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DOMINO, doxycycline 40 mg vs. minocycline 100 mg in the treatment of rosacea: a randomized, single-blinded, noninferiority trial, comparing efficacy and safety.
van der Linden, M M D; van Ratingen, A R; van Rappard, D C; Nieuwenburg, S A; Spuls, Ph I.
Afiliação
  • van der Linden MMD; Department of Dermatology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.
  • van Ratingen AR; Department of Dermatology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.
  • van Rappard DC; Department of Dermatology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.
  • Nieuwenburg SA; Department of Dermatology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.
  • Spuls PI; Department of Dermatology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.
Br J Dermatol ; 176(6): 1465-1474, 2017 Jun.
Article em En | MEDLINE | ID: mdl-27797396
ABSTRACT

BACKGROUND:

There is a lack of evidence for minocycline in the treatment of rosacea.

OBJECTIVES:

To compare the efficacy and safety of doxycycline 40 mg vs. minocycline 100 mg in papulopustular rosacea.

METHODS:

In this randomized, single-centre, 1  1 allocation, assessor-blinded, noninferiority trial, patients with mild-to-severe papulopustular rosacea were randomly allocated to either oral doxycycline 40 mg or minocycline 100 mg for a 16-week period with 12 weeks of follow-up. Our primary outcomes were the change in lesion count and change in patient's health-related quality of life (using RosaQoL). Intention-to-treat and per protocol analyses were performed.

RESULTS:

Of the 80 patients randomized (40 minocycline, 40 doxycycline), 71 were treated for 16 weeks. Sixty-eight patients completed the study. At week 16, the median change in lesion count was comparable in both groups doxycycline vs. minocycline, respectively 13 vs. 14 fewer lesions. The RosaQoL scores were decreased for both doxycycline and minocycline, respectively by 0·62 and 0·86. Secondary outcomes were comparable except for Investigator's Global Assessment success, which was seen significantly more often in the minocycline group than in the doxycycline group (60% vs. 18%, P < 0·001). At week 28, outcomes were comparable, except for RosaQoL scores and PaGA, which were significantly different in favour of minocycline (P = 0·005 and P = 0·043, respectively), and fewer relapses were recorded in the minocycline group than in the doxycycline group (7% and 48%, respectively; P < 0·001). No serious adverse reactions were reported.

CONCLUSIONS:

Minocycline 100 mg is noninferior to doxycycline 40 mg in efficacy over a 16- week treatment period. At follow-up, RosaQoL and PaGA were statistically significantly more improved in the minocycline group than in the doxycycline group, and minocycline 100 mg gives longer remission. In this study there was no significant difference in safety between these treatments; however, based on previous literature minocycline has a lower risk-to-benefit ratio than doxycycline. Minocycline 100 mg may be a good alternative treatment for those patients who, for any reason, are unable or unwilling to take doxycycline 40 mg.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doxiciclina / Rosácea / Fármacos Dermatológicos / Dermatoses Faciais / Minociclina / Antibacterianos Tipo de estudo: Clinical_trials / Guideline Limite: Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doxiciclina / Rosácea / Fármacos Dermatológicos / Dermatoses Faciais / Minociclina / Antibacterianos Tipo de estudo: Clinical_trials / Guideline Limite: Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article