Liu Jia, Jiang Zhong-Xing, Xie Xin-Sheng, Wan Ding-Ming, Cao Wei-Jie, Wang Meng, Liu Zhen-Zhen, Dong Zhen-Kun, Wang Hai-Qiong, Lu Run-Qing, Zhang Yin-Yin, Cheng Qian-Qian, Fan Ji-Xin, Li Wei, He Fei, Guo Rong
Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Hematopoietic Stem Cell Transplantation Center, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Front Oncol. 2021 Aug 16;11:710545. doi: 10.3389/fonc.2021.710545. eCollection 2021.
Post-transplant relapse remains a principal leading cause of failure after allogeneic hematopoietic stem cell transplantation (allo-HSCT) in patients with adult acute lymphoblastic leukemia (ALL). The aim of this study was to investigate the efficacy and safety of low-dose decitabine on the prevention of adult ALL relapse after allo-HSCT.
In this prospective study, we enrolled 34 patients with ALL who underwent allo-HSCT from August 2016 to April 2020 and received low-dose decitabine maintenance treatment after transplantation. The primary objectives were cumulative incidence of relapse rate (CIR), overall survival (OS), and disease-free survival (DFS). The secondary objectives were graft--host disease (GVHD) and safety.
Among the enrolled 34 patients, 6 patients relapsed and 6 patients died. The 2-year CIR, OS, and DFS were 20.2, 77.5, and 73.6%, respectively. Subgroup analysis revealed the 2-year CIR, OS, and DFS rates of 12 patients with T-ALL/lymphoblastic lymphoma (LBL) were 8.3, 90, and 81.5%, respectively. None of the seven patients with T-ALL relapsed. During maintenance treatment, only one patient (2.9%) developed grade IV acute GVHD and four (11.8%) patients had severe chronic GVHD. Thirty-two patients (94.1%) developed only grade I to II myelosuppression, and two patients (5.8%) developed grade III to IV granulocytopenia.
Maintenance treatment with low-dose decitabine after allo-HSCT may be used as a therapeutic option to reduce relapse in patients with adult ALL, especially in patients with T-ALL. Our findings require confirmation in larger-scale controlled trials.
Chinese Clinical Trials Registry, identifier ChiCTR1800014888.
移植后复发仍然是成人急性淋巴细胞白血病(ALL)患者异基因造血干细胞移植(allo-HSCT)失败的主要原因。本研究旨在探讨低剂量地西他滨预防allo-HSCT后成人ALL复发的疗效和安全性。
在这项前瞻性研究中,我们纳入了2016年8月至2020年4月接受allo-HSCT并在移植后接受低剂量地西他滨维持治疗的34例ALL患者。主要目标是复发率的累积发生率(CIR)、总生存期(OS)和无病生存期(DFS)。次要目标是移植物抗宿主病(GVHD)和安全性。
在纳入的34例患者中,6例复发,6例死亡。2年的CIR、OS和DFS分别为20.2%、77.5%和73.6%。亚组分析显示,12例T-ALL/淋巴母细胞淋巴瘤(LBL)患者的2年CIR、OS和DFS率分别为8.3%、90%和81.5%。7例T-ALL患者均未复发。在维持治疗期间,仅1例患者(2.9%)发生IV级急性GVHD,4例患者(11.8%)发生严重慢性GVHD。32例患者(94.1%)仅发生I至II级骨髓抑制,2例患者(5.8%)发生III至IV级粒细胞减少。
allo-HSCT后低剂量地西他滨维持治疗可作为降低成人ALL患者复发的一种治疗选择,尤其是T-ALL患者。我们的研究结果需要在更大规模的对照试验中得到证实。
中国临床试验注册中心,标识符ChiCTR1800014888