TY - JOUR
T1 - Efficacy of apheresis as maintenance therapy for patients with ulcerative colitis in an open-label prospective multicenter randomised controlled trial
AU - for the CAPTAIN study Group
AU - Naganuma, Makoto
AU - Yokoyama, Yoko
AU - Motoya, Satoshi
AU - Watanabe, Kenji
AU - Sawada, Koji
AU - Hirai, Fumito
AU - Yamamoto, Takayuki
AU - Hanai, Hiroyuki
AU - Omori, Teppei
AU - Kanai, Takanori
AU - Hibi, Toshifumi
AU - Naganuma, Makoto
AU - Sugimoto, Shinya
AU - Nanki, Kosaku
AU - Mizuno, Shinta
AU - Ogata, Haruhiko
AU - Nagase, Kazuko
AU - Nakamura, Shiro
AU - Tanaka, Hiroki
AU - Nasuno, Masanao
AU - Miyagawa, Maki
AU - Shimoyama, Takahiro
AU - Ikeya, Kentaro
AU - Itoh, Ayumi
AU - Yokoyama, Kaoru
AU - Mitsuyama, Keiichi
AU - Yamazaki, Hiroshi
AU - Sakata, Yasuhisa
AU - Yoshimura, Naoki
AU - Shirai, Takayuki
AU - Suzuki, Yasuo
AU - Matsuura, Minoru
AU - Tanaka, Shinji
AU - Hayashi, Kohei
AU - Ueno, Yositaka
AU - Sakemi, Ryosuke
AU - Ishiguro, Yo
AU - Yoshida, Atsushi
AU - Endo, Yutaka
AU - Yamagami, Hirokazu
AU - Sakurai, Toshiharu
AU - Iwabuchi, Masahiro
AU - Sugimura, Mikako
AU - Iizuka, Masahiro
AU - Nagino, Ko
AU - Kobayashi, Taku
AU - Ohnishi, Kunio
AU - Yoshino, Takuya
AU - Ohmori, Toshihide
AU - Teramoto, Tadashi
N1 - Funding Information:
We would like to thank the late Professor Takayuki Matsumoto (Hyogo College of Medicine) for his significant contribution to the study protocol. We would also like to thank Editage (http://www.editage.jp) for English language editing and Dr. Kiyoso Yamataga (Kureha Special Laboratory, Tokyo, Japan) for the statistical analysis. Members in the CAPTAIN Study Group are Makoto Naganuma, Shinya Sugimoto, Kosaku Nanki, Shinta Mizuno, Haruhiko Ogata, Takanori Kanai (Keio University School of Medicine), Yoko Yokoyama, Kenji Watanabe, Kazuko Nagase, Shiro Nakamura (Hyogo College of Medicine), Satoshi Motoya, Hiroki Tanaka, Masanao Nasuno, Maki Miyagawa (Sapporo Kosei General Hospital), Koji Sawada (Dojima General and Gastroenterology Clinic), Fumito Hirai (Fukuoka University Chikushi Hospital), Takayuki Yamamoto, Takahiro Shimoyama (Yokkaichi Hazu Medical Center), Kentaro Ikeya, Hiroyuki Hanai (Hamamatsu South Hospital), Ayumi Itoh, Teppei Omori (Tokyo Women’s Medical University), Kaoru Yokoyama (Kitasato University), Keiichi Mitsuyama, Hiroshi Yamazaki (Kurume University School of Medicine), Yasuhisa Sakata (Saga Universtiy), Naoki Yoshimura (Tokyo Yamate Medical Center), Takayuki Shirai (Tokai University Hachioji Hospital), Yasuo Suzuki (Toho University Sakura Medical Center), Minoru Matsuura (Kyoto University), Shinji Tanaka, Kohei Hayashi, Yositaka Ueno (Hiroshima University), Ryosuke Sakemi (Tobata Kyoritsu Hospital), Yo Ishiguro (Hirosaki National Hospital), Atsushi Yoshida, Yutaka Endo (Ofuna Chuo Hospital), Hirokazu Yamagami (Osaka City Universtiy), Toshiharu Sakurai (Kindai University), Masahiro Iwabuchi, Mikako Sugimura (Sendai Medical Center), Masahiro Iizuka (Akita Red Cross Hospital). Ko Nagino (Yamagata City Hospital Saiseikan), Taku Kobayashi, Toshifumi Hibi (Kitasato University Kitasato Institute Hospital), Kunio Ohnishi (Ikoma Clinic), Takuya Yoshino (Kitano Hospital), Toshihide Ohmori (Toshihide Ohmori Gastrointestinal Clinic), Tadashi Teramoto (Machida Gastrointestinal Hospital).
Publisher Copyright:
© 2019, Japanese Society of Gastroenterology.
PY - 2020/4/1
Y1 - 2020/4/1
N2 - Background: Apheresis therapy involves the selective removal of leukocytes and is used to induce remission in ulcerative colitis (UC) patients. The aim of this study was to demonstrate the efficacy and safety of apheresis therapy for maintaining UC remission. Methods: We conducted a multicenter, prospective, randomised-control trial of patients with remitting UC induced by granulocyte and monocyte adsorption apheresis or leukocytapheresis. Patients were randomly assigned to the apheresis group (twice per month for 12 months) or the control group (no apheresis treatment) using a 1:1 allocation ratio. The primary endpoint was the rate of cumulative clinical remission (Mayo score ≤ 2) at 12 months. The secondary endpoints were the rates of clinical remission, endoscopic remission, and complete endoscopic remission at 12 months. Results: Between March 2013 and March 2017, 164 patients were enrolled. The cumulative remission rate at 12 months was 46.6% in the apheresis group and 36.4% in the control group (p = 0.1621). The rate of endoscopic remission at 12 months was significantly higher in the apheresis group than in the control group (42.5% vs. 25.9%) p = 0.0480). The rate of clinical remission (47.5% vs.32.1%, p = 0.0540) and complete endoscopic remission (33.8% vs.19.8%, p = 0.0513) tended to be higher in the apheresis than in the control group; however, the difference was not significant. No severe adverse events were observed in either group. Conclusions: Apheresis was well tolerated as maintenance therapy for UC although the cumulative clinical remission rate at 12 months was comparable between the apheresis and control groups.
AB - Background: Apheresis therapy involves the selective removal of leukocytes and is used to induce remission in ulcerative colitis (UC) patients. The aim of this study was to demonstrate the efficacy and safety of apheresis therapy for maintaining UC remission. Methods: We conducted a multicenter, prospective, randomised-control trial of patients with remitting UC induced by granulocyte and monocyte adsorption apheresis or leukocytapheresis. Patients were randomly assigned to the apheresis group (twice per month for 12 months) or the control group (no apheresis treatment) using a 1:1 allocation ratio. The primary endpoint was the rate of cumulative clinical remission (Mayo score ≤ 2) at 12 months. The secondary endpoints were the rates of clinical remission, endoscopic remission, and complete endoscopic remission at 12 months. Results: Between March 2013 and March 2017, 164 patients were enrolled. The cumulative remission rate at 12 months was 46.6% in the apheresis group and 36.4% in the control group (p = 0.1621). The rate of endoscopic remission at 12 months was significantly higher in the apheresis group than in the control group (42.5% vs. 25.9%) p = 0.0480). The rate of clinical remission (47.5% vs.32.1%, p = 0.0540) and complete endoscopic remission (33.8% vs.19.8%, p = 0.0513) tended to be higher in the apheresis than in the control group; however, the difference was not significant. No severe adverse events were observed in either group. Conclusions: Apheresis was well tolerated as maintenance therapy for UC although the cumulative clinical remission rate at 12 months was comparable between the apheresis and control groups.
KW - Endoscopic remission
KW - Granulocyte and monocyte adsorption apheresis
KW - Leukocytapheresis ulcerative colitis
KW - Maintenance therapy
UR - http://www.scopus.com/inward/record.url?scp=85076304024&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076304024&partnerID=8YFLogxK
U2 - 10.1007/s00535-019-01651-0
DO - 10.1007/s00535-019-01651-0
M3 - Article
C2 - 31811562
AN - SCOPUS:85076304024
SN - 0944-1174
VL - 55
SP - 390
EP - 400
JO - Journal of gastroenterology
JF - Journal of gastroenterology
IS - 4
ER -