Leng Yun, Hou Jian, Jin Jie, Zhang Mei, Ke Xiaoyan, Jiang Bin, Pan Ling, Yang Linhua, Zhou Fang, Wang Jianmin, Wang Zhao, Liu Li, Li Wei, Shen Zhixiang, Qiu Lugui, Chang Naibai, Li Jianyong, Liu Jing, Pang Hongyan, Meng Haitao, Wei Peng, Jiang Hua, Liu Yan, Zheng Xiangjun, Yang Shifang, Chen Wenming
Department of Hematology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Department of Hematology, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China.
Cancer Chemother Pharmacol. 2017 Jun;79(6):1141-1149. doi: 10.1007/s00280-017-3310-0. Epub 2017 May 12.
Circularly permuted TRAIL (CPT) has exhibited promising efficacy as a mono-therapy or in combination with thalidomide for patients with multiple myeloma (MM). In this phase 2 study, the safety and efficacy of CPT in combination with thalidomide and dexamethasone (CPT + TD) was evaluated in patients with pretreated relapsed/refractory MM (RRMM).
Patients who received at least two previous therapies for MM were randomly assigned at a 2:1 ratio to receive treatment with CPT + TD or thalidomide and dexamethasone (TD). The primary endpoint was the overall response rate (ORR), and the secondary endpoints included progression-free survival (PFS), duration of response (DOR) and safety.
Overall, 47 patients were assigned to the CPT + TD group, and 24 patients were recruited to the TD group. The ORR in the CPT + TD group was 38.3 vs. 25.0% in the TD group. The median PFS time was 6.7 months for the CPT + TD group and 3.1 months for the TD group. The median DORs for the CPT + TD and TD groups were 7.1 and 3.2 months, respectively. Most of the adverse effects (AEs) were grade 1 or 2. Serious AEs were reported in 19.7% of the patients. No treatment-related deaths were reported.
CPT plus TD could serve as a new therapeutic strategy for patients with RRMM. A randomized, double-blind, placebo-controlled confirmatory study is currently under way.
环化排列的肿瘤坏死因子相关凋亡诱导配体(CPT)作为单一疗法或与沙利度胺联合用于多发性骨髓瘤(MM)患者已显示出有前景的疗效。在这项2期研究中,评估了CPT联合沙利度胺和地塞米松(CPT + TD)用于预处理的复发/难治性MM(RRMM)患者的安全性和疗效。
接受过至少两种先前MM治疗的患者按2:1的比例随机分配,接受CPT + TD或沙利度胺和地塞米松(TD)治疗。主要终点是总缓解率(ORR),次要终点包括无进展生存期(PFS)、缓解持续时间(DOR)和安全性。
总体而言,47例患者被分配到CPT + TD组,24例患者被招募到TD组。CPT + TD组的ORR为38.3%,而TD组为25.0%。CPT + TD组的中位PFS时间为6.7个月,TD组为3.1个月。CPT + TD组和TD组的中位DOR分别为7.1个月和3.2个月。大多数不良反应(AE)为1级或2级。19.7%的患者报告了严重AE。未报告与治疗相关的死亡。
CPT加TD可作为RRMM患者的一种新治疗策略。目前正在进行一项随机、双盲、安慰剂对照的验证性研究。