G-CSF-combined conditioning in allogeneic transplantation for non-remission acute myeloid leukemia with inv(3)(q21q26.2)/t(3;3)(q21;q26.2)

G-CSF联合预处理用于异基因移植治疗伴有inv(3)(q21q26.2)/t(3;3)(q21;q26.2)的非缓解性急性髓系白血病

阅读:1

Abstract

Acute myeloid leukemia (AML) with inv(3)(q21q26.2) or t(3;3)(q21;q26.2) has a dismal prognosis and poor response to conventional chemotherapy. Allogeneic hematopoietic cell transplantation (HCT) is a potentially curative treatment for adult AML with inv(3)/t(3;3) during complete remission (CR). Nevertheless, because fewer than half of patients achieve a CR with induction conventional chemotherapy, allogeneic HCT is frequently performed for AML with inv(3)/t(3;3) in non-remission. Here, we report six patients with adult AML with inv(3)/t(3;3) in non-remission who underwent allogeneic HCT at our institute between 2010 and 2024. The median age at the time of HCT was 43.5 years (range, 28-53 years). The median proportion of blasts in the bone marrow at HCT was 47.5% (range, 0.7-75.0%). The median duration from diagnosis to HCT was 65.5 days (range, 41-123 days). A total of five patients received single-unit cord blood transplantation, and one received bone marrow transplantation from an HLA-matched sibling donor. All patients received a myeloablative conditioning regimen, including 12 Gy total body irradiation and granulocyte colony-stimulating factor (G-CSF) combined with high-dose cytarabine, as well as standard cyclosporine and methotrexate for graft-versus-host disease prophylaxis. With a median follow-up of 41 months for survivors, three patients experienced relapse at 18, 5, and 2 months, whereas the remaining three patients were alive and disease-free at 173, 110, and 30 months after HCT. Our data demonstrate that G-CSF-combined myeloablative conditioning following allogeneic HCT could lead to favorable long-term remission for adult AML with inv(3)/t(3;3) in non-remission at HCT.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。