Füreder W, Weltermann A, Chott A, Gisslinger H, Valent P, Jäger U, Geissler K, Lechner K
Department of Internal Medicine I, University of Vienna, Austria.
Wien Klin Wochenschr. 1999 Dec 23;111(24):1027-30.
Hairy cell leukemia is a rare lymphoproliferative disorder resistant to conventional chemotherapeutic agents. Recently, the purine analogue cladribine (2-chlorodeoxyadenosine, 2-CdA) was introduced for the treatment of this disease. We report on 14 patients with hairy cell leukemia who were treated with 2-CdA at our department between 1993 and 1997. The patients received a single cycle of 2-CdA at a dose of 0.07 or 0.09 mg/kg/day by continuous infusion, over a seven-day period. Five patients were previously untreated, while the others had received prior treatment with interferon-alpha (seven patients), interferon-alpha and splenectomy (one patient) or interferon-alpha, splenectomy and pentostatin (one patient). Six patients achieved complete remission, three a good partial response and three partial remission. Two patients did not respond to treatment and one of them died from septicemia in aplasia. Relapse of the disease occurred in two patients. Side effects such as fever (WHO grade 2) and/or neutropenia (WHO grade 4) were noted in eight patients. Thus, 2-CdA is an effective treatment of hairy cell leukemia that can induce long lasting remissions in both, previously treated and untreated patients.
毛细胞白血病是一种罕见的淋巴细胞增殖性疾病,对传统化疗药物耐药。最近,嘌呤类似物克拉屈滨(2-氯脱氧腺苷,2-CdA)被用于治疗该疾病。我们报告了1993年至1997年间在我们科室接受2-CdA治疗的14例毛细胞白血病患者。患者接受单周期2-CdA治疗,剂量为0.07或0.09mg/kg/天,持续静脉输注7天。5例患者此前未接受过治疗,其余患者曾接受过α干扰素治疗(7例)、α干扰素联合脾切除术(1例)或α干扰素、脾切除术联合喷司他丁(1例)。6例患者达到完全缓解,3例为良好部分缓解,3例为部分缓解。2例患者对治疗无反应,其中1例死于再生障碍性贫血合并败血症。2例患者疾病复发。8例患者出现发热(世界卫生组织2级)和/或中性粒细胞减少(世界卫生组织4级)等副作用。因此,2-CdA是治疗毛细胞白血病的有效方法,可使既往治疗和未治疗的患者均获得持久缓解。