Successful treatment with tocilizumab every 4 weeks of a low disease activity group who achieve a drug-free remission in patients with systemic-onset juvenile idiopathic arthritis

被引:11
作者
Kostik, Mikhail M. [1 ]
Dubko, Margarita F. [1 ]
Masalova, Vera V. [1 ]
Snegireva, Ludmila S. [1 ]
Komishina, Tatyana L. [1 ]
Chikova, Irina A. [1 ]
Isupova, Eugenia A. [1 ]
Kuchinskaya, Ekaterina M. [1 ]
Glebova, Natalia I. [1 ]
Buchinskaya, Natalia V. [1 ]
Kalashnikova, Olga V. [1 ]
Chasnyk, Vyacheslav G. [1 ]
机构
[1] St Petersburg State Pediat Med Univ, Hosp Pediat Dept, St Petersburg 194100, Russia
关键词
Systemic-onset juvenile idiopathic arthritis; Interleukine-6; Tocilizumab; Biologic free remission; Low disease activity; High disease activity; ANTI-INTERLEUKIN-6 RECEPTOR ANTIBODY; IL-6; RECEPTOR; DOUBLE-BLIND; EFFICACY; CHILDREN; TRIAL; SAFETY;
D O I
10.1186/1546-0096-13-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Systemic juvenile idiopathic arthritis (SoJIA) is the most striking form of juvenile idiopathic arthritis. The aim of our study was to evaluate the clinical responses and outcomes of children with SoJIA to IL-6 blockade using two different tocilizumab (TCZ) treatment protocols designed for milder and more severe SoJIA patient groups, and evaluate the possibility of achieving biologic-free remission. Methods: Thirty-seven active SoJIA children who have failed treatment with corticosteroids and other DMARDs were included in our retrospective study. TCZ doses were prescribed in two treatment approaches: every 2 weeks TCZ dosing (Q2W) and every 4 weeks TCZ dosing (Q4W). The patients were assigned to these two groups by the study physicians depending on the severity of the SoJIA disease as judged by each clinician. Results: Thirty-three of the 37 children successfully completed the trial. TCZ was discontinued in 11patients during the trial. Seven children achieved inactive disease and were allowed to stop the TCZ and 4 had severe adverse events requiring drug cessation. Currently 7 patients continue to have TCZ-free remission [4/7 remission off-medication, 3/7 still on methotrexate (MTX)]. This mixed group had a median treatment duration of 1002 days. The children in remission off of all medications, TCZ and MTX, had a median remission duration of 1162 days (ranged 932-1301 days). Compared to the patients assigned to the Q2W TCZ treatment group, the patients assigned to the Q4W TCZ group had a milder SoJIA course. The patients had higher levels of hemoglobin, total proteins, and serum albumins. They had lower white blood cell counts (WBC), % granulocytes, CRP, ESR, ferritins, and LDH. These children had a lower frequency of internal organ involvement, fewer relapses during TCZ treatment, and no macrophage activation syndrome episodes. Conclusions: Our experience with TCZ for SoJIA supports the excellent result of other studies. What may be novel is our finding that this IL-6 blockade with TCZ may be able to be utilized at a less frequent dosing schedule in mild SoJIA compared to severe SoJIA. We discuss other factors that may increase the probability of a patient reaching TCZ-free remission.
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页数:9
相关论文
共 26 条
[1]  
Brunner HI, 2013, ARTHRITIS RHEUM-US, V65, pS335
[2]   Randomized Trial of Tocilizumab in Systemic Juvenile Idiopathic Arthritis [J].
De Benedetti, Fabrizio ;
Brunner, Hermine I. ;
Ruperto, Nicolino ;
Kenwright, Andrew ;
Wright, Stephen ;
Calvo, Inmaculada ;
Cuttica, Ruben ;
Ravelli, Angelo ;
Schneider, Rayfel ;
Woo, Patricia ;
Wouters, Carine ;
Xavier, Ricardo ;
Zemel, Lawrence ;
Baildam, Eileen ;
Burgos-Vargas, Ruben ;
Dolezalova, Pavla ;
Garay, Stella M. ;
Merino, Rosa ;
Joos, Rik ;
Grom, Alexei ;
Wulffraat, Nico ;
Zuber, Zbigniew ;
Zulian, Francesco ;
Lovell, Daniel ;
Martini, Alberto .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (25) :2385-2395
[3]  
DeBenedetti F, 1997, J RHEUMATOL, V24, P1403
[4]   SERUM-SOLUBLE INTERLEUKIN-6 (IL-6) RECEPTOR AND IL-6 SOLUBLE IL-6 RECEPTOR COMPLEX IN SYSTEMIC JUVENILE RHEUMATOID-ARTHRITIS [J].
DEBENEDETTI, F ;
MASSA, M ;
PIGNATTI, P ;
ALBANI, S ;
NOVICK, D ;
MARTINI, A .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (05) :2114-2119
[5]   CORRELATION OF SERUM INTERLEUKIN-6 LEVELS WITH JOINT INVOLVEMENT AND THROMBOCYTOSIS IN SYSTEMIC JUVENILE RHEUMATOID-ARTHRITIS [J].
DEBENEDETTI, F ;
MASSA, M ;
ROBBIONI, P ;
RAVELLI, A ;
BURGIO, GR ;
MARTINI, A .
ARTHRITIS AND RHEUMATISM, 1991, 34 (09) :1158-1163
[6]   Consensus treatment plans for new-onset systemic juvenile idiopathic arthritis [J].
Dewitt, Esi Morgan ;
Kimura, Yukiko ;
Beukelman, Timothy ;
Nigrovic, Peter A. ;
Onel, Karen ;
Prahalad, Sampath ;
Schneider, Rayfel ;
Stoll, Matthew L. ;
Angeles-Han, Sheila ;
Milojevic, Diana ;
Schikler, Kenneth N. ;
Vehe, Richard K. ;
Weiss, Jennifer E. ;
Weiss, Pamela ;
Ilowite, Norman T. ;
Wallace, Carol A. .
ARTHRITIS CARE & RESEARCH, 2012, 64 (07) :1001-1010
[7]   The pattern of response to anti-interleukin-1 treatment distinguishes two subsets of patients with systemic-onset juvenile idiopathic arthritis [J].
Gattorno, Marco ;
Piccini, Alessandra ;
Lasiglie, Denise ;
Tassi, Sara ;
Brisca, Giacomo ;
Carta, Sonia ;
Delfino, Laura ;
Ferlito, Francesca ;
Pelagatti, Maria Antonietta ;
Caroli, Francesco ;
Buoncompagni, Antonella ;
Viola, Stefania ;
Loy, Anna ;
Sironi, Marina ;
Vecchi, Annunciata ;
Ravelli, Angelo ;
Martini, Alberto ;
Rubartelli, Anna .
ARTHRITIS AND RHEUMATISM, 2008, 58 (05) :1505-1515
[8]  
Giannini EH, 1997, ARTHRITIS RHEUM, V40, P1202
[9]   Systemic Arthritis in Children: A Review of Clinical Presentation and Treatment [J].
Gurion, R. ;
Lehman, T. J. A. ;
Moorthy, L. N. .
INTERNATIONAL JOURNAL OF INFLAMMATION, 2012, 2012
[10]   Tocilizumab for Systemic Juvenile Idiopathic Arthritis [J].
Hagino, Noboru ;
Yamaguchi, Ken-ichi ;
Ohara, Yuri .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (13) :1256-1256