Abstract
Original language | English |
---|---|
Pages (from-to) | 465-479 |
Number of pages | 15 |
Journal | Nature Reviews Rheumatology |
Volume | 18 |
Issue number | 8 |
Early online date | 2022 |
DOIs | |
Publication status | Published - 1 Aug 2022 |
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Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) : updated treatment recommendations for psoriatic arthritis 2021. / the GRAPPA Treatment Recommendations domain subcommittees.
In: Nature Reviews Rheumatology, Vol. 18, No. 8, 01.08.2022, p. 465-479.Research output: Contribution to journal › Article › Academic › peer-review
TY - JOUR
T1 - Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA)
T2 - updated treatment recommendations for psoriatic arthritis 2021
AU - Coates, Laura C.
AU - Soriano, Enrique R.
AU - Corp, Nadia
AU - Bertheussen, Heidi
AU - Callis Duffin, Kristina
AU - Campanholo, Cristiano B.
AU - Chau, Jeffrey
AU - Eder, Lihi
AU - Fernández-Ávila, Daniel G.
AU - FitzGerald, Oliver
AU - Garg, Amit
AU - Gladman, Dafna D.
AU - Goel, Niti
AU - Helliwell, Philip S.
AU - Husni, M. Elaine
AU - Jadon, Deepak R.
AU - Katz, Arnon
AU - Laheru, Dhruvkumar
AU - Latella, John
AU - Leung, Ying-Ying
AU - Lindsay, Christine
AU - Lubrano, Ennio
AU - Mazzuoccolo, Luis Daniel
AU - Mease, Philip J.
AU - O’Sullivan, Denis
AU - Ogdie, Alexis
AU - Olsder, Wendy
AU - Palominos, Penelope Esther
AU - Schick, Lori
AU - Steinkoenig, Ingrid
AU - de Wit, Maarten
AU - van der Windt, D. A.
AU - Kavanaugh, Arthur
AU - Campanholo, Cristiano
AU - the GRAPPA Treatment Recommendations domain subcommittees
AU - Fitzgerald, Oliver
AU - Gladman, Dafna
AU - Helliwell, Philip
AU - Husni, M. Elaine
AU - Laheru, Dhrukumar
AU - Leung, Ying-Ying
AU - Lubrano, Ennio
AU - Mazzuoccolo, Luis Daniel
AU - Mease, Philip J.
AU - Ogdie, Alexis
AU - Palominos, Penelope Esther
N1 - Funding Information: L.C.C. has received grants/research support from AbbVie, Amgen, Celgene, Eli Lilly, Novartis and Pfizer; worked as a paid consultant for AbbVie, Amgen, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Eli Lilly, Gilead, Galapagos, Janssen, Novartis, Pfizer and UCB; and has been paid as a speaker for AbbVie, Amgen, Biogen, Celgene, Eli Lilly, Galapagos, Gilead, Janssen, Medac, Novartis, Pfizer and UCB. E.R.S. has participated in advisory boards, given conferences or received grants from AbbVie, Amgen, Bristol Myers Squibb, Eli Lilly, Glaxo, Janssen, Novartis, Pfizer, Sandoz, Roche and UCB. H.B. has received consultancy funding from Pfizer. K.C.D. has received research funding from Amgen, Abbvie, Celgene, Lilly, Novartis, Pfizer, Boehringer-Ingelheim, Stiefel, Janssen, UCB, and honoraria for consulting/advising from Abbvie, Celgene, Lilly, Novartis, Pfizer, Boehringer-Ingelheim, Regeneron, Janssen, Ortho Dermatologic, UCB, Bristol-Myers Squibb, and Astra Zeneca. C.B.C. has received honoraria for consulting/advising and fees for educational consulting from AbbVie, Bristol, Janssen, Lilly, Novartis, Pfizer, and UCB. L.E. has received educational/research grants and consultation fees from Abbvie, Janssen, Novartis, UCB, Eli Lily, Sandoz and Pfizer. D.F.-A. declares that they have acted as a consultant of Abbvie, UCB, Roche, Janssen, Pfizer, Amgen and Brystol, and received grant/research support from Abbvie, UCB, Roche, Janssen, Pfizer, Amgen and Brystol. O.F. has received grant/research support from AbbVie, Bristol-Myers Squibb, Eli Lilly, Novartis, Pfizer Inc and UCB; has received consulting fees from Bristol-Myers Squibb, Celgene, Eli Lilly, Janssen and Pfizer Inc; and has been on speakers’ bureaus for AbbVie, Janssen, Biogen and Pfizer Inc. A.G. is an adviser for AbbVie, Anaptys Bio, Boehringer Ingelheim, Bristol Myers Squibb, Incyte, InflaRx, Janssen, Novartis, Pfizer, UCB, and Viela Biosciences, and receives honoraria; A.G. receives research grants from AbbVie, UCB and National Psoriasis Foundation. D.D.G. has received grant support from Abbvie, Amgen, Eli Lilly, Janssen, Novartis, Pfizer and UCB, and received honoraria/consulting fees from Abbvie, Amgen, BMS, Galapagos, Gilead, Eli Lilly, Janssen, Novartis, Pfizer and UCB. N.G. owns stock in UCB Pharma Ltd. P.S.H. received consultancy fees from Eli Lilly and fees for educational services from Pfizer, Novartis and Janssen. M.E.H. reports honoraria/consulting fees from Abbvie, Amgen, BMS, Lilly, Novartis, Janssen, Pfizer and UCB. D.R.J. has received education and/or research grants from AbbVie, Amgen, Biogen, BMS, Celgene, Celltrion Healthcare, Eli Lilly, Fresenius-Kabi, Galapagos, GSK, Janssen, MSD, Novartis, Pfizer, Roche, Sandoz, Sanofi and UCB; D.R.J. has acted on advisory boards for AbbVie, Eli Lilly, Galapagos, GSK, Janssen, MSD, Novartis, Pfizer, Sandoz and UCB; D.R.J. has been a paid speaker for AbbVie, Celgene, Eli Lilly, Janssen, Novartis, Pfizer and UCB. D.L. declares educational Honoraria for lectures from Abbvie, Leo Pharma and UCB Pharma. Y.-Y.L. has been paid as a speaker for AbbVie, DKSH, Janssen, Novartis and Pfizer. C.L. has Amgen stock and is employed by Aurinia Pharma US Inc. E.L. reports honoraria/Consultant fees from Alfasigma, AbbVie, Galapagos, Janssen, Lilly, MSD, Novartis, Pfizer. L.D.M. has been a paid speaker for Abbvie, Elli Lilly, Novartis, Amgen, Janssen, UCB, Boehringer Ingelheim. P.J.M. declares research grants, consultation fees, and/or speaker honoraria from Abbvie, Amgen, Bristol Myers, Boehringer Ingelheim, Galapagos, Gilead, GlaxoSmithKline, Inmagene, Janssen, Lilly, Merck, Novartis, Pfizer, SUN Pharma, and UCB. A.O. declares that she has consulted for Abbvie, Amgen, BMS, Celgene, CorEvitas, Gilead, Janssen, Lilly, Novartis, Pfizer and UCB and has received grants from Abbvie, Novartis and Pfizer to University of Pennsylvania and Amgen to Forward databank; A.O.’s spouse has received royalties from Novartis. P.E.P. declares honoraria/research grants from AbbVie, Janssen, Novartis, Pfizer and UCB. M.d.W. declares that Stichting Tools has received fees for lectures or consultancy provided by M.d.W. from Celgene, Eli Lilly, Pfizer and UCB. A.K. has worked as a consultant to AbbVie, Bristol Myers Squibb, Eli Lilly, Gilead, Janssen, Novartis, Pfizer and UCB. N.C., J.C., A.K., J.L., D.O’S., W.O., L.S., I.S. and D.A.v.d.W. declare no competing interests. Publisher Copyright: © 2022, Springer Nature Limited.
PY - 2022/8/1
Y1 - 2022/8/1
N2 - Since the second version of the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) treatment recommendations were published in 2015, therapeutic options for psoriatic arthritis (PsA) have advanced considerably. This work reviews the literature since the previous recommendations (data published 2013–2020, including conference presentations between 2017 and 2020) and reports high-quality, evidence-based, domain-focused recommendations for medication selection in PsA developed by GRAPPA clinicians and patient research partners. The overarching principles for the management of adults with PsA were updated by consensus. Principles considering biosimilars and tapering of therapy were added, and the research agenda was revised. Literature searches covered treatments for the key domains of PsA: peripheral arthritis, axial disease, enthesitis, dactylitis, and skin and nail psoriasis; additional searches were performed for PsA-related conditions (uveitis and inflammatory bowel disease) and comorbidities. Individual subcommittees used a GRADE-informed approach, taking into account the quality of evidence for therapies, to generate recommendations for each of these domains, which were incorporated into an overall schema. Choice of therapy for an individual should ideally address all disease domains active in that patient, supporting shared decision-making. As safety issues often affect potential therapeutic choices, additional consideration was given to relevant comorbidities. These GRAPPA treatment recommendations provide up-to-date, evidence-based guidance on PsA management for clinicians and people with PsA.
AB - Since the second version of the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) treatment recommendations were published in 2015, therapeutic options for psoriatic arthritis (PsA) have advanced considerably. This work reviews the literature since the previous recommendations (data published 2013–2020, including conference presentations between 2017 and 2020) and reports high-quality, evidence-based, domain-focused recommendations for medication selection in PsA developed by GRAPPA clinicians and patient research partners. The overarching principles for the management of adults with PsA were updated by consensus. Principles considering biosimilars and tapering of therapy were added, and the research agenda was revised. Literature searches covered treatments for the key domains of PsA: peripheral arthritis, axial disease, enthesitis, dactylitis, and skin and nail psoriasis; additional searches were performed for PsA-related conditions (uveitis and inflammatory bowel disease) and comorbidities. Individual subcommittees used a GRADE-informed approach, taking into account the quality of evidence for therapies, to generate recommendations for each of these domains, which were incorporated into an overall schema. Choice of therapy for an individual should ideally address all disease domains active in that patient, supporting shared decision-making. As safety issues often affect potential therapeutic choices, additional consideration was given to relevant comorbidities. These GRAPPA treatment recommendations provide up-to-date, evidence-based guidance on PsA management for clinicians and people with PsA.
UR - http://www.scopus.com/inward/record.url?scp=85133751616&partnerID=8YFLogxK
U2 - 10.1038/s41584-022-00798-0
DO - 10.1038/s41584-022-00798-0
M3 - Article
C2 - 35761070
SN - 1759-4790
VL - 18
SP - 465
EP - 479
JO - Nature Reviews Rheumatology
JF - Nature Reviews Rheumatology
IS - 8
ER -