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维奈托克联合地西他滨用于异基因造血细胞移植后复发的T细胞急性淋巴细胞白血病

Venetoclax in Combination with Decitabine for Relapsed T-Cell Acute Lymphoblastic Leukemia after Allogeneic Hematopoietic Cell Transplant.

作者信息

Rahmat Leena T, Nguyen Anna, Abdulhaq Haifaa, Prakash Sonam, Logan Aaron C, Mannis Gabriel N

机构信息

Department of Hematologic Malignancies and Blood and Marrow Transplant, University of California, San Francisco, CA, USA.

Department of Pathology, University of California, San Francisco, CA, USA.

出版信息

Case Rep Hematol. 2018 Aug 26;2018:6092646. doi: 10.1155/2018/6092646. eCollection 2018.

Abstract

Long-term disease-free survival in adults with T-cell acute lymphoblastic leukemia (T-ALL) remains poor, particularly after relapse, with few available salvage options. Preclinical data suggest that inhibition of the antiapoptotic protein BCL-2 (B-cell lymphoma 2) either alone or in combination with other agents, may be a unique therapeutic approach for the treatment of T-ALL. We present a case of a young male with T-ALL, relapsed after allogeneic hematopoietic stem cell transplant, who achieved a second complete remission following salvage therapy with combined venetoclax and decitabine. Assessment of measurable residual disease by next generation sequencing showed no evidence of residual disease of a sensitivity of 1 × 10. While the combination of venetoclax and hypomethylating agents has shown promise in the treatment of relapsed/refractory AML, and to our knowledge, this is the first report of this combination demonstrating clinical activity in relapsed/refractory T-ALL.

摘要

成人T细胞急性淋巴细胞白血病(T-ALL)患者的长期无病生存率仍然很低,尤其是在复发后,可用的挽救治疗方案很少。临床前数据表明,单独或与其他药物联合抑制抗凋亡蛋白BCL-2(B细胞淋巴瘤2)可能是治疗T-ALL的一种独特治疗方法。我们报告了一例年轻男性T-ALL患者,在异基因造血干细胞移植后复发,在用维奈克拉和地西他滨联合进行挽救治疗后实现了第二次完全缓解。通过下一代测序评估可测量的残留疾病,结果显示没有灵敏度为1×10的残留疾病证据。虽然维奈克拉与低甲基化药物联合在复发/难治性急性髓系白血病(AML)的治疗中已显示出前景,但据我们所知,这是该联合用药在复发/难治性T-ALL中显示临床活性的首例报告。

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