Micol Romano1, Z Serap Arici2, David Piskin1, Sara Alehashemi3, Daniel Aletaha4, Karyl Barron5, Susanne Benseler6, Roberta A Berard1, Lori Broderick7, Fatma Dedeoglu8, Michelle Diebold1, Karen Durrant9, Polly Ferguson10, Dirk Foell11, Jonathan S Hausmann12, Olcay Y Jones13, Daniel Kastner14, Helen J Lachmann15, Ronald M Laxer16, Dorelia Rivera17, Nicola Ruperto18, Anna Simon19, Marinka Twilt6, Joost Frenkel20, Hal M Hoffman7, Adriana A de Jesus3, Jasmin B Kuemmerle-Deschner21, Seza Ozen22, Marco Gattorno18, Raphaela Goldbach-Mansky3, Erkan Demirkaya1. 1. University of Western Ontario, London, Ontario, Canada. 2. Sanliurfa Training and Research Hospital, Sanliurfa, Turkey. 3. National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland. 4. Medical University of Vienna, Vienna, Austria. 5. National Institute of Allergy and Immunology, NIH, Bethesda, Maryland. 6. University of Calgary, Calgary, Alberta, Canada. 7. University of California and Rady Children's Hospital, San Diego, California. 8. Harvard Medical School, Boston, Massachusetts. 9. Autoinflammatory Alliance and Kaiser Foundation Hospital, San Francisco, California. 10. University of Iowa, Iowa City. 11. University of Muenster, Muenster, Germany. 12. Boston Children's Hospital and Beth Israel Deaconess Medical Center, Boston, Massachusetts. 13. Walter Reed National Military Medical Center, Bethesda, Maryland. 14. National Human Genome Research Institute, NIH, Bethesda, Maryland. 15. University College London, London, UK. 16. The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada. 17. Autoinflammatory Alliance, San Francisco, California. 18. IRCCS Istituto Giannina Gaslini, Genoa, Italy. 19. Radboud University Medical Centre, Nijmegen, The Netherlands. 20. Wilhelmina Kinderziekenhuis, Utrecht, The Netherlands. 21. University Hospital Tubingen, Tubingen, Germany. 22. Hacettepe University, Ankara, Turkey.
Abstract
BACKGROUND: The interleukin-1 (IL-1) mediated systemic autoinflammatory diseases, including the cryopyrin- associated periodic syndromes (CAPS), tumour necrosis factor receptor-associated periodic syndrome (TRAPS), mevalonate kinase deficiency (MKD) and deficiency of the IL-1 receptor antagonist (DIRA), belong to a group of rare immunodysregulatory diseases that primarily present in early childhood with variable multiorgan involvement. When untreated, patients with severe clinical phenotypes have a poor prognosis, and diagnosis and management of these patients can be challenging. However, approved treatments targeting the proinflammatory cytokine IL-1 have been life changing and have significantly improved patient outcomes. OBJECTIVE: To establish evidence-based recommendations for diagnosis, treatment and monitoring of patients with IL-1 mediated autoinflammatory diseases to standardise their management. METHODS: A multinational, multidisciplinary task force consisting of physician experts, including rheumatologists, patients or caregivers and allied healthcare professionals, was established. Evidence synthesis, including systematic literature review and expert consensus (Delphi) via surveys, was conducted. Consensus methodology was used to formulate and vote on statements to guide optimal patient care. RESULTS: The task force devised five overarching principles, 14 statements related to diagnosis, 10 on therapy, and nine focused on long-term monitoring that were evidence and/or consensus-based for patients with IL-1 mediated diseases. An outline was developed for disease-specific monitoring of inflammation-induced organ damage progression and reported treatments of CAPS, TRAPS, MKD and DIRA. CONCLUSION: The 2021 EULAR/American College of Rheumatology points to consider represent state-of-the-art knowledge based on published data and expert opinion to guide diagnostic evaluation, treatment and monitoring of patients with CAPS, TRAPS, MKD and DIRA, and to standardise and improve care, quality of life and disease outcomes.
BACKGROUND: The interleukin-1 (IL-1) mediated systemic autoinflammatory diseases, including the cryopyrin- associated periodic syndromes (CAPS), tumour necrosis factor receptor-associated periodic syndrome (TRAPS), mevalonate kinase deficiency (MKD) and deficiency of the IL-1 receptor antagonist (DIRA), belong to a group of rare immunodysregulatory diseases that primarily present in early childhood with variable multiorgan involvement. When untreated, patients with severe clinical phenotypes have a poor prognosis, and diagnosis and management of these patients can be challenging. However, approved treatments targeting the proinflammatory cytokine IL-1 have been life changing and have significantly improved patient outcomes. OBJECTIVE: To establish evidence-based recommendations for diagnosis, treatment and monitoring of patients with IL-1 mediated autoinflammatory diseases to standardise their management. METHODS: A multinational, multidisciplinary task force consisting of physician experts, including rheumatologists, patients or caregivers and allied healthcare professionals, was established. Evidence synthesis, including systematic literature review and expert consensus (Delphi) via surveys, was conducted. Consensus methodology was used to formulate and vote on statements to guide optimal patient care. RESULTS: The task force devised five overarching principles, 14 statements related to diagnosis, 10 on therapy, and nine focused on long-term monitoring that were evidence and/or consensus-based for patients with IL-1 mediated diseases. An outline was developed for disease-specific monitoring of inflammation-induced organ damage progression and reported treatments of CAPS, TRAPS, MKD and DIRA. CONCLUSION: The 2021 EULAR/American College of Rheumatology points to consider represent state-of-the-art knowledge based on published data and expert opinion to guide diagnostic evaluation, treatment and monitoring of patients with CAPS, TRAPS, MKD and DIRA, and to standardise and improve care, quality of life and disease outcomes.
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