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SQ house dust mite sublingual immunotherapy tablet subgroup efficacy and local application site reaction duration.
Bernstein, David I; Kleine-Tebbe, Joerg; Nelson, Harold S; Bardelas, Jose A; Sussman, Gordon L; Lu, Susan; Rehm, Dorte; Svanholm Fogh, Bodil; Nolte, Hendrik.
Afiliación
  • Bernstein DI; Bernstein Clinical Research Center and Department of Medicine and Environmental Health, University of Cincinnati, Cincinnati, Ohio.
  • Kleine-Tebbe J; Allergy & Asthma Center Westend, Berlin, Germany.
  • Nelson HS; Department of Medicine, National Jewish Health, Denver, Colorado.
  • Bardelas JA; Allergy and Asthma Center of North Carolina, High Point, North Carolina.
  • Sussman GL; Department of Medicine, University of Toronto, Toronto, Canada.
  • Lu S; Merck & Co., Inc., Kenilworth, New Jersey.
  • Rehm D; ALK-Abelló A/S, Hørsholm, Denmark.
  • Svanholm Fogh B; ALK-Abelló A/S, Hørsholm, Denmark.
  • Nolte H; ALK-Abelló A/S, Hørsholm, Denmark. Electronic address: Hendrik.nolte@alk.net.
Ann Allergy Asthma Immunol ; 121(1): 105-110, 2018 07.
Article en En | MEDLINE | ID: mdl-29656145
ABSTRACT

BACKGROUND:

Allergic rhinitis with or without conjunctivitis (AR/C) is common, necessitating evaluation of SQ house dust mite (HDM) sublingual immunotherapy (SLIT)-tablet efficacy in various subgroups.

OBJECTIVE:

To evaluate 12 SQ-HDM efficacy and safety across subgroups, and the onset, duration, and recurrence of local application site reactions.

METHODS:

Subgroup (age, sex, race, asthma status, and allergen sensitization) efficacy was assessed using pooled data from 2 previously described trials of daily 12 SQ-HDM vs placebo for AR/C (n = 2,138). Efficacy was measured by average total combined rhinitis score (TCRS; rhinitis daily symptom plus medication score) during the last 8 weeks of treatment. Safety in subgroups and local application site reaction onset, duration, and recurrence were evaluated using pooled data from 5 previously described trials of SQ HDM SLIT-tablet (n = 2,923).

RESULTS:

Significant (based on 95% confidence intervals [CIs]) reduction in TCRS was seen with 12 SQ-HDM relative to placebo across all subgroups, with TCRS improvements ranging from 15% to 25%. The AE profile was generally similar within subgroups. Approximately 95% of local application site reactions were mild to moderate in severity. Median duration on day 1 of treatment for the most common local application site reactions (throat irritation, oral pruritus, ear pruritus, and lip swelling) ranged from 30 to 60 minutes; median first day of onset ranged from days 1 to 4 of treatment; median days that reactions recurred ranged from 3 to 12 days.

CONCLUSION:

Treatment with 12 SQ-HDM consistently improved symptoms and was well tolerated in relevant subgroups of subjects with HDM AR/C. Local application site reactions to 12 SQ-HDM were typically mild to moderate and transient.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Alérgenos / Conjuntivitis / Antígenos Dermatofagoides / Inmunoterapia Sublingual / Rinitis Alérgica Tipo de estudio: Clinical_trials / Etiology_studies Límite: Adolescent / Adult / Aged / Aged80 / Animals / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Allergy Asthma Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Alérgenos / Conjuntivitis / Antígenos Dermatofagoides / Inmunoterapia Sublingual / Rinitis Alérgica Tipo de estudio: Clinical_trials / Etiology_studies Límite: Adolescent / Adult / Aged / Aged80 / Animals / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Allergy Asthma Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2018 Tipo del documento: Article