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Biological treatments for paediatric psoriasis : a retrospective observational study on biological drug survival in daily practice in childhood psoriasis.
Phan, C; Beauchet, A; Burztejn, A-C; Severino-Freire, M; Barbarot, S; Girard, C; Lasek, A; Reguiai, Z; Hadj-Rabia, S; Abasq, C; Brenaut, E; Droitcourt, C; Perrussel, M; Mallet, S; Phan, A; Lacour, J-P; Khemis, A; Bourrat, E; Chaby, G; Deborde, R; Plantin, P; Maruani, A; Piram, M; Maccari, F; Fougerousse, A-C; Kupfer-Bessaguet, I; Balguérie, X; Barthelemy, H; Martin, L; Quiles-Tsimaratos, N; Mery-Brossard, L; Pallure, V; Lons-Danic, D; Bouilly-Auvray, D; Beylot-Barry, M; Puzenat, E; Aubin, F; Mahé, E.
Afiliación
  • Phan C; Service de Dermatologie, Hôpital Victor Dupouy, Argenteuil, France.
  • Beauchet A; Département de Santé Publique, Centre Hospitalier Universitaire Ambroise Paré, Assistance Publique-Hôpitaux de Paris, Boulogne-Billancourt, France.
  • Burztejn AC; Service de Dermatologie, Hôpital Brabois, Vandoeuvre Les Nancy, France.
  • Severino-Freire M; Service de Dermatologie, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
  • Barbarot S; Service de Dermatologie, Hôtel Dieu, Nantes, France.
  • Girard C; Service de Dermatologie, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
  • Lasek A; Service de Dermatologie, Hôpital Saint Vincent de Paul, Université Catholique de Lille, Lille, France.
  • Reguiai Z; Service de Dermatologie, Polyclinique Courlancy, Hôpital Robert Debré, Reims, France.
  • Hadj-Rabia S; Service de Dermatologie, INSERM U1163 & Institut Imagine, Centre Hospitalier Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Université Paris Descartes - Sorbonne, Paris Cité, Paris, France.
  • Abasq C; Service de Dermatologie, Centre Hospitalier Universitaire de Brest, Brest, France.
  • Brenaut E; Service de Dermatologie, Centre Hospitalier Universitaire de Brest, Brest, France.
  • Droitcourt C; Service de Dermatologie, Centre Hospitalier Universitaire Pontchaillou, Université de Rennes, Rennes, France.
  • Perrussel M; Service de Dermatologie, Centre Hospitalier Universitaire Pontchaillou, Université de Rennes, Rennes, France.
  • Mallet S; Service de Dermatologie, Vénéréologie et Cancérologie Cutanée, Hôpital de la Timone, Assistance-publique-Hôpitaux de Marseille, Marseille, France.
  • Phan A; Service de Pédiatrie, Hôpital Femme-Mère-Enfant, Hospices Civils de Lyon, Bron, France.
  • Lacour JP; Service de Dermatologie, Hôpital Archet 2, ESPIC CHU-Lenval, Nice, France.
  • Khemis A; Service de Dermatologie, Hôpital Archet 2, ESPIC CHU-Lenval, Nice, France.
  • Bourrat E; Service de Pédiatrie Générale, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Chaby G; Service de Dermatologie, Hôpital Sud, Amiens, France.
  • Deborde R; Service de Rhumatologie Pédiatrique, Hôpital Femme-Mère-Enfant, Hospices Civils de Lyon, Bron, France.
  • Plantin P; Service de Dermatologie, Centre Hospitalier de Cornuaille, Quimper, France.
  • Maruani A; Service de Dermatologie, Unité de Dermatologie Pédiatrique, Centre Hospitalier Universitaire de Tours, Université de Tours, Tours, France.
  • Piram M; Service de Rhumatologie Pédiatrique, Centre Hospitalier Universitaire Bicêtre, Université Paris Sud-Saclay, UVSQ, Assistance Publique-Hôpitaux de Paris HP, Le Kremlin Bicêtre, France.
  • Maccari F; Service de Dermatologie, Hôpital d'Instruction des Armées Bégin, Saint Mandé, France.
  • Fougerousse AC; Service de Dermatologie, Hôpital d'Instruction des Armées Bégin, Saint Mandé, France.
  • Kupfer-Bessaguet I; Service de Dermatologie, Hôpital de Niort, Niort, France.
  • Balguérie X; Service de Dermatologie, Centre Hospitalier Universitaire Charles-Nicolle, Rouen, France.
  • Barthelemy H; Service de Dermatologie, Hôpital d'Auxerre, Auxerre, France.
  • Martin L; Service de Dermatologie, Centre Hospitalier Universitaire d'Angers, Angers, France.
  • Quiles-Tsimaratos N; Service de Dermatologie, Hôpital Saint-Joseph, Marseille, France.
  • Mery-Brossard L; Service de Dermatologie, Hôpital François Quesnay, Mantes la Jolie, France.
  • Pallure V; Service de Dermatologie, Hôpital de Perpignan, Perpignan, France.
  • Lons-Danic D; Service de Dermatologie, Hôpital Saint-Joseph, Paris, France.
  • Bouilly-Auvray D; Service de Dermatologie, Hôpital du Bocage, Dijon, France.
  • Beylot-Barry M; Service de Dermatologie, Hôpital Saint-André, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
  • Puzenat E; Service de Dermatologie, Centre Hospitalier Régional Universitaire de Besançon Université de Franche Comté, Besançon, France.
  • Aubin F; Service de Dermatologie, Centre Hospitalier Régional Universitaire de Besançon Université de Franche Comté, Besançon, France.
  • Mahé E; Service de Dermatologie, Hôpital Victor Dupouy, Argenteuil, France.
J Eur Acad Dermatol Venereol ; 33(10): 1984-1992, 2019 Oct.
Article en En | MEDLINE | ID: mdl-30883928
ABSTRACT

BACKGROUND:

Three biotherapies - etanercept, adalimumab and ustekinumab - are licensed in childhood psoriasis. The few data available on their efficacy and tolerance are mainly derived from industry trials. However, biological drug survival impacts long-term performance in real-life settings.

OBJECTIVE:

The objective of this study was to evaluate the survival rates of biological therapies in children with psoriasis in real-life conditions. Secondary objectives were to evaluate the factors associated with the choice of the biological therapy and to report severe adverse events. MATERIALS AND

METHODS:

This study was an observational retrospective study. Data were extracted from the clinical records of 134 children. Kaplan-Meier estimates were used to analyse drug survival overall and in subgroups of plaque psoriasis, bio-naïve and non-naïve patients.

RESULTS:

We analysed 184 treatment courses 70 with etanercept, 68 with adalimumab and 46 with ustekinumab. Factors associated with the choice of first-line biological agent were age at initiation (younger for adalimumab, P < 0.0001), age at onset of psoriasis (younger for adalimumab and etanercept, P = 0.03) and baseline Psoriasis Assessment Severity Index and Physician global assessment (both higher for adalimumab, P < 0.001). Drug survival rates were higher for ustekinumab than for adalimumab and etanercept (P < 0.0001) for all treatment and all psoriasis types, plaque-type psoriasis (P = 0.0003), patients naïve for biological agents (P = 0.0007) and non-naïve patients (P = 0.007). We reported eight serious adverse events (SAEs) severe infections (n = 3), significant weight gain (n = 2), psoriasis flare (n = 1) and malaise (n = 1). Biological therapy was discontinued in three children (one with psoriasis flare and two with weight gain). Only the two cases of weight gain resulted in an unfavourable outcome.

CONCLUSIONS:

Our real-life comparative study found that ustekinumab had the best drug survival outcome. The profile of SAEs in children was comparable to that in adults. These results will assist dermatologists in the decision-making process when choosing treatment options for children with psoriasis in daily practice.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis / Fármacos Dermatológicos / Adalimumab / Ustekinumab / Etanercept Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2019 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis / Fármacos Dermatológicos / Adalimumab / Ustekinumab / Etanercept Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2019 Tipo del documento: Article País de afiliación: Francia