Literature DB >> 25188673

Amphotericin B lipid soluble formulations versus amphotericin B in cancer patients with neutropenia.

Helle Krogh Johansen1, Peter C Gøtzsche.   

Abstract

BACKGROUND: Patients with cancer who are treated with chemotherapy or receive a bone marrow transplant have an increased risk of acquiring fungal infections. Such infections can be life-threatening. Antifungal drugs are therefore often given prophylactically to such patients, or when they have a fever.
OBJECTIVES: To compare the benefits and harms of lipid soluble formulations of amphotericin B with conventional amphotericin B in cancer patients with neutropenia. SEARCH
METHODS: We searched PubMed from 1966 to 7 July 2014 and the reference lists of identified articles. SELECTION CRITERIA: Randomised clinical trials comparing lipid soluble formulations of amphotericin B with conventional amphotericin B. DATA COLLECTION AND ANALYSIS: The two review authors independently assessed trial eligibility and risk of bias and abstracted data. MAIN
RESULTS: We found 13 trials (1960 patients). Lipid-based amphotericin B was not more effective than conventional amphotericin B on mortality (relative risk (RR) 0.5; 95% confidence interval (CI) 0.64 to 1.14) but decreased invasive fungal infection (RR 0.65; 95% CI 0.44 to 0.97), nephrotoxicity defined as a 100% increase in serum creatinine (RR 0.45; 95% CI 0.37 to 0.54), and number of dropouts (RR 0.78; 95% CI 0.62 to 0.97).For the drug used in most patients, AmBisome (4 trials, 1214 patients), there was no significant difference in mortality (RR 0.77; 95% CI 0.54 to 1.10) whereas it tended to be more effective than conventional amphotericin B on invasive fungal infection (RR 0.63; 95% CI 0.39 to 1.01, P value 0.053).AmBisome, amphotericin B in Intralipid (6 trials, 379 patients), amphotericin B colloidal dispersion (ABCD) (2 trials, 262 patients), and amphotericin B lipid complex (ABLC) (1 trial, 105 patients) all decreased the occurrence of nephrotoxicity, but conventional amphotericin B was rarely administered under optimal circumstances. AUTHORS'
CONCLUSIONS: It is not clear whether there are any advantages of lipid-based formulations if conventional amphotericin B is administered under optimal circumstances, and their high cost prohibits routine use in most settings. There is a need for large trials comparing lipid-based formulations of amphotericin B with conventional amphotericin B given in the same dose, with routine premedication for prevention of infusion-related toxicity, and with supplementation with fluid, potassium, and magnesium for prevention of nephrotoxicity.

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Year:  2014        PMID: 25188673      PMCID: PMC6457843          DOI: 10.1002/14651858.CD000969.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  36 in total

1.  Liposomal amphotericin B for fever and neutropenia.

Authors:  D J Winston; G J Schiller; M C Territo
Journal:  N Engl J Med       Date:  1999-10-07       Impact factor: 91.245

2.  Liposomal amphotericin B for fever and neutropenia.

Authors:  T Fischer; G Heussel; C Huber
Journal:  N Engl J Med       Date:  1999-10-07       Impact factor: 91.245

Review 3.  Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients.

Authors:  Pablo J Cagnoni
Journal:  J Antimicrob Chemother       Date:  2002-02       Impact factor: 5.790

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Authors:  U Eriksson; B Seifert; A Schaffner
Journal:  BMJ       Date:  2001-03-10

5.  Pharmacoeconomic analysis of liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients.

Authors:  P J Cagnoni; T J Walsh; M M Prendergast; D Bodensteiner; S Hiemenz; R N Greenberg; C A Arndt; M Schuster; N Seibel; V Yeldandi; K B Tong
Journal:  J Clin Oncol       Date:  2000-06       Impact factor: 44.544

Review 6.  Amphotericin B lipid soluble formulations vs amphotericin B in cancer patients with neutropenia.

Authors:  H K Johansen; P C Gotzsche
Journal:  Cochrane Database Syst Rev       Date:  2000

7.  Comparison of the toxicity of amphotericin B in 5% dextrose with that of amphotericin B in fat emulsion in a randomized trial with cancer patients.

Authors:  M Nucci; M Loureiro; F Silveira; A R Casali; L F Bouzas; E Velasco; N Spector; W Pulcheri
Journal:  Antimicrob Agents Chemother       Date:  1999-06       Impact factor: 5.191

8.  Amphotericin B in children with malignant disease: a comparison of the toxicities and pharmacokinetics of amphotericin B administered in dextrose versus lipid emulsion.

Authors:  C E Nath; P J Shaw; R Gunning; A J McLachlan; J W Earl
Journal:  Antimicrob Agents Chemother       Date:  1999-06       Impact factor: 5.191

9.  Liposomal amphotericin B for empirical therapy in patients with persistent fever and neutropenia. National Institute of Allergy and Infectious Diseases Mycoses Study Group.

Authors:  T J Walsh; R W Finberg; C Arndt; J Hiemenz; C Schwartz; D Bodensteiner; P Pappas; N Seibel; R N Greenberg; S Dummer; M Schuster; J S Holcenberg
Journal:  N Engl J Med       Date:  1999-03-11       Impact factor: 91.245

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Authors:  E S Sandler; M M Mustafa; I Tkaczewski; M L Graham; V A Morrison; M Green; M Trigg; M Abboud; V M Aquino; M Gurwith; L Pietrelli
Journal:  J Pediatr Hematol Oncol       Date:  2000 May-Jun       Impact factor: 1.289

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