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Topical tretinoin in chronic rhinosinusitis with nasal polyps: a randomized clinical trial.
Antonio, Marcelo Augusto; Marson, Fernando Augusto Lima; Toro, Mariana Dalbo Contrera; Sampaio, Marcelo Hamilton; Barreto, Icleia Siqueira; Dertkigil, Sérgio San Juan; Sakuma, Emerson Taro Inoue; Guadagnini, Dioze; Sakano, Eulalia.
  • Antonio MA; Department of Ophthalmology and Otorhinolaryngology, University of Campinas (Unicamp), Campinas, São Paulo, Brazil.
  • Marson FAL; Department of Medical Genetics and Genomic Medicine, Unicamp, Campinas, São Paulo, Brazil.
  • Toro MDC; Laboratory of Cell and Molecular Tumor Biology and Bioactive Compounds and Laboratory of Human and Medical Genetics, Postgraduate Program in Health Science, University of São Francisco, Bragança Paulista, São Paulo, Brazil.
  • Sampaio MH; Department of Ophthalmology and Otorhinolaryngology, University of Campinas (Unicamp), Campinas, São Paulo, Brazil.
  • Barreto IS; Department of Ophthalmology and Otorhinolaryngology, University of Campinas (Unicamp), Campinas, São Paulo, Brazil.
  • Dertkigil SSJ; Department of Pathological Anatomy, Unicamp, Campinas, São Paulo, Brazil.
  • Sakuma ETI; Department of Radiology, Unicamp, Campinas, São Paulo, Brazil.
  • Guadagnini D; Department of Radiology, Unicamp, Campinas, São Paulo, Brazil.
  • Sakano E; Department of Internal Medicine, Faculty of Medical Sciences, Unicamp, Campinas, São Paulo, Brazil.
Int Forum Allergy Rhinol ; 11(8): 1187-1196, 2021 08.
Article en En | MEDLINE | ID: mdl-33583149
ABSTRACT

BACKGROUND:

Chronic rhinosinusitis with nasal polyps (CRSwNP) is usually treated with corticosteroids, given their anti-inflammatory effects. Unlike the nasal administration, the oral and ocular use of tretinoin, an immunoregulatory drug, is well established. Therefore, tretinoin was thought to act on nasal polyps, and possible adverse and/or therapeutic effects were investigated.

METHODS:

A first-in-human open-label trial was conducted enrolling patients with CRSwNP randomized into a control group (CTR, n = 15), treated with budesonide for 24 weeks; and an intervention group (TRT, n = 15), who received budesonide and 0.1% tretinoin in the last 12 weeks. Primary endpoint included histopathological analysis and tissue immunoassay (Multiplex) for tumor necrosis factor α (TNF-α), interleukin (IL)-1ß, IL-4, IL-5, IL-13, and matrix metalloproteinase 9 (MMP-9) at 12 and 24 weeks. Secondary endpoints were adverse events report, endoscopy (modified Lund-Kennedy scoring system [LKS]), quality of life (22-item Sino-Nasal Outcome Test [SNOT-22]), and olfactory test (Connecticut Chemosensory Clinical Research Center) at baseline, at 12 weeks, and at 24 weeks, in addition to serum biochemistry and tomographic findings (Lund-Mackay computed tomography [CT] staging system [LMS]) at baseline and 24 weeks.

RESULTS:

TRT showed less microscopic edema (2/13 [15.4%] vs 8/13 [61.5%]; p = 0.044) as well as no increase in cytokines levels. All adverse events were categorized as "grade 1" (asymptomatic; mild). The most interesting part of this study was the improvement in smell between baseline (T0) and week 24 (T2) in TRT only (p = 0.041).

CONCLUSION:

Transnasal tretinoin associated with budesonide was safe and well tolerated, and it should be investigated as a treatment option for some CRSwNP endotypes. ©2021 ARSAAOA, LLC.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sinusitis / Rinitis / Pólipos Nasales Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sinusitis / Rinitis / Pólipos Nasales Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article