Ruxolitinib combined with prednisone, thalidomide and danazol in patients with myelofibrosis: Results of a pilot study

鲁索利替尼 医学 骨髓纤维化 达那唑 强的松 骨髓增生性肿瘤 内科学 贫血 不利影响 胃肠病学 沙利度胺 血红蛋白 血小板 外科 骨髓 多发性骨髓瘤 子宫内膜异位症
作者
Shiqiang Qu,Zefeng Xu,Tiejun Qin,Bing Li,Lijuan Pan,Jia Chen,Xin Yan,Junying Wu,Shouxin Zhang,Peihong Zhang,Robert Peter Gale,Zhijian Xiao
出处
期刊:Hematological Oncology [Wiley]
卷期号:40 (4): 787-795 被引量:6
标识
DOI:10.1002/hon.3026
摘要

Abstract Ruxolitinib is a safe and effective therapy of myeloproliferative neoplasm‐associated (MPN) myelofibrosis. However, often there are dose reductions and/or therapy interruptions because of therapy‐related adverse events (AEs), especially anemia and thrombocytopenia. We previously reported combined therapy with prednisone, thalidomide and danazol (PTD) reversed anemia and thrombocytopenia in people with MPN‐associated myelofibrosis. We wondered whether adding PTD to ruxolitinib might mitigate the hematologic AEs and thereby avoid the dose reduction of ruxolitinib and improve the efficacy. To test this hypothesis, we conducted a baseline hemoglobin and platelet concentration assignment prospective observational study in 72 patients comparing 3‐month dose adjustment and efficacy of ruxolitinib with ( N = 53, the study group) or without ( N = 19, the control group) PTD. According to the platelet counts, the median daily ruxolitinib doses in the study group increased from 30 to 40 mg by week 12, whereas in the control group it remained at 30 mg ( p = 0.019). In the study group 35 patients had a hemoglobin increase ≥10 g/L compared with no patient receiving ruxolitinib only ( p < 0.001). Platelet increases >100 × 10E+9/L were seen in 56.6% and 5.3% of patients in the two groups, respectively ( p < 0.001). In patients with anemia and thrombocytopenia, 18 patients in the study group had an anemia response at week 12 and 12 had a platelet increase of ≥50 × 10E+9/L. No patient in the control group achieved either response ( p < 0.001 and p = 0.078). The study group had a more spleen response than the control group ( p = 0.046). Peripheral edema and transaminase elevation were the main nonhematologic AEs of PTD. These AEs can be alleviated by adjusting the danazol dose. In conclusion, adding PTD to ruxolitinib improved ruxolitinib‐associated anemia and thrombocytopenia, and resulted in a higher ruxolitinib dose.
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