First experience of allogeneic haematopoietic stem cell transplantation in patients with mantle cell lymphoma with a mutation in the TP53 gene

Author:

Koroleva D. A.1ORCID,Gabeeva N. G.1ORCID,Drokov M. Yu.1ORCID,Vasilyeva V. A.1ORCID,Biderman B. V.1ORCID,Tsygankova S. V.2ORCID,Bulygina E. S.2ORCID,Galstyan G. M.1ORCID,Sudarikov A. B.1ORCID,Obukhova T. N.1ORCID,Kuzmina L. A.1ORCID,Zvonkov E. E.1ORCID,Parovichnikova E. N.1ORCID,Savchenko V. G.1ORCID

Affiliation:

1. National Research Center for Hematology

2. National Research Center “Kurchatov institute”

Abstract

Introduction. Mutations in the TP53 gene in patients with mantle cell lymphoma (MCL TP53+) are associated with a low response to intensive chemotherapy (CT) and adverse outcomes. Allogeneic haematopoietic stem cells transplantation (allo-HSCT) is a curative approach in MCL-TP53+ patients.Aim. Efficacy and safety assessment of allo-HSCT in MCL-TP53+ patients.Main findings. During 2016–2020, allo-HSCT in MCL TP53+ was performed in three patients. Two of them were grafted from HLA-identical unrelated donors, and one — from a haploidentical donor. Pre-transplant conditioning was “fludarabine + treosulfan + melphalan” in one case, and “fludarabine + busulfan” — in the other two. In three patients, leukocyte and platelet counts were recovered at days +18 and +20, +17 and +21, +19 and +16 after allo-HSCT, respectively. Acute graft-versushost disease (aGVHD) was observed in all patients (grade I — in 2 patients, grade IV — in 1 patient). One patient developed chronic GVHD (cGVHD) of moderate grade. All three patients exhibited complete remission and 100% donor chimerism in allo-HSCT follow-up of 6, 15 and 40 months, respectively.

Publisher

National Medical Research Center of Hematology of the Ministry of Health of the Russian Federation

Subject

Hematology

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