Rieger C T, Dittmer M, Ostermann H
Medizinische Klinik und Poliklinik III, Abteilung für Hämatologie und Onkologie, Klinikum der Universität München - Campus Grosshadern, München, Deutschland.
Dtsch Med Wochenschr. 2007 Oct;132(40):2062-6. doi: 10.1055/s-2007-985641.
Activity and efficacy of liposomal amphotericin B have been established for the treatment of severe fungal infections. Nephrotoxic side effects, especially during prolonged administration, are regarded as a major disadvantage. In this study we examined the response rates and side effects, particularly nephrotoxicity, of treatment with liposomal amphotericin B in a large cohort of patients.
406 patients treated with liposomal amphotericin B between January 1999 and August 2003 in participating German hospitals were included. Documentation included demographic and clinical data, reason for the treatment with liposomal amphotericin B, length of treatment, response to antifungal treatment and side effects.
42.4% of the 406 patients were females. Their ages ranged from 1 day to 77 years. 83 % of the patients had malignancies and 65.5 % had fever of unknown origin (FUO). Mean duration of treatment with liposomal amphotericin B was 20 +/- 20 days, at an average dose of 2.3 mg/kg/d. 209 patients (51.5 %) showed complete response (CR),105 patients (25.9 %) partial response (PR) and 51 (12.6 %) patients died during the observation. 80.0 % of patients with FUO showed complete or partial response of symptoms. Mean serum creatinine increased from 0.9 mg/kg before start of therapy with liposomal amphotericin B to 1.1 mg/kg during treatment. Side effects (common toxicity criteria > grade 1) occurred in 94 patients (23/2 %). Among these hypokalemia (6.2 %) and liver damage (5,2 %) were the most common. Nephrotoxicity was documented in 17 patients (4.2 %).
Liposomal amphotericin B is a safe and efficacious antifungal drug in the treatment of severe invasive fungal infections and fever of unknown origin. Nephrotoxicity is usually not a limiting factor when using liposomal amphotericin B, if it is administered in approved dosage.
脂质体两性霉素B治疗严重真菌感染的活性和疗效已得到确立。肾毒性副作用,尤其是在长期给药期间,被视为一个主要缺点。在本研究中,我们在一大群患者中检查了脂质体两性霉素B治疗的缓解率和副作用,特别是肾毒性。
纳入了1999年1月至2003年8月期间在参与研究的德国医院接受脂质体两性霉素B治疗的406例患者。记录内容包括人口统计学和临床数据、使用脂质体两性霉素B治疗的原因、治疗时长、抗真菌治疗反应和副作用。
406例患者中42.4%为女性。年龄范围从1天至77岁。83%的患者患有恶性肿瘤,65.5%的患者有不明原因发热(FUO)。脂质体两性霉素B的平均治疗时长为20±20天,平均剂量为2.3mg/kg/天。209例患者(51.5%)显示完全缓解(CR),105例患者(25.9%)部分缓解(PR),51例(12.6%)患者在观察期间死亡。80.0%的不明原因发热患者症状显示完全或部分缓解。血清肌酐均值从脂质体两性霉素B治疗开始前的0.9mg/kg升至治疗期间的1.1mg/kg。94例患者(占23.2%)出现副作用(常见毒性标准>1级)。其中低钾血症(6.2%)和肝损伤(5.2%)最为常见。17例患者(4.2%)记录有肾毒性。
脂质体两性霉素B是治疗严重侵袭性真菌感染和不明原因发热的一种安全有效的抗真菌药物。如果按批准剂量给药,使用脂质体两性霉素B时肾毒性通常不是限制因素。