TY - JOUR
T1 - An open-label prospective randomized multicenter study shows very rapid remission of ulcerative colitis by intensive granulocyte and monocyte adsorptive apheresis as compared with routine weekly treatment
AU - Sakuraba, Atsushi
AU - Motoya, Satoshi
AU - Watanabe, Kenji
AU - Nishishita, Masakazu
AU - Kanke, Kazunari
AU - Matsui, Toshiyuki
AU - Suzuki, Yasuo
AU - Oshima, Tadayuki
AU - Kunisaki, Reiko
AU - Matsumoto, Takayuki
AU - Hanai, Hiroyuki
AU - Fukunaga, Ken
AU - Yoshimura, Naoki
AU - Chiba, Toshimi
AU - Funakoshi, Shinsuke
AU - Aoyama, Nobuo
AU - Andoh, Akira
AU - Nakase, Hiroshi
AU - Mizuta, Yohei
AU - Suzuki, Ryoichi
AU - Akamatsu, Taiji
AU - Iizuka, Masahiro
AU - Ashida, Toshifumi
AU - Hibi, Toshifumi
PY - 2009/12
Y1 - 2009/12
N2 - OBJECTIVES: Granulocyte and monocyte adsorptive apheresis (GMA) has shown efficacy in patients with active ulcerative colitis (UC). However, with routine weekly treatment, it may take several weeks to achieve remission, and to date, the efficacy of a more frequent treatment schedule remains unknown. The aim of this study was to assess the clinical efficacy and safety of intensive GMA treatment in patients with active UC. METHODS: This was an open-label, prospective, randomized multicenter study to compare an intensive, two GMA sessions per week, with the routine, one GMA session per week. A total of 163 patients with mild-to-moderately active UC were randomly assigned to routine weekly treatment or intensive treatment. The maximum number of sessions of GMA permitted was 10. However, when patients achieved remission, GMA was discontinued. Remission rate at the end of the study, time to remission, and adverse events were assessed in both groups. RESULTS: Of the 163 patients, 149 were available for efficacy analysis as per protocol, 76 were in weekly GMA, and 73 were in intensive GMA. At the end of the study period, clinical remission was achieved in 41 of 76 patients (54.0%) in weekly GMA and in 52 of 73 patients (71.2%) in intensive GMA (P0.029). The mean time to remission was 28.116.9 days in the weekly GMA treatment group and 14.99.5 days in the intensive GMA group (P0.0001). Intensive GMA was well tolerated without GMA-related serious adverse side effects. CONCLUSIONS: Intensive GMA in patients with active UC seems to be more efficacious than weekly treatment, and significantly reduced the patients' morbidity time without increasing the incidence of side effects.
AB - OBJECTIVES: Granulocyte and monocyte adsorptive apheresis (GMA) has shown efficacy in patients with active ulcerative colitis (UC). However, with routine weekly treatment, it may take several weeks to achieve remission, and to date, the efficacy of a more frequent treatment schedule remains unknown. The aim of this study was to assess the clinical efficacy and safety of intensive GMA treatment in patients with active UC. METHODS: This was an open-label, prospective, randomized multicenter study to compare an intensive, two GMA sessions per week, with the routine, one GMA session per week. A total of 163 patients with mild-to-moderately active UC were randomly assigned to routine weekly treatment or intensive treatment. The maximum number of sessions of GMA permitted was 10. However, when patients achieved remission, GMA was discontinued. Remission rate at the end of the study, time to remission, and adverse events were assessed in both groups. RESULTS: Of the 163 patients, 149 were available for efficacy analysis as per protocol, 76 were in weekly GMA, and 73 were in intensive GMA. At the end of the study period, clinical remission was achieved in 41 of 76 patients (54.0%) in weekly GMA and in 52 of 73 patients (71.2%) in intensive GMA (P0.029). The mean time to remission was 28.116.9 days in the weekly GMA treatment group and 14.99.5 days in the intensive GMA group (P0.0001). Intensive GMA was well tolerated without GMA-related serious adverse side effects. CONCLUSIONS: Intensive GMA in patients with active UC seems to be more efficacious than weekly treatment, and significantly reduced the patients' morbidity time without increasing the incidence of side effects.
UR - http://www.scopus.com/inward/record.url?scp=72949090370&partnerID=8YFLogxK
U2 - 10.1038/ajg.2009.453
DO - 10.1038/ajg.2009.453
M3 - 学術論文
C2 - 19724269
AN - SCOPUS:72949090370
SN - 0002-9270
VL - 104
SP - 2990
EP - 2995
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 12
ER -