Florida · USMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USSt Bartholomew's Hospital · GBThe University of Texas MD Anderson Cancer Center · USUniversity Hospital Münster · DEUniversity of Milan · ITUniversity of Washington · USWashington University in St. Louis · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

Mature T-cell lymphomas constitute the most common indication for allogeneic hematopoietic cell transplantation (allo-HCT) of all lymphomas. Large studies evaluating contemporary outcomes of allo-HCT in mature T-cell lymphomas relative to commonly used donor sources are not available. Included in this registry study were adult patients who had undergone allo-HCT for anaplastic large cell lymphoma, angioimmunoblastic T-cell lymphoma (AITL), or peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) between 2008 and 2018. Hematopoietic cell transplantation (HCT) platforms compared were posttransplant cyclophosphamide-based haploidentical (haplo-)HCT, matched sibling donor (MSD) HCT, matched unrelated donor HCT with in vivo T-cell depletion (MUD TCD+), and matched unrelated donor HCT without in vivo T-cell depletion (MUD TCD-). Coprimary end points were overall survival (OS) and progression-free survival (PFS); secondary end points included nonrelapse mortality (NRM), and relapse/progression incidence (RI). A total of 1942 patients were eligible (237 haplo-HCT; 911 MSD; 468 MUD TCD+; 326 MUD TCD-). Cohorts were comparable for baseline characteristics with the exception of higher proportions of patients with decreased performance status (PS) and marrow graft recipients in the haplo-HCT group. Using univariate and multivariate comparisons, OS, PFS, RI, and NRM were not significantly different among the haplo-HCT, MSD, MUD TCD+, and MUD TCD- cohorts, with 3-year OS and PFS of 60%, 63%, 59%, and 64%, respectively, and 50%, 50%, 48%, and 52%, respectively. Significant predictors of inferior OS and PFS on multivariate analysis were active disease status at HCT and decreased PS. AITL was associated with significantly reduced relapse risk and better PFS compared with PTCL-NOS. Allo-HCT can provide durable PFS in patients with mature T-cell lymphoma (TCL). Outcomes of haplo-HCT were comparable to those of matched donor allo-HCT.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLymphoma, T-Cell, PeripheralAdultHumansNeoplasm Recurrence, LocalTransplantation, Homologous

Identifiers

PMID34861680
PMCPMC8945300
OpenAlexW3217075939

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.