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吉瑞替尼治疗FLT3/NPM1突变型急性髓系白血病异基因干细胞移植后早期复发的长期缓解情况。

Long-term remissions with Gilteritinib in early relapse after allogeneic stem cell transplantation of FLT3/NPM1 mutated acute myeloid leukemia.

作者信息

Tamellini E, Sorio M, Andreini A, Tecchio C, Nadali G, Bernardelli A, Ferrarini I, Crosera L, Vatteroni A, Simio C, Benedetti F, Krampera M, Tanasi I

机构信息

Department of Engineering for Innovation Medicine, Section of Hematology, University of Verona, Verona, Italy.

Hematology and Bone Marrow Transplant Unit, Azienda Ospedaliera Universitaria Integrata di Verona, Verona, Italy.

出版信息

Blood Cell Ther. 2024 Jun 14;7(3):75-78. doi: 10.31547/bct-2024-005. eCollection 2024 Aug 25.

Abstract

Early post-allogeneic hematopoietic stem cell transplantation (allo-HSCT) relapse in patients with acute myeloid leukemia (AML) has an almost invariably dismal prognosis. Recent studies have demonstrated that FLT3 inhibition enhances the graft-versus-leukemia effect in vitro and in vivo. Thus, FLT-3 inhibitors may be viable treatment options in this setting. Here, we report three patients with FLT3 and NPM1 mutated AML who relapsed early after allo-HSCT and were treated with gilteritinib (associated with donor lymphocyte Infusion in two patients) to achieve long-term remission without a second transplantation.

摘要

急性髓系白血病(AML)患者异基因造血干细胞移植(allo-HSCT)后早期复发,其预后几乎总是很差。最近的研究表明,FLT3抑制在体外和体内均可增强移植物抗白血病效应。因此,FLT-3抑制剂可能是这种情况下可行的治疗选择。在此,我们报告了3例FLT3和NPM1突变的AML患者,他们在allo-HSCT后早期复发,并接受了吉瑞替尼治疗(2例患者联合供体淋巴细胞输注),从而在未进行二次移植的情况下实现了长期缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6814/11384128/a64b4e0e51c8/2432-7026-7-3-0075-g001.jpg

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