• 1. Department of Dermatology, The First Hospital of China Medical University, Key Laboratory of Immunodermatology, Ministry of Health, Shenyang 110001, China; 2. Department of Emergence, Shengjing Hospital of China Medical University, Shenyang 110001, China;3. Department of Dermatology, Dalian Economic and Technological Development District Hospital, Dalian 116600, China;
GAO Xinghua, Email: gaobarry@hotmail.com
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Objective  To assess the efficacy and safety of adalimumab on plaque psoriasis.
Methods  We searched the MEDLINE (1966 to December 2009), Cochrane Central Register of Controlled Trials (The Cochrane Library, Issue 12, 2009), EMbase (1980 to December 2009), CBM (1978 to December 2009), and CNKI (1979 to December 2009) to collect randomized controlled trials (RCTs) of adalimumab for plaque psoriasis. The language was confined to English and Chinese. We screened the retrieved studies according to the predefined inclusion and exclusion criteria, evaluated the quality of included studies, and performed meta-analyses by using the Cochrane Collaboration’s RevMan 4.2 software.
Results  Three RCTs involving 1?630 patients with chronic moderate or severe plaque psoriasis were included and assessed. At the end of 4th, 8th, 12th and 16th week, the PASI 75s of subcutaneous injection every other week in adalimumab (EOW) group were obviously higher than that of placebo group and methotrexate group. While at the end of 24th week and 60th week, the PASI 75s showed no difference between adalimumab EOW and placebo group. Twelve weeks after subcutaneous injection each week with adalimumab (QW), PASI 75 was obviously higher than those of placebo and EOW groups. However, at the end of 24th week and 60th week, there was no significant difference between adalimumab QW and placebo followed by adalimumab EOW. At end of week 12-16, there was no difference between adalimumab EOW group and placebo group in the incidence of adverse effects, with the exception of pain on injection site and upper respiration viral infection. At week 12-60, there was no difference between adalimumab QW and EOW groups in the incidence of adverse effects, with the exception of all serious adverse effects.
Conclusion  The limited evidence indicates that subcutaneous injection of adalimumab every other week for 12-16 weeks is safe and efficient for patients with moderate or severe plaque psoriasis. The efficacy can’t be enhanced when the treatment is prolonged to 24 weeks. The once-a-week protocol has no obvious advantage over every other week protocol. More RCTs are required to verify these conclusions owing to the limitations of the present study.

Citation: SUN Yan,WU Yan,CHEN Lianghong,LIU Yubo,GAO Xinghua. Efficacy and Safety of Adalimumab for Plaque Psoriasis: A Systematic Review. Chinese Journal of Evidence-Based Medicine, 2010, 10(9): 1085-1095. doi: 10.7507/1672-2531.20100549 Copy

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