dc.contributor.author | Montoro, Juan | |
dc.contributor.author | Ngoya, Maud | |
dc.contributor.author | Kulagin, Alexander | |
dc.contributor.author | Giebel, Sebastian | |
dc.contributor.author | Broers, Annoek E. C. | |
dc.contributor.author | Bramanti, Stefania | |
dc.contributor.author | Halahleh, Khalid | |
dc.date.accessioned | 2025-01-12T18:54:50Z | |
dc.date.available | 2025-01-12T18:54:50Z | |
dc.date.issued | 2024 | |
dc.identifier.issn | 2473-9529 | |
dc.identifier.issn | 2473-9537 | |
dc.identifier.uri | https://doi.org/10.1182/bloodadvances.2024013328 | |
dc.identifier.uri | http://hdl.handle.net/11446/4988 | |
dc.description.abstract | Studies 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 CNIbased prophylaxis in adult patients with HL undergoing HSCT from HLA-matched donors. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Blood Advances | en_US |
dc.identifier.doi | 10.1182/bloodadvances.2024013328 | |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Versus-Host-Disease | en_US |
dc.subject | Bone-Marrow-Transplantation | en_US |
dc.subject | Posttransplantation Cyclophosphamide | en_US |
dc.subject | Haploidentical Transplantation | en_US |
dc.subject | Cell Transplantation | en_US |
dc.subject | Outcomes | en_US |
dc.subject | Malignancies | en_US |
dc.subject | Prevention | en_US |
dc.subject | Registry | en_US |
dc.subject | Blood | en_US |
dc.title | PTCy vs CNI-based GVHD prophylaxis in HLA-matched transplants for Hodgkin lymphoma: a study of the LWP of the EBMT | en_US |
dc.type | article | en_US |
dc.department | DBÜ | en_US |
dc.identifier.issue | 15 | en_US |
dc.identifier.volume | 8 | en_US |
dc.identifier.startpage | 3985 | en_US |
dc.identifier.endpage | 3992 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | [Montoro, Juan; Sanz, Jaime] Univ Sci, Hue Univ, Fac Informat Technol, Hue 530000, Vietnam; [Montoro, Juan; Giebel, Sebastian] Univ Catolica Valencia, Dept Hematol, Valencia, Spain; [Ngoya, Maud] EBMT Lymphoma Working Party, Dept Biostat, Paris, France; [Kulagin, Alexander] Pavlov Univ, RM Gorbacheva Res Inst, St Petersburg, Russia; [Kulagin, Alexander] Fdn Ratunek Dzieciom Choroba Nowotworowa, Dept Bone Marrow Transplantat & Oncohematol, Gliwice, Poland; [Broers, Annoek E. C.] Erasmus MC Canc Inst, Dept Hematol, Rotterdam, Netherlands; [Bramanti, Stefania] IRCCS, Human Res Hosp, Dept Oncol & Haematol, Transplantat Unit, Milan, Italy; [Halahleh, Khalid] King Hussein Canc Ctr, Adult BMT Program, Amman, Jordan; [Perez-Simon, Jose A.] Univ Seville, Hosp Univ Virgen Rocio, CSIC, Inst Biomed Sevilla,Dept Hematol, Seville, Spain; [Solano, Carlos] Univ Valencia, Hosp Clin Univ, INCLIVA, Valencia, Spain; [Ozcelik, Tulay] Demiroglu Bilim Univ, Istanbul Florence Nightingale Hosp, Istanbul, Turkiye; [Blaise, Didier] Programme Transplantat & Therapie Cellulaire, Marseille, France; [Sanz, Jaime] Univ Valencia, Dept Med, Valencia, Spain; [Henriques, Marta] Univ Hosp Sao Joao, Dept Hematol, Porto, Portugal; [de Latour, Regis Peffault] St Louis H | en_US |
dc.authorid | Blaise, Didier/0000-0002-5684-9447 | |
dc.authorid | Montoro, Juan/0000-0003-0024-8068 | |
dc.authorid | Perez-Simon, Jose A/0000-0003-3616-6101 | |
dc.authorid | Bramanti, Stefania/0000-0002-4117-7991 | |
dc.authorid | Ngoya, Maud/0000-0002-7810-6900 | |
dc.authorid | Sanz, Jaime/0000-0001-6934-4619 | |
dc.authorid | MARTINO, RODRIGO/0000-0001-5143-4042 | |
dc.identifier.pmid | 38810260 | en_US |
dc.identifier.scopus | 2-s2.0-85201479742 | en_US |
dc.identifier.wos | WOS:001285285300001 | en_US |
dc.authorwosid | Pérez-Martínez, Antonio/AAF-5797-2019 | |
dc.authorwosid | Kulagin, Alexander/L-9795-2014 | |
dc.authorwosid | Blaise, Didier/R-2483-2016 | |
dc.authorwosid | Bramanti, Stefania/LIC-6851-2024 | |
dc.authorwosid | Sanz, Jaime/K-7141-2019 | |
dc.authorscopusid | 7005575750 | |
dc.authorscopusid | 57226109363 | |
dc.authorscopusid | 57788890000 | |
dc.authorscopusid | 26643020200 | |
dc.authorscopusid | 7004099697 | |
dc.authorscopusid | 8513545500 | |
dc.authorscopusid | 56815013300 | |