Background: Recent reports have suggested that the topical formulation of sirolimus is effective in treating facial angiofibromas in tuberous sclerosis complex (TSC). Here, we determined the safety and efficacy of 0.2% topical sirolimus for the treatment of facial angiofibroma and compared its effects based on age. Method: This was a retrospective study which involved 36 TSC patients with facial angiofibromas who were treated with 0.2% sirolimus ointment. Its effect was evaluated using the Facial Angiofibroma Severity Index (FASI). In order to observe its comparative effect based on patient age, a subgroup analysis was performed, between the adult group (> 18 years old) and the pediatric group (≤18 years old). Results: The total FASI as well as its subcategories (erythema, size, and extent) showed statistically significant improvements after the topical treatment with 0.2% sirolimus ointment (FASI before treatment: 7.2 ± 1.1, FASI after treatment: 4.4± 1.4, p < 0.001). Among the subcategories of FASI, the erythema was most significantly reduced with the fastest response to the treatment. In a subgroup analysis, the pediatric group showed significantly greater improvements in FASI (improvement of FASI in the pediatric group = 49.7 ± 12.2%, adult group = 27.9 ± 15.6%, p < 0.001). The serial improvement analysis also showed that the pediatric group achieved a consistently greater improvement in FASI at all visits. Its 1-year application in 3 patients demonstrated a continuous maintenance effect. No significant adverse effects were observed. Conclusion: 0.2% sirolimus ointment is safe and effective for facial angiofibromas. Considering its higher efficacy in younger patients, an early initiation of the treatment is recommended.

1.
Schwartz RA, Fernandez G, Kotulska K, Jozwiak S: Tuberous sclerosis complex: advances in diagnosis, genetics, and management. J Am Acad Dermatol 2007; 57: 189–202.
2.
Salido R, Garnacho-Saucedo G, Cuevas-Asencio I, Ruano J, Galan-Gutierrez M, Velez A, Moreno-Gimenez JC: Sustained clinical effectiveness and favorable safety profile of topical sirolimus for tuberous sclerosis – associated facial angiofibroma. J Eur Acad Dermatol Venereol 2012; 26: 1315–1318.
3.
Balestri R, Neri I, Patrizi A, Angileri L, Ricci L, Magnano M: Analysis of current data on the use of topical rapamycin in the treatment of facial angiofibromas in tuberous sclerosis complex. J Eur Acad Dermatol Venereol 2015; 29: 14–20.
4.
Sadowski K, Kotulska K, Jozwiak S: Management of side effects of mTOR inhibitors in tuberous sclerosis patients. Pharmacol Rep 2016; 68: 536–542.
5.
Haemel AK, O’Brian AL, Teng JM: Topical rapamycin: a novel approach to facial angiofibromas in tuberous sclerosis. Arch Dermatol 2010; 146: 715–718.
6.
Cinar SL, Kartal D, Bayram AK, Canpolat M, Borlu M, Ferahbas A, Per H: Topical sirolimus for the treatment of angiofibromas in tuberous sclerosis. Indian J Dermatol Venereol Leprol 2017; 83: 27–32.
7.
Jozwiak S, Sadowski K, Kotulska K, Schwartz RA: Topical use of mammalian target of rapamycin (mTOR) inhibitors in tuberous sclerosis complex – a comprehensive review of the literature. Pediatr Neurol 2016; 61: 21–27.
8.
Samanta D: Topical mTOR (mechanistic target of rapamycin) inhibitor therapy in facial angiofibroma. Indian J Dermatol Venereol Leprol 2015; 81: 540–541.
9.
Pynn EV, Collins J, Hunasehally PR, Hughes J: Successful topical rapamycin treatment for facial angiofibromata in two children. Pediatr Dermatol 2015; 32:e120–e123.
10.
Wheless JW, Almoazen H: A novel topical rapamycin cream for the treatment of facial angiofibromas in tuberous sclerosis complex. J Child Neurol 2013; 28: 933–936.
11.
Wataya-Kaneda M, Nakamura A, Tanaka M, Hayashi M, Matsumoto S, Yamamoto K, Katayama I: Efficacy and safety of topical sirolimus therapy for facial angiofibromas in the tuberous sclerosis complex : a randomized clinical trial. JAMA Dermatol 2017; 153: 39–48.
12.
Salido-Vallejo R, Ruano J, Garnacho-Saucedo G, Godoy-Gijon E, Llorca D, Gomez-Fernandez C, Moreno-Gimenez JC: Facial Angiofibroma Severity Index (FASI): reliability assessment of a new tool developed to measure severity and responsiveness to therapy in tuberous sclerosis-associated facial angiofibroma. Clin Exp Dermatol 2014; 39: 888–893.
13.
Kawashiri S, Kumagai S, Nakagawa K, Yamamoto E, Imai K: Juvenile xanthogranuloma occurring in the oral cavity: case report and histopathological findings. J Oral Pathol Med 1997; 26: 484–487.
14.
Schultz KD Jr, Petronio J, Narad C, Hunter SB: Solitary intracerebral juvenile xanthogranuloma. Case report and review of the literature. Pediatr Neurosurg 1997; 26: 315–321.
15.
Nascimento AG: A clinicopathologic and immunohistochemical comparative study of cutaneous and intramuscular forms of juvenile xanthogranuloma. Am J Surg Pathol 1997; 21: 645–652.
16.
Jimenez-Heffernan JA, Hardisson D, Gutierrez J, Contreras F: Rosai-Dorfman disease and juvenile xanthogranuloma. Pediatr Pathol Lab Med 1997; 17: 527–530.
17.
Neveling U, Kahn LB, Valderrama E, Poustchi-Amin M, Uckan D, Shende A: Deep juvenile xanthogranuloma: an unusual presentation. Pediatr Pathol Lab Med 1997; 17: 503–511.
18.
Newman CC, Raimer SS, Sanchez RL: Nonlipidized juvenile xanthogranuloma: a histologic and immunohistochemical study. Pediatr Dermatol 1997; 14: 98–102.
19.
Kaufman McNamara E, Curtis AR, Fleischer AB Jr: Successful treatment of angiofibromata of tuberous sclerosis complex with rapamycin. J Dermatolog Treat 2012; 23: 46–48.
20.
Hofbauer GF, Marcollo-Pini A, Corsenca A, Kistler AD, French LE, Wuthrich RP, Serra AL: The mTOR inhibitor rapamycin significantly improves facial angiofibroma lesions in a patient with tuberous sclerosis. Br J Dermatol 2008; 159: 473–475.
21.
Koenig MK, Hebert AA, Roberson J, Samuels J, Slopis J, Woerner A, Northrup H: Topical rapamycin therapy to alleviate the cutaneous manifestations of tuberous sclerosis complex: a double-blind, randomized, controlled trial to evaluate the safety and efficacy of topically applied rapamycin. Drugs R D 2012; 12: 121–126.
22.
Karar J, Maity A: PI3K/AKT/mTOR pathway in angiogenesis. Front Mol Neurosci 2011; 4: 51.
23.
Tu J, Foster RS, Bint LJ, Halbert AR: Topical rapamycin for angiofibromas in paediatric patients with tuberous sclerosis: follow-up of a pilot study and promising future directions. Australas J Dermatol 2014; 55: 63–69.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.