TY - JOUR
T1 - Tocilizumab in adult-onset still's disease
T2 - The Israeli experience
AU - Elkayam, Ori
AU - Jiries, Nizar
AU - Dranitzki, Zvi
AU - Kivity, Shay
AU - Lidar, Merav
AU - Levy, Ofer
AU - Ablin, Jacob
AU - Abu-Shakra, Mahmoud
AU - Savargyl-Maman, Hagit
AU - Padova, Hagit
AU - Caspi, Dan
AU - Rosner, Itzhak
PY - 2014/2
Y1 - 2014/2
N2 - Objective. To describe the Israeli experience of treating adult-onset Still's disease (AOSD) with tocilizumab (TCZ). Methods. Israeli rheumatologists who treated AOSD with TCZ filled in questionnaires on symptoms, number of tender and swollen joints, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and dosage of prednisone at initial TCZ administration, after 6 months, and at the end of followup. Results. Nine male and 6 female patients, aged 33 ± 12 years, mean disease duration 9 years (range: 1-25) were identified. They had used a mean of 3.6 disease-modifying drugs, including 10 patients with tumor necrosis factor blockers. Intravenous TCZ 8 mg/kg was administered every 4 weeks (12 patients) or every 2 weeks (3 patients). All patients completed at least 6 months of treatment. The mean followup period was 15.7 ± 9 months. At the onset of therapy, despite the use of prednisone (27.6 ± 26.3 mg/d), all patients reported joint pain. Fever was reported in 9 patients, rash in 7, pleuritis in 3, and hepatitis in 2 before TCZ use, with mean ESR and CRP levels of 60 ± 28 mm/h and 11.6 ± 15 mg/dl, respectively. After 6 months of treatment and at the end of followup, the number of tender and swollen joints, the ESR and CRP levels, and the prednisone dosage decreased significantly. Only 2 patients still complained of mild arthralgias, and none reported systemic symptoms at the end of followup. Conclusion. TCZ 8 mg/kg was extremely efficacious in treating adult patients with refractory Still's disease. Both TCZ and interleukin 1 blockade should be considered in the treatment algorithm of AOSD. Randomized controlled studies are needed to validate these findings. (First Release Jan 15 2014; J Rheumatol 2014;41:244-7; doi:10.3899/jrheum.130881).
AB - Objective. To describe the Israeli experience of treating adult-onset Still's disease (AOSD) with tocilizumab (TCZ). Methods. Israeli rheumatologists who treated AOSD with TCZ filled in questionnaires on symptoms, number of tender and swollen joints, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and dosage of prednisone at initial TCZ administration, after 6 months, and at the end of followup. Results. Nine male and 6 female patients, aged 33 ± 12 years, mean disease duration 9 years (range: 1-25) were identified. They had used a mean of 3.6 disease-modifying drugs, including 10 patients with tumor necrosis factor blockers. Intravenous TCZ 8 mg/kg was administered every 4 weeks (12 patients) or every 2 weeks (3 patients). All patients completed at least 6 months of treatment. The mean followup period was 15.7 ± 9 months. At the onset of therapy, despite the use of prednisone (27.6 ± 26.3 mg/d), all patients reported joint pain. Fever was reported in 9 patients, rash in 7, pleuritis in 3, and hepatitis in 2 before TCZ use, with mean ESR and CRP levels of 60 ± 28 mm/h and 11.6 ± 15 mg/dl, respectively. After 6 months of treatment and at the end of followup, the number of tender and swollen joints, the ESR and CRP levels, and the prednisone dosage decreased significantly. Only 2 patients still complained of mild arthralgias, and none reported systemic symptoms at the end of followup. Conclusion. TCZ 8 mg/kg was extremely efficacious in treating adult patients with refractory Still's disease. Both TCZ and interleukin 1 blockade should be considered in the treatment algorithm of AOSD. Randomized controlled studies are needed to validate these findings. (First Release Jan 15 2014; J Rheumatol 2014;41:244-7; doi:10.3899/jrheum.130881).
KW - Adult-onset still's disease
KW - Biologics
KW - Cytokines
KW - Disease-modifying antirheumatic drugs
KW - Inflammation
UR - http://www.scopus.com/inward/record.url?scp=84893590547&partnerID=8YFLogxK
U2 - 10.3899/jrheum.130881
DO - 10.3899/jrheum.130881
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AN - SCOPUS:84893590547
SN - 0315-162X
VL - 41
SP - 244
EP - 247
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 2
ER -