Donor Lymphocyte Infusions After Allogeneic Stem Cell Transplantation in Acute Leukemia: A Survey From the Gruppo Italiano Trapianto Midollo Osseo (GITMO).

acute leukemia allogeneic stem cell transplantation donor lymphocyte infusions pre-emptive treatment relapse

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2020
Historique:
received: 15 06 2020
accepted: 27 08 2020
entrez: 12 11 2020
pubmed: 13 11 2020
medline: 13 11 2020
Statut: epublish

Résumé

We conducted a retrospective multicenter study including pediatric and adult patients with acute leukemia (AL) who received donor lymphocyte infusions (DLIs) after allogeneic hematopoietic stem cell transplantation (HCT) between January 1, 2010 and December 31, 2015, in order to determine the efficacy and toxicity of the immune treatment. Two hundred fifty-two patients, median age 45.1 years (1.6-73.4), were enrolled from 34 Italian transplant centers. The underlying disease was acute myeloid leukemia in 180 cases (71%). Donors were HLA identical or 1 locus mismatched sibling (40%), unrelated (40%), or haploidentical (20%). The first DLI was administered at a median time of 258 days (55-3,784) after HCT. The main indication for DLI was leukemia relapse (73%), followed by mixed chimerism (17%), and pre-emptive/prophylactic use (10%). Ninety-six patients (38%) received one single infusion, whereas 65 (26%), 42 (17%), and 49 patients (19%) received 2, 3, or ≥4 infusions, respectively, with a median of 31 days between two subsequent DLIs. Forty percent of evaluable patients received no treatment before the first DLI, whereas radiotherapy, conventional chemotherapy or targeted treatments were administered in 3, 39, and 18%, respectively. In informative patients, a few severe adverse events were reported: grade III-IV graft versus host disease (GVHD) (3%), grade III-IV hematological toxicity (11%), and DLI-related mortality (9%). Forty-six patients (18%) received a second HCT after a median of 232 days (32-1,390) from the first DLI. With a median follow-up of 461 days (2-3,255) after the first DLI, 1-, 3-, and 5- year overall survival (OS) of the whole group from start of DLI treatment was 55, 39, and 33%, respectively. In multivariate analysis, older recipient age, and transplants from haploidentical donors significantly reduced OS, whereas DLI for mixed chimerism or as pre-emptive/prophylactic treatment compared to DLI for AL relapse and a schedule including more than one DLI significantly prolonged OS. This GITMO survey confirms that DLI administration in absence of overt hematological relapse and multiple infusions are associated with a favorable outcome in AL patients. DLI from haploidentical donors had a poor outcome and may represent an area of further investigation.

Identifiants

pubmed: 33178602
doi: 10.3389/fonc.2020.572918
pmc: PMC7593406
doi:

Types de publication

Journal Article

Langues

eng

Pagination

572918

Informations de copyright

Copyright © 2020 Patriarca, Sperotto, Lorentino, Oldani, Mammoliti, Isola, Picardi, Arcese, Saporiti, Sorasio, Mordini, Cavattoni, Musso, Borghero, Micò, Fanin, Bruno, Ciceri and Bonifazi.

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Auteurs

Francesca Patriarca (F)

Clinica Ematologica e Centro Trapianti, Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.
Department of Medical Area (DAME) Università di Udine, Udine, Italy.

Alessandra Sperotto (A)

Clinica Ematologica e Centro Trapianti, Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.

Francesca Lorentino (F)

Unitá Operativa Complessa (UOC) Ematologia e Trapianto, Istituto di Ricovero e Cura a carattere scientifico (IRCSS) Ospedale San Raffaele, Milan, Italy.

Elena Oldani (E)

Unitá Operativa Complessa (UOC) Ematologia e Trapianto, Azienda Socio Sanitaria Territoriale (ASST) Papa Giovanni XXIII, Bergamo, Italy.

Sonia Mammoliti (S)

Trial Office Gruppo Trapianto Di Midollo Osseo e Terapie Cellulari (GITMO), Genova, Italy.

Miriam Isola (M)

Istituto di Statistica, Department of Medical Area (DAME) Università di Udine, Udine, Italy.

Alessandra Picardi (A)

Unitá Operativa Complessa (UOC) Ematologia con Trapianto, Azienda Ospedaliera (AO) Cardarelli, Naples, Italy.

William Arcese (W)

Unitá Operativa Complessa (UOC) Ematologia, Azienda Ospedaliera Universitaria (AOU) Policlinico Tor Vergata, Rome, Italy.

Giorgia Saporiti (G)

Ematologia-Centro Trapianti di Midollo-Fondazione Istituto di Ricovero e Cura a carattere scientifico (IRCSS) Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Roberto Sorasio (R)

Unitá Operativa Complessa (UOC) Ematologia, Azienda Ospedaliera (AO) S. Croce, Cuneo, Italy.

Nicola Mordini (N)

Unitá Operativa Complessa (UOC) Ematologia, Azienda Ospedaliera (AO) S. Croce, Cuneo, Italy.

Irene Cavattoni (I)

UOC Ematologia, Azienda Ospedaliera (AO) di Bolzano, Genova, Italy.

Maurizio Musso (M)

Unitá Operativa Onco-ematologia e (UO) Oncoematologia e Trapianto Midollo Osseo (TMO), Ospedale LaMaddalena, Palermo, Italy.

Carlo Borghero (C)

Unitá Operativa Complessa (UOC) Ematologia, Ospedale San Bortolo, Vicenza, Italy.

Caterina Micò (C)

Unitá Operativa Complessa (UOC) Ematologia e Trapianto, Azienda Socio Sanitaria Territoriale (ASST) Papa Giovanni XXIII, Bergamo, Italy.

Renato Fanin (R)

Clinica Ematologica e Centro Trapianti, Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.
Department of Medical Area (DAME) Università di Udine, Udine, Italy.

Benedetto Bruno (B)

Unitá Operativa Complessa (UOC) Ematologia, Azienda Ospedaliera Universitaria (AOU) Città della Salute e della Scienza, Turin, Italy.

Fabio Ciceri (F)

Unitá Operativa Complessa (UOC) Ematologia e Trapianto, Istituto di Ricovero e Cura a carattere scientifico (IRCSS) Ospedale San Raffaele, Milan, Italy.

Francesca Bonifazi (F)

Ematologia, Azienda Ospedaliera-Universitaria di Bologna, Bologna, Italy.

Classifications MeSH