[Haploidentical hematopoietic stem cell transplant: How to choose the best donor? Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)].

Greffe de cellules souches hématopoïétiques haplo-identiques avec cyclophosphamide en post-greffe : comment choisir le meilleur donneur en 2019 ? Recommandations de la Société francophone de greffe de mœlle et de thérapie cellulaire (SFGM-TC).

Journal

Bulletin du cancer
ISSN: 1769-6917
Titre abrégé: Bull Cancer
Pays: France
ID NLM: 0072416

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 28 05 2019
revised: 25 07 2019
accepted: 31 07 2019
pubmed: 7 10 2019
medline: 4 3 2020
entrez: 7 10 2019
Statut: ppublish

Résumé

Haploidentical hematopoietic stem cell transplantation has been growing steadily since 2012. The SFGM-TC has twice published guidelines concerning T-cell repleted haploidentical grafts with high dose cyclophosphamide post-transplantation. The 2013 workshop recommended using the non-myeloablative Baltimore protocol with bone marrow and developed prospective protocols to evaluate these transplantations. The 2015 workshop reported improved results of reduced conditioning regimens in Hodgkin's lymphoma and intensive conditioning in myeloid hemopathies, and a similar outcome with 10/10 HLA matched donor with the same disease-risk score thus raising the question of the qualifier "alternative" for haploidentical transplants. The current work concerns the criteria for selecting the donor. The main criterion remains the absence of anti-HLA antibodies directed against the donor present in the recipient sera (DSA - Donor Specific Antibodies). In case of DSA and in the absence of an alternative donor, desensitization protocols exist. The other criteria are impossible to prioritize: age, sex, CMV, and blood type. The degree of relatedness and the number of HLA incompatibilities do not seem to be a criterion of choice. The 'ideal' donor would be a young man, CMV-matched, without major ABO incompatibility with a marrow transplant. There is insufficient data for the KIR-ligand and NIMA/NIPA mismatch. Peripheral stem cell grafts appear to yield more acute GVHD than bone marrow grafts after intensive conditioning, but with comparable survival rates. Based on the literature review, the comparison of haploidentical with unrelated donors encourages inclusion in existing national protocols randomizing these different donors.

Identifiants

pubmed: 31586527
pii: S0007-4551(19)30302-9
doi: 10.1016/j.bulcan.2019.07.011
pii:
doi:

Substances chimiques

HLA Antigens 0
Immunosuppressive Agents 0
Cyclophosphamide 8N3DW7272P

Types de publication

Consensus Development Conference Journal Article Practice Guideline Review

Langues

fre

Sous-ensembles de citation

IM

Pagination

S72-S84

Informations de copyright

Copyright © 2019. Published by Elsevier Masson SAS.

Auteurs

Valérie Dubois (V)

EFS Auvergne Rhône Alpes, laboratoire HLA, 111, rue Elisée-Reclus, 69150 Décines, France.

Kahina Amokrane (K)

Hôpital Saint-Louis, laboratoire d'immunologie et histocompatibilité, 01, avenue Claude-Vellefaux, 75010 Paris, France.

Yves Beguin (Y)

CHU de Liège, service d'hématologie, 1, avenue de l'Hôpital, 4000 Liège, Belgique.

Bénédicte Bruno (B)

CHU de Lille, hématologie pédiatrique, 59000 Lille, France.

Patrice Chevallier (P)

CHU de l'Hôtel-Dieu, service d'hématologie clinique, place A. Ricordeau, 44093 Nantes cedex, France.

Florent Delbos (F)

EFS centre Pays de la Loire, laboratoire HLA, 34, rue Jean-Monnet, 44000 Nantes, France.

Raynier Devillier (R)

Aix-Marseille Université, institut Paoli-Calmettes, CNRS, CRCM, Inserm, 13000 Marseille, France.

Catherine Giannoli (C)

EFS Auvergne Rhône Alpes, laboratoire HLA, 111, rue Elisée-Reclus, 69150 Décines, France.

Gwendaline Guidicelli (G)

CHU de Pellegrin, laboratoire immunologie et immunogénétique, place Amélie-Raba-Leon, 33076 Bordeaux cedex, France.

Mhamed Harif (M)

CHU d'Ibn-Rochd, service d'hématologie et oncologie pédiatrique, 6, rue Larjoun, quartier des Hôpitaux, 20360 Casablanca, Maroc.

Pascale Loiseau (P)

Hôpital Saint-Louis, laboratoire d'immunologie et histocompatibilité, 01, avenue Claude-Vellefaux, 75010 Paris, France.

Paul-Olivier Rouzaire (PO)

CHU de Clermont-Ferrand, université Clermont-Auvergne, service d'histocompatibilité, Inserm U1240, 58, rue Montalembert, 63003 Clermont-Ferrand, France.

Pauline Varlet (P)

CHU de Lille, université de Lille, laboratoire immunologie HLA, LIRIC, Inserm U995, 59000 Lille, France.

Ibrahim Yakoub-Agha (I)

CHU de Lille, université de Lille, LIRIC, Inserm U995, 59000 Lille, France.

Stéphanie Nguyen (S)

Université Paris 6 Pierre-et-Marie-Curie, groupe hospitalier Pitié-Salpêtrière, centre d'immunologie et des maladies infectieuses (CIMI-Paris), service d'hématologie clinique, UPMC CR7, CNRS ERL8255, Inserm U1135, 75013 Paris, France. Electronic address: stephanie.nguyen-quoc@aphp.fr.

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Classifications MeSH