Randomized comparison of the type 4 phosphodiesterase inhibitor cipamfylline cream, cream vehicle and hydrocortisone 17-butyrate cream for the treatment of atopic dermatitis

被引:40
作者
Griffiths, CEM
Van Leent, EJM
Gilbert, M
Traulsen, J
机构
[1] Univ Manchester, Hope Hosp, Dermatol Ctr, Salford M6 8HD, Lancs, England
[2] Univ Amsterdam, Acad Med Ctr, Dept Dermatol, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Laval, Hop Enfant Jesus, Dermatol Serv, Quebec City, PQ, Canada
[4] Leo Pharmaceut Prod, DK-2750 Ballerup, Denmark
关键词
atopic dermatitis; cipamfylline; hydrocortisone; 17-butyrate;
D O I
10.1046/j.1365-2133.2002.04894.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Therapeutic options to treat atopic dermatitis are limited. Leukocytes from atopic patients have an abnormally high activity of cyclic adenosine monophosphate (AMP)-phosphodiesterase (PDE), which can be normalized in vitro by PDE inhibitors. Cipamfylline is a new potent and selective inhibitor of PDE-4. Objectives To compare the efficacy and safety of up to 14 days' topical treatment with cipamfylline (0.15%) cream with vehicle and with hydrocortisone 17-butyrate (0.1%) cream. Patient and methods International, multicentre, prospective, randomized double-blind, left-right studies of cipamfylline vs. vehicle and cipamfylline vs. hydrocortisone 17-butyrate in adult patients with stable symmetrical atopic dermatitis on the arms. Results Both cipamfylline and hydrocortisone 17-butyrate reduced the Total Severity Score significantly (P < 0.001). The reduction with cipamfylline was significantly greater than that with vehicle (difference vehicle-cipamfylline 1.67 95% confidence interval (CI) 1.06, 2.28; P < 0.001) and was significantly less than with hydrocortisone 17-butyrate (difference hydrocortisone-cipamfylline -2.10 95% CI -2.93, -1.27; P < 0.001). Investigator and patient assessments of the overall treatment response showed a similar picture. Conclusions Cipamfylline cream is significantly more effective than vehicle, but significantly less effective than hydrocortisone 17-butyrate cream in the treatment of atopic dermatitis.
引用
收藏
页码:299 / 307
页数:9
相关论文
共 20 条
[1]  
[Anonymous], ACTA DERM VENERE S92, DOI [10.2340/00015555924447, DOI 10.2340/00015555924447]
[2]   INCREASED LEUKOCYTE HISTAMINE-RELEASE WITH ELEVATED CYCLIC AMP-PHOSPHODIESTERASE ACTIVITY IN ATOPIC-DERMATITIS [J].
BUTLER, JM ;
CHAN, SC ;
STEVENS, S ;
HANIFIN, JM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1983, 71 (05) :490-497
[3]   INCREASED INTERLEUKIN-4 PRODUCTION BY ATOPIC MONONUCLEAR LEUKOCYTES CORRELATES WITH INCREASED CYCLIC ADENOSINE-MONOPHOSPHATE PHOSPHODIESTERASE ACTIVITY AND IS REVERSIBLE BY PHOSPHODIESTERASE INHIBITION [J].
CHAN, SC ;
LI, SH ;
HANIFIN, JM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 100 (05) :681-684
[4]  
Coleman R, 1997, BRIT J DERMATOL, V136, P1
[5]   PHOSPHODIESTERASE INHIBITION BY RO 20-1724 REDUCES HYPER-IGE SYNTHESIS BY ATOPIC-DERMATITIS CELLS-INVITRO [J].
COOPER, KD ;
KANG, K ;
CHAN, SC ;
HANIFIN, JM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1985, 84 (06) :477-482
[6]  
*CYT SOFTW CORP, 1992, STATX STAT SOFTW EX
[7]   ELEVATED LEUKOCYTE CYCLIC-AMP PHOSPHODIESTERASE IN ATOPIC DISEASE - A POSSIBLE MECHANISM FOR CYCLIC-AMP AGONIST HYPORESPONSIVENESS [J].
GREWE, SR ;
CHAN, SC ;
HANIFIN, JM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1982, 70 (06) :452-457
[8]  
Hanifin J, 1996, DERMATOL THER, V1, P9
[9]   Type 4 phosphodiesterase inhibitors have clinical and in vitro anti-inflammatory effects in atopic dermatitis [J].
Hanifin, JM ;
Chan, SC ;
Cheng, JB ;
Tofte, SJ ;
Henderson, WR ;
Kirby, DS ;
Weiner, ES .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (01) :51-56
[10]   MONOCYTE PHOSPHODIESTERASE ABNORMALITIES AND DYSREGULATION OF LYMPHOCYTE FUNCTION IN ATOPIC-DERMATITIS [J].
HANIFIN, JM ;
CHAN, SC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (01) :S84-S88