Comparison of the efficacy of IGIV-C, 10% (caprylate/chromatography) and IGIV-SD, 10% as replacement therapy in primary immune deficiency - A randomized double-blind trial

被引:104
作者
Roifman, CM
Schroeder, H
Berger, M
Sorensen, R
Ballow, M
Buckley, RH
Gewurz, A
Korenblat, P
Sussman, G
Lemm, G
机构
[1] Hosp Sick Children, Div Allergy Immunol, Toronto, ON M5G 1X8, Canada
[2] Univ Alabama, Birmingham, AL USA
[3] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[4] LSU, Hlth Sci Ctr, New Orleans, LA USA
[5] Childrens Hosp Buffalo, Buffalo, NY USA
[6] Duke Univ, Ctr Med, Durham, NC USA
[7] Rush Presbyterian St Lukes Med Ctr, Chicago, IL 60612 USA
[8] Clin Res Ctr, LLC, St Louis, MO USA
[9] Wellesley Cent Hosp, Toronto, ON, Canada
[10] Bayer Healthcare, Biol Prod Div, Res Triangle Pk, NC USA
关键词
D O I
10.1016/S1567-5769(03)00134-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A novel method of large-scale chromatography has been developed to improve recovery and purity of immunoglobulin G (IgG) from pooled plasma. The current study compares safety, toxicity and efficacy of two intravenous immunoglobulin products: a novel formulation, IGIV caprylate/chromatography (IGIV-C; Gamunex(TM), 10%) and a licensed solvent/detergent-treated product, Garmmune(R)N, 10% (IGIV-SD). The study, a randomized, double-blind, parallel group, therapeutic equivalence trial, was conducted at 25 treatment centers in Canada and the United States. Patients (n = 172) having confirmed chronic primary immunodeficiency (PID), aged 1-75 years, and receiving IGIV therapy were enrolled. For 9 months, patients were treated with IGIV-C or IGIV-SD in accordance with the patient's individualized treatment regimen utilized before study entry. The primary endpoint was the proportion of patients with greater than or equal to1 validated acute sinopulmonary infection during the treatment period. Secondary endpoints included the proportion of patients with all infections, time to first infection, annual infection rates, lung function parameters, infusion-related safety and viral safety. The annual validated infection rate in the IGIV-C group was 0.18 compared to 0.43 in the IGIV-SD group (p = 0.023). Nine patients receiving IGIV-C experienced validated infections, compared to 17 patients in IGIV-SD group (p = 0.06). Acute sinusitis (validated plus clinically defined) was less frequent in the IGIV-C group (p = 0.012). Presence of bronchiectasis did not affect efficacy. Adverse reactions were similar in frequency and severity in both groups. No evidence of viral transmission was. observed. IGIV-C appears to be superior to IGIV-SD in preventing validated sinopulmonary infections, especially acute sinusitis, in patients with PID. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1325 / 1333
页数:9
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