Evidence map›Paper›PMID 30723110›Full record

ArticleBlood advances2019

PTCy-based haploidentical vs matched related or unrelated donor reduced-intensity conditioning transplant for DLBCL.

Peter Dreger, Anna Sureda, Kwang Woo Ahn, Mary Eapen, Carlos Litovich, Herve Finel, Ariane Boumendil, Ajay Gopal, Alex F Herrera, Christoph Schmid and 16 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 3 pooled it
12.0field-weighted citation impact, top 1% 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

61 citing papers in PubMed, 3 syntheses or guidelines pooled it, 113 citations in OpenAlex.

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1 more citing papers are in PubMed but not listed here.

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 17 institutions in 6 countries.

Peter DregerDepartment Medicine V, University of Heidelberg, Heidelberg, Germany.
Anna SuredaHematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Kwang Woo AhnDivision of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, WI.
Mary EapenCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Carlos LitovichCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Herve FinelEuropean Society for Blood and Marrow Transplantation, Paris, France.
Ariane BoumendilEuropean Society for Blood and Marrow Transplantation, Paris, France.
Ajay GopalDivision of Medical Oncology, Clinical Research Division, Department of Medicine, University of Washington, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, Seattle, WA.
Alex F HerreraCity of Hope, Duarte, CA.
Christoph SchmidKlinikum Augsburg, Augsburg, Germany.
José Luis Diez-MartinHospital Gregorio Marañón, Madrid, Spain.
Ephraim FuchsJohns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD.
Javier Bolaños-MeadeJohns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD.
Mahasweta GooptuDana-Farber Cancer Institute, Boston, MA.
Monzr M Al MalkiCity of Hope, Duarte, CA.
Luca CastagnaIstituto Clinico Humanitas, Rozzano Milan, Italy.
Stefan O CiureaUniversity of Texas, MD Anderson Cancer Center, Houston, TX.
Alida DominiettoDivisione Ematologia e Trapianto di Midollo, Istituto di Ricovero e Cura a Carattere Scientifico San Martino, Genoa, Italy.
Didier BlaiseProgramme de Transplantation and Thérapie Cellulaire-Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.
Fabio CiceriHematology and Bone Marrow Transplantation Unit, San Raffaele Scientific Institute, Milan, Italy.
Johanna TischerDepartment of Internal Medicine III, Campus Großhadern, University of Munich, Munich, Germany.
Paolo CorradiniDepartment of Oncology and Hematology, University of Milan, Milan, Italy.
Silvia MontotoEuropean Society for Blood and Marrow Transplantation, Paris, France.
Stephen RobinsonEuropean Society for Blood and Marrow Transplantation, Paris, France.
Zafer GülbasAnadolu Medical Center Hospital, Kocaeli, Turkey.
Mehdi HamadaniCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Medical College of Wisconsin · USCity of Hope · USEuropean Society for Blood and Marrow Transplantation · FRSidney Kimmel Comprehensive Cancer Center · USCancer Research Center · USCentre de Recherche en Cancérologie de Marseille · FRDana-Farber Cancer Institute · USFondazione Humanitas per la Ricerca · ITHeidelberg University · DEHospital General Universitario Gregorio Marañón · ESInstitut Català d'Oncologia · ESLudwig-Maximilians-Universität München · DESt Bartholomew's Hospital · GBThe University of Texas MD Anderson Cancer Center · USUniversity Hospital Augsburg · DEUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity of Milan · IT

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

This study retrospectively compared long-term outcomes of nonmyeloablative/reduced intensity conditioning (NMC/RIC) allogeneic hematopoietic cell transplantation (allo-HCT) from a haploidentical family donor (haplo-HCT) using posttransplant cyclophosphamide (PTCy) with those of matched sibling donor (MSD) and matched unrelated donor (MUD) with or without T-cell depletion (TCD+/TCD-) in patients with relapsed diffuse large B-cell lymphoma (DLBCL). Adult patients with DLBCL who had undergone their first NMC/RIC allo-HCT between 2008 and 2015 were included. Recipients of haplo-HCT were limited to those receiving graft-versus-host disease (GVHD) prophylaxis with PTCy. GVHD prophylaxis in MSD was limited to calcineurin inhibitor (CNI)-based approaches without in vivo TCD, while MUD recipients received CNI-based prophylaxis with or without TCD. Outcome analyses for overall survival (OS) and progression-free survival (PFS), nonrelapse mortality (NRM), and disease relapse/progression were calculated. A total of 1438 patients (haplo, 132; MSD, 525; MUD TCD+, 403; and MUD TCD-, 378) were included. Patients with haplo donors were significantly older, had a better performance status and had more frequently received total body irradiation-based conditioning regimens and bone marrow grafts than MSD and MUD TCD+ or TCD-. 3-year OS, PFS, NRM and relapse/progression incidence after haplo-HCT was 46%, 38%, 22%, and 41%, respectively, and not significantly different from outcomes of matched donor transplants on multivariate analyses. Haplo-HCT was associated with a lower cumulative incidence of chronic GVHD compared with MSD, MUD TCD+/TCD-. NMC/RIC haplo-HCT with PTCy seems to be a valuable alternative for patients with DLBCL considered for allo-HCT but lacking a matched donor.

Indexed as

AdultAgedFemaleHematopoietic Stem Cell TransplantationHumansLymphoma, Large B-Cell, DiffuseMaleMiddle AgedRetrospective StudiesTissue DonorsTransplantation ConditioningYoung Adult

Identifiers

PMID30723110
PMCPMC6373757
OpenAlexW2914763076

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.