TY - JOUR
T1 - Omalizumab for the Treatment of Multiple Food Allergies
AU - Wood, Robert A.
AU - Togias, Alkis
AU - Sicherer, Scott H.
AU - Shreffler, Wayne G.
AU - Kim, Edwin H.
AU - Jones, Stacie M.
AU - Leung, Donald Y.M.
AU - Vickery, Brian P.
AU - Andrew Bird, J.
AU - Spergel, Jonathan M.
AU - Iqbal, Ahmar
AU - Olsson, Julie
AU - Ligueros-Saylan, Monica
AU - Uddin, Alkaz
AU - Calatroni, Agustin
AU - Huckabee, Charmaine Marquis
AU - Rogers, Nicole H.
AU - Yovetich, Nancy
AU - Dantzer, Jennifer
AU - Mudd, Kim
AU - Wang, Julie
AU - Groetch, Marion
AU - Pyle, David
AU - Keet, Corinne A.
AU - Kulis, Michael
AU - Sindher, Sayantani B.
AU - Long, Andrew
AU - Scurlock, Amy M.
AU - Lanser, Bruce J.
AU - Lee, Tricia
AU - Parrish, Christopher
AU - Brown-Whitehorn, Terri
AU - Rudman Spergel, Amanda K.
AU - Veri, Maria
AU - Hamrah, Sanaz Daneshfar
AU - Brittain, Erica
AU - Poyser, Julian
AU - Wheatley, Lisa M.
AU - Chinthrajah, R. Sharon
N1 - Publisher Copyright:
Copyright © 2024 Massachusetts Medical Society.
PY - 2024/3/7
Y1 - 2024/3/7
N2 - BACKGROUND Food allergies are common and are associated with substantial morbidity; the only approved treatment is oral immunotherapy for peanut allergy. METHODS In this trial, we assessed whether omalizumab, a monoclonal anti-IgE antibody, would be effective and safe as monotherapy in patients with multiple food allergies. Persons 1 to 55 years of age who were allergic to peanuts and at least two other trial-specified foods (cashew, milk, egg, walnut, wheat, and hazelnut) were screened. Inclusion required a reaction to a food challenge of 100 mg or less of peanut protein and 300 mg or less of the two other foods. Participants were randomly assigned, in a 2:1 ratio, to receive omalizumab or placebo administered subcutaneously (with the dose based on weight and IgE levels) every 2 to 4 weeks for 16 to 20 weeks, after which the challenges were repeated. The primary end point was ingestion of peanut protein in a single dose of 600 mg or more without dose-limiting symptoms. The three key secondary end points were the consumption of cashew, of milk, and of egg in single doses of at least 1000 mg each without dose-limiting symptoms. The first 60 participants (59 of whom were children or adolescents) who completed this first stage were enrolled in a 24-week open-label extension. RESULTS Of the 462 persons who were screened, 180 underwent randomization. The analysis population consisted of the 177 children and adolescents (1 to 17 years of age). A total of 79 of the 118 participants (67%) receiving omalizumab met the primary end-point criteria, as compared with 4 of the 59 participants (7%) receiving placebo (P<0.001). Results for the key secondary end points were consistent with those of the primary end point (cashew, 41% vs. 3%; milk, 66% vs. 10%; egg, 67% vs. 0%; P<0.001 for all comparisons). Safety end points did not differ between the groups, aside from more injection-site reactions in the omalizumab group. CONCLUSIONS In persons as young as 1 year of age with multiple food allergies, omalizumab treatment for 16 weeks was superior to placebo in increasing the reaction threshold for peanut and other common food allergens.
AB - BACKGROUND Food allergies are common and are associated with substantial morbidity; the only approved treatment is oral immunotherapy for peanut allergy. METHODS In this trial, we assessed whether omalizumab, a monoclonal anti-IgE antibody, would be effective and safe as monotherapy in patients with multiple food allergies. Persons 1 to 55 years of age who were allergic to peanuts and at least two other trial-specified foods (cashew, milk, egg, walnut, wheat, and hazelnut) were screened. Inclusion required a reaction to a food challenge of 100 mg or less of peanut protein and 300 mg or less of the two other foods. Participants were randomly assigned, in a 2:1 ratio, to receive omalizumab or placebo administered subcutaneously (with the dose based on weight and IgE levels) every 2 to 4 weeks for 16 to 20 weeks, after which the challenges were repeated. The primary end point was ingestion of peanut protein in a single dose of 600 mg or more without dose-limiting symptoms. The three key secondary end points were the consumption of cashew, of milk, and of egg in single doses of at least 1000 mg each without dose-limiting symptoms. The first 60 participants (59 of whom were children or adolescents) who completed this first stage were enrolled in a 24-week open-label extension. RESULTS Of the 462 persons who were screened, 180 underwent randomization. The analysis population consisted of the 177 children and adolescents (1 to 17 years of age). A total of 79 of the 118 participants (67%) receiving omalizumab met the primary end-point criteria, as compared with 4 of the 59 participants (7%) receiving placebo (P<0.001). Results for the key secondary end points were consistent with those of the primary end point (cashew, 41% vs. 3%; milk, 66% vs. 10%; egg, 67% vs. 0%; P<0.001 for all comparisons). Safety end points did not differ between the groups, aside from more injection-site reactions in the omalizumab group. CONCLUSIONS In persons as young as 1 year of age with multiple food allergies, omalizumab treatment for 16 weeks was superior to placebo in increasing the reaction threshold for peanut and other common food allergens.
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U2 - 10.1056/NEJMoa2312382
DO - 10.1056/NEJMoa2312382
M3 - Article
C2 - 38407394
AN - SCOPUS:85187197753
SN - 0028-4793
VL - 390
SP - 889
EP - 899
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 10
ER -