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Sunitinib reduces recurrent pelvic adhesions in a rabbit model

Authors :
Mark Puder
Bo R. Rueda
Arthur Nedder
Sarah J. Carlson
Deepika Nehra
Alexis K. Potemkin
Erica M. Fallon
Paul Mitchell
Source :
Journal of Surgical Research. 178:860-865
Publication Year :
2012
Publisher :
Elsevier BV, 2012.

Abstract

Background Adhesions represent a major problem after abdominal and pelvic procedures. The purpose of the present study was to determine the effect of sunitinib (Sutent, SU11248), a Food and Drug Administration-approved receptor tyrosine kinase inhibitor, on recurrent pelvic adhesion formation after pelvic adhesiolysis in a rabbit model. Materials and methods A total of 20 New Zealand white rabbits underwent a uterine abrasion procedure, followed by an adhesiolysis procedure 4 weeks later. Before adhesiolysis, the rabbits were randomized to sunitinib at 10 mg/kg/d or placebo. These were administered as 1 dose preoperatively followed by 10 doses postoperatively. The rabbits were killed 30 d after the adhesiolysis procedure. At death, the adhesions were scored, and a total adhesion score (presented as the median and interquartile range [IQR]) was calculated according to the percentage of uterine involvement and the tenacity of the adhesions. Results All the rabbits survived the operative procedures without complications. The sunitinib-treated rabbits (n = 10) had a significantly lower uterine involvement score (median 2.0, IQR 1.0–3.0) than the placebo-treated rabbits (median 4.0, IQR 3.0–4.0; P = 0.02). The sunitinib-treated rabbits also had median tenacity score of 3.0 (IQR 3.0–4.0) compared with a median of 4.0 (IQR 4.0–4.0; P = 0.04) in the placebo-treated rabbits (n = 10). The median total score in the sunitinib-treated rabbits was 5.0 (IQR 4.0–6.25) compared with 8.0 (IQR 6.75, 8.0) in the placebo-treated rabbits (P = 0.01). Conclusions Sunitinib treatment might be an efficacious strategy to reduce recurrent adhesion formation after pelvic procedures.

Details

ISSN :
00224804
Volume :
178
Database :
OpenAIRE
Journal :
Journal of Surgical Research
Accession number :
edsair.doi.dedup.....f4fe3ad175a431f34a28ac244c5545ca
Full Text :
https://doi.org/10.1016/j.jss.2012.07.038