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地西他滨和维奈克拉作为挽救治疗及桥接治疗用于一名多药耐药急性髓系白血病患者单倍体相合造血干细胞移植的疗效

Efficacy of Decitabine and Venetoclax as Salvage and Bridge Therapy to Haploidentical Hematopoietic Stem Cell Transplantation in a Multiresistant Acute Myeloid Leukemia Patient.

作者信息

Serio Bianca, Giudice Valentina, Morini Denise, Guariglia Roberto, Vitolo Rosa, Manzo Paola, Langella Maddalena, Selleri Carmine

机构信息

Hematology and Transplant Center, University Hospital "San Giovanni di Dio e Ruggi d'Aragona,", Salerno, Italy.

Department of Medicine, Surgery, and Dentistry, University of Salerno, Baronissi, Italy.

出版信息

Case Rep Oncol. 2022 Jun 7;15(2):593-598. doi: 10.1159/000524952. eCollection 2022 May-Aug.

Abstract

Treatment of relapsed/refractory or elderly unfit acute myeloid leukemia (AML) is still challenging, and hypomethylating agents in combination with venetoclax, an oral selective BCL2 inhibitor, might be successfully used as salvage therapy. However, clinical trials evaluating the efficacy and safety of this combination in the setting of multiresistant AML treatment also as a bridge to transplant are still ongoing. Here, we reported a 50-year-old male diagnosed with AML with normal cytogenetics and wild type for fms-like tyrosine kinase 3, nucleophosmin 1, and KIT, and treated with decitabine and venetoclax as the fifth line of therapy and after a relapse post-allogeneic transplant. The patient achieved a complete remission and successfully underwent a haploidentical transplant with an overall survival of 48.6 months.

摘要

复发/难治性或老年体弱急性髓系白血病(AML)的治疗仍然具有挑战性,而低甲基化药物与口服选择性BCL2抑制剂维奈克拉联合使用,可能成功用作挽救治疗。然而,评估这种联合用药在多药耐药AML治疗中的疗效和安全性以及作为移植桥梁的临床试验仍在进行中。在此,我们报告了一名50岁男性,诊断为细胞遗传学正常且fms样酪氨酸激酶3、核磷蛋白1和KIT为野生型的AML患者,在异基因移植后复发,接受地西他滨和维奈克拉作为第五线治疗。该患者实现了完全缓解,并成功接受了单倍体移植,总生存期为48.6个月。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e4b/9247557/55dd559d534f/cro-0015-0593-g01.jpg

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