Matching-Adjusted Indirect Comparison of Long-Term Efficacy and Safety Outcomes for Calcipotriol Plus Betamethasone Dipropionate Foam Versus Halobetasol Proprionate Plus Tazarotene Lotion in the Treatment of Plaque Psoriasis

被引:2
|
作者
Adam, David N. [1 ,2 ,3 ]
Bernasconi, Marie Y. Jablonski [4 ]
Thoning, Henrik [4 ]
Wu, Jashin J. [5 ]
机构
[1] Univ Toronto, Temerty Dept Med, Div Dermatol, Toronto, ON, Canada
[2] CCA Med Res, Ajax, ON, Canada
[3] Prob Med Res, Waterloo, ON, Canada
[4] Leo Pharma, Ballerup, Denmark
[5] Univ Miami, Miller Sch Med, Dept Dermatol, Miami, FL 33136 USA
关键词
Betamethasone dipropionate; Calcipotriol; Foam; Halobetasol propionate; Psoriasis; Tazarotene; SUPERIOR EFFICACY; AEROSOL FOAM; MANAGEMENT; ARTHRITIS; VULGARIS; QUALITY;
D O I
10.1007/s13555-022-00824-9
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction To date, there have been no head-to-head clinical studies comparing calcipotriol 0.005% plus betamethasone dipropionate 0.064% (Cal/BD) aerosol foam and halobetasol propionate 0.01% plus tazarotene 0.045% (HP/Taz) lotion for the treatment of plaque psoriasis. However, the efficacy of 4 weeks of Cal/BD foam and 8 weeks of HP/Taz lotion has been compared using a matching-adjusted indirect comparison (MAIC) approach. Here, we compare the efficacy and safety of Cal/BD foam and HP/Taz lotion for up to 52 weeks. Methods An unanchored MAIC was conducted using individual patient data from the PSO-LONG Cal/BD foam trial and a 52-week, open-label phase 3 study of HP/Taz lotion (NCT02462083). Key outcomes of interest were Physician's Global Assessment (PGA) success (PGA 0/1 with >= 2-point improvement) after 4 or 8 weeks of open-label therapy; the proportion of patients who had body surface area affected (BSA) <= 3 after open-label therapy who maintained BSA <= 3 to week 52; and adverse events (AEs). Results After matching, patients were statistically significantly more likely to have PGA success after 4 weeks of Cal/BD foam than after 8 weeks of HP/Taz lotion (84.5% versus 54.4%; p < 0.01). At week 52, 92.5% and 92.4% of patients receiving proactive and reactive Cal/BD foam, respectively, maintained BSA <= 3, compared with 49.3% of those treated with HP/Taz lotion (both p < 0.01). Treatment-related AEs, AEs leading to withdrawal, and AEs associated with drug application (dermatitis, application site pain, and pruritus) were significantly rarer with Cal/BD foam than with HP/Taz lotion (all p < 0.01). Conclusions Cal/BD aerosol foam demonstrated significantly greater efficacy than HP/Taz lotion, and had a more favorable safety profile, compared with HP/Taz lotion, for up to 52 weeks. Proactive Cal/BD foam maintenance therapy and reactive use of Cal/BD foam following relapse both had significant advantages over HP/Taz lotion.
引用
收藏
页码:2589 / 2600
页数:12
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