High dose cytarabine, mitoxantrone, pegasapargase (HAM-pegA) in combination with dasatinib for the first-line treatment of Philadelphia chromosome positive mixed phenotype acute leukemia.

American journal of leukemia research Pub Date : 2020-01-01 Epub Date: 2020-10-15
Ciera L Patzke, Ashkan Emadi
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Abstract

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.

高剂量阿糖胞苷、米托蒽醌、pegasgasase (HAM-pegA)联合达沙替尼一线治疗费城染色体阳性混合表型急性白血病
由于骨髓性和淋巴性白血病的疾病特征,混合表型急性白血病(MPAL)的治疗具有挑战性。历史上用于治疗急性淋巴细胞白血病的方案经常用于治疗MPAL,特别是那些疾病也具有费城染色体(Ph+)的患者。在这里,我们提出了一种新的方案,HAM-pegA加达沙替尼,用于治疗两名新诊断的Ph+ MPAL患者。该方案是骨髓靶向和淋巴靶向化疗药物的混合,并作为一个单周期的强化化疗,随后口服达沙替尼维持治疗。在不进行同种异体移植的情况下,该方案产生了18个月甚至更长时间的持久缓解。这种新方案提供了一个令人兴奋的替代方案,其他强化方案需要多个周期的强化化疗和同种异体移植在首次缓解。
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