Systemic treatments for atopic dermatitis (eczema): Systematic review and network meta- analysis of randomized trials

被引:41
|
作者
Chu, Alexandro W. L. [1 ,2 ]
Wong, Melanie M. [1 ,2 ]
Rayner, Daniel G. [3 ]
Guyatt, Gordon H. [1 ,2 ,3 ]
Martinez, Juan Pablo Diaz [3 ]
Ceccacci, Renata [1 ,2 ]
Zhao, Irene X. [1 ,2 ]
McMullen, Eric [1 ,2 ]
Srivastava, Archita [2 ,4 ]
Wang, Jason [1 ,2 ]
Wen, Aaron [1 ,2 ]
Wang, Fang Chi [2 ,5 ]
Brignardello-Petersen, Romina [3 ]
Izcovich, Ariel [6 ]
Oykhman, Paul [1 ,2 ]
Wheeler, Kathryn E. [7 ]
Wang, Julie [8 ]
Spergel, Jonathan M. [9 ,10 ,12 ]
Singh, Jasvinder A. [11 ]
Silverberg, Jonathan I. [15 ]
Ong, Peck Y. [13 ,14 ]
O'Brien, Monica [15 ]
Martin, Stephen A. [16 ]
Lio, Peter A. [17 ,18 ]
Lind, Mary Laura [19 ]
LeBovidge, Jennifer [20 ,21 ]
Kim, Elaine [22 ]
Huynh, Joey [23 ]
Greenhawt, Matthew [24 ,25 ]
Gardner, Donna D. [26 ]
Frazier, Winfred T. [28 ]
Ellison, Kathy [27 ]
Chen, Lina [2 ,28 ]
Capozza, Korey [29 ]
De Benedetto, Anna [24 ,31 ]
Boguniewicz, Mark [24 ,30 ]
Begolka, Wendy Smith [31 ]
Asiniwasis, Rachel N. [32 ]
Schneider, Lynda C. [20 ]
Chu, Derek K. [1 ,2 ,3 ,33 ,34 ]
机构
[1] McMaster Univ, Dept Med, Hamilton, ON, Canada
[2] McMaster Univ, Evidence Allergy Grp, Hamilton, ON, Canada
[3] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON, Canada
[4] Western Univ, Dept Internal Med, London, England
[5] Western Univ, Schulich Sch Med & Dent, London, England
[6] Hosp Aleman, Serv Clin Med, Buenos Aires, Argentina
[7] Univ Florida, Dept Pediat, Gainesville, FL USA
[8] Icahn Sch Med Mt Sinai, Dept Pediat, Div Pediat Allergy & Immunol, New York, NY USA
[9] Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA USA
[10] Childrens Hosp Philadelphia, Div Allergy & Immunol, Philadelphia, PA USA
[11] Univ Alabama Birmingham, Dept Med, Birmingham, AL USA
[12] George Washington Univ, Sch Med & Hlth Sci, Dept Dermatol, Washington, DC USA
[13] Childrens Hosp Los Angeles, Div Clin Immunol & Allergy, Los Angeles, CA USA
[14] USC, Keck Sch Med, Dept Pediat, Los Angeles, CA USA
[15] Tufts Univ, Sch Med, Boston, MA USA
[16] UMass Chan Med Sch, Worcester, MA USA
[17] Northwestern Univ, Feinberg Sch Med, Dept Dermatol, Chicago, IL USA
[18] Northwestern Univ, Feinberg Sch Med, Dept Pediat, Chicago, IL USA
[19] Arizona State Univ, Sch Engn Matter Transport & Energy, Tempe, AZ USA
[20] Boston Childrens Hosp, Div Immunol, Boston, MA USA
[21] Harvard Med Sch, Boston, MA USA
[22] Sepulveda VA Med Ctr, North Hills, CA USA
[23] Univ Colorado, Dept Pediat, Sch Med, Boulder, CO USA
[24] Childrens Hosp Colorado, Sect Allergy & Immunol, Aurora, CO USA
[25] Allergy & Asthma Network, Fairfax, VA USA
[26] UPMC St Margaret, Dept Family Med, Pittsburgh, PA USA
[27] McMaster Univ, Dept Pediat, Hamilton, ON, Bermuda
[28] Global Parents Eczema Res, Santa Barbara, CA USA
[29] Univ Rochester, Med Ctr, Dept Dermatol, Rochester, NY USA
[30] Natl Eczema Assoc, Novato, CA USA
[31] Univ Saskatchewan, Dept Dermatol, Regina, SK, Canada
[32] Res Inst St Joes Hamilton, Hamilton, ON, Canada
[33] McMaster Univ, Dept Med, Hamilton, ON L8S 4K1, Canada
[34] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON L8S 4K1, Canada
关键词
Atopic dermatitis (eczema); systemic treatments and phototherapy (light therapy; immunosuppressants; immunomodula-tors; DMARDs; cyclosporine; methotrexate; azathioprine; mycophe-nolate; cortiosteroids; narrow-band UVB); biologics (dupilumab; lebrikizumab; tralokinumab; nemolizumab); Janus kinase (JAK) in-hibitors (upadacitinib; abrocitinib; baricitinib); patient-important outcomes and adverse events or adverse reactions; disease severity; itch; sleep; itch and sleep disturbance quality of life; network meta-analysis (comparative effectiveness; multiple treatment comparison); QUALITY-OF-LIFE; L-HISTIDINE SUPPLEMENTATION; PLACEBO-CONTROLLED TRIAL; LOW-DOSE CYCLOSPORINE; DOUBLE-BLIND; TOPICAL CORTICOSTEROIDS; CARDIOVASCULAR EVENTS; ADULT PATIENTS; INTRAVENOUS IMMUNOGLOBULIN; RHEUMATOID-ARTHRITIS;
D O I
10.1016/j.jaci.2023.08.029
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Atopic dermatitis (AD) is an inflammatory skin condition with multiple systemic treatments and uncertainty regarding their comparative impact on AD outcomes. Objective: We sought to systematically synthesize the benefits and harms of AD systemic treatments. Methods: For the 2023 American Academy of Allergy, Asthma & Immunology and American College of Allergy, Asthma, and Immunology Joint Task Force on Practice Parameters AD guidelines, we searched MEDLINE, EMBASE, CENTRAL, Web of Science, and GREAT databases from inception to November 29, 2022, for randomized trials addressing systemic treatments and phototherapy for AD. Paired reviewers independently screened records, extracted data, and assessed risk of bias. Random-effects network meta-analyses addressed AD severity, itch, sleep, AD-related quality of life, flares, and harms. The Grading of Recommendations Assessment, Development and Evaluation approach informed certainty of evidence ratings. This review is registered in the Open Science Framework (https://osf.io/e5sna). Results: The 149 included trials (28,686 patients with moderate to-severe AD) evaluated 75 interventions. With high-certainty evidence, high-dose upadacitinib was among the most effective for 5 of 6 patient-important outcomes; high-dose abrocitinib and low-dose upadacitinib were among the most effective for 2 outcomes. These Janus kinase inhibitors were among the most harmful in increasing adverse events. With high-certainty evidence, dupilumab, lebrikizumab, and tralokinumab were of intermediate effectiveness and among the safest, modestly increasing conjunctivitis. Low-dose baricitinib was among the least effective. Efficacy and safety of azathioprine, oral corticosteroids, cyclosporine, methotrexate, mycophenolate, phototherapy, and many novel agents are less certain. Conclusions: Among individuals with moderate-to-severe AD, high-certainty evidence demonstrates that high-dose upadacitinib is among the most effective in addressing multiple patient-important outcomes, but also is among the most harmful. High-dose abrocitinib and low-dose upadacitinib are effective, but also among the most harmful. Dupilumab, lebrikizumab, and tralokinumab are of intermediate effectiveness and have favorable safety. (J Allergy Clin Immunol 2023;152:1470-92.)
引用
收藏
页码:1470 / 1492
页数:23
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