Haploidentical stem cell transplantation after a reduced-intensity conditioning regimen for the treatment of advanced hematologic malignancies: posttransplantation CD8-depleted donor lymphocyte infusions contribute to improve T-cell recovery

被引:58
作者
Dodero, Anna
Carniti, Cristiana
Raganato, Anna
Vendramin, Antonio
Farina, Lucia
Spina, Francesco
Carlo-Stella, Carmelo [2 ,3 ]
Di Terlizzi, Simona
Milanesi, Marco [2 ]
Longoni, Paolo [2 ]
Gandola, Lorenza [4 ]
Lombardo, Claudia [5 ]
Corradini, Paolo [1 ,6 ]
机构
[1] Ist Nazl Tumori, Div Hematol & Bone Marrow Transplantat, Fdn Ist Ricovero & Cura Carattere Sci, I-20133 Milan, Italy
[2] Ist Nazl Tumori, Cristina Gandini Div Med Oncol, I-20133 Milan, Italy
[3] Univ Milan, Chair Oncol, Milan, Italy
[4] Ist Nazl Tumori, Dept Radiotherapy, Fdn Ist Ricovero & Cura Carattere Sci, I-20133 Milan, Italy
[5] Ist Nazl Tumori, HLA Typing Lab, Fdn Ist Ricovero & Cura Carattere Sci, I-20133 Milan, Italy
[6] Univ Milan, Chair Hematol, Milan, Italy
关键词
VERSUS-HOST-DISEASE; CD3/CD19; DEPLETION; ACUTE-LEUKEMIA; HIGH-RISK; MARROW; RECONSTITUTION; OUTCOMES; ADULTS;
D O I
10.1182/blood-2008-10-183723
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Haploidentical hematopoietic stem cell transplantation provides an option for patients with advanced hematologic malignancies lacking a compatible donor. In this prospective phase 1/2 trial, we evaluated the role of reduced-intensity conditioning (RIC) followed by early add-backs of CD8-depleted donor lymphocyte infusions (DLIs). The RIC regimen consisted of thiotepa, fludarabine, cyclophosphamide, and 2 Gy total body irradiation. Twenty-eight patients with advanced lym-phoproliferative diseases (n = 24) or acute myeloid leukemia ( n = 4) were enrolled. Ex vivo and in vivo T-cell depletion was carried out by CD34(+) cell selection and alemtuzumab treatment. The 2-year cumulative incidence of nonrelapse mortality was 26% and the 2-year overall survival (OS) was 44%, with a better outcome for patients with chemosensitive disease (OS, 75%). Overall, 54 CD8-depleted DLIs were administered to 23 patients (82%) at 3 different dose levels without loss of engraftment or acute toxicities. Overall, 6 of 23 patients ( 26%) developed grade II-IV graft-versus-host disease, mainly at dose level 2. In conclusion, our RIC regimen allowed a stable engraftment with a rather low nonrelapse mortality in poor-risk patients; OS is encouraging with some long-term remissions in lymphoid malignancies. CD8-depleted DLIs are feasible and promote the immune reconstitution. (Blood. 2009;113:4771-4779)
引用
收藏
页码:4771 / 4779
页数:9
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