Patzke Ciera L, Emadi Ashkan
University of Maryland Greenebaum Comprehensive Cancer Center, 22 S Greene St Baltimore MD 21201, USA.
University of Maryland School of Medicine, 655 W Baltimore St Baltimore MD 21201, USA.
Am J Leuk Res. 2020;4(1). Epub 2020 Oct 15.
The treatment of mixed phenotype acute leukemia (MPAL) is challenging due to the presence of disease characteristics of both myeloid and lymphoid leukemia. Regimens historically used to treat acute lymphoblastic leukemia are often used to treat MPAL, particularly for patients whose diseases also possess the Philadelphia chromosome (Ph+). Here we present a novel regimen, HAM-pegA plus dasatinib, for the treatment of two patients with newly diagnosed Ph+ MPAL. This regimen is a blend of both myeloid-targeted and lymphoid-targeted chemotherapy agents, and is given as a single cycle of intensive chemotherapy followed by oral dasatinib maintenance therapy. Without proceeding to allogeneic transplant, this regimen produced durable remissions of 18 months and longer. This novel regimen offers an exciting alternative to other intensive regimens that require multiple cycles of intensive chemotherapy and allogeneic transplant in first remission.
混合表型急性白血病(MPAL)的治疗具有挑战性,因为它同时具有髓系和淋系白血病的疾病特征。历史上用于治疗急性淋巴细胞白血病的方案常被用于治疗MPAL,特别是对于那些疾病也携带费城染色体(Ph+)的患者。在此,我们介绍一种新型方案,即HAM-pegA加达沙替尼,用于治疗两名新诊断的Ph+ MPAL患者。该方案是一种髓系靶向和淋系靶向化疗药物的组合,作为一个强化化疗周期给药,随后进行口服达沙替尼维持治疗。在未进行异基因移植的情况下,该方案产生了18个月及更长时间的持久缓解。这种新型方案为其他需要在首次缓解期进行多个强化化疗周期和异基因移植的强化方案提供了令人兴奋的替代选择。