Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York.
The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer. 2018 Jan 15;124(2):325-334. doi: 10.1002/cncr.31138. Epub 2017 Dec 6.
Outcomes for patients with relapsed or refractory acute myeloid leukemia (AML) are poor. Guadecitabine, a next-generation hypomethylating agent, could be useful in treating such patients.
In this multicenter, open-label, phase 2 dose-expansion study, AML patients from 10 North American medical centers were first randomized (1:1) to receive subcutaneous guadecitabine at 60 or 90 mg/m on 5 consecutive days in each 28-day cycle (5-day regimen). Subsequently, another cohort was treated for 10 days with 60 mg/m (10-day regimen).
Between June 15, 2012, and August 19, 2013, 108 patients with previously treated AML consented to enroll in the study, and 103 of these patients were treated; 5 patients did not receive the study treatment. A total of 103 patients were included in the safety and efficacy analyses (24 and 26 patients who were randomly assigned to 60 and 90 mg/m /d, respectively [5-day regimen] and 53 patients who were assigned to 60 mg/m /d [10-day regimen]). The 90 mg/m dose showed no benefit in clinical outcomes in comparison with 60 mg/m in the randomized cohort. Composite complete response (CRc) and complete response (CR) rates were higher with the 10-day regimen versus the 5-day regimen (CRc, 30.2% vs 16.0%; P = .1061; CR, 18.9% vs 8%; P = .15). Adverse events (grade ≥ 3) were mainly hematologic, with a higher incidence on the 10-day regimen. Early all-cause mortality was low and similar between regimens. Twenty patients (8 on the 5-day regimen and 12 on the 10-day regimen) were bridged to hematopoietic cell transplantation.
Guadecitabine has promising clinical activity and an acceptable safety profile and thus warrants further development in this population. Cancer 2018;124:325-34. © 2017 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
复发或难治性急性髓系白血病(AML)患者的预后较差。作为一种新型低甲基化药物,地西他滨可能对治疗此类患者有效。
在这项多中心、开放性、2 期剂量扩展研究中,来自北美 10 个医疗中心的 AML 患者首先按照 1:1 的比例随机(1:1)接受皮下注射地西他滨,剂量分别为 60 或 90mg/m2,连续 5 天,每 28 天为一个周期(5 天疗程)。随后,另一队列接受 60mg/m2 的 10 天疗程(10 天疗程)。
2012 年 6 月 15 日至 2013 年 8 月 19 日,108 例先前治疗过的 AML 患者同意参加该研究,其中 103 例接受了治疗;5 例患者未接受研究治疗。共有 103 例患者纳入安全性和疗效分析(随机分配至 60 和 90mg/m2/d(5 天疗程)的患者各 24 例和 26 例,以及分配至 60mg/m2/d(10 天疗程)的患者 53 例)。与 60mg/m2 相比,90mg/m2 剂量并未显示出在临床结局方面的优势。与 5 天疗程相比,10 天疗程的复合完全缓解(CRc)和完全缓解(CR)率更高(CRc:30.2% vs 16.0%;P=0.1061;CR:18.9% vs 8%;P=0.15)。不良事件(≥3 级)主要为血液学毒性,10 天疗程的发生率更高。早期全因死亡率较低,且各治疗方案之间相似。20 例患者(5 天疗程 8 例,10 天疗程 12 例)桥接至造血细胞移植。
地西他滨具有良好的临床活性和可接受的安全性,因此值得在该人群中进一步研究。癌症 2018;124:325-34。© 2017 美国癌症协会。这是在知识共享署名非商业许可下的许可,允许在任何媒体中不受限制地使用、分发和复制,前提是原始作品正确引用,并不得用于商业目的。