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Research Article
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Published Online: 15 June 2006

Treatment with Intramuscular Vascular Endothelial Growth Factor Gene Compared with Placebo for Patients with Diabetes Mellitus and Critical Limb Ischemia: A Double-Blind Randomized Trial

Publication: Human Gene Therapy
Volume 17, Issue Number 6

Abstract

Despite advances in revascularization techniques, limb salvage and relief of pain cannot be achieved in many diabetic patients with diffuse peripheral vascular disease. Our objective was to determine the effect of intramuscular administration of phVEGF165 (vascular endothelial growth factor gene-carrying plasmid) on critical limb ischemia (CLI) compared with placebo (0.9% NaCl). A double-blind, placebo-controlled study was performed in 54 adult diabetic patients with CLI. The primary end point was the amputation rate at 100 days. Secondary end points were a 15% increase in pressure indices (ankle-to-brachial index and toe-to-brachial index), clinical improvement (skin, pain, and Quality of Life score), and safety. In patients (n = 27) treated with placebo versus phVEGF165-treated patients (n = 27) the following results were found: 6 amputations versus 3 (p = not significant [NS]); hemodynamic improvement in 1 versus 7 (p = 0.05); improvement in skin ulcers, 0 versus 7 (p = 0.01); decrease in pain, 2 versus 5 (p = NS); and overall, 3 versus 14 responding patients (p = 0.003). No grade 3 or 4 adverse effects were seen in these patients. We conclude that this small, randomized gene therapy study failed to meet the primary objective of significant amputation reduction. However, significant and meaningful improvement was found in patients treated with a VEGF165-containing plasmid. There were no substantial adverse events.

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Published In

cover image Human Gene Therapy
Human Gene Therapy
Volume 17Issue Number 6June 2006
Pages: 683 - 691
PubMed: 16776576

History

Published online: 15 June 2006
Published in print: June 2006

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    Y.H. Kusumanto
    Department of Internal Medicine, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    V. van Weel
    Department of Vascular Surgery, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
    N.H. Mulder
    Department of Medical Oncology, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    A.J. Smit
    Department of Internal Medicine, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    J.J.A.M. van den Dungen
    Department of Vascular Surgery, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    J.M.M. Hooymans
    Department of Ophthalmology, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    W.J. Sluiter
    Department of Pathology and Laboratory Medicine, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    R.A. Tio
    Department of Cardiology, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    P.H.A. Quax
    Gaubius Laboratory TNO-PG, 2301 CE, Leiden, The Netherlands.
    R.O.B. Gans
    Department of Internal Medicine, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    R.P.F. Dullaart
    Department of Endocrinology, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
    Dr. G.A.P. Hospers
    Department of Medical Oncology, University of Groningen and University Medical Center Groningen, 9700 RB Groningen, The Netherlands.

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