TY - JOUR
T1 - A multicenter phase II prospective clinical trial of glucocorticoid for patients with untreated IgG4-related disease
AU - Masaki, Yasufumi
AU - Matsui, Shoko
AU - Saeki, Takako
AU - Tsuboi, Hiroto
AU - Hirata, Shintaro
AU - Izumi, Yasumori
AU - Miyashita, Taiichiro
AU - Fujikawa, Keita
AU - Dobashi, Hiroaki
AU - Susaki, Kentaro
AU - Morimoto, Hisanori
AU - Takagi, Kazutaka
AU - Kawano, Mitsuhiro
AU - Origuchi, Tomoki
AU - Wada, Yoko
AU - Takahashi, Naoki
AU - Horikoshi, Masanobu
AU - Ogishima, Hiroshi
AU - Suzuki, Yasunori
AU - Kawanami, Takafumi
AU - Kawanami Iwao, Haruka
AU - Sakai, Tomoyuki
AU - Fujita, Yoshimasa
AU - Fukushima, Toshihiro
AU - Saito, Masatoshi
AU - Suzuki, Ritsuro
AU - Morikawa, Yuko
AU - Yoshino, Tadashi
AU - Nakamura, Shigeo
AU - Kojima, Masaru
AU - Kurose, Nozomu
AU - Sato, Yasuharu
AU - Tanaka, Yoshiya
AU - Sugai, Susumu
AU - Sumida, Takayuki
N1 - Publisher Copyright:
© 2016 Japan College of Rheumatology.
PY - 2017/9/3
Y1 - 2017/9/3
N2 - Objective: Although glucocorticoids are effective for patients with IgG4-related disease, the treatment has not yet been standardized. Therefore, the treatment strategy should be established. Patients and methods: Patients who fulfilled the comprehensive diagnostic criteria for definite IgG4-related disease were started on prednisolone (0.6 mg/kg body weight) with the dose reduced every two weeks. The subsequent maintenance dose and need for prednisolone were determined for individual patients. The primary endpoint was the complete remission (CR) rate at one year. Secondary endpoints included overall response rate (ORR), the maintenance dose, the relapse rate, and adverse events. Results: This study enrolled 61 patients. After clinicopathological review, three patients were excluded, and one, 13, and 44 patients were diagnosed with probable, possible, and definite IgG4-related disease, respectively. Of the 44 patients with definite IgG4-RD, 29 (65.9%) achieved CR, and the ORR was 93.2%. No patient was refractory to primary treatment. The most frequent adverse events were glucose intolerance. Six patients relapsed. Conclusions: Glucocorticoid treatment is usually effective for patients with IgG4-RD, and we should examine the possibility of other disorders when a patient is glucocorticoid refractory. Some patients are misdiagnosed, making central clinicopathological review of diagnosis very important in conducting clinical studies.
AB - Objective: Although glucocorticoids are effective for patients with IgG4-related disease, the treatment has not yet been standardized. Therefore, the treatment strategy should be established. Patients and methods: Patients who fulfilled the comprehensive diagnostic criteria for definite IgG4-related disease were started on prednisolone (0.6 mg/kg body weight) with the dose reduced every two weeks. The subsequent maintenance dose and need for prednisolone were determined for individual patients. The primary endpoint was the complete remission (CR) rate at one year. Secondary endpoints included overall response rate (ORR), the maintenance dose, the relapse rate, and adverse events. Results: This study enrolled 61 patients. After clinicopathological review, three patients were excluded, and one, 13, and 44 patients were diagnosed with probable, possible, and definite IgG4-related disease, respectively. Of the 44 patients with definite IgG4-RD, 29 (65.9%) achieved CR, and the ORR was 93.2%. No patient was refractory to primary treatment. The most frequent adverse events were glucose intolerance. Six patients relapsed. Conclusions: Glucocorticoid treatment is usually effective for patients with IgG4-RD, and we should examine the possibility of other disorders when a patient is glucocorticoid refractory. Some patients are misdiagnosed, making central clinicopathological review of diagnosis very important in conducting clinical studies.
KW - 18FDG-PET
KW - Glucocorticoid
KW - Lymphoma
KW - Multicentric Castleman's disease
KW - Prospective trial
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U2 - 10.1080/14397595.2016.1259602
DO - 10.1080/14397595.2016.1259602
M3 - Article
C2 - 27846767
AN - SCOPUS:85006127287
SN - 1439-7595
VL - 27
SP - 849
EP - 854
JO - Japanese Journal of Rheumatology
JF - Japanese Journal of Rheumatology
IS - 5
ER -