Outcomes of Reduced Intensity Conditioning Allogeneic Hematopoietic Stem Cell Transplantation for Hodgkin Lymphomas: A Retrospective Multicenter Experience by the Rete Ematologica Pugliese (REP).


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
01 2019
Historique:
received: 01 06 2018
revised: 28 07 2018
accepted: 21 08 2018
pubmed: 9 10 2018
medline: 23 2 2020
entrez: 9 10 2018
Statut: ppublish

Résumé

Hodgkin lymphoma (HL) is a potentially curable disease, and modern therapy is expected to successfully cure more than 80% of the patients. However, patients progressing after intensive treatments, such as autologous stem cell transplantation (SCT), have a very poor outcome. Allogeneic SCT offers the only strategy with a curative potential for these patients. This study reports a retrospective multicenter experience of the Rete Ematologica Pugliese (REP) over the past 17 years, aiming to define the impact of each patient's disease and transplant-related characteristics on outcomes. We retrospectively studied 72 patients with HL who received allogeneic SCT from 2000 to 2017. At the time of allogeneic SCT, 33 (46%) patients had chemosensitive disease, and 39 (54%) were chemo-refractory. All patients received reduced-intensity conditioning, 50% received grafts from a matched sibling donor, and 50% from a matched-unrelated donor. With a median follow-up of 48 months (range, 3-195 months), 30 patients are alive, and 42 have died. The Kaplan-Meier estimates of overall survival and progression-free survival at 5 years were 35% and 34%, respectively. Following transplantation, 12 (17%) patients died of non-relapse mortality at a median of 90 days (range, 1 day-20 months). The causes of death included infection (n = 7), graft-versus-host disease (n = 3), and multi-organ failure (n = 2). Allogeneic SCT results extend survival in selected patients with relapsed/refractory HL, showing low treatment-related mortality. Patients with active disease at the time of allogeneic transplantation have poor outcomes. Allogeneic SCT may be an effective salvage strategy for patients who relapse after an autologous SCT.

Sections du résumé

BACKGROUND
Hodgkin lymphoma (HL) is a potentially curable disease, and modern therapy is expected to successfully cure more than 80% of the patients. However, patients progressing after intensive treatments, such as autologous stem cell transplantation (SCT), have a very poor outcome. Allogeneic SCT offers the only strategy with a curative potential for these patients. This study reports a retrospective multicenter experience of the Rete Ematologica Pugliese (REP) over the past 17 years, aiming to define the impact of each patient's disease and transplant-related characteristics on outcomes.
PATIENTS AND METHODS
We retrospectively studied 72 patients with HL who received allogeneic SCT from 2000 to 2017. At the time of allogeneic SCT, 33 (46%) patients had chemosensitive disease, and 39 (54%) were chemo-refractory. All patients received reduced-intensity conditioning, 50% received grafts from a matched sibling donor, and 50% from a matched-unrelated donor.
RESULTS
With a median follow-up of 48 months (range, 3-195 months), 30 patients are alive, and 42 have died. The Kaplan-Meier estimates of overall survival and progression-free survival at 5 years were 35% and 34%, respectively. Following transplantation, 12 (17%) patients died of non-relapse mortality at a median of 90 days (range, 1 day-20 months). The causes of death included infection (n = 7), graft-versus-host disease (n = 3), and multi-organ failure (n = 2).
CONCLUSIONS
Allogeneic SCT results extend survival in selected patients with relapsed/refractory HL, showing low treatment-related mortality. Patients with active disease at the time of allogeneic transplantation have poor outcomes. Allogeneic SCT may be an effective salvage strategy for patients who relapse after an autologous SCT.

Identifiants

pubmed: 30293754
pii: S2152-2650(18)30578-0
doi: 10.1016/j.clml.2018.08.012
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

35-40

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Francesco Gaudio (F)

Haematology, Policlinico Hospital, Bari, Italy. Electronic address: fragaudio@alice.it.

Patrizio Mazza (P)

Haematology, "G.Moscati" Hospital, Taranto, Italy.

Angelo Michele Carella (AM)

Haematology, "Casa Sollievo della sofferenza" Hospital, San Giovanni Rotondo (FG), Italy.

Anna Mele (A)

Haematology, "G.Panico" Hospital, Tricase (LE), Italy.

Giulia Palazzo (G)

Haematology, "G.Moscati" Hospital, Taranto, Italy.

Giovanni Pisapia (G)

Haematology, "G.Moscati" Hospital, Taranto, Italy.

Paola Carluccio (P)

Haematology, Policlinico Hospital, Bari, Italy.

Domenico Pastore (D)

Haematology, "A.Perrino" Hospital, Brindisi, Italy.

Nicola Cascavilla (N)

Haematology, "Casa Sollievo della sofferenza" Hospital, San Giovanni Rotondo (FG), Italy.

Giorgina Specchia (G)

Haematology, Policlinico Hospital, Bari, Italy.

Vincenzo Pavone (V)

Haematology, "G.Panico" Hospital, Tricase (LE), Italy.

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