The University of Chicago Pritzker School of Medicine, Chicago, IL.
Section of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL.
Blood Adv. 2024 Nov 26;8(22):5735-5743. doi: 10.1182/bloodadvances.2024013215.
Myelofibrosis (MF) in the chronic phase is a challenging disease to treat, and conventional treatment options are geared toward symptom palliation. In this prospective, multicenter, phase 2 trial, 21 patients with MF (18 chronic phase, 2 accelerated phase, and 1 blast phase) were treated with a 10-day schedule of subcutaneous decitabine at 0.3 mg/kg per day. The overall response rate was 33% (95% confidence interval, 15-57), primarily manifested as an improvement in cytopenias. The median duration of response was 7 months (range, 3-44). A high International Prognostic Scoring System risk score, high baseline fetal hemoglobin level, and sustained decrease in circulating CD34+ cell counts were associated with response to decitabine. All patients experienced at least 1 grade 3/4 cytopenia. Nonhematologic toxicities were less frequent, with fatigue, anorexia, and hypocalcemia being the most common. Given the lack of effective therapies in MF with severe cytopenias, this study supports further investigation into the use of hypomethylating agents as single agents or in combination therapies. This trial was registered at www.ClinicalTrials.gov as #NCT00095784.
骨髓纤维化(MF)慢性期是一种具有挑战性的疾病,常规治疗方法侧重于缓解症状。在这项前瞻性、多中心、2 期临床试验中,21 例 MF 患者(18 例慢性期、2 例加速期和 1 例急变期)接受了每日皮下注射 0.3mg/kg 地西他滨的 10 天疗程。总缓解率为 33%(95%置信区间,15-57),主要表现为细胞减少症的改善。缓解的中位持续时间为 7 个月(范围为 3-44)。国际预后评分系统风险评分高、基线胎儿血红蛋白水平高和循环 CD34+细胞计数持续下降与对地西他滨的反应相关。所有患者均至少经历了 1 级 3/4 级血细胞减少症。非血液学毒性较少见,最常见的是疲劳、厌食和低钙血症。鉴于 MF 伴严重血细胞减少症缺乏有效治疗方法,本研究支持进一步研究低甲基化剂作为单一药物或联合治疗的应用。该试验在 www.ClinicalTrials.gov 上注册为 #NCT00095784。