摘要
目的:观察沙利度胺联合干扰素α-2b治疗原发性骨髓纤维化(IMF)的疗效。方法:IMF患者9例,口服沙利度胺100~250mg/d,分2~3次口服。干扰素α-2b300万U/次,皮下注射,3次/周,治疗3个月以上。根据治疗前后白细胞计数、血红蛋白测定、血小板计数、脾脏大小的变化、腹胀的改善及骨髓活检来评定疗效。结果:9例脾肿大患者均明显缩小,其中4例巨脾患者缩小更显著;5例白细胞升高患者,3例恢复正常,2例明显降低;4例轻中度贫血患者2例恢复正常,2例有所上升;3例血小板升高患者,均恢复正常;6例腹胀患者,4例消失,2例明显减轻;复查骨髓活检(髂后),9例IMF患者治疗前后骨髓纤维化无明显进展。结论:沙利度胺联合干扰素α-2b是治疗IMF的有效方法之一。
Objective: To observe the therapeutic effect of thalidomide combined with interfero-α-2b for treatment of idiopathic myelofibrosis (IMF). Methods: Nine patients with IMF were enrolled into the study. All the patients received thalidomide 100-250 mg/d orally and interferon-α-2b 3 million units hypodermicly 3 times a week for more than 3 months. Therapeutic effect was evaluated by leucocyte count, hemoglobin determination, blood platelet count, the size of spleen, the relief of abdominal distention and bone marrow biopsy before and after treatment. Results: The size of spleen was smaller obviously in 9 patients, and more prominent in 4 cases with huge spleen. Among 5 cases with high leucocytie count, 3 cases recovered, 2 cases decreased obviously. Among 4 cases with ane mia, 2 cases recovered, 2 cases improved. All 5 cases with high blood platelet count recovered. Among 6 cases of abdominal distention, 4 cases disappeared, 2 cases improved obviously. There was no obviously aggravation of myelofibrosis before and after treatment in 9 cases with IMF. Conclusions: Thalidomide combined with interferon-α-2b is one of the effective methods for treatment of idiopathic myelofibrosis.
出处
《内科急危重症杂志》
2009年第2期93-94,共2页
Journal of Critical Care In Internal Medicine