Abstract
Original language | English |
---|---|
Pages (from-to) | 1899-1911 |
Number of pages | 13 |
Journal | Journal of allergy and clinical immunology |
Volume | 149 |
Issue number | 6 |
Early online date | 2022 |
DOIs | |
Publication status | Published - Jun 2022 |
Keywords
- Atopic dermatitis
- clinical trials
- core outcome sets
- eczema
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In: Journal of allergy and clinical immunology, Vol. 149, No. 6, 06.2022, p. 1899-1911.
Research output: Contribution to journal › Article › Academic › peer-review
TY - JOUR
T1 - The HOME Core outcome set for clinical trials of atopic dermatitis
AU - Williams, Hywel C.
AU - Schmitt, Jochen
AU - Thomas, Kim S.
AU - Spuls, Phyllis I.
AU - Simpson, Eric L.
AU - Apfelbacher, Christian J.
AU - Chalmers, Joanne R.
AU - Furue, Masutaka
AU - Katoh, Norito
AU - Gerbens, Louise A. A.
AU - Leshem, Yael A.
AU - Howells, Laura
AU - Singh, Jasvinder A.
AU - HOME Initiative
AU - Boers, Maarten
N1 - Funding Information: The following people contributed to 1 or more HOME consensus meeting: K. Abuabara, S. Admani, J. Ahn, R. Allsopp, V. Aoki, C. Apfelbacher, Y. Arakawa, M. Ardeleanu, J. Armstrong, J. Austin, M. Awici-Rasmussen, J. Bae, B. Bang, A. Bansal, S. Barbarot, T. Berents, T. Berger, J.N. Bergman, K.B. Clemmensen, J. Block, M. Boers, N. Borok, M. Bradley, A. Bragg, C. Bruijnzeel-Koomen, M. Bruin-Weller, A. Bullock, T. Burton, L. Butler, B. Calimlim, J. Chalmers, S. Chamlin, C. Charman, T. Chubachi, A. Cohen, A. Cresswell-Melville, S. Deckert, C. DeKlotz, A. DeLozier, M. Dinesen, M. Dohil, A. Drucker, T. Ebata, L. Eckert, L. Eichenfield, C. Feeney, A. Finlay, C. Flohr, R. Fujimoto, F. Fukuie, M. Furue, M. Futamura, M. Gabes, A. Gadkari, M. Garg, L. Gerbens, U. Gieler, E. Gjerde, A. Graff, L. Graff, I. Guillemin, J. Gutermuth, J. Hanifin, C. Hawkes, A. Hebert, D. Heinl, L. Hooft, L. Howells, L. Howie, R. Humphreys, D. Hun Lee, S. Ichiyama, K. Igawa, I. Ikegami, Y. Imai, H. Ishii, H. Jung, Y. Kataoka, I. Katayama, N. Katoh, R. Kisa, W. Kouwenhoven, S. Langan, M. Lanigan, Y. Leshem, S. Lewis-Jones, D. Margolis, B. Marquort, K. Maru, E. Maruyama, M. Massuel, S. Merhand, P. Mina-Osorio, R. Minnillo, H. Mizutani, M. Murakami, H. Murota, D. Murrell, C. Na, T. Nakahara, H. Nankervis, I. Nasr, K. Nograles, F. Nunes, U. Nygaard, M. Nygardas, M. Ogino, Y. Ohya, E. Ono, A. Oranje, I. Osterloh, H. Otsuka, J. Pander, C. Paul, C. Prinsen, L. Purkins, E. Rehbinder, M. Ridd, A. Roberts, P. Rodgers, E. Roekevisch, N. Rogers, G. Romeijn, Y. Rosenbluth, T. Sach, H. Saeki, E. Simpson, J. Schmitt, M. Schram, M. Schuttelaar, A. Sears, S. Shindo, J. Singh, S. Smirnova, P. Spuls, J. Srour, J.-F. Stalder, D. Stölzl, B. Stuart, V. Sultana, A. Sulzer, Å. Svensson, E. Synnøve Gjerde, R. Takaoka, G. Talmo, H. Talmo, M. Tauber, H. Teixeira, A. Teper, K.S. Thomas, J. Thyssen, G. Todd, W. Tom, F. Torchet, H. Toyama, K. van Halewijn, A. Volke, L. von Kobyletzk, C. Wahlgren, L. Wang, S. Weidinger, E. Weisshaar, Y. Weng Yew, H. Williams, A. Wollenberg, K. Yamaga, A. Yasui, K. Yoshida, T. Young Han, M. Zaniboni, S. Zelt, and C. Zhao. 2022 HOME Executive: Christian Apfelbacher (Co-Chair), Eric Simpson (Co-Chair), Hywel C. Williams, Phyllis I. Spuls, Louise A.A. Gerbens, Yael Leshem, Laura Howells, Jochen Schmitt, Kim S. Thomas, Norito Katoh, and Mike Jacobson, Working group leads:, Symptoms: Phyllis Spuls and Louise Gerbens, Signs: Eric Simpson and Yael Leshem, Quality of life: Christian Apfelbacher, Long-term control: Kim Thomas and Laura Howells, The following local organizing committees planned and organized HOME consensus meetings in collaboration with the HOME Executive Committee: • HOME VII: N. Katoh, M. Furue, T. Nakahara, and H. Saeki • HOME V: S. Barbarot and J.-F. Stalder • HOME IV: Å. Svensson and L. von Kobyletzki • HOME III: M. Dohil, L. Eichenfield, and E. Simpson • HOME II: M. Schram, P. Spuls, and E. Roekevisch, The following people contributed to systematic reviews and other studies that were used in the development of the COS: K. Abuabara, V. Aoki, C. Apfelbacher, H. Aubert, M. Augustin, N. Ball, S. Barbarot, A. Bhanot, C. Blome, J. Bos, L. Bradshaw, B. Carter, J. Chalmers, C. Chambers, S. Chamlin, C. Charman, R. Chopra, A. Drucker, C. Flohr, M. Furue, M. Futamura, M. Gabes, K. Garfield, D. Gaunt, L. Gerbens, D. Grindlay, E. Grinich, R. Guy, T. Hajar, J. Hanifin, D. Heinl, S. Hollinghurst, L. Howells, D. Hsu, R. Humphreys, S. Immaneni, R. Kantor, D. Kuster, S. Langan, M. Leeflang, Y. Leshem, J. Limpens, R. Lindeboom, D. Margolis, C. Metcalfe, L. Naldi, H. Nankervis, R. Ofenloch, J. Oja, C. O'Leary, N. Patel, R. Pattinson, C. Paul, T. Pawlitschek, T. Peters, C. Prinsen, S. Purdy, S. Ratib, N. Redmond, M. Ridd, N.K. Rogers, T. Sach, R. Sacotte, J. Schmitt, D. Schoch, M. Schuttelaar, L. Shaw, J. Silverberg, E. Simpson, M. Schram, S. Smith, R. Sommer, P. Spuls, S. Stander, B. Stuart, A. Svensson, M. Tauber, C. Terwee, K.S. Thomas, C. Tischer, P. Vakharia, A. Volke, L. von Kobyletzki, S. Weidinger, E. Weisshaar, T. White, S. Wilkes, H. Williams, A. Wollenberg, and J. Zhang. The following people provided additional support to the HOME initiative: Barbara Maston provided assistance with premeeting preparations. Martin Boers and Jasvinder Singh acted as independent moderators at HOME consensus meetings. Carron Layfield and Masaki Futumura supported the planning and delivery of the patient introduction sessions at HOME V and HOME VII, respectively. Yukiyasu Arakawa and Susumu Ichiyama translated for Japanese patient representatives. Natasha Rogers kindly assisted with manuscript preparations for HOME meeting reports and for this article. Development of individual instruments that HOME subsequently evaluated for the core outcome set have been funded separately. Details of funding for each of the consensus meetings is outlined in the published meeting reports. The following additional funding sources contributed to facilitating the HOME COS development: • National Institute for Health and Care Research Senior Investigator award to Prof Hywel Williams (RE 2374) funded travel costs to enable UK patients to participate in HOME meetings • National Institute for Health and Care Research Programme Grant for Applied Research RP-PG-0407-10177 “Setting Priorities and Reducing Uncertainties for the Prevention and Treatment of Skin Disease (SPRUSD)” was used to support completion of the some of the systematic reviews, the cost of meetings and patient and public involvement (Prof Kim Thomas) • NIH NIAMS A Community-based Assessment of Skin Care, Allergies, and Eczema: The CASCADE Trial grant number 5 R01 AR071057-05 and Oregon Clinical and Translational Research Institute (OCTRI) assisted with outcome evaluations and associated travel costs (Prof Eric Simpson) • Laura Howells received a PhD studentship from the British Skin Foundation (Ref: 8016) for studies that informed this work Funding disclaimer: This study presents independent research commissioned by the National Institute for Health & Care Research (NIHR) under its Programme Grants for Applied Research funding scheme (RP-PG-0407-10177). The views expressed in this study are those of the author(s) and are not necessarily those of the NHS, the NIHR or the Department of Health. Disclosure of potential conflict of interest: The following people were involved with the development of the following instruments and present at a HOME consensus meeting at which these were considered: Atopic Dermatitis Control Test (L. Eckert, A. Gadkari, and E. Simpson), ADQoL-J (Y. Kataoka), BODE (A. Drucker), Childhood Atopic Dermatitis Impact Scale (CADIS)/Skindex Teen (S. Chamlin), CADIS short form (C. Apfelbacher, S. Chamlin, and M. Gabes), Dermatology Life Quality Index (DLQI), Children's Dermatology Life Quality Index (CDLQI), Dermatitis Family Impact (DFI), FDLQI, FROM-16, EDI, Infants’ Dermatitis Quality of Life Index (IDQoL) (A. Finlay), Eczema Area Severity Index (EASI) (L. Eichenfield, J. Hanifin, and Y. A. Leshem), Japanese versions of Patient-Oriented Eczema Measure (POEM), DLQI, CDLQI, DFI, IDQoL, POEM, QPCAD, PQCAD short form (Y. Ohya), NESS (H. Williams), POEM (H. Williams), PO-SCORAD (S. Barbarot, J.-F. Stalder, Å. Svensson, and A. Wollenberg), Recap of atopic eczema (C. Apfelbacher, T. Burton, J. Chalmers, L. Howells, L. Howie, P. Spuls, and K. Thomas), visual analogue scale (E. Weisshaar), and Ziarco Itch Diary (L. Purkins). L. Howells has received consultancy fees from the University of Oxford on an educational grant funded by Pfizer, unrelated to the submitted work. J. A. Singh has received consultant fees from Crealta/Horizon, Medisys, Fidia, PK Med, Two Labs, Inc, Adept Field Solutions, Clinical Care Options, Clearview Healthcare Partners, Putnam Associates, Focus Forward, Navigant Consulting, Spherix, MedIQ, Jupiter Life Science, UBM LLC, Trio Health, Medscape, WebMD, and Practice Point Communications; and the National Institutes of Health and the American College of Rheumatology; owns stock options in TPT Global Tech, Vaxart Pharmaceuticals, Atyu Biopharma, Adaptimmune Therapeutics, GeoVax Labs, Pieris Pharmaceuticals, Enzolytics, Inc, Seres Therapeutics, and Charlotte's Web Holdings, Inc; previously owned stock options in Amarin, Viking, and Moderna Pharmaceuticals; is on the speaker's bureau of Simply Speaking; and is a member of the executive of Outcomes Measures in Rheumatology, an organization that develops outcome measures in rheumatology and receives arms-length funding from 8 companies. Y. A. Leshem has received honoraria as a consultant from AbbVie, Sanofi, Genentech, Regeneron Pharmaceuticals, Pfizer, Janssen, and Dexcel Pharma, an independent research grant from AbbVie, and has, without personal compensation, provided investigator services for Eli Lilly, Pfizer, and AbbVie. N. Katoh has received honoraria as a speaker/consultant for Sanofi, Maruho, Abbvie, Ely-Lilly Japan, Taiho Pharmaceutical, Jansen Pharma, Mitsubishi Tanabe Pharma, Abbvie, Kyowa Kirin, Celgene Japan, and Leo Pharma, and has received grants as an investigator from Sanofi, Maruho, Abbvie, Mitsubishi Tanabe Pharma, Ely-Lilly Japan, Kyowa Kirin, Sun Pharma, Taiho Pharmaceutical, and Leo Pharma. P. I. Spuls has done consultancies in the past for Sanofi 111017 and AbbVie 041217 (unpaid), receives departmental independent research grants for TREAT NL registry, for which she is Chief Investigator (CI), from pharma companies since December 2019, and is involved in performing clinical trials with many pharmaceutical industries that manufacture drugs used for the treatment of, for example, psoriasis and atopic dermatitis, for which financial compensation is paid to the department/hospital. C. J. Apfelbacher has received institutional funding from the Dr Wolff Group and Bionorica, and consultancy fees from the Dr Wolff Group, Sanofi-Genzyme, Sanofi-Aventis, AstraZeneca, LeoPharma, and Bionorica. M. Boers is a consultant for Novartis. J. Schmitt acted as a paid consultant for Novartis, Sanofi, and ALK; received institutional grants for investigator-initiated research from Sanofi, Lilly, Pfizer, ALK, and Novartis; and is the lead investigator of the German eczema registry TREATgermany. E. L. Simpson reports grants and fees for participation as a consultant and principal investigator for Eli Lilly and Company, LEO Pharma, Pfizer, and Regeneron; grants for participation as a principal investigator from Galderma and Merck; and fees for consultant services from AbbVie, Boehringer-Ingelheim, Dermavant Incyte, Forte Bio, Pierre Fabre Dermo, and Sanofi-Genzyme. The rest of the authors declare that they have no relevant conflicts of interest. Funding Information: Funding disclaimer: This study presents independent research commissioned by the National Institute for Health & Care Research (NIHR) under its Programme Grants for Applied Research funding scheme (RP-PG-0407-10177). The views expressed in this study are those of the author(s) and are not necessarily those of the NHS, the NIHR or the Department of Health. Publisher Copyright: © 2022 The Authors
PY - 2022/6
Y1 - 2022/6
N2 - Core outcome sets are critically important outcomes that should be measured in clinical trials. Their absence in atopic dermatitis is a form of research waste and impedes combining evidence to inform patient care. Here, we articulate the rationale for core outcome sets in atopic dermatitis and review the work of the international Harmonising Outcome Measures for Eczema group from its inception in Munich, 2010. We describe core domain determination (what should be measured), to instrument selection (how domains should be measured), culminating in the complete core outcome measurement set in Tokyo, 2019. Using a “road map,” Harmonising Outcome Measures for Eczema includes diverse research methods including Delphi and nominal group techniques informed by systematic reviews of properties of candidate instruments. The 4 domains and recommended instruments for including in all clinical trials of atopic dermatitis are patient symptoms, measured by Patient-Oriented Eczema Measure and peak Numerical Rating Scale 11 for itch intensity over 24 hours, clinical signs measured using the Eczema Area and Severity Index, quality of life measured by the Dermatology Life Quality Index series for adults, children, and infants, and long-term control measured by either Recap of atopic eczema or Atopic Dermatitis Control Tool.
AB - Core outcome sets are critically important outcomes that should be measured in clinical trials. Their absence in atopic dermatitis is a form of research waste and impedes combining evidence to inform patient care. Here, we articulate the rationale for core outcome sets in atopic dermatitis and review the work of the international Harmonising Outcome Measures for Eczema group from its inception in Munich, 2010. We describe core domain determination (what should be measured), to instrument selection (how domains should be measured), culminating in the complete core outcome measurement set in Tokyo, 2019. Using a “road map,” Harmonising Outcome Measures for Eczema includes diverse research methods including Delphi and nominal group techniques informed by systematic reviews of properties of candidate instruments. The 4 domains and recommended instruments for including in all clinical trials of atopic dermatitis are patient symptoms, measured by Patient-Oriented Eczema Measure and peak Numerical Rating Scale 11 for itch intensity over 24 hours, clinical signs measured using the Eczema Area and Severity Index, quality of life measured by the Dermatology Life Quality Index series for adults, children, and infants, and long-term control measured by either Recap of atopic eczema or Atopic Dermatitis Control Tool.
KW - Atopic dermatitis
KW - clinical trials
KW - core outcome sets
KW - eczema
UR - http://www.scopus.com/inward/record.url?scp=85129445332&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.jaci.2022.03.017
DO - https://doi.org/10.1016/j.jaci.2022.03.017
M3 - Article
C2 - 35351441
SN - 0091-6749
VL - 149
SP - 1899
EP - 1911
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 6
ER -