The Journal of Practical Medicine ›› 2024, Vol. 40 ›› Issue (12): 1719-1724.doi: 10.3969/j.issn.1006-5725.2024.12.018

• Drugs and Clinic Practice • Previous Articles     Next Articles

Efficacy and safety of Roxadustat in the treatment of refractory NSAA and low-risk MDS-related anemia

Qinglin HU,Ziqi WAN,Chen YANG,Miao CHEN,Bing HAN()   

  1. Department of Hematology,Peking Union Medical College Hospital,Chinese Academy of Medical Science and Peking Union Medical College,Beijing 100730,China
  • Received:2023-12-22 Online:2024-06-25 Published:2024-06-14
  • Contact: Bing HAN E-mail:hanbingtg123@163.com

Abstract:

Objective To investigate the overall and subgroup efficacy, subgroup differences, predictors of efficacy and safety of roxadustat in the treatment of refractory non-severe aplastic anemia (NSAA) and low-risk myelodysplastic syndromes (LR-MDS). Methods Patients with refractory NSAA and LR-MDS who were admitted to the Department of Hematology, Peking Union Medical College Hospital from August 2020 to December 2022 were enrolled. All patients received first-line standard treatment, including recombinant human erythropoietin (rhEPO) for at least 3 months before roxadustat treatment. All patients received roxadustat 2.5 mg/kg every other day for at least 3 months, and were followed up for at least 8 months. The clinical characteristics of patients, roxadustat efficacy, predictors of efficacy, adverse effects,relapse and disease clonal evolution were analyzed. Results A total of 40 patients including 24 refractory NSAA and 16 LR-MDS were included. median age was 56 (18 ~ 81) years and 40% were males. 65% of the patients were transfusion dependent. Median follow-up was 21 (9 ~ 34) months. 22.5%, 25.0%, 47.5% , 55.0%, 57.5%, 60.0% and 50.0% of the patients achieved haematological improvement-erythroid (HI-E) at months 1, 2, 3, 4, 5, 6, and end of the follow-up period, respectively, and no factors affecting HI-E were identified.The hemoglobin change from baseline was statistically different between the two groups at the end of the follow-up period. 50% of patients were relieved from transfusion dependence. Adverse reactions were reported in 22.5% of patients. 28.5% of patients relapsed after achieving HI-E, with a median time to relapse of 7(4 ~ 12) months. No clonal evolution was observed at the end of the follow-up period. Conclusions Our preliminary findings suggested that Roxadustat may be effective for patients with NSAA or LR-MDS refractory to conventional therapies and rhEPO, with mild adverse effects and low relapse rate.The degree of hemoglobin improvement may be better in the refractory NSAA patients.

Key words: Roxadustat, refractory, non-severe aplastic anemia, low risk myelodysplastic syndromes

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