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Pilot study of the safety and efficacy of angiogenic therapy in diabetic foot syndrome

https://doi.org/10.14341/DM9644

Abstract

BACKGROUND: The syndrome of diabetic foot remains the main cause of non-traumatic amputation of the lower extremity in the world. Even with the provision of comprehensive medical care in the conditions of a specialized center, 10-15% of patients do not succeed in healing the ulcerative defect due to the ischemic component.


AIMS: The objective of this study is evaluation of safety and efficacy of pl-VEGF165 transfer in patients with neuroischemic type of diabetic foot syndrome.


METHODS: The pilot study included 35 diabetic patients with neuroischemic foot ulcers (Wagner stage 1-2) who were not candidates for revascularization procedures (NCT02538705). The patients were closely monitored after repeated pl-VEGF165 intramuscular gene transfer (2,4 mg) at 1, 3, and 6 months after treatment. The primary efficacy endpoint was the surface area of the ulcers (sq.cm), the secondary endpoints were transcutaneous oxygen tension (Tcp02), ankle-brachial index (ABI), neuropathy disability score (NDS), neuropathy symptoms score (NSS), and Michigan neuropathy screening instrument (MNSI). Adverse events were monitored throughout the study.


RESULTS: The use of pl-VEGF165 as part of complex treatment allowed to achieve wound healing in 65,7% of patients with chronic ulcerative defects, the safety of the target limb was 84%. Carrying out therapeutic angiogenesis as a part of the combined therapy ensured a reduction in the average area of the resistant to treatment defects from 3.6 [1.0; 7.05] cm2 to 0.0 [0.0;2.0] cm2 (p=0,001), which correlated with an increase in the TcPo2 index by 15% from 35 [29.5; 40.5] to 40.5 [36.0; 46.5] mm Hg (p= p=0,005) and in the ABI by 16% from 0.96 [0.82;1.08] to 1.11 [0.85; 1.24] (p=0,062). The decrease in the signs of diabetic neuropathy was determined - the scores of NSS scales and VAT decreased from 6,5 [5.75; 8.0) to 6.0 [5.25; 7.0] (p=0,004) and from 9.0 [8.0; 13.5] to 8.0 [7.0; 12.7] (p=0,001), respectively. No adverse effects associated with the use of pl-VEGF165 were recorded.


CONCLUSIONS: Thus, preliminary results of the pilot study show that the use of pl-VEGF165 gene transfer in combination therapy allows for complete healing of neuroischemic diabetic foot ulcers in the majority of patients.

About the Authors

Igor L. Plaksa
Human Stem Cells Institute; Moscow City Oncology Hospital No 62
Russian Federation


Nina D. Mzhavanadze
Ryazan State Medical University
Russian Federation

MD, PhD



Roman E. Kalinin
Ryazan State Medical University
Russian Federation

MD, PhD, Professor



Igor A. Suchkov
Ryazan State Medical University
Russian Federation

MD, PhD, Professor



Michail U. Bakunov
City Clinical Hospital No 4 of the Moscow Department of Health
Russian Federation


Vyacheslav T. Krivichin
M.F. Vladimirsky Moscow Regional Research and Clinical Institute
Russian Federation

MD, PhD, Professor



Sergey A. Matveev
National Medical and Surgical Center named after N.I. Pirogov
Russian Federation

MD, PhD, Professor



Artur A. Isaev
Human Stem Cells Institute
Russian Federation


Roman V. Deev
Human Stem Cells Institute; North-Western State Medical University named after I.I. Mechnikov
Russian Federation

MD, PhD, associate professor



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Supplementary files

1. Fig. 1. Design of a pilot clinical study (scheme): LPI - ankle-brachial index; TKNA - transcutaneous oxygen tension; VAT - neuropathic dysfunctional account; NSS - neuropathic symptomatic score; AE - adverse events; SNA - serious adverse events.
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2. Fig. 2. Dynamics of the area of the ulcerous defect (cm2): * - the difference between the indicator and the previous value is statistically significant (p <0.01).
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Review

For citations:


Plaksa I.L., Mzhavanadze N.D., Kalinin R.E., Suchkov I.A., Bakunov M.U., Krivichin V.T., Matveev S.A., Isaev A.A., Deev R.V. Pilot study of the safety and efficacy of angiogenic therapy in diabetic foot syndrome. Diabetes mellitus. 2019;22(6):559-567. (In Russ.) https://doi.org/10.14341/DM9644

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ISSN 2072-0351 (Print)
ISSN 2072-0378 (Online)