Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
German Cancer Research Center (DKFZ), Heidelberg, Germany.
Blood Adv. 2021 Jul 27;5(14):2901-2908. doi: 10.1182/bloodadvances.2020004144.
Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative therapy for most children with juvenile myelomonocytic leukemia (JMML). Novel therapies controlling the disorder prior to HSCT are needed. We conducted a phase 2, multicenter, open-label study to evaluate the safety and antileukemic activity of azacitidine monotherapy prior to HSCT in newly diagnosed JMML patients. Eighteen patients enrolled from September 2015 to November 2017 were treated with azacitidine (75 mg/m2) administered IV once daily on days 1 to 7 of a 28-day cycle. The primary end point was the number of patients with clinical complete remission (cCR) or clinical partial remission (cPR) after 3 cycles of therapy. Pharmacokinetics, genome-wide DNA-methylation levels, and variant allele frequencies of leukemia-specific index mutations were also analyzed. Sixteen patients completed 3 cycles and 5 patients completed 6 cycles. After 3 cycles, 11 patients (61%) were in cPR and 7 (39%) had progressive disease. Six of 16 patients (38%) who needed platelet transfusions were transfusion-free after 3 cycles. All 7 patients with intermediate- or low-methylation signatures in genome-wide DNA-methylation studies achieved cPR. Seventeen patients received HSCT; 14 (82%) were leukemia-free at a median follow-up of 23.8 months (range, 7.0-39.3 months) after HSCT. Azacitidine was well tolerated and plasma concentration--time profiles were similar to observed profiles in adults. In conclusion, azacitidine monotherapy is a suitable option for children with newly diagnosed JMML. Although long-term safety and efficacy remain to be fully elucidated in this population, these data demonstrate that azacitidine provides valuable clinical benefit to JMML patients prior to HSCT. This trial was registered at www.clinicaltrials.gov as #NCT02447666.
异基因造血干细胞移植(HSCT)是大多数儿童幼年型粒单核细胞白血病(JMML)的唯一治愈性治疗方法。在 HSCT 之前,需要有控制疾病的新型治疗方法。我们进行了一项 2 期、多中心、开放性标签研究,以评估新诊断的 JMML 患者在 HSCT 之前接受阿扎胞苷单药治疗的安全性和抗白血病活性。2015 年 9 月至 2017 年 11 月,共纳入 18 例患者,接受阿扎胞苷(75mg/m2)静脉输注,每天 1 次,28 天为 1 个周期,连用 7 天。主要终点是 3 个周期治疗后达到临床完全缓解(cCR)或临床部分缓解(cPR)的患者数量。还分析了药代动力学、全基因组 DNA 甲基化水平和白血病特异性指标突变的变异等位基因频率。16 例患者完成 3 个周期,5 例患者完成 6 个周期。3 个周期后,11 例(61%)患者为 cPR,7 例(39%)患者疾病进展。需要血小板输注的 6 例患者中有 3 例在 3 个周期后无需输注。全基因组 DNA 甲基化研究中具有中或低甲基化特征的 7 例患者均达到 cPR。17 例患者接受了 HSCT;在 HSCT 后中位随访 23.8 个月(7.0-39.3 个月)时,14 例(82%)患者无白血病。阿扎胞苷耐受性良好,药代动力学-时间曲线与成人观察到的曲线相似。总之,阿扎胞苷单药治疗是新诊断为 JMML 的儿童的一种合适选择。尽管在该人群中,长期安全性和疗效仍有待充分阐明,但这些数据表明,阿扎胞苷在 HSCT 之前为 JMML 患者提供了有价值的临床获益。该试验在 www.clinicaltrials.gov 上注册为 #NCT02447666。