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Oral Immunotherapy for Peanut Allergy in Children 1 to Less Than 4 Years of Age.
Du Toit, George; Brown, Kari R; Vereda, Andrea; Irani, Anne-Marie; Tilles, Stephen; Ratnayake, Anoshie; Jones, Stacie M; Vickery, Brian P.
Afiliação
  • Du Toit G; Guy's and St. Thomas' National Health Service Foundation Trust and Kings College, London.
  • Brown KR; Aimmune Therapeutics, Nestlé Health Science, Brisbane, CA.
  • Vereda A; Aimmune Therapeutics, Nestlé Health Science, London.
  • Irani AM; Aimmune Therapeutics, Nestlé Health Science, Brisbane, CA.
  • Tilles S; Aimmune Therapeutics, Nestlé Health Science, Brisbane, CA.
  • Ratnayake A; Aimmune Therapeutics, Nestlé Health Science, Brisbane, CA.
  • Jones SM; University of Arkansas for Medical Sciences and Arkansas Children's Hospital, Little Rock.
  • Vickery BP; Emory University School of Medicine, Atlanta.
NEJM Evid ; 2(11): EVIDoa2300145, 2023 Nov.
Article em En | MEDLINE | ID: mdl-38320526
ABSTRACT

BACKGROUND:

Peanut allergy is a common childhood allergy, and the only approved treatment for children 4 to 17 years of age is peanut allergen powder-dnfp (PTAH) oral immunotherapy.

METHODS:

For this phase 3, randomized, double-blind, placebo-controlled trial, we enrolled peanut-allergic children 1 to <4 years of age who experienced dose-limiting symptoms from ≤300 mg peanut protein during a screening double-blind, placebo-controlled food challenge (DBPCFC). Participants received PTAH or placebo, randomized in a 21 ratio, for approximately 12 months. At the trial conclusion, all participants underwent an exit BDPCFC. The primary end point was desensitization (i.e., tolerating a ≥600-mg single dose of peanut protein with only mild allergy symptoms).

RESULTS:

In the PTAH-treated group (n=98), 73.5% of participants tolerated a single dose of ≥600 mg peanut protein at exit DBPCFC compared with 6.3% in the placebo group (n=48). Most participants experienced an adverse event (98.0% of PTAH-treated and 97.9% of placebo-treated participants), which was mild or moderate in grade for 93.2% of participants (92.9% in PTAH-treated and 93.8% in placebo-treated participants). Treatment-related adverse events, which were mild to moderate, were experienced by 75.5% of PTAH-treated and 58.3% of placebo-treated participants. Three treatment-related systemic allergic reactions, none of which were severe or serious in grade, were noted in two PTAH-treated participants (2%).

CONCLUSIONS:

In peanut-allergic children 1 to <4 years of age treated with PTAH for approximately 12 months, the majority tolerated all peanut protein dose levels assessed. PTAH-treated patients had more treatment-related adverse events, which were mild to moderate severity. (Funded by Aimmune Therapeutics; ClinicalTrials.gov number, NCT03736447.)
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipersensibilidade a Amendoim Tipo de estudo: Clinical_trials Limite: Child / Humans Idioma: En Revista: NEJM Evid Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipersensibilidade a Amendoim Tipo de estudo: Clinical_trials Limite: Child / Humans Idioma: En Revista: NEJM Evid Ano de publicação: 2023 Tipo de documento: Article