Topical Rapamycin as a Treatment for Fibrofolliculomas in Birt-Hogg-Dube Syndrome: A Double-Blind Placebo-Controlled Randomized Split-Face Trial

被引:33
作者
Gijezen, LiekeM. C. [1 ]
Vernooij, Marigje [1 ]
Martens, Herm [1 ]
Oduber, Charlene E. U. [1 ]
Henquet, Charles J. M. [1 ]
Starink, Theo M. [2 ]
Prins, Martin H. [3 ]
Menko, Fred H. [4 ]
Nelemans, Patty J. [3 ]
van Steensel, Maurice A. M. [1 ,5 ,6 ]
机构
[1] Maastricht Univ, Med Ctr, GROW Sch Oncol & Dev Biol, Dept Dermatol, Maastricht, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Dermatol, Amsterdam, Netherlands
[3] Maastricht Univ, Med Ctr, CAPHRI Res Sch Publ Hlth Primary Care, Dept Epidemiol, Maastricht, Netherlands
[4] Vrije Univ Amsterdam Med Ctr, Dept Clin Genet, Amsterdam, Netherlands
[5] Maastricht Univ, Med Ctr, GROW Sch Oncol & Dev Biol, Dept Clin Genet, Maastricht, Netherlands
[6] Inst Med Biol, Singapore, Singapore
关键词
TUBEROUS-SCLEROSIS; FACIAL-ANGIOFIBROMAS; SPONTANEOUS PNEUMOTHORAX; FLUOCINOLONE ACETONIDE; POLYCYSTIC KIDNEYS; MTOR ACTIVATION; BHD GENE; NEOPLASIA; VEHICLE; FOLLICULIN;
D O I
10.1371/journal.pone.0099071
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Birt-Hogg-Dube syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence of benign, mostly facial, skin tumours called fibrofolliculomas, multiple lung cysts, spontaneous pneumothorax and an increased renal cancer risk. Current treatments for fibrofolliculomas have high rates of recurrence and carry a risk of complications. It would be desirable to have a treatment that could prevent fibrofolliculomas from growing. Animal models of BHD have previously shown deregulation of mammalian target of rapamycin (mTOR). Topical use of the mTOR inhibitor rapamycin is an effective treatment for the skin tumours (angiofibromas) in tuberous sclerosis complex, which is also characterised by mTOR deregulation. In this study we aimed to determine if topical rapamycin is also an effective treatment for fibrofolliculomas in BHD. Methods: We performed a double blinded, randomised, facial left-right controlled trial of topical rapamycin 0.1% versus placebo in 19 BHD patients. Trial duration was 6 months. The primary outcome was cosmetic improvement as measured by doctors and patients. Changes in fibrofolliculoma number and size were also measured, as was occurrence of side effects. Results: No change in cosmetic status of fibrofolliculomas was reported in the majority of cases for the rapamycin treated (79% by doctors, 53% by patients) as well as the placebo treated facial sides (both 74%). No significant differences between rapamycin and placebo treated facial halves were observed (p = 1.000 for doctors opinion, p = 0.344 for patients opinion). No significant difference in fibrofolliculoma number or change in size of the fibrofolliculomas was seen after 6 months. Side effects occurred more often after rapamycin treatment (68% of patients) than after placebo (58% of patients; p = 0.625). A burning sensation, erythema, itching and dryness were most frequently reported. Conclusions: This study provides no evidence that treatment of fibrofolliculomas with topical rapamycin in BHD results in cosmetic improvement.
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页数:8
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