Olverembatinib treatment in adult patients with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia

IF 3 3区 医学 Q2 HEMATOLOGY Annals of Hematology Pub Date : 2024-10-14 DOI:10.1007/s00277-024-06027-w
Yiyan Zhu, Jiayi Huang, Ying Wang, Yue Han, Shengli Xue, Yonggong Yang, Yu Zhu, Wenzhi Cai, Suning Chen
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Abstract

Olverembatinib is a novel orally administered third-generation tyrosine kinase inhibitor (TKI) with definitive responses in T315I-mutant chronic myeloid leukemia (CML) patients. However, its value in newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) remained unclarified. In this multiple-center study, 20 patients with de novo Ph + ALL were treated with olverembatinib-based regimens as frontline therapy. All patients acquired complete remission (CR) after induction. 85% of patients achieved complete molecular response (CMR) within three months, contributed mainly by the addition of blinatumomab. A total of 45% of patients experienced mild hematological treatment-related adverse events (TRAEs). Olverembatinib-based treatment led to promising outcomes in de novo Ph + ALL patients but warranted further studies to investigate the best-combined strategy.

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新诊断的费城染色体阳性急性淋巴细胞白血病成人患者的奥韦拉替尼治疗。
奥罗巴替尼是一种新型口服第三代酪氨酸激酶抑制剂(TKI),对T315I突变型慢性髓性白血病(CML)患者有确切的疗效。然而,它在新诊断的费城染色体阳性急性淋巴细胞白血病(Ph + ALL)中的价值仍未得到明确。在这项多中心研究中,20名新发Ph + ALL患者接受了以奥罗瑞巴替尼为基础的方案作为一线疗法。所有患者在诱导治疗后都获得了完全缓解(CR)。85%的患者在三个月内获得了完全分子反应(CMR),这主要得益于加用了blinatumomab。共有45%的患者出现了轻微的血液治疗相关不良事件(TRAEs)。基于奥罗瑞巴替尼的治疗为新发Ph + ALL患者带来了可喜的结果,但仍需进一步研究最佳联合策略。
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来源期刊
Annals of Hematology
Annals of Hematology 医学-血液学
CiteScore
5.60
自引率
2.90%
发文量
304
审稿时长
2 months
期刊介绍: Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.
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