• Ming-Hua Yang, Wu-Qing Wan, Jie-Si Luo, Min-Cui Zheng, Ke Huang, Li-Hua Yang, Hui-Rong Mai, Jian Li, Hui-Qin Chen, Xiao-Fei Sun, Ri-Yang Liu, Guo-Hua Chen, Xiaoqin Feng, Zhi-Yong Ke, Bin Li, Yan-Lai Tang, Li-Bin Huang, and Xue-Qun Luo.
• Department of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.
• Am. J. Hematol. 2018 Dec 1; 93 (12): 1467-1473.

AbstractIntravenous arsenic trioxide (ATO) has been adopted as the first-line treatment for acute promyelocytic leukemia (APL). Another arsenic compound named the Realgar-Indigo naturalis formula (RIF), an oral traditional Chinese medicine containing As4 S4 , has been shown to be highly effective in treating adult APL. In the treatment of pediatric APL, the safety and efficacy of RIF remains to be confirmed. This randomized, multicenter, and noninferiority trial was conducted to determine whether intravenous ATO can be substituted by oral RIF in the treatment of pediatric APL. From September 2011 to January 2017, among 92 patients who were 16 years old or younger with newly diagnosed PML-RARa positive APL, 82 met eligible criteria and were randomly assigned to ATO (n = 42) or RIF (n = 40) group. The remaining 10 patients did not fulfilled eligible criteria because five did not accept randomization, four died and one had hemiplegia prior to arsenic randomization due to intracranial hemorrhage or cerebral thrombosis. Induction and consolidation treatment contained ATO or RIF, all-trans-retinoic acid and low intensity chemotherapy. End points included event-free survival (EFS), adverse events and hospital days. After a median 3-year follow-up, the estimated 5-year EFS was 100% in both groups, and adverse events were mild. However, patients in the RIF group had significantly less hospital stay than those in the ATO group. This interim analysis shows that oral RIF is as effective and safe as intravenous ATO for the treatment of pediatric APL, with the advantage of reducing hospital stay. Final trial analysis will reveal mature outcome data.© 2018 The Authors. American Journal of Hematology published by Wiley Periodicals, Inc.

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