Comparison of amphotericin B lipid complex (ABLC) vs. AmBisome in the treatment of suspected or documented fungal infections in patients with leukemia

被引:99
作者
Fleming, RV [1 ]
Kantarjian, HM [1 ]
Husni, R [1 ]
Rolston, K [1 ]
Lim, J [1 ]
Raad, I [1 ]
Pierce, S [1 ]
Cortes, J [1 ]
Estey, E [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
关键词
fungal infections; leukemia; ABLC; Abelcet; AmBisome; amphotericin B;
D O I
10.3109/10428190109097650
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fungal infections remain a major cause of treatment failure and death in acute leukemia. New liposomal preparations of amphotericin B are now available. While less tonic, their comparative efficacy and toxicity profiles are unknown. In this study the comparative efficacy and safety of ABLC vs. AmBisome was evaluated in seventy-five patients with leukemia who developed 82 episodes of suspected or documented mycosis, and were treated (1:1) with either ABLC (n=43) or AmBisome (n=39). Both drugs were dosed accordingly from 3 to 5mg/kg/day. Using an intent-to-treat analysis, the overall response to therapy was 27/43 (63%) for ABLC and 15/39 (39%) for AmBisome (p=0.03). Median doss and duration of treatment was 10 days at 3mg/kg for ABLC and 15 days at 4 mg/kg for AmBisome. Acute, not dose-limiting infusion side effects were seen in 70% vs. 36% (p=0.002). ABLC vs. AmBisome. Increase of bilirubin > 1.5 times from baseline was 38% vs. 59%. ABLC vs. AmBisome (p=0.05). ABLC and AmBisome were squally effective for the treatment of suspected or documented fungal infections. While, acute infusion-toxicity was greater with ABLC, infusion tonicity requiring discontinuation was similar for both drugs. AmBisome was better tolerated than ABLC but was associated with mild abnormalities in liver function tests at the end of therapy.
引用
收藏
页码:511 / 520
页数:10
相关论文
共 26 条
[1]   TREATMENT OF INVASIVE ASPERGILLOSIS - RELATION OF EARLY DIAGNOSIS AND TREATMENT TO RESPONSE [J].
AISNER, J ;
SCHIMPFF, SC ;
WIERNIK, PH .
ANNALS OF INTERNAL MEDICINE, 1977, 86 (05) :539-543
[2]   Safety and efficacy of liposomal amphotericin B in allogeneic bone marrow transplant recipients [J].
Andstrom, EE ;
Ringden, O ;
Remberger, M ;
Svahn, BM ;
Tollemar, J .
MYCOSES, 1996, 39 (5-6) :185-193
[3]  
Bohme A, 1996, MYCOSES, V39, P419, DOI 10.1111/j.1439-0507.1996.tb00090.x
[4]   FAVORABLE OUTCOME OF INVASIVE ASPERGILLOSIS IN PATIENTS WITH ACUTE-LEUKEMIA [J].
BURCH, PA ;
KARP, JE ;
MERZ, WG ;
KUHLMAN, JE ;
FISHMAN, EK .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (12) :1985-1993
[5]  
Fleming R, 1996, BLOOD, V88, P319
[6]  
GILBERT D, 1999, SANFORD GUIDE ANTIMI, P78
[7]  
GOLDSTONE AH, 1994, BONE MARROW TRANSPL, V14, pS15
[8]  
Hiemenz JW, 1995, BLOOD, V86, P3383
[9]  
HIEMENZ JW, 1996, CLIN INFECT DIS S2, V22, P133
[10]   Lipid formulations of amphotericin B [J].
Janknegt, R ;
vanEtten, EWM ;
deMarie, S .
CURRENT OPINION IN INFECTIOUS DISEASES, 1996, 9 (06) :403-406