Post-transplant cyclophosphamide-based graft-versus-host disease prophylaxis in HLA-matched and haploidentical donor transplants for patients with Hodgkin lymphoma: a comparative study of the LWP EBMT.: GVHD prophylaxis for patients with Hodgkin lymphoma.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
01 Dec 2023
Historique:
received: 10 10 2023
revised: 15 11 2023
accepted: 25 11 2023
medline: 4 12 2023
pubmed: 4 12 2023
entrez: 3 12 2023
Statut: aheadofprint

Résumé

Post-transplant cyclophosphamide (PTCy) has emerged as a promising approach for preventing graft-versus-host disease (GVHD) in allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, there is a lack of studies examining the impact of this GVHD prophylaxis when different donor types are used in patients with Hodgkin lymphoma (HL). To compare the outcomes of patients with HL undergoing HSCT from both HLA-matched donors, which include matched sibling donors (MSD) and matched unrelated donors (MUD), and haploidentical donors, using PTCy as GVHD prophylaxis approach in all cohorts. We retrospectively compared transplant outcomes of allo-HSCT from 166 HLA-matched donors (96 siblings and 70 unrelated) and 694 haploidentical donors using PTCy-based GVHD prophylaxis in patients with HL registered in the EBMT database from 2010 to 2020. Haploidentical transplantation showed significantly lower platelet engraftment (86% vs 94%, p<0.001) and higher rates of grades II-IV acute GVHD (24% vs 34%, p=0.01) compared to HLA-matched transplantation. The 2-year cumulative incidence of non-relapse mortality (NRM) was significantly lower in the HLA-matched cohort compared to haploidentical cohort (10% vs 18%, p=0.02), resulting in a higher overall survival (OS) rate (82% vs 70%, p=0.002). There were no significant differences observed in terms of relapse, progression-free survival, or GVHD-free relapse-free survival between the groups. In multivariable analysis, haploidentical transplantation was associated with an increased risk of grades II-IV acute GVHD, NRM, and worse OS compared to HLA-matched transplantation. Our findings suggest that, in the context of PTCy-based GVHD prophylaxis, transplantation from HLA-matched donors appears to be a more favorable option compared to haploidentical transplantation.

Sections du résumé

BACKGROUND BACKGROUND
Post-transplant cyclophosphamide (PTCy) has emerged as a promising approach for preventing graft-versus-host disease (GVHD) in allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, there is a lack of studies examining the impact of this GVHD prophylaxis when different donor types are used in patients with Hodgkin lymphoma (HL).
OBJECTIVE OBJECTIVE
To compare the outcomes of patients with HL undergoing HSCT from both HLA-matched donors, which include matched sibling donors (MSD) and matched unrelated donors (MUD), and haploidentical donors, using PTCy as GVHD prophylaxis approach in all cohorts.
STUDY DESIGN METHODS
We retrospectively compared transplant outcomes of allo-HSCT from 166 HLA-matched donors (96 siblings and 70 unrelated) and 694 haploidentical donors using PTCy-based GVHD prophylaxis in patients with HL registered in the EBMT database from 2010 to 2020.
RESULTS RESULTS
Haploidentical transplantation showed significantly lower platelet engraftment (86% vs 94%, p<0.001) and higher rates of grades II-IV acute GVHD (24% vs 34%, p=0.01) compared to HLA-matched transplantation. The 2-year cumulative incidence of non-relapse mortality (NRM) was significantly lower in the HLA-matched cohort compared to haploidentical cohort (10% vs 18%, p=0.02), resulting in a higher overall survival (OS) rate (82% vs 70%, p=0.002). There were no significant differences observed in terms of relapse, progression-free survival, or GVHD-free relapse-free survival between the groups. In multivariable analysis, haploidentical transplantation was associated with an increased risk of grades II-IV acute GVHD, NRM, and worse OS compared to HLA-matched transplantation.
CONCLUSIONS CONCLUSIONS
Our findings suggest that, in the context of PTCy-based GVHD prophylaxis, transplantation from HLA-matched donors appears to be a more favorable option compared to haploidentical transplantation.

Identifiants

pubmed: 38043802
pii: S2666-6367(23)01710-4
doi: 10.1016/j.jtct.2023.11.021
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest There are no conflicts of interest to report.

Auteurs

J Montoro (J)

Department of Hematology, Hospital Universitario y Politécnico La Fe, Valencia, Spain; Universidad Católica de Valencia, Spain. Electronic address: juanmontorogomez@gmail.com.

A Boumendil (A)

EBMT Lymphoma Working Party, Paris, France.

H Finel (H)

EBMT Lymphoma Working Party, Paris, France.

S Bramanti (S)

Department of Oncology/Hematology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

L Castagna (L)

Department of Oncology/Hematology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

D Blaise (D)

Programme de Transplantation and Therapie Cellulaire, Marseille, France.

A Dominietto (A)

U.O. Ematologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

A Kulagin (A)

RM Gorbacheva Research Institute, Pavlov University, Saint Petersburg, Russia.

I Yakoub-Agha (I)

CHU de Lille, University of Lille, Lille, France.

A Tbakhi (A)

King Hussein Cancer Centre, Amman, Jordania.

C Solano (C)

Hematology Department, Hospital Clínico Universitario-INCLIVA, Valencia, Spain.

S Giebel (S)

The Department of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.

Z Gulbas (Z)

Anadolu Health Center Avliated John Hopkins, Kocaeli, Gebze, Turkey.

L López Corral (L)

Hospital Clínico Salamanca, Salamanca, Spain.

J A Pérez-Simón (JA)

Servicio de Hematología, Hospital Universitario Virgen del Rocío, Instituto de Biomedicina de Sevilla (IBIS), CSIC, Universidad de Sevilla, Spain.

J L Díez Martín (JL)

Hospital Gregorio Marañon, Madrid, Spain.

J Sanz (J)

Department of Hematology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.

L Farina (L)

University of Milan. Hematology Division, Fondazione IRCCS Istituto. Nazionale dei Tumori di Milano, Milan, Italy.

Y Koc (Y)

Medical Park Hospitals, Beylikduzu, Istanbul, Turkey.

G Socié (G)

Department of Hematology - BMT, Hematology Transplantation, Paris, France.

M Arat (M)

Demiroglu Bilim University Istanbul Florence Nightingale Hospital, Hematopoietic SCT Unit, Istanbul, Turkey.

M Jurado (M)

Hospital Virgen De Las Nieves, Granada, Spain.

A Bermudez (A)

Hospital Universitario Marqués de Valdecilla (IDIVAL), Santander, Spain.

H Labussière-Wallet (H)

Centre Hospitalier Lyon Sud, Lyon, France.

M Villalba (M)

Department of Hematology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.

F Ciceri (F)

Hematology and Bone Marrow Transplantation Unit, Milano, Italy.

C Martinez (C)

Hematopoietic Stem Cell Transplantation Unit, Hospital Clínic de Barcelona, Institute of Cancer and Blood Diseases, Barcelona, Spain.

A Nagler (A)

Hematology Division, Chaim Sheba Medical Center, Tel-Hashomer, Ramat-Gan, Israel.

A Sureda (A)

Hematology Department. Institut Català d'Oncologia, Hospital Duran i Reynals. Institut d'Investigació Biomèdica de Bellvitge (IDIBELL). Universitat de Barcelona, Barcelona, Spain.

B Glass (B)

Department of Hematology, Oncology and Stem Cell Transplantation, Asklepios Klinik St. Georg, Hamburg, Germany.

Classifications MeSH