Department of Hematology.
Department of Oncology.
Blood Adv. 2022 Jan 25;6(2):521-527. doi: 10.1182/bloodadvances.2021006139.
Secondary myelodysplastic syndromes and acute myeloid leukemia (sMDS/AML) are rare in children and adolescents and have a dismal prognosis. The mainstay therapy is hematopoietic cell transplantation (HCT), but there has been no innovation in cytoreductive regimens. CP X-351, a fixed 5:1 molar ratio of liposomal cytarabine to daunorubicin, has shown favorable safety and efficacy in elderly individuals with secondary AML and children with relapsed de novo AML. We report the outcomes of 7 young patients (6 with newly diagnosed sMDS/AML and 1 with primary MDS/AML) uniformly treated with CP X-351. Five patients had previously received chemotherapy for osteosarcoma, Ewing sarcoma, neuroblastoma, or T-cell acute lymphoblastic leukemia; 1 had predisposing genomic instability disorder (Cornelia de Lange syndrome) and 1 had MDS-related AML and multiorgan failure. The median age at diagnosis of myeloid malignancy was 17 years (range, 13-23 years). Patients received 1 to 3 cycles of CP X-351 (cytarabine 100 mg/m2 plus daunorubicin 44 mg/m2) on days 1, 3, and 5, resulting in complete morphologic remission without overt toxicity or treatment-related mortality. This approach allowed for adding an FLT3 inhibitor as individualized therapy in 1 patient. Six patients were alive and leukemia-free at 0.5 to 3.3 years after HCT. One patient died as a result of disease progression before HCT. To summarize, CP X-351 is an effective and well-tolerated regimen for cytoreduction in pediatric sMDS/AML that warrants prospective studies.
继发性骨髓增生异常综合征和急性髓系白血病(sMDS/AML)在儿童和青少年中较为罕见,且预后较差。主要治疗方法是造血细胞移植(HCT),但细胞减灭方案没有创新。CP X-351 是一种脂质体阿糖胞苷与柔红霉素摩尔比为 5:1 的固定混合物,在老年继发性 AML 患者和复发的初发 AML 儿童中显示出良好的安全性和疗效。我们报告了 7 名年轻患者(6 名新诊断的 sMDS/AML 和 1 名原发性 MDS/AML)接受 CP X-351 治疗的结果。5 名患者之前曾接受过骨肉瘤、尤文肉瘤、神经母细胞瘤或 T 细胞急性淋巴细胞白血病的化疗;1 名患者有易患的基因组不稳定性疾病(Cornelia de Lange 综合征),1 名患者有 MDS 相关的 AML 和多器官衰竭。髓系恶性肿瘤的中位诊断年龄为 17 岁(范围,13-23 岁)。患者接受了 1-3 个周期的 CP X-351(阿糖胞苷 100 mg/m2 加柔红霉素 44 mg/m2),于第 1、3 和 5 天给药,导致完全形态缓解,无明显毒性或治疗相关死亡。这种方法允许在 1 名患者中添加 FLT3 抑制剂作为个体化治疗。6 名患者在 HCT 后 0.5-3.3 年内无白血病存活。1 名患者在 HCT 前因疾病进展而死亡。总之,CP X-351 是一种有效且耐受性良好的儿童 sMDS/AML 细胞减灭方案,值得进行前瞻性研究。