Ault Patricia, Cortes Jorge, Koller Charles, Kaled Elizabeth S, Kantarjian Hagop
Department of Leukemia, M.D. Anderson Cancer Center, University of Texas, 1515 Holcombe Boulevard, Box 428, Houston, TX 77030, USA.
Leuk Res. 2002 Sep;26(9):881-4. doi: 10.1016/s0145-2126(02)00046-2.
Idiopathic hypereosinophilic syndrome (HES) is a rare hematologic disorder characterized by persistent eosinophilia with organ involvement. Patients with HES have a poor prognosis, but the disease course can be heterogeneous. Treatment of HES has included corticosteroids, chemotherapeutic agents such as cyclophosphamide, vincristine, hydroxyrea, and most recently interferon-alpha (IFN-alpha) which has shown long-term beneficial effects. We herein report on a patient with HES who had disease resistant to steroids, and chemotherapy with 2-chlorodeoxyadenosine and cytarabine, but who had a significant response after only 8 days of treatment with imatinib mesylate 100mg daily. The possible mechanism of response is discussed. This observation may lead to a better understanding of the pathophysiology of HES, and may provide a new form of effective therapy for the disease.
特发性嗜酸性粒细胞增多综合征(HES)是一种罕见的血液系统疾病,其特征为持续性嗜酸性粒细胞增多并伴有器官受累。HES患者预后较差,但病程可能具有异质性。HES的治疗方法包括使用皮质类固醇、化疗药物如环磷酰胺、长春新碱、羟基脲,以及最近显示出长期有益效果的α-干扰素(IFN-α)。我们在此报告一名HES患者,该患者对类固醇和使用2-氯脱氧腺苷及阿糖胞苷的化疗均耐药,但在每天服用100mg甲磺酸伊马替尼仅8天后就有显著反应。文中讨论了可能的反应机制。这一观察结果可能有助于更好地理解HES的病理生理学,并可能为该疾病提供一种新的有效治疗形式。