Can topical mitomycin prevent laryngotracheal stenosis?

Citation
R. Eliashar et al., Can topical mitomycin prevent laryngotracheal stenosis?, LARYNGOSCOP, 109(10), 1999, pp. 1594-1600
Citations number
35
Categorie Soggetti
Otolaryngology
Journal title
LARYNGOSCOPE
ISSN journal
0023852X → ACNP
Volume
109
Issue
10
Year of publication
1999
Pages
1594 - 1600
Database
ISI
SICI code
0023-852X(199910)109:10<1594:CTMPLS>2.0.ZU;2-B
Abstract
Objectives/Hypothesis: Early topical application of mitomycin to a laryngot racheal lesion may prevent or reduce laryngotracheal stenosis (LTS), Study Design: Prospective controlled animal study, Methods: LTS was induced in 60 dogs randomly assigned to four groups. Controls received an immediate topi cal application of normal saline. The suction-control group received an imm ediate application of normal saline followed by suction of secretions on da y 2, The mitomycin group received immediate application of 0.7 mt mitomycin (0.2 mg/mL), The repeat-mitomycin group received an immediate application of mitomycin and a second application on day 2, after secretions were sucti oned, The laryngeal lumens were measured endoscopically at baseline, day 12 , and day 21, Animals were euthanatized if stenosis approximated 95% or at day 21, Results: All dogs in the mitomycin groups survived to day 21, compa red with 12 in the suction group and only 2 controls. No side effects of mi tomycin were observed. At day 21, surviving controls had 85% and 95% stenos is, In the mitomycin group, median stenosis was 27% (interquartile range, 2 9% to 42%); in the repeat-mitomycin group, 30% (22% to 40%); and in the suc tion-control group, 84.5% (72.5% to 93.5%). The mitomycin group differed si gnificantly from controls on day 12 (median difference = 85%, 95% CI = 80%- 94%, P <.0001) and day 21 (difference 63.9%, 95% CI = 58%-85%, P =.031), Co nclusion: A single topical application of mitomycin significantly reduces t he severity of LTS in dogs. Reapplication after 2 days does not improve res ults. Prospective clinical studies are warranted to assess the efficacy in humans.