TY - JOUR
T1 - Safety and effectiveness responses to etanercept for rheumatoid arthritis in Japan
T2 - A sub-analysis of a post-marketing surveillance study focusing on the duration of rheumatoid arthritis
AU - Koike, Takao
AU - Harigai, Masayoshi
AU - Inokuma, Shigeko
AU - Ishiguro, Naoki
AU - Ryu, Junnosuke
AU - Takeuchi, Tsutomu
AU - Tanaka, Yoshiya
AU - Yamanaka, Hisashi
AU - Fujii, Koichi
AU - Yoshinaga, Takunari
AU - Freundlich, Bruce
AU - Suzukawa, Michio
N1 - Funding Information:
Acknowledgments The authors wish to acknowledge the contributions of the late Professor Kazuhiko Inoue, MD, PhD, who participated in this work. The authors wish to thank all participating physicians and registered patients. The Etanercept Post-Marketing Surveillance Committee of the Japan College of Rheumatology was created in response to a request for assistance from the Ministry of Health, Labor, and Welfare (MHLW) of Japan. The role of the committee is to provide independent advice to Wyeth K. K. on the conduct of the Post-Marketing Surveillance Program mandated by the MHLW and on the results thereof. Participation on this committee is not compensated. This manuscript was prepared with the assistance of Joanne Foehl (previously of Pfizer Inc., Global Medical Affairs) and BioMedCom Consultants inc., Montreal, Canada. This study was sponsored by Wyeth (Wyeth was integrated into Pfizer in October 2009), and clinical fees were shared by Wyeth K. K. and Takeda Pharmaceutical Company Limited, Wyeth K. K.’s co-promotion partner for etanercept in Japan.
PY - 2012/6
Y1 - 2012/6
N2 - The aim is to investigate the relationship of duration of rheumatoid arthritis (RA) with safety and effectiveness of etanercept (ETN) in Japan. Post-marketing surveillance data for 7,099 patients treated with ETN were analyzed. Baseline characteristics, treatment effectiveness, incidence of adverse events (AEs), and serious AEs (SAEs) in relation to duration of RA were studied. At baseline, patients with RA for longer duration were older, weighed less, had more comorbidities, allergies, and corticosteroid use, but smoked less and had less morning stiffness. By 2-5 years with RA, more than half of the patients had advanced to Steinbrocker radiographic stage III or IV. Methotrexate (MTX) was the most commonly used pretreatment disease-modifying antirheumatic drug; however, concomitant MTX use and its dose were lower among patients with longer duration of RA. Remission rates (26.6%) were greatest among patients having RA for <2 years. Less AEs and SAEs were observed among patients with shorter duration of RA. These results suggest that RA treatment in Japan in the era pre-biologics may not have been adequate to control disease activity and prevent joint destruction. Patients with shorter duration of RA may have better physical status which allows the opportunity to treat more intensively putting a higher percentage of patients in remission and possibly decreasing exposure to SAEs.
AB - The aim is to investigate the relationship of duration of rheumatoid arthritis (RA) with safety and effectiveness of etanercept (ETN) in Japan. Post-marketing surveillance data for 7,099 patients treated with ETN were analyzed. Baseline characteristics, treatment effectiveness, incidence of adverse events (AEs), and serious AEs (SAEs) in relation to duration of RA were studied. At baseline, patients with RA for longer duration were older, weighed less, had more comorbidities, allergies, and corticosteroid use, but smoked less and had less morning stiffness. By 2-5 years with RA, more than half of the patients had advanced to Steinbrocker radiographic stage III or IV. Methotrexate (MTX) was the most commonly used pretreatment disease-modifying antirheumatic drug; however, concomitant MTX use and its dose were lower among patients with longer duration of RA. Remission rates (26.6%) were greatest among patients having RA for <2 years. Less AEs and SAEs were observed among patients with shorter duration of RA. These results suggest that RA treatment in Japan in the era pre-biologics may not have been adequate to control disease activity and prevent joint destruction. Patients with shorter duration of RA may have better physical status which allows the opportunity to treat more intensively putting a higher percentage of patients in remission and possibly decreasing exposure to SAEs.
KW - Antirheumatic agents/adverse effects
KW - Antirheumatic agents/therapeutic use
KW - Arthritis
KW - Japan
KW - Postmarketing/statistics & numerical data
KW - Product surveillance
KW - Receptors
KW - Rheumatoid/drug therapy
KW - Tumor necrosis factor/therapeutic use
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U2 - 10.1007/s00296-010-1784-8
DO - 10.1007/s00296-010-1784-8
M3 - Article
C2 - 21327436
AN - SCOPUS:84863869931
SN - 0172-8172
VL - 32
SP - 1511
EP - 1519
JO - Rheumatology International
JF - Rheumatology International
IS - 6
ER -