TY - JOUR
T1 - First-line options for systemic juvenile idiopathic arthritis treatment
T2 - an observational study of Childhood Arthritis and Rheumatology Research Alliance Consensus Treatment Plans
AU - for the CARRA FROST Investigators
AU - Beukelman, Timothy
AU - Tomlinson, George
AU - Nigrovic, Peter A.
AU - Dennos, Anne
AU - Del Gaizo, Vincent
AU - Jelinek, Marian
AU - Riordan, Mary Ellen
AU - Schanberg, Laura E.
AU - Mohan, Shalini
AU - Pfeifer, Erin
AU - Kimura, Yukiko
AU - Agbayani, R.
AU - Akoghlanian, S.
AU - Allenspach, E.
AU - Anderson, E.
AU - Ardoin, S.
AU - Armendariz, S.
AU - Balboni, I.
AU - Ballenger, L.
AU - Ballinger, S.
AU - Barbar-Smiley, F.
AU - Baszis, K.
AU - Bell-Brunson, H.
AU - Benham, H.
AU - Bernal, W.
AU - Bigley, T.
AU - Binstadt, B.
AU - Blakley, M.
AU - Bohnsack, J.
AU - Brown, A.
AU - Buckley, M.
AU - Bullock, D.
AU - Cameron, B.
AU - Canna, S.
AU - Cassidy, E.
AU - Chang, J.
AU - Chauhan, V.
AU - Chinn, T.
AU - Chira, P.
AU - Cooper, A.
AU - Cooper, J.
AU - Correll, C.
AU - Curiel-Duran, L.
AU - Curry, M.
AU - Dalrymple, A.
AU - De Ranieri, D.
AU - Dedeoglu, F.
AU - DeGuzman, M.
AU - Delnay, N.
AU - Dempsey, V.
AU - Dowling, J.
AU - Drew, J.
AU - Driest, K.
AU - Du, Q.
AU - Durkee, D.
AU - Eckert, M.
AU - Edens, C.
AU - Elder, M.
AU - Fadrhonc, S.
AU - Favier, L.
AU - Feldman, B.
AU - Ferguson, I.
AU - Ferreira, B.
AU - Fogel, L.
AU - Fox, E.
AU - Fuhlbrigge, R.
AU - Fuller, J.
AU - George, N.
AU - Gerstbacher, D.
AU - Gillispie-Taylor, M.
AU - Goh, I.
AU - Goldsmith, D.
AU - Grevich, S.
AU - Griffin, T.
AU - Guevara, M.
AU - Guittar, P.
AU - Hager, M.
AU - Hahn, T.
AU - Halyabar, O.
AU - Hance, M.
AU - Haro, S.
AU - Harris, J.
AU - Hausmann, J.
AU - Hayward, K.
AU - Henderson, L.
AU - Hersh, A.
AU - Hillyer, S.
AU - Hiraki, L.
AU - Hiskey, M.
AU - Hobday, P.
AU - Hoffart, C.
AU - Holland, M.
AU - Hollander, M.
AU - Horwitz, M.
AU - Hsu, J.
AU - Huber, A.
AU - Ibarra, M.
AU - Inman, C.
AU - Jackson, S.
AU - James, K.
AU - Janow, G.
AU - Jones, S.
AU - Jones, K.
AU - Jones, J.
AU - Justice, C.
AU - Khalsa, U.
AU - Kienzle, B.
AU - Kim, S.
AU - Kimura, Y.
AU - Kitcharoensakkul, M.
AU - Klausmeier, T.
AU - Klein, K.
AU - Klein-Gitelman, M.
AU - Kramer, S.
AU - Lai, J.
AU - Lang, B.
AU - Lapidus, S.
AU - Lawson, E.
AU - Laxer, R.
AU - Lee, P.
AU - Lee, T.
AU - Lerman, M.
AU - Levy, D.
AU - Li, S.
AU - Lin, C.
AU - Ling, N.
AU - Lo, M.
AU - Lvovich, S.
AU - Maller, J.
AU - Martyniuk, A.
AU - McConnell, K.
AU - McHale, I.
AU - Meidan, E.
AU - Mellins, E.
AU - Miller, M.
AU - Modica, R.
AU - Moore, K.
AU - Moussa, T.
AU - Mruk, V.
AU - Muscal, E.
AU - Nanda, K.
AU - Nassi, L.
AU - Neely, J.
AU - Newhall, L.
AU - Nigrovic, P.
AU - Nolan, B.
AU - Oberle, E.
AU - Okeke, O.
AU - Oliver, M.
AU - O’Neil, K.
AU - Oz, R.
AU - Paller, A.
AU - Patel, J.
AU - Pepmueller, P.
AU - Phillippi, K.
AU - Pooni, R.
AU - Protopapas, S.
AU - Puplava, B.
AU - Radhakrishna, S.
AU - Ramsey, S.
AU - Reid, H.
AU - Ringold, S.
AU - Riordan, M.
AU - Riskalla, M.
AU - Ritter, M.
AU - Rodriquez, M.
AU - Rojas, K.
AU - Rosenkranz, M.
AU - Rubinstein, T.
AU - Sandborg, C.
AU - Scalzi, L.
AU - Schikler, K.
AU - Schmidt, K.
AU - Schmitt, E.
AU - Schneider, R.
AU - Seper, C.
AU - Shalen, J.
AU - Sheets, R.
AU - Shenoi, S.
AU - Shirley, J.
AU - Silverman, E.
AU - Sivaraman, V.
AU - Smith, C.
AU - Soep, J.
AU - Son, M.
AU - Spiegel, L.
AU - Stapp, H.
AU - Stern, S.
AU - Stevens, A.
AU - Stevens, B.
AU - Stewart, K.
AU - Stringer, E.
AU - Sundel, R.
AU - Sutter, M.
AU - Syed, R.
AU - Syed, R.
AU - Tanner, T.
AU - Tarshish, G.
AU - White, A.
AU - Yomogida, K.
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) developed consensus treatment plans (CTPs) to compare treatment initiation strategies for systemic juvenile idiopathic arthritis (sJIA). First-line options for sJIA treatment (FROST) was a prospective observational study to assess CTP outcomes using the CARRA Registry. Methods: Patients with new-onset sJIA were enrolled if they received initial treatment according to the biologic CTPs (IL-1 or IL-6 inhibitor) or non-biologic CTPs (glucocorticoid (GC) monotherapy or methotrexate). CTPs could be used with or without systemic GC. Primary outcome was achievement of clinical inactive disease (CID) at 9 months without current use of GC. Due to the small numbers of patients in the non-biologic CTPs, no statistical comparisons were made between the CTPs. Results: Seventy-three patients were enrolled: 63 (86%) in the biologic CTPs and 10 (14%) in the non-biologic CTPs. CTP choice appeared to be strongly influenced by physician preference. During the first month of follow-up, oral GC use was observed in 54% of biologic CTP patients and 90% of non-biologic CTPs patients. Five (50%) non-biologic CTP patients subsequently received biologics within 4 months of follow-up. Overall, 30/53 (57%) of patients achieved CID at 9 months without current GC use. Conclusion: Nearly all patients received treatment with biologics during the study period, and 46% of biologic CTP patients did not receive oral GC within the first month of treatment. The majority of patients had favorable short-term clinical outcomes. Increased use of biologics and decreased use of GC may lead to improved outcomes in sJIA.
AB - Background: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) developed consensus treatment plans (CTPs) to compare treatment initiation strategies for systemic juvenile idiopathic arthritis (sJIA). First-line options for sJIA treatment (FROST) was a prospective observational study to assess CTP outcomes using the CARRA Registry. Methods: Patients with new-onset sJIA were enrolled if they received initial treatment according to the biologic CTPs (IL-1 or IL-6 inhibitor) or non-biologic CTPs (glucocorticoid (GC) monotherapy or methotrexate). CTPs could be used with or without systemic GC. Primary outcome was achievement of clinical inactive disease (CID) at 9 months without current use of GC. Due to the small numbers of patients in the non-biologic CTPs, no statistical comparisons were made between the CTPs. Results: Seventy-three patients were enrolled: 63 (86%) in the biologic CTPs and 10 (14%) in the non-biologic CTPs. CTP choice appeared to be strongly influenced by physician preference. During the first month of follow-up, oral GC use was observed in 54% of biologic CTP patients and 90% of non-biologic CTPs patients. Five (50%) non-biologic CTP patients subsequently received biologics within 4 months of follow-up. Overall, 30/53 (57%) of patients achieved CID at 9 months without current GC use. Conclusion: Nearly all patients received treatment with biologics during the study period, and 46% of biologic CTP patients did not receive oral GC within the first month of treatment. The majority of patients had favorable short-term clinical outcomes. Increased use of biologics and decreased use of GC may lead to improved outcomes in sJIA.
KW - Biologics
KW - Juvenile idiopathic arthritis
KW - Still’s disease
KW - Systemic juvenile idiopathic arthritis
KW - Treatment
UR - http://www.scopus.com/inward/record.url?scp=85143553706&partnerID=8YFLogxK
U2 - 10.1186/s12969-022-00768-6
DO - 10.1186/s12969-022-00768-6
M3 - Article
C2 - 36482434
AN - SCOPUS:85143553706
SN - 1546-0096
VL - 20
JO - Pediatric Rheumatology
JF - Pediatric Rheumatology
IS - 1
M1 - 113
ER -