TY - JOUR
T1 - A Phase 2 Randomized Controlled Multisite Study Using Omalizumab-facilitated Rapid Desensitization to Test Continued vs Discontinued Dosing in Multifood Allergic Individuals
AU - Andorf, Sandra
AU - Purington, Natasha
AU - Kumar, Divya
AU - Long, Andrew
AU - O'Laughlin, Katherine L.
AU - Sicherer, Scott
AU - Sampson, Hugh
AU - Cianferoni, Antonella
AU - Whitehorn, Terri Brown
AU - Petroni, Daniel
AU - Makhija, Melanie
AU - Robison, Rachel G.
AU - Lierl, Michelle
AU - Logsdon, Stephanie
AU - Desai, Manisha
AU - Galli, Stephen J.
AU - Rael, Efren
AU - Assa'ad, Amal
AU - Chinthrajah, Sharon
AU - Pongracic, Jacqueline
AU - Spergel, Jonathan M.
AU - Tam, Jonathan
AU - Tilles, Stephen
AU - Wang, Julie
AU - Nadeau, Kari
N1 - Funding Information:
Dr. Kari Nadeau: NIAID CoFAR, NIAID Immune Tolerance Network, NHLBI Data and Safety Monitoring Board, NIEHS grant awardee, EPA grant awardee, FARE Center of Excellence Director, WAO Center of Excellence Director, site principal investigator (Aimmune Phase 3, DBV phase 3, AnaptysBio Phase 1, Astellas Phase 1). Dr. Sharon Chinthrajah receives grant support from CoFAR NIAID, Aimmune, DBV Technologies, Astellas, AnaptysBio, and is on the Regional Advisory Board for Aimmune. Dr. Julie Wang: NIAID CoFAR, Aimmune, DBV Technologies, UpToDate. Dr. Scott Sicherer: NIAID CoFAR, HAL-Allergy, UpToDate, Johns Hopkins University Press, Board of Directors of the American Academy of Allergy, Asthma and Immunology, and is associate editor of J Allergy Clin Immunol Pract. Dr. Hugh Sampson: NIAID and is the Chief Scientific Officer at DBV Technologies (60%) and a consultant for Allertein Therapeutics, LLC. Dr. Jonathan Spergel receives grant support from DBV Technologies, Aimmune and NIH, is a consultant with Regeneron and Shire, and is on the Scientific Advisory Board at DBV Technologies. Dr. Whitehorn is a consultant and principal investigator for DBV Technologies. Dr. Cianferoni receives funding from DBV Technologies. Dr. Stephen J. Galli receives grant support from NIAID, NIAMS, and the Tobacco-Related Disease Research Program (U. California). Dr. Assa'ad is a principal investigator for DBV Technologies, Aimmune Pharmaceuticals, Astellas, and the National Institute of Health. All other authors declare no conflicts of interest.
Funding Information:
Sean N. Parker Center for Allergy and Asthma Research at Stanford University, Jeff and MacKenzie Bezos, NIAID AADCRC U19AI104209.Funding sources include Sean N. Parker Center for Allergy and Asthma Research at Stanford University, Jeff and MacKenzie Bezos, NIAID AADCRC U19AI104209 (Galli, Nadeau, and Chinthrajah), Myra Reinhard Foundation, FARE Center of Excellence, EAT (End Allergies Together), Trip Advisor Foundation, CHOP-FARE, Children's Hospital of Philadelphia's Food Allergy Fund, The Sunshine Foundation, the Crown Family Philanthropies, and NCATS (NIH) Grant# UL1TR001422 (Pongracic). All medications and study drug (omalizumab) were purchased as commercially available products. We thank the nurses, dieticians, study coordinators, and patients and their families who participated in the study. We also thank Jennifer Bosworth, RN, Jennifer Howard, RN, Melissa Jain, RN, Michelle Catalano, LPN, Nashmia Qamar, DO, Rajesh Kumar, MD, Amanda Johnson, RD, Stefanie McCormack, BS, Christine Szychlinski, APN, CPNP, Jennifer Fishman, Jennifer Heimall, Lisa Clark, Jennifer Jennings, RN, Christina McDougall, Jane Robertson, Megan Lewis, Rushani Saltzman, Vanitha Sampath, PhD, Wendy Davidson, PhD, Marshall Plaut, MD, and Lisa Wheatley, MD, for reading and editing the manuscript. The funders of the study had no role in study design, data collection, data analysis, data interpretation, writing of the report, or decision to submit the paper for publication. The funder did not fund any serological or cellular mechanistic studies. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication. All of the individual participant data collected during the trial (after de-identification), study protocol, statistical analysis plan, informed consent form, and clinical study report will be available immediately to anyone who wishes to access the data for any purpose. Data will be available indefinitely at Stanford University.
Funding Information:
Funding sources include Sean N. Parker Center for Allergy and Asthma Research at Stanford University , Jeff and MacKenzie Bezos , NIAID AADCRC U19AI104209 (Galli, Nadeau, and Chinthrajah), Myra Reinhard Foundation , FARE Center of Excellence, EAT (End Allergies Together), Trip Advisor Foundation , CHOP -FARE, Children's Hospital of Philadelphia 's Food Allergy Fund, The Sunshine Foundation , the Crown Family Philanthropies , and NCATS (NIH) Grant# UL1TR001422 (Pongracic). All medications and study drug (omalizumab) were purchased as commercially available products. We thank the nurses, dieticians, study coordinators, and patients and their families who participated in the study. We also thank Jennifer Bosworth, RN, Jennifer Howard, RN, Melissa Jain, RN, Michelle Catalano, LPN, Nashmia Qamar, DO, Rajesh Kumar, MD, Amanda Johnson, RD, Stefanie McCormack, BS, Christine Szychlinski, APN, CPNP, Jennifer Fishman, Jennifer Heimall, Lisa Clark, Jennifer Jennings, RN, Christina McDougall, Jane Robertson, Megan Lewis, Rushani Saltzman, Vanitha Sampath, PhD, Wendy Davidson, PhD, Marshall Plaut, MD, and Lisa Wheatley, MD, for reading and editing the manuscript.
Publisher Copyright:
© 2018
PY - 2019/1
Y1 - 2019/1
N2 - Background: As there is limited data on the sustainability of desensitization of multifood-oral immunotherapy (multifood-OIT), we conducted a multisite multifood-OIT study to compare the efficacy of successful desensitization with sustained dosing vs discontinued dosing after multifood-OIT. Methods: We enrolled 70 participants, aged 5–22 years with multiple food allergies confirmed by double-blind placebo-controlled food challenges (DBPCFCs). In the open-label phase of the study, all participants received omalizumab (weeks 1–16) and multi-OIT (2–5 allergens; weeks 8–30) and eligible participants (on maintenance dose of each allergen by weeks 28–29) were randomized 1:1:1 to 1 g, 300 mg, or 0 mg arms (blinded, weeks 30–36) and then tested by food challenge at week 36. Success was defined as passing 2 g food challenge to at least 2 foods in week 36. Findings: Most participants were able to reach a dose of 2 g or higher of each of 2, 3, 4, and 5 food allergens (as applicable to the participant's food allergens in OIT) in week 36 food challenges. Using an intent-to-treat analysis, we did not find evidence that a 300 mg dose was effectively different than a 1 g dose in maintaining desensitization, and both together were more effective than OIT discontinuation (0 mg dose) (85% vs 55%, P = 0.03). Fifty-five percent of the intent-to-treat participants and 69% of per protocol participants randomized to the 0 mg arm showed no objective reactivity after 6 weeks of discontinuation. Cross-desensitization was found between cashew/pistachio and walnut/pecan when only one of the foods was part of OIT. No statistically significant safety differences were found between the three arms. Interpretation: These results suggest that sustained desensitization after omalizumab-facilitated multi-OIT best occurs through continued maintenance OIT dosing of either 300 mg or 1 g of each food allergen as opposed to discontinuation of multi-OIT. Funding: Sean N. Parker Center for Allergy and Asthma Research at Stanford University, Jeff and MacKenzie Bezos, NIAID AADCRC U19AI104209. Trial Registration Number: ClinicalTrials.gov number, NCT02626611.
AB - Background: As there is limited data on the sustainability of desensitization of multifood-oral immunotherapy (multifood-OIT), we conducted a multisite multifood-OIT study to compare the efficacy of successful desensitization with sustained dosing vs discontinued dosing after multifood-OIT. Methods: We enrolled 70 participants, aged 5–22 years with multiple food allergies confirmed by double-blind placebo-controlled food challenges (DBPCFCs). In the open-label phase of the study, all participants received omalizumab (weeks 1–16) and multi-OIT (2–5 allergens; weeks 8–30) and eligible participants (on maintenance dose of each allergen by weeks 28–29) were randomized 1:1:1 to 1 g, 300 mg, or 0 mg arms (blinded, weeks 30–36) and then tested by food challenge at week 36. Success was defined as passing 2 g food challenge to at least 2 foods in week 36. Findings: Most participants were able to reach a dose of 2 g or higher of each of 2, 3, 4, and 5 food allergens (as applicable to the participant's food allergens in OIT) in week 36 food challenges. Using an intent-to-treat analysis, we did not find evidence that a 300 mg dose was effectively different than a 1 g dose in maintaining desensitization, and both together were more effective than OIT discontinuation (0 mg dose) (85% vs 55%, P = 0.03). Fifty-five percent of the intent-to-treat participants and 69% of per protocol participants randomized to the 0 mg arm showed no objective reactivity after 6 weeks of discontinuation. Cross-desensitization was found between cashew/pistachio and walnut/pecan when only one of the foods was part of OIT. No statistically significant safety differences were found between the three arms. Interpretation: These results suggest that sustained desensitization after omalizumab-facilitated multi-OIT best occurs through continued maintenance OIT dosing of either 300 mg or 1 g of each food allergen as opposed to discontinuation of multi-OIT. Funding: Sean N. Parker Center for Allergy and Asthma Research at Stanford University, Jeff and MacKenzie Bezos, NIAID AADCRC U19AI104209. Trial Registration Number: ClinicalTrials.gov number, NCT02626611.
KW - Food allergen
KW - Food allergy
KW - Omalizumab
KW - Oral immunotherapy
KW - Sustained unresponsiveness
UR - http://www.scopus.com/inward/record.url?scp=85064149807&partnerID=8YFLogxK
U2 - 10.1016/j.eclinm.2018.12.006
DO - 10.1016/j.eclinm.2018.12.006
M3 - Article
AN - SCOPUS:85064149807
SN - 2589-5370
VL - 7
SP - 27
EP - 38
JO - eClinicalMedicine
JF - eClinicalMedicine
ER -