A phase II multicenter, double-blind, randomized, placebo-controlled study of three dosages of an immunomodulator (PGG-glucan) in high-risk surgical patients
T. J. Babineau, A. Hackford, A. Kenler, B. Bistrian, R. A. Forse, P. G. Fairchild, S. Heard, M. Keroack, P. Caushaj and P. Benotti
Department of Surgery, Deaconess Hospital, Harvard Medical School, Boston.
OBJECTIVE: To examine the safety and efficacy of multiple doses of
PGG-glucan (poly-[1-6]-B-D-glucopyranosyl-[1-3]-B-D-glucopyranose) in
high-risk patients undergoing major thoracic or abdominal surgery. DESIGN:
An interventional, multicenter, double-blind, randomized,
placebo-controlled study. SETTING: Four university-affiliated medical
centers. PATIENTS: Sixty-seven high-risk patients undergoing major thoracic
or abdominal surgery. INTERVENTION: Patients were randomized in a 1:1:1:1
ratio to receive saline placebo or PGG-glucan at a dose of 0.1 mg/kg, 0.5
mg/kg, and 1.0 mg/kg or 2.0 mg/kg. One dose was administered before surgery
and three doses were administered after surgery. MAIN OUTCOME MEASURES: To
examine the safety and efficacy of PGG-glucan infusion and to identify
potentially important factors for a planned phase III study. RESULTS: A
dose-response trend with regard to infection incidence among patients who
received PGG-glucan was observed. Serious infections occurred in four
patients who received placebo and in three patients who received PGG-glucan
at a dose of 0.1 mg/kg. However, only one patient who received PGG-glucan
at a high dose had a serious infection. The incidence and severity of
adverse events was comparable in all groups. CONCLUSIONS: PGG-glucan was
generally safe and well tolerated, may decrease postoperative infection
rates, and warrants further investigation in a planned phase III trial.
The effect of PGG-{beta}-glucan on neutrophil chemotaxis in vivo
LeBlanc et al.
J. Leukoc. Biol. 2006;79:667-675.
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The Lectin-Like Domain of Complement Receptor 3 Protects Endothelial Barrier Function from Activated Neutrophils
Tsikitis et al.
J. Immunol. 2004;173:1284-1291.
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Polysaccharide Immunomodulators as Therapeutic Agents: Structural Aspects and Biologic Function
Tzianabos
Clin. Microbiol. Rev. 2000;13:523-533.
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The influence of glucan polymer structure and solution conformation on binding to (1->3)-{beta}-D-glucan receptors in a human monocyte-like cell line
Mueller et al.
Glycobiology 2000;10:339-346.
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Effect of PGG-glucan on the Rate of Serious Postoperative Infection or Death Observed After High-Risk Gastrointestinal Operations
Dellinger et al.
Arch Surg 1999;134:977-983.
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Modulation of Endotoxin- and Enterotoxin-Induced Cytokine Release by In Vivo Treatment with beta -(1,6)-Branched beta -(1,3)-Glucan
Soltys and Quinn
Infect. Immun. 1999;67:244-252.
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A Novel Carbohydrate-Glycosphingolipid Interaction between a beta -(1-3)-Glucan Immunomodulator, PGG-glucan, and Lactosylceramide of Human Leukocytes
Zimmerman et al.
J. Biol. Chem. 1998;273:22014-22020.
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Prophylactic Anti-Infective Activity of Poly-[1-6]-beta -D-Glucopyranosyl-[1-3]-beta -D-Glucopyranose Glucan in a Guinea Pig Model of Staphylococcal Wound Infection
Kernodle et al.
Antimicrob. Agents Chemother. 1998;42:545-549.
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Utilization of a chromogenic Limulus amebocyte lysate blood assay in a multi-center study of sepsis
Ketchum et al.
Innate Immunity 1997;4:9-16.
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Preclinical and clinical evaluation of carbohydrate immunopharmaceuticals in the prevention of sepsis and septic sequelae
Williams et al.
Innate Immunity 1995;2:203-208.
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