Use of mTOR inhibitors (rapalogs) for the treatment of skin changes in tuberous sclerosis complex

D Farges1, N Sigg2, D Ville3

  • 1Service de Neuropédiatrie et Neurochirurgie de l'enfant, CHU d'Angers, 49000 Angers, France; Service de Neurologie, CHU d'Angers, 49000 Angers, France.

Abstract

Insights

Topical rapamycin effectively treats facial angiofibromas in Tuberous Sclerosis Complex (TSC), with significant improvements in size and visibility. Maintenance therapy is crucial for sustained results, though cost and accessibility remain key concerns for patients.

Area of Science:

  • Dermatology
  • Medical Genetics
  • Pharmacology

Background:

  • Tuberous Sclerosis Complex (TSC) affects over 90% of patients with skin manifestations.
  • Facial angiofibromas (AF) are a hallmark skin feature of TSC, causing significant aesthetic concerns.
  • Reviewing rapamycin and everolimus for TSC skin conditions is crucial.

Purpose of the Study:

  • To review existing data on oral and topical rapamycin/everolimus for TSC skin lesions.
  • To report preliminary findings from Angers University Hospital on treating facial AF.

Main Methods:

  • Literature search using terms: rapamycin, sirolimus, everolimus, tuberous sclerosis complex, skin, trial.
  • Categorized findings into systemic and topical rapalog use for TSC.
  • Analyzed clinical trial data and hospital patient experience.

Main Results:

  • Topical rapamycin shows significant, though temporary, efficacy in reducing AF size and visibility.
  • Long-term studies (up to 136 weeks) indicate sustained response with good tolerance, necessitating maintenance therapy.
  • Approximately 80% of patients in the Angers University Hospital study experienced impressive and sustained facial AF response.

Conclusions:

  • Topical rapamycin offers a promising treatment for facial angiofibromas in TSC.
  • Standardizing topical rapamycin formulations and improving access/reimbursement are critical for patient care.
  • Further research is needed for other TSC-related skin changes like shagreen plaques and hypomelanotic macules.

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