TY - JOUR
T1 - Delphi consensus recommendations for a treatment algorithm in pulmonary sarcoidosis
AU - Rahaghi, Franck F.
AU - Baughman, Robert P.
AU - Saketkoo, Lesley Ann
AU - Sweiss, Nadera J.
AU - Barney, Joseph B.
AU - Birring, Surinder S.
AU - Costabel, Ulrich
AU - Crouser, Elliott D.
AU - Drent, Marjolein
AU - Gerke, Alicia K.
AU - Grutters, Jan C.
AU - Hamzeh, Nabeel Y.
AU - Huizar, Isham
AU - James, W. Ennis
AU - Kalra, Sanjay
AU - Kullberg, Susanna
AU - Li, Huiping
AU - Lower, Elyse E.
AU - Maier, Lisa A.
AU - Mirsaeidi, Mehdi
AU - Müller-Quernheim, Joachim
AU - Carmona Porquera, Eva M.
AU - Samavati, Lobelia
AU - Valeyre, Dominique
AU - Scholand, Mary Beth
N1 - Funding Information:
Conflict of interest: F.F. Rahaghi reports grants and consulting fees from Mallinckrodt, during the conduct of the study. R.P. Baughman reports grants and personal fees from Malllinckrodt, Novartis and Celgene, grants from Gilead, Genentech, Bayer and West Pharmaceutical, during the conduct of the study. L.A. Saketkoo has nothing to disclose. N.J. Sweiss has nothing to disclose. J.B. Barney has nothing to disclose. S.S. Birring has nothing to disclose. U. Costabel has nothing to disclose. E.D. Crouser has no relevant conflicts of interest to disclose. M. Drent has nothing to disclose. A.K. Gerke has nothing to disclose. J.C. Grutters has nothing to disclose. N.Y. Hamzeh has a patent pending from Prothena Inc. I. Huizar has no relevant conflicts of interest to disclose. W.E. James has nothing to disclose. S. Kalra has nothing to disclose. S. Kullberg has nothing to disclose. H. Li has nothing to disclose. E.E. Lower has nothing to disclose. L.A. Maier reports grants from National Institutes of Health: 1R01 HL127461-01A, 1R01HL11487-01A1, R01HL136681-01A1, 1R21 128738A-02, R21 HL140012-1, outside the submitted work. M. Mirsaeidi reports grants and personal fees from Mallinckrodt, outside the submitted work. J. Müller-Quernheim has nothing to disclose. E.M. Carmona Porquera reports other from ReSaph (Gilead), personal fees from American College of Chest Physicians (CHEST), outside the submitted work. L. Samavati participated in the Questcor Advisory Board Meeting 2014 and received $6500 compensation. D. Valeyre reports personal fees from Roche, Boehringer Ingelheim, AstraZeneca and Boehringer Ingelheim, outside the submitted work. M.B. Scholand reports other from Boehringer Ingelheim, Fibrogen, Global Blood Therapeutics and Genetech, outside the submitted work. In addition, M.B. Scholand has a patent Apparatus, Compositions and Methods for Assessment of Chronic Obstructive Pulmonary Disease Progression among Rapid and Slow Decline Conditions issued.
Publisher Copyright:
© ERS 2020.
PY - 2020/3
Y1 - 2020/3
N2 - Pulmonary sarcoidosis presents substantial management challenges, with limited evidence on effective therapies and phenotypes. In the absence of definitive evidence, expert consensus can supply clinically useful guidance in medicine. An international panel of 26 experts participated in a Delphi process to identify consensus on pharmacological management in sarcoidosis with the development of preliminary recommendations. The modified Delphi process used three rounds. The first round focused on qualitative data collection with open-ended questions to ensure comprehensive inclusion of expert concepts. Rounds 2 and 3 applied quantitative assessments using an 11-point Likert scale to identify consensus. Key consensus points included glucocorticoids as initial therapy for most patients, with non-biologics (immunomodulators), usually methotrexate, considered in severe or extrapulmonary disease requiring prolonged treatment, or as a steroid-sparing intervention in cases with high risk of steroid toxicity. Biologic therapies might be considered as additive therapy if non-biologics are insufficiently effective or are not tolerated with initial biologic therapy, usually with a tumour necrosis factor-α inhibitor, typically infliximab. The Delphi methodology provided a platform to gain potentially valuable insight and interim guidance while awaiting evidenced-based contributions.
AB - Pulmonary sarcoidosis presents substantial management challenges, with limited evidence on effective therapies and phenotypes. In the absence of definitive evidence, expert consensus can supply clinically useful guidance in medicine. An international panel of 26 experts participated in a Delphi process to identify consensus on pharmacological management in sarcoidosis with the development of preliminary recommendations. The modified Delphi process used three rounds. The first round focused on qualitative data collection with open-ended questions to ensure comprehensive inclusion of expert concepts. Rounds 2 and 3 applied quantitative assessments using an 11-point Likert scale to identify consensus. Key consensus points included glucocorticoids as initial therapy for most patients, with non-biologics (immunomodulators), usually methotrexate, considered in severe or extrapulmonary disease requiring prolonged treatment, or as a steroid-sparing intervention in cases with high risk of steroid toxicity. Biologic therapies might be considered as additive therapy if non-biologics are insufficiently effective or are not tolerated with initial biologic therapy, usually with a tumour necrosis factor-α inhibitor, typically infliximab. The Delphi methodology provided a platform to gain potentially valuable insight and interim guidance while awaiting evidenced-based contributions.
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U2 - 10.1183/16000617.0146-2019
DO - 10.1183/16000617.0146-2019
M3 - Article
C2 - 32198218
AN - SCOPUS:85082092403
SN - 0905-9180
VL - 29
JO - European Respiratory Review
JF - European Respiratory Review
IS - 155
M1 - 190146
ER -