Tolerance of high doses of amphotericin B by infusion of a liposomal formulation in children with cancer

Conventional amphotericin B (Amph-B) is the drug of choice for treating systemic fungal infections. Recently, a new formulation has become available, encapsulated in liposomes (Amph-lip). This new form of administration was developed in order to lower the acute side effects and to offer the possibil...

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Veröffentlicht in:Annals of hematology 1994, Vol.68 (1), p.27-31
Hauptverfasser: EMMINGER, W, GRANINGER, W, EMMINGER-SCHMIDMEIER, W, ZOUBEK, A, PILLWEIN, K, SUSANI, M, WASSERER, A, GADNER, H
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container_end_page 31
container_issue 1
container_start_page 27
container_title Annals of hematology
container_volume 68
creator EMMINGER, W
GRANINGER, W
EMMINGER-SCHMIDMEIER, W
ZOUBEK, A
PILLWEIN, K
SUSANI, M
WASSERER, A
GADNER, H
description Conventional amphotericin B (Amph-B) is the drug of choice for treating systemic fungal infections. Recently, a new formulation has become available, encapsulated in liposomes (Amph-lip). This new form of administration was developed in order to lower the acute side effects and to offer the possibility of administering high doses of amphotericin B. Experience with Amph-lip is limited, especially in children. We treated four children with documented systemic fungal infections with Amph-lip and administered it empirically to 12 children. Fifteen of these 16 children were severely granulocytopenic oncologic patients. One 3-month-old baby suffered from systemic candidiasis. Amph-lip was preferred to conventional Amph-B in children with organ dysfunction developing as a consequence of conventional chemotherapy or bone marrow transplantation, after failure of conventional Amph-B to improve a fungal infection, and after adverse drug reactions had occurred. The daily doses of Amph-lip ranged from 1 to 6 mg/kg (median 3 mg/kg), the cumulative doses from 13 to 311 mg/kg (median 75 mg/kg). Acute adverse reactions or organ function abnormalities attributable to Amph-lip did not occur in 402 administrations. Amph-lip has proven to be well tolerated by children in terms of acute toxicity and in the long term. Although large cumulative doses were given, organ function abnormalities attributable to Amph-lip doses were not detected in any of ten long-term survivors over a median observation time of 36 months (range 30-44 months). Amph-lip appears to be a promising alternative antifungal treatment, especially for patients with impaired organ function, when high doses of amphotericin B are necessary.
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Recently, a new formulation has become available, encapsulated in liposomes (Amph-lip). This new form of administration was developed in order to lower the acute side effects and to offer the possibility of administering high doses of amphotericin B. Experience with Amph-lip is limited, especially in children. We treated four children with documented systemic fungal infections with Amph-lip and administered it empirically to 12 children. Fifteen of these 16 children were severely granulocytopenic oncologic patients. One 3-month-old baby suffered from systemic candidiasis. Amph-lip was preferred to conventional Amph-B in children with organ dysfunction developing as a consequence of conventional chemotherapy or bone marrow transplantation, after failure of conventional Amph-B to improve a fungal infection, and after adverse drug reactions had occurred. The daily doses of Amph-lip ranged from 1 to 6 mg/kg (median 3 mg/kg), the cumulative doses from 13 to 311 mg/kg (median 75 mg/kg). Acute adverse reactions or organ function abnormalities attributable to Amph-lip did not occur in 402 administrations. Amph-lip has proven to be well tolerated by children in terms of acute toxicity and in the long term. Although large cumulative doses were given, organ function abnormalities attributable to Amph-lip doses were not detected in any of ten long-term survivors over a median observation time of 36 months (range 30-44 months). 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Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal agents</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Drug Carriers</topic><topic>Hematologic Diseases - therapy</topic><topic>Humans</topic><topic>Immunocompromised Host</topic><topic>Infant</topic><topic>Leukemia - therapy</topic><topic>Liposomes</topic><topic>Lymphoma - therapy</topic><topic>Medical sciences</topic><topic>Mycoses - drug therapy</topic><topic>Mycoses - prevention &amp; control</topic><topic>Pharmacology. 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Recently, a new formulation has become available, encapsulated in liposomes (Amph-lip). This new form of administration was developed in order to lower the acute side effects and to offer the possibility of administering high doses of amphotericin B. Experience with Amph-lip is limited, especially in children. We treated four children with documented systemic fungal infections with Amph-lip and administered it empirically to 12 children. Fifteen of these 16 children were severely granulocytopenic oncologic patients. One 3-month-old baby suffered from systemic candidiasis. Amph-lip was preferred to conventional Amph-B in children with organ dysfunction developing as a consequence of conventional chemotherapy or bone marrow transplantation, after failure of conventional Amph-B to improve a fungal infection, and after adverse drug reactions had occurred. The daily doses of Amph-lip ranged from 1 to 6 mg/kg (median 3 mg/kg), the cumulative doses from 13 to 311 mg/kg (median 75 mg/kg). 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source MEDLINE; SpringerNature Complete Journals
subjects Adolescent
Agranulocytosis - drug therapy
Amphotericin B - administration & dosage
Amphotericin B - adverse effects
Amphotericin B - therapeutic use
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antifungal agents
Biological and medical sciences
Bone Marrow Transplantation
Child
Child, Preschool
Drug Carriers
Hematologic Diseases - therapy
Humans
Immunocompromised Host
Infant
Leukemia - therapy
Liposomes
Lymphoma - therapy
Medical sciences
Mycoses - drug therapy
Mycoses - prevention & control
Pharmacology. Drug treatments
Time Factors
Treatment Outcome
title Tolerance of high doses of amphotericin B by infusion of a liposomal formulation in children with cancer
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