Reduced-intensity versus conventional myeloablative conditioning allogeneic stem cell transplantation for patients with acute lymphoblastic leukemia: a retrospective study from the European Group for Blood and Marrow Transplantation

Author:

Mohty Mohamad1,Labopin Myriam2,Volin Liisa3,Gratwohl Alois4,Socié Gérard5,Esteve Jordi6,Tabrizi Reza7,Nagler Arnon8,Rocha Vanderson5,

Affiliation:

1. Service d'Hématologie Clinique, Centre Hospitalier Universitaire Hôtel Dieu, Université de Nantes, Centre d'Investigation Clinique en Cancerologie and Inserm U892, Nantes, France;

2. European Group for Blood and Marrow Transplantation, Acute Leukemia Working Party, Paris office Hôpital Saint Antoine, Service d'Hématologie et Thérapie Cellulaire, Assistance Publique–Hôpitaux de Paris (AP-HP), Université Pierre et Marie Curie, Université de Paris 06, Unité Mixte de Recherche S 938, CEREST-TC European Group for Blood and Marrow Transplantation, Paris, France;

3. Department of Medicine, Helsinki University Central Hospital, Helsinki, Finland;

4. Division of Hematology, Department of Medicine, University Hospital Basel, Basel, Switzerland;

5. Department of Hematology, Hopital Saint-Louis, AP-HP, Paris, France;

6. Hospital Clínic, Barcelona, Spain;

7. Centre Hospitalo-Universitaire de Bordeaux, Hôpital Haut-Leveque, Pessac, France; and

8. Tel-Aviv University, Chaim Sheba Medical Center, Tel-Hashomer, Israel

Abstract

This retrospective study assessed the outcome of 576 adult acute lymphoblastic leukemia patients aged ≥ 45 years, and who received a reduced-intensity conditioning (RIC; n = 127) or myeloablative conditioning (MAC; n = 449) allogeneic stem cell transplantation (allo-SCT) from a human leukocyte antigen-identical sibling while in complete remission. With a median follow-up of 16 months, at 2 years, the cumulative incidences of nonrelapse mortality and relapse incidence were 29% ± 2% (MAC) versus 21% ± 5% (RIC; P = .03), and 31% ± 2% (MAC) versus 47% ± 5% (RIC; P < .001), respectively. In a multivariate analysis, nonrelapse mortality was decreased in RIC recipients (P = .0001, hazard ratio [HR] = 1.98) whereas it was associated with higher relapse rate (P = .03, HR = 0.59). At 2 years, LFS was 38% ± 3% (MAC) versus 32% ± 6% (RIC; P = .07). In multivariate analysis, the type of conditioning regimen (RIC vs. MAC) was not significantly associated with leukemia-free survival (P = .23, HR = 0.84). Despite the need for randomized trials, we conclude that RIC allo-SCT from a human leukocyte antigen-identical donor is a potential therapeutic option for acute lymphoblastic leukemia patients aged ≥ 45 years in complete remission and not eligible for MAC allo-SCT.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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