Chen Shu, Qin Weiwei, Lu Xiaohong, Liu Li, Zheng Yinsuo, Lu Xinhua, Wang Xiaohui, Zhang Xiaojuan, Gong Sha, Wei Suhua, Zhang Huiyun, Ding Hanru, Seifollah Ranjbarha, Li Jing, Zhang Haitao, Wu Di, Abiona Olubukola, He Pengcheng, Zhang Rong, Wald David, Wang Huaiyu
Department of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi Province.
Department of Hematology, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi Province.
Haematologica. 2025 Mar 1;110(3):621-628. doi: 10.3324/haematol.2024.285905.
Realgar-Indigo naturalis formula (RIF) is an oral form of arsenic that is effective against acute promyelocytic leukemia (APL). This multicenter, randomized, controlled trial compared the efficacy of all-trans retinoic acid (ATRA) plus RIF with ATRA plus arsenic trioxide (ATO) in a simplified regimen for non-high-risk APL. Following induction therapy with ATRA and ATO, participants were randomly assigned to receive either ATRA plus ATO or ATRA plus RIF both in a 2-week on 2-week off schedule for consolidation therapy. Once achieving molecular complete remission, the regimen was administered for a total of six cycles. All of 108 eligible patients achieved hematological complete remission after induction therapy. The median follow-up time was 29 months. The primary endpoint of 2-year disease-free survival was 97% in the ATRA-RIF arm and 98% in the ATRA-ATO arm, respectively (the ATRA-RIF arm was found to be non-inferior to the ATRA-ATO arm, [P<0.01], with a percentage difference of -1% [95% confidence interval: -4.8 to 6.9]). No deaths have been observed. Most adverse events were moderate. This study confirms the non-inferiority of RIF to ATO for non-high-risk APL, while also offering a more favorable regimen schedule for post-remission therapy (clinicaltrials gov. identifier: NCT02899169).
雄黄-靛玉红天然配方(RIF)是一种口服砷剂,对急性早幼粒细胞白血病(APL)有效。这项多中心、随机、对照试验比较了全反式维甲酸(ATRA)联合RIF与ATRA联合三氧化二砷(ATO)在非高危APL简化方案中的疗效。在接受ATRA和ATO诱导治疗后,参与者被随机分配接受ATRA联合ATO或ATRA联合RIF,均采用2周治疗、2周休息的巩固治疗方案。一旦达到分子完全缓解,该方案共进行六个周期。108例符合条件的患者在诱导治疗后均达到血液学完全缓解。中位随访时间为29个月。ATRA-RIF组和ATRA-ATO组的2年无病生存率主要终点分别为97%和98%(发现ATRA-RIF组不劣于ATRA-ATO组,[P<0.01],百分比差异为-1%[95%置信区间:-4.8至6.9])。未观察到死亡病例。大多数不良事件为中度。本研究证实了RIF在非高危APL中不劣于ATO,同时也为缓解后治疗提供了更有利的方案安排(临床试验.gov标识符:NCT02899169)。