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  4. Clinical effectiveness and safety experience with alefacept in the treatment of patients with moderate-to-severe chronic plaque psoriasis in Taiwan: Results of an open-label, single-arm, multicentre pilot study
 
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Clinical effectiveness and safety experience with alefacept in the treatment of patients with moderate-to-severe chronic plaque psoriasis in Taiwan: Results of an open-label, single-arm, multicentre pilot study

Journal
Journal of the European Academy of Dermatology and Venereology
Journal Volume
22
Journal Issue
8
Pages
923-930
Date Issued
2008
Author(s)
Huang P.H.
YI-HUA LIAO  
Wei C.C.
Tseng Y.H.
Ho J.C.
TSEN-FANG TSAI  
DOI
10.1111/j.1468-3083.2007.02575.x
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-52249110434&doi=10.1111%2fj.1468-3083.2007.02575.x&partnerID=40&md5=642b908427f8a5b8211251c1df3660b0
https://scholars.lib.ntu.edu.tw/handle/123456789/517703
Abstract
Background: The effectiveness and safety of alefacept for the treatment of moderate-to-severe chronic plaque psoriasis has been established in several clinical trials conducted in the United States and Europe. No clinical trial of alefacept has been conducted in Asia. Objective: To determine the effectiveness and safety of alefacept in the treatment of psoriasis in Chinese population. Design and methods: This was an open-label, single-arm, multicentre pilot study conducted at three centres. Patients with a body surface area ? 10% and psoriasis area and severity Index (PASI) ? 12 were given 15 mg alefacept intramuscularly once a week for 12 weeks and were then followed up for a further 12 weeks. Results: A total of 46 patients was enrolled. Only one subject (2%) achieved a ? 75% improvement in PASI at week 14. The median improvement in PASI at week 14 after the 12-week treatment was 39%. At any time during the 6-month course, 3 subjects (7%) achieved a Physician Global Assessment (PGA) of 'almost clear', and a ? 50% and ? 75% improvement in PASI was seen in 46% and 9%, respectively. There is a trend for decreased counts of CD4+ and CD8+ cells after alefacept treatment, but subjects who achieved PASI50 showed a lesser degree of decrease in CD4+ and CD8+ counts compared with those in patients who did not achieve PASI50. Conclusions: This small pilot study indicated that intramuscular alefacept was effective and safe in psoriasis in Chinese patients over 12 weeks of treatment. Further studies are needed to clarify the reason for low PASI 75 effectiveness and the paradoxical lesser decline of CD4+ and CD8+ T cells in those who responded. ? 2008 The Authors.
SDGs

[SDGs]SDG3

Other Subjects
alefacept; corticosteroid; emollient agent; adolescent; adult; arthralgia; article; Asia; body surface; CD4 lymphocyte count; CD8+ T lymphocyte; cerebrovascular accident; Chinese; clinical article; clinical effectiveness; connective tissue disease; controlled study; disease severity; dizziness; drug withdrawal; female; follow up; headache; human; malaise; male; mouth ulcer; musculoskeletal disease; myalgia; pilot study; polyarthritis; population; priority journal; psoriasis vulgaris; quality of life; rash; sore throat; Taiwan; treatment duration; upper respiratory tract infection; Adolescent; Adult; Dermatologic Agents; Female; Humans; Injections, Intramuscular; Male; Middle Aged; Pilot Projects; Psoriasis; Recombinant Fusion Proteins; Safety; Severity of Illness Index; Taiwan; Treatment Outcome
Type
journal article

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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