TY - JOUR
T1 - Comparison of combination therapy of prednisolone and cyclosporine with corticosteroid pulse therapy in Vogt–Koyanagi–Harada disease
AU - The Japan VKH Disease Treatment Study Group
AU - Ono, Takashi
AU - Goto, Hiroshi
AU - Sakai, Tsutomu
AU - Nitta, Fumihiko
AU - Mizuki, Nobuhisa
AU - Takase, Hiroshi
AU - Kaneko, Yutaka
AU - Hori, Junko
AU - Nakano, Satoko
AU - Nao-I, Nobuhisa
AU - Ohguro, Nobuyuki
AU - Miyata, Kazunori
AU - Tomita, Makoto
AU - Mochizuki, Manabu
AU - Mochizuki, Manabu
AU - Komizo, Takashi
AU - Miyata, Kazurori
AU - Umazume, Akihiko
AU - Usui, Yoshihiko
AU - Kohno, Hideo
AU - Aoyagi, Ranko
AU - Maruyama, Kazuichi
AU - Shibuya, Etsuko
AU - Ida, Yasutsugu
AU - Horie, Shintaro
AU - Ide, Mitsunao
AU - Iwasaki, Yuko
AU - Kamoi, Koju
AU - Terada, Yukiko
AU - Yui, Tomoko
AU - Takeda, Ayaka
N1 - Funding Information:
A list of Study Group Members and Safety and Efficacy Monitoring Committee Members are Miyata Eye Hospital, Miyakonojo, Japan: Manabu Mochizuki, MD, PhD, Takashi Ono, MD, Takashi Komizo, MD, Kazurori Miyata, MD, PhD; Department of Ophthalmology, Tokyo Medical University, Tokyo, Japan: Hiroshi Goto, MD, PhD, Akihiko Umazume, MD, PhD, Yoshihiko Usui, MD, PhD; Department of Ophthalmology, Jikei University School of Medicine, Tokyo, Japan: Tsutomu Sakai, MD, PhD, Hideo Kohno, MD, Ranko Aoyagi, MD; Department of Ophthalmology and Visual Science, Tohoku University Graduate School of Medicine, Sendai, Japan: Fumihiko Nitta, MD, PhD, Kazuichi Maruyama, MD, PhD; Department of Ophthalmology, Yokohama City University School of Medicine, Yokohama, Japan: Nobuhisa Mizuki, MD, PhD, Etsuko Shibuya, MD, Yasutsugu Ida, MD; Department of Ophthalmology & Visual Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan: Hiroshi Takase, MD, PhD, Shintaro Horie, MD, PhD, Mitsunao Ide, MD, Yuko Iwasaki, MD, PhD, Koju Kamoi, MD, PhD, Yukiko Terada, MD; Department of Ophthalmology and Visual Sciences, Yamagata University Faculty of Medicine, Yamagata, Japan: Yutaka Kaneko, MD, PhD; Department of Ophthalmology, Nippon Medical School, Tokyo, Japan: Junko Hori, MD, PhD, Tomoko Yui, MD, Ayaka Takeda, MD; Department of Ophthalmology, Oita University, Faculty of Medicine, Oita, Japan: Satoko Nakano, MD, PhD; Department of Ophthalmology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan: Nobuhisa Nao-I, MD, PhD; Department of Ophthalmology, Japan Community Health Care Organization Osaka Hospital, Osaka, Japan: Nobuyuki Ohguro, MD, PhD; School of Data Science, Yokohama City University, Kanagawa, Japan: Makoto Tomita, PhD; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan: Ko-hei Sonoda, MD, PhD; Department of Ophthalmology, Japan Community Health Care Organization Tokyo Shinjuku Medical Center, Tokyo, Japan: Yujiro Fujino, MD, PhD; Biostatistical Research Corporation, Tokyo, Japan: Toshihito Furukawa, PhD; Department of Renal Transplantation, Masuko Memorial Hospital, Nagoya, Japan: Kunio Morozumi, MD, PhD. And also a list of Study Group Members and Safety and Efficacy Monitoring Committee Members is available online. The authors are grateful for the support of the Safety and Efficacy Monitoring Committee members, including Koh-Hei Sonoda, M.D., PhD. (Kyushu University); Yujiro Fujino, M.D., Ph.D. (Japan Community Health Care Organization Tokyo Shinjuku Medical Center); Toshihito Furukawa, Ph.D. (Biostatistical Research Corporation); and Kunio Morozumi, M.D., Ph.D. (Masuko Memorial Hospital).
Publisher Copyright:
© 2021, Japanese Ophthalmological Society.
PY - 2022/3
Y1 - 2022/3
N2 - Purpose: To compare the efficacy and safety of a combination therapy of prednisolone and cyclosporine and corticosteroid pulse therapy in Vogt–Koyanagi–Harada (VKH) disease. Study design: A prospective, multicenter, randomized, non-inferiority trial. Methods: Patients of new-onset acute VKH disease at 11 centers in Japan between 2014 and 2018 were randomized to a combination (oral prednisolone 60 mg daily with gradual taper-off to 35 mg/day and cyclosporine 3 mg/kg/day) and corticosteroid (methylprednisolone 1000 mg for 3 days followed by oral prednisolone) groups, and were followed for 1 year. Results: Thirty-four were assigned to the combination and thirty-six patients to the corticosteroid group. Recurrence/worsening risk was 0.15 (95% confidence-interval [CI] 0.03–0.27) in the combination group and 0.25 (95% CI 0.11–0.39) in the corticosteroid group, with a risk difference of − 0.10 (90% CI − 0.27 to 0.06), demonstrating non-inferiority of the combination group with a non-inferiority margin of 0.20 (P = 0.0013). Serious adverse events occurred in three patients (two with hyponatremia and one with severe headaches) in the combination group and none in the corticosteroid group. Sunset glow fundus grades and cataract rates at 1 year were 0.57 (95% CI 0.42–71) and 4.3% in the combination group and 0.91 (95% CI 0.78–1.04) and 34.0% in the corticosteroid group, respectively. Conclusions: Combination therapy was noninferior to corticosteroid therapy with respect to recurrence/worsening risk. Notably, the recurrence/worsening risk, sunset glow fundus grade, and cataract rate were lower in the combination group than in the corticosteroid group.
AB - Purpose: To compare the efficacy and safety of a combination therapy of prednisolone and cyclosporine and corticosteroid pulse therapy in Vogt–Koyanagi–Harada (VKH) disease. Study design: A prospective, multicenter, randomized, non-inferiority trial. Methods: Patients of new-onset acute VKH disease at 11 centers in Japan between 2014 and 2018 were randomized to a combination (oral prednisolone 60 mg daily with gradual taper-off to 35 mg/day and cyclosporine 3 mg/kg/day) and corticosteroid (methylprednisolone 1000 mg for 3 days followed by oral prednisolone) groups, and were followed for 1 year. Results: Thirty-four were assigned to the combination and thirty-six patients to the corticosteroid group. Recurrence/worsening risk was 0.15 (95% confidence-interval [CI] 0.03–0.27) in the combination group and 0.25 (95% CI 0.11–0.39) in the corticosteroid group, with a risk difference of − 0.10 (90% CI − 0.27 to 0.06), demonstrating non-inferiority of the combination group with a non-inferiority margin of 0.20 (P = 0.0013). Serious adverse events occurred in three patients (two with hyponatremia and one with severe headaches) in the combination group and none in the corticosteroid group. Sunset glow fundus grades and cataract rates at 1 year were 0.57 (95% CI 0.42–71) and 4.3% in the combination group and 0.91 (95% CI 0.78–1.04) and 34.0% in the corticosteroid group, respectively. Conclusions: Combination therapy was noninferior to corticosteroid therapy with respect to recurrence/worsening risk. Notably, the recurrence/worsening risk, sunset glow fundus grade, and cataract rate were lower in the combination group than in the corticosteroid group.
KW - Corticosteroid pulse therapy
KW - Cyclosporine
KW - Recurrence or worsening risk
KW - Sunset-glow fundus
KW - Vogt–Koyanagi–Harada disease
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U2 - 10.1007/s10384-021-00878-w
DO - 10.1007/s10384-021-00878-w
M3 - Article
C2 - 34689288
AN - SCOPUS:85125551109
SN - 0021-5155
VL - 66
SP - 119
EP - 129
JO - Japanese Journal of Ophthalmology
JF - Japanese Journal of Ophthalmology
IS - 2
ER -