Betticher D C, Hsu Schmitz S F, Ratschiller D, von Rohr A, Egger T, Pugin P, Stalder M, Hess U, Fey M F, Cerny T
Institute of Medical Oncology, Inselspital, Berne, Switzerland.
Br J Haematol. 1997 Nov;99(2):358-63. doi: 10.1046/j.1365-2141.1997.3923206.x.
Clinical trials with intravenous cladribine infusions in pretreated patients with Waldenström's macroglobulinaemia have shown a response rate of 40%. Our pharmacokinetic studies revealed that the bioavailability of subcutaneous cladribine is complete but that the concentration-time profile is very different from intravenous administration. We designed this phase II multi-institutional trial to study the activity and toxicity of cladribine given as s.c. bolus injections in patients with symptomatic Waldenström's macroglobulinaemia. Between May 1993 and October 1995, 25 patients were accrued: male/female 18/7, median age 65 years (range 44-85). All except one patient had been pretreated with more than one regimen (median 2, range 0-10). 18 patients had progressed under previous therapy and six were in relapse. All patients received cladribine for a total dose of 0.5 mg/kg per cycle as s.c. bolus injections divided over 5 d at > or = 4 week intervals, for a maximum of six cycles. All 25 patients were evaluable for toxicity and response. A total of 67 cycles were administered (median 3 cycles, range 1-6). Overall response rate including disease stabilization which had been progressive under previous therapy was 68%. 10 patients (40%, 95% CI 21-61%) achieved a partial remission. Seven responders had been progressive under previous therapy. Maximum responses were reached no later than the third cycle. Median time to treatment failure and remission duration were 4.4 (range 0.5-33) and 8 months (5-29), respectively. Four patients (16%) suffered from infections W.H.O. grade > or = 2 (pneumonia grade 2, Staphylococcus septicaemia grade 3, viral encephalitis and pneumonia, both grade 4 with complete resolution). No other severe adverse events were observed. Cladribine given as s.c. 5 d bolus injections was found to be active in pretreated Waldenström's macroglobulinaemia and resulted in durable remissions.
对先前接受过治疗的华氏巨球蛋白血症患者进行静脉注射克拉屈滨的临床试验显示,缓解率为40%。我们的药代动力学研究表明,皮下注射克拉屈滨的生物利用度良好,但浓度-时间曲线与静脉给药有很大不同。我们设计了这项II期多机构试验,以研究皮下推注克拉屈滨对有症状的华氏巨球蛋白血症患者的活性和毒性。1993年5月至1995年10月,共纳入25例患者:男/女为18/7,中位年龄65岁(范围44 - 85岁)。除1例患者外,所有患者均接受过一种以上治疗方案(中位2种,范围0 - 10种)。18例患者在先前治疗中病情进展,6例复发。所有患者接受克拉屈滨治疗,每周期总剂量为0.5 mg/kg,皮下推注,分5天给药,间隔≥4周,最多6个周期。所有25例患者均可评估毒性和疗效。共给药67个周期(中位3个周期,范围1 - 6个周期)。包括在先前治疗中病情进展但病情稳定的患者在内,总体缓解率为68%。10例患者(40%,95%可信区间21 - 61%)获得部分缓解。7例缓解患者在先前治疗中病情进展。最大缓解在不晚于第3个周期时达到。治疗失败的中位时间和缓解持续时间分别为4.4个月(范围0.5 - 33个月)和8个月(5 - 29个月)。4例患者(16%)发生WHO≥2级感染(2级肺炎、3级金黄色葡萄球菌败血症、病毒性脑炎和肺炎,均为4级且完全缓解)。未观察到其他严重不良事件。皮下5天推注克拉屈滨在先前接受过治疗的华氏巨球蛋白血症患者中显示出活性,并导致持久缓解。