Savona Michael R, Odenike Olatoyosi, Roboz Gail J, Amin Harshad, DeZern Amy E, Griffiths Elizabeth A, Dao Kim-Hien, Zeidan Amer M, Bhatnagar Bhavana, Buckstein Rena, Leber Brian, Keating Mary-Margaret, Ball Somedeb, Oganesian Aram, Sano Yuri, Keer Harold N, Garcia-Manero Guillermo
Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
University of Chicago and the University of Chicago Comprehensive Cancer Center, Chicago, Illinois, USA.
Br J Haematol. 2025 Aug;207(2):432-444. doi: 10.1111/bjh.20203. Epub 2025 Jun 16.
DNA methyltransferase inhibitors (DNMTis) are commonly used in treating chronic myelomonocytic leukaemia (CMML); however, data from prospective studies of DNMTis in CMML are limited. The present analysis evaluated the efficacy, safety and pharmacodynamics of the oral DNMTi decitabine/cedazuridine in the subset of patients with CMML from the phase 2 and 3 trials, which led to the approval of this agent for myelodysplastic syndromes and CMML in the United States and Canada. Potential prognostic factors also were analysed. In all, 34 patients with CMML were screened and 33 were treated. Most patients (76% [n = 25]) had myelodysplastic type-CMML and 77% (n = 24/31 with DNA available for sequencing) had intermediate-2 or high-risk disease noted by CMML-specific prognostic scoring systems. The overall response rate was 76%, with 21% (n = 7) of patients achieving a complete response. Nearly half of the 11 patients who were red blood cell-transfusion dependent at baseline (46%) attained transfusion independence for ≥12 weeks, which was associated with survival. Median overall and transformation-free survival were 35.7 and 28.3 months, respectively, and the safety profile was similar to that previously reported for decitabine. This analysis described the use of decitabine/cedazuridine in CMML from consecutive, prospective, randomised trials and illustrated a median survival of nearly 3 years.
DNA甲基转移酶抑制剂(DNMTis)常用于治疗慢性粒单核细胞白血病(CMML);然而,关于DNMTis治疗CMML的前瞻性研究数据有限。本分析评估了口服DNMTi地西他滨/西扎珠苷在2期和3期试验中CMML患者亚组中的疗效、安全性和药效学,这两项试验促使该药物在美国和加拿大被批准用于治疗骨髓增生异常综合征和CMML。还分析了潜在的预后因素。总共筛选了34例CMML患者,33例接受了治疗。大多数患者(76%[n = 25])患有骨髓增生异常型CMML,77%(n = 24/31,可进行DNA测序)根据CMML特异性预后评分系统被判定为中危2或高危疾病。总缓解率为76%,21%(n = 7)的患者达到完全缓解。基线时依赖红细胞输血的11例患者中,近一半(46%)实现了≥12周的输血独立,这与生存相关。总生存期和无转化生存期的中位数分别为35.7个月和28.3个月,安全性与先前报道的地西他滨相似。本分析描述了地西他滨/西扎珠苷在连续、前瞻性、随机试验中的CMML患者中的应用,并显示中位生存期接近3年。