Two-year post-treatment outcomes following peanut oral immunotherapy in the Probiotic and Peanut Oral Immunotherapy-003 Long-Term (PPOIT-003LT) study

被引:4
作者
Loke, Paxton [1 ,2 ,3 ]
Wang, Xiaofang [1 ]
Lloyd, Melanie [1 ,4 ]
Ashley, Sarah E. [1 ,2 ,5 ]
Lozinsky, Adriana C. [1 ]
Gold, Michael [6 ,7 ]
O'Sullivan, Michael D. [8 ,9 ,10 ]
Quinn, Patrick [6 ,7 ]
Robinson, Marnie [1 ,5 ]
Galvin, Audrey Dunn [11 ,12 ]
Orsini, Francesca [1 ]
Tang, Mimi L. K. [1 ,2 ,5 ]
机构
[1] Murdoch Childrens Res Inst, 50 Flemington Rd, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Paediat, Parkville, Vic, Australia
[3] Monash Childrens Hosp, Monash Hlth, Clayton, Vic, Australia
[4] Monash Univ, Ctr Med Use & Safety, Parkville, Vic, Australia
[5] Royal Childrens Hosp, Dept Allergy & Immunol, Parkville, Vic, Australia
[6] Univ Adelaide, Adelaide Med Sch, Dept Paediat, Adelaide, SA, Australia
[7] Womens & Childrens Hosp Adelaide, North Adelaide, SA, Australia
[8] Perth Childrens Hosp, Immunol Dept, Child & Adolescent Hlth Serv, Nedlands, WA, Australia
[9] Univ Western Australia, Med Sch, Discipline Paediat, Perth, WA, Australia
[10] Telethon Kids Inst, Nedlands, WA, Australia
[11] Univ Coll Cork, Sch Appl Psychol, Cork Univ Hosp, Cork, Ireland
[12] Allergy Res Network, Cork, Ireland
关键词
desensitization; health-related quality of life; oral immunotherapy; peanut allergy; peanut oral immunotherapy; probiotic; remission; sustained unresponsiveness; ADVERSE FOOD REACTIONS; ALLERGY; CHILDREN; ANAPHYLAXIS; PREVALENCE; CHILDHOOD; QUESTIONNAIRE;
D O I
10.1111/all.16262
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Few studies have examined long-term outcomes following oral immunotherapy (OIT); none have examined long-term risks and benefits associated with distinct clinical outcomes (desensitization, remission). Methods: Participants completing the probiotic and peanut oral immunotherapy (PPOIT) -003 randomized trial were enrolled in a follow-on study, PPOIT-003LT. Peanut ingestion, reactions, and health-related quality of life (HRQOL) were monitored prospectively. Outcomes at 1-year and 2-years post-treatment were examined by treatment group and by post-OIT clinical outcome (remission, desensitization without remission [DWR], allergic). Results: 86% (151/176) of eligible children enrolled. Post-treatment peanut ingestion at 2-years post-treatment were similar for PPOIT (86.7%) and OIT (78.7%) groups, both higher than placebo (10.3%). Reactions reduced over time for all treatment and clinical outcome groups (PPOIT 31.7% to 23.3%, OIT 37.7% to 19.7%, placebo 13.8% to 6.9%; remission 27.5% to 15.9%; DWR 57.9% to 36.8%; allergic 11.6% to 7%). At 2-years post-treatment, similar proportions of remission and allergic participants reported reactions (RD 0.09 (95%CI -0.03, 0.20), p = .127), whereas more DWR participants reported reactions than remission (remission vs DWR: RD -0.21 (95%CI -0.39; -0.03), p = .02) and allergic (DWR vs allergic: RD 0.30 (95%CI 0.13, 0.47), p = .001) participants. At 2-years post-treatment, 0% remission versus 5.3% DWR versus 2.3% allergic participants reported adrenaline injector usage. Remission participants had significantly greater HRQOL improvement (adjusted for baseline) compared with both DWR (MD -0.54 (95%CI -0.99, -0.10), p = .017) and allergic (MD -0.82 (95%CI -1.25, -0.38), p < .001). Conclusion: By 2-years post-treatment, remission participants reported fewer reactions, less severe reactions and greater HRQOL improvement compared with DWR and allergic participants, indicating that remission is the patient-preferred treatment outcome over desensitization or remaining allergic.
引用
收藏
页码:2759 / 2774
页数:16
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