Evidence map›Paper›PMID 38810260›Full record

ArticleBlood advances2024

PTCy vs CNI-based GVHD prophylaxis in HLA-matched transplants for Hodgkin lymphoma: a study of the LWP of the EBMT.

Juan Montoro, Maud Ngoya, Alexander Kulagin, Sebastian Giebel, Annoek E C Broers, Stefania Bramanti, Khalid Halahleh, Jose A Pérez-Simón, Carlos Solano, Tulay Ozcelik and 15 more

Abstract readComparative Study
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

25 authors.

Juan MontoroDepartment of Hematology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.ORCID 0000-0003-0024-8068
Maud NgoyaDepartment of Biostatistics, EBMT Lymphoma Working Party, Paris, France.ORCID 0000-0002-7810-6900
Alexander KulaginRM Gorbacheva Research Institute, Pavlov University, Saint-Petersburg, Russia.
Sebastian GiebelDepartment of Bone Marrow Transplantation and Oncohematology, Fundacja Na Ratunek Dzieciom z Chorobą Nowotworową, Gliwice, Poland.ORCID 0000-0002-4827-4401
Annoek E C BroersDepartment of Hematology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Stefania BramantiIRCCS Humanitas Research Hospital, Transplantation Unit Department of Oncology and Haematology, Milan, Italy.ORCID 0000-0002-4117-7991
Khalid HalahlehKing Hussein Cancer Centre, Adult BMT Program, Amman, Jordan.ORCID 0000-0002-1161-9138
Jose A Pérez-SimónDepartment of Hematology. Hospital Universitario Virgen del Rocío, Instituto de Biomedicina de Sevilla, CISC, Universidad de Sevilla, Seville, Spain.
Carlos SolanoHospital Clínico Universitario-INCLIVA, University of Valencia, Valencia, Spain.
Tulay OzcelikDemiroglu Bilim University, Istanbul Florence Nightingale Hospital, Istanbul, Turkey.
Didier BlaiseProgramme de Transplantation & Therapie Cellulaire, Marseille, France.ORCID 0000-0002-5684-9447
Jaime SanzDepartment of Hematology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.ORCID 0000-0001-6934-4619
Marta HenriquesDepartment of Hematology, Unversity Hospital Sao Joao, Oporto, Portugal.
Régis Peffault de LatourSaint-Louis Hospital, BMT Unit, Paris, France.
Rodrigo MartinoDepartment of Hematology, Hospital Santa Creu i Sant Pau, Barcelona, Spain.ORCID 0000-0001-5143-4042
Christof ScheidDepartment of Internal Medicine, University of Cologne, Cologne, Germany.ORCID 0009-0007-6539-226X
Laura FoxDepartment of Hematology, Hospital Vall d`Hebron, Barcelona, Spain.
Tomasz GromekDepartment of Hematology, Samodzielny Publiczny Szpital Kliniczny, Lublin, Poland.
Manuel JuradoDepartment of Hematology, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Ioanna SakellariDepartment of Hematology, George Papanicolaou General Hospital, Thessaloniki, Greece.
Gwendolyn Van GorkomDivision of Hematology, Department of Internal Medicine, GROW School for Oncology and Development Biology, Maastricht, The Netherlands.
Paola MatteucciDepartment of Hematology, University of Milano, Milan, Italy.
Arnon NaglerChaim Sheba Medical Center, Tel-Hashomer, Israel.
Yener KocDepartment of Hematology, Medicana International Hospital Istanbul, Istanbul, Turkey.
Bertram GlassDepartment of Hematology, Oncology, and Stem Cell Transplantation, Asklepios Klinik St. Georg, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractStudies comparing the efficacy of posttransplant cyclophosphamide (PTCy) to conventional calcineurin inhibitor (CNI)-based graft-versus-host disease (GVHD) prophylaxis regimens in patients with Hodgkin lymphoma (HL) are scarce. This study aimed to compare the outcomes of patients with HL undergoing hematopoietic stem cell transplantation (HSCT) from HLA-matched donors who received GVHD prophylaxis with either PTCy- or conventional CNI-based regimens, using data reported in the European Society for Blood and Marrow Transplantation database between January 2015 and December 2022. Among the cohort, 270 recipients received conventional CNI-based prophylaxis and 176 received PTCy prophylaxis. Notably, PTCy prophylaxis was associated with delayed hematopoietic recovery but also with a lower risk of chronic (25% vs 43%; P < .001) and extensive chronic GVHD (13% vs 28%; P = .003) compared with the CNI-based cohort. The 2-year cumulative incidence of nonrelapse mortality and relapse was 11% vs 17% (P = .12) and 17% vs 30% (P = .007) for PTCy- and CNI-based, respectively. Moreover, the 2-year overall survival (OS), progression-free survival (PFS), and GVHD-free, relapse-free survival (GRFS) were all significantly better in the PTCy group compared with the CNI-based group: 85% vs 72% (P = .005), 72% vs 53% (P < .001), and 59% vs 31% (P < .001), respectively. In multivariable analysis, PTCy was associated with a lower risk of chronic and extensive chronic GVHD, reduced relapse, and better OS, PFS, and GRFS than the CNI-based platform. Our findings suggest that PTCy as GVHD prophylaxis offers more favorable outcomes than conventional CNI-based prophylaxis in adult patients with HL undergoing HSCT from HLA-matched donors.

Indexed as

CyclophosphamideGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHodgkin DiseaseAdolescentAdultCalcineurin InhibitorsFemaleHLA AntigensHumansMaleMiddle AgedYoung AdultCalcineurin InhibitorsCyclophosphamideHLA Antigens

Identifiers

PMID38810260
PMCPMC11331730

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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.