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两性霉素B脂质复合物治疗548例儿童和青少年侵袭性真菌感染的疗效与安全性。

Efficacy and safety of amphotericin B lipid complex in 548 children and adolescents with invasive fungal infections.

作者信息

Wiley Joseph M, Seibel Nita L, Walsh Thomas J

机构信息

Department of Pediatrics, Division of Hematology/Oncology, Sinai Hospital of Baltimore, Baltimore, MD 21215, USA.

出版信息

Pediatr Infect Dis J. 2005 Feb;24(2):167-74. doi: 10.1097/01.inf.0000153183.51258.b8.

Abstract

BACKGROUND

The safety and efficacy of amphotericin B lipid complex injection (ABELCET; Enzon Pharmaceuticals, Piscataway, NJ) was assessed in 548 children and adolescents 0-20 years of age who were enrolled in the Collaborative Exchange of Antifungal Research (CLEAR) registry. To our knowledge, this is the largest series of pediatric patients treated for invasive mycoses with a single agent. All patients had cancer or had received a bone marrow, cord blood or solid organ transplant and were treated with amphotericin B lipid complex for documented or suspected fungal infection.

METHODS

The CLEAR database was queried for all patients 0-20 years of age from 1996 to 2000. Data gathered included demographic variables, underlying disease type, reasons for the use of amphotericin B lipid complex injection, dosing information, clinical response and renal effects.

RESULTS

Most patients were either intolerant of or refractory to conventional antifungal therapy, and almost one-half were neutropenic at treatment onset. Of the 548 patients, 300 (54.7%) were transplant recipients and 393 (71.7%) had received one or more concomitant nephrotoxins. Candida and Aspergillus were the most commonly isolated species in patients with proven or probable infections. Response data were evaluable for 255 of the 285 patients with documented single or multiple pathogens. A complete (cured) or partial (improved) response was achieved in 54.9% of patients, with an additional 16.9% of patients having a stable outcome. Among patients with proven Aspergillus infection, the response rates (cured + improved) were 40.5 and 37.5% in transplant and nontransplant patients, respectively. When stable responses were added, the response rates were 48.6 and 71.9%, respectively. There were few clinically significant deleterious effects on renal function. There was no significant difference between the rates of new hemodialysis versus baseline hemodialysis. Elevations in serum creatinine of >1.5 x baseline and >2.5 x baseline values were seen in 24.8 and 8.8% of all patients, respectively.

CONCLUSIONS

The safety and efficacy data from this large pediatric population support the use of amphotericin B lipid complex injection for treatment of invasive fungal infections in immunocompromised children and adolescents, including the high risk subgroup of transplant recipients. The overall response rate and safety profile in pediatric patients who were largely intolerant of or refractory to conventional antifungal therapy were consistent with earlier reported findings of smaller trials.

摘要

背景

两性霉素B脂质体复合物注射液(ABELCET;Enzon制药公司,新泽西州皮斯卡塔韦)的安全性和有效性在548名0至20岁的儿童和青少年中进行了评估,这些患者被纳入抗真菌研究协作交流(CLEAR)登记处。据我们所知,这是使用单一药物治疗侵袭性真菌病的最大系列儿科患者。所有患者均患有癌症或接受了骨髓、脐血或实体器官移植,并接受两性霉素B脂质体复合物治疗已记录或疑似的真菌感染。

方法

查询CLEAR数据库中1996年至2000年所有0至20岁的患者。收集的数据包括人口统计学变量、基础疾病类型、使用两性霉素B脂质体复合物注射液的原因、给药信息、临床反应和肾脏影响。

结果

大多数患者对传统抗真菌治疗不耐受或难治,近一半患者在治疗开始时中性粒细胞减少。在548例患者中,300例(54.7%)是移植受者,393例(71.7%)接受了一种或多种伴随的肾毒素。念珠菌和曲霉菌是已证实或可能感染患者中最常见的分离菌种。在285例记录有单一或多种病原体的患者中,255例患者的反应数据可评估。54.9%的患者获得了完全(治愈)或部分(改善)反应,另有16.9%的患者病情稳定。在确诊为曲霉菌感染的患者中,移植患者和非移植患者的反应率(治愈+改善)分别为40.5%和37.5%。加上病情稳定的反应,反应率分别为48.6%和71.9%。对肾功能几乎没有临床上显著的有害影响。新的血液透析率与基线血液透析率之间没有显著差异。所有患者中,血清肌酐升高>1.5倍基线值和>2.5倍基线值的比例分别为24.8%和8.8%。

结论

来自这一大型儿科人群的安全性和有效性数据支持使用两性霉素B脂质体复合物注射液治疗免疫受损儿童和青少年的侵袭性真菌感染,包括移植受者这一高风险亚组。在对传统抗真菌治疗大多不耐受或难治的儿科患者中,总体反应率和安全性与早期较小规模试验报告的结果一致。

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