Collagenase Clostridium Histolyticum for the Treatment of Edematous Fibrosclerotic Panniculopathy (Cellulite): A Randomized Trial

被引:31
作者
Sadick, Neil S. [1 ]
Goldman, Mitchel P. [2 ,3 ,4 ]
Liu, Genzhou [5 ]
Shusterman, Neil H. [6 ]
McLane, Michael P. [7 ]
Hurley, David [8 ]
Young, V. Leroy [9 ]
机构
[1] Cornell Univ, Weill Cornell Med Coll, Dept Dermatol, 911 Pk Ave,Suite 1A, New York, NY 10075 USA
[2] Cosmet Laser Dermatol, San Diego, CA USA
[3] Univ Calif San Diego, Dept Dermatol, San Diego, CA 92103 USA
[4] West Dermatol, Irvine, CA USA
[5] Endo Pharmaceut Inc, Biostat, Malvern, PA USA
[6] Endo Pharmaceut Inc, Res & Dev, Malvern, PA USA
[7] Endo Pharmaceut Inc, Clin Dev, Malvern, PA USA
[8] Endo Pharmaceut Inc, Med Affairs, Malvern, PA USA
[9] Mercy Res, Washington, MO USA
关键词
SUBCISION; TISSUE;
D O I
10.1097/DSS.0000000000001803
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BACKGROUND Edematous fibrosclerotic panniculopathy (EFP; cellulite) is associated with thickening and contraction of collagen-rich subdermal septae. Collagenase clostridium histolyticum (CCH) may disrupt collagen-rich septae. OBJECTIVE To evaluate the safety and efficacy of CCH for treatment of EFP. MATERIALS AND METHODS In a randomized, double-blind study, women with moderate or severe EFP of the buttocks or posterolateral thighs (i.e., Clinician Reported Photonumeric Cellulite Severity Scale [CR-PCSS] and Patient Reported Photonumeric Cellulite Severity Scale [PR-PCSS] ratings of 3 to 4, and Hexsel Cellulite Severity Scale score <= 13) received up to 3 treatment sessions (Days 1, 22, and 43) of subcutaneous CCH 0.84 mg or placebo injections. End points included the percentage of 2-level and 1-level composite responders (i.e., had >= 2-level or >= 1-level improvement in CR-PCSS and PR-PCSS) at Day 71. RESULTS Three hundred seventy-five women (mean age, 46.5 years; 86.4% white) were randomly assigned to CCH (n = 189) or placebo (n = 186). At Day 71, the percentages of 2-level and 1-level composite responders were greater with CCH (10.6% and 44.6%, respectively) versus placebo (1.6% and 17.9%; p < .001 for both). The most common adverse events were injection-site related. CONCLUSION CCH significantly improved EFP appearance versus placebo; further evaluation of CCH for EFP (cellulite) is warranted.
引用
收藏
页码:1047 / 1056
页数:10
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