FIRST EXPERIENCE OF ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION IN PATIENTS WITH MANTLE CELL LYMPHOMA WITH A MUTATION IN THE TP53 GENE

被引:2
作者
Koroleva, D. A. [1 ]
Gabeeva, N. G. [1 ]
Drokov, M. Yu [1 ]
Vasilyeva, V. A. [1 ]
Biderman, B., V [1 ]
Tsygankova, S., V [2 ]
Bulygina, E. S. [2 ]
Galstyan, G. M. [1 ]
Sudarikov, A. B. [1 ]
Obukhova, T. N. [1 ]
Kuzmina, L. A. [1 ]
Zvonkov, E. E. [1 ]
Parovichnikova, E. N. [1 ]
Savchenko, V. G. [1 ]
机构
[1] Natl Res Ctr Hematol, Moscow 125167, Russia
[2] Natl Res Ctr, Kurchatov Inst, Moscow 123182, Russia
来源
GEMATOLOGIYA I TRANSFUZIOLOGIYA | 2020年 / 65卷 / 04期
关键词
mantle cell lymphoma; mutation of TP53 gene; allo-HCT; GVHD; next generation sequencing;
D O I
10.35754/0234-5730-2020-65-4-483-500
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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-versus host 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.
引用
收藏
页码:483 / 500
页数:18
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