Preventative treatment of tuberous sclerosis complex with sirolimus: Phase I safety and efficacy results

• Published in: Annals of the Child Neurology Society 2024-06, Vol.2 (2), p.106-119
• Main Authors: Capal, Jamie K., Ritter, David M., Franz, David Neal, Griffith, Molly, Currans, Kristn, Kent, Bridget, Martina Bebin, E., Northrup, Hope, Koenig, Mary Kay, Mizuno, Tomoyuki, Vinks, Alexander A., Galandi, Stephanie L., Zhang, Wujuan, Setchell, Kenneth D.R., Kremer, Kelly M., Prada, Carlos M., Greiner, Hansel M., Holland‐Bouley, Katherine, Horn, Paul S., Krueger, Darcy A.
• Format: Article
• Language: English
• Subjects: safety; seizures; sirolimus; tuberous sclerosis complex
• ISSN: 2831-3267; 2831-3267
• DOI: 10.1002/cns3.20070

Objective Tuberous sclerosis complex (TSC) results from overactivity of the mechanistic target of rapamycin (mTOR). Sirolimus and everolimus are mTOR inhibitors that treat most facets of TSC but are understudied in infants. We sought to understand the safety and potential efficacy of preventative sirolimus in infants with TSC. Methods We conducted a phase 1 clinical trial of sirolimus, treating five patients until 12 months of age. Enrolled infants had to be younger than 6 months of age with no history of seizures and no clinical indication for sirolimus treatment. Adverse events (AEs), tolerability, and blood concentrations of sirolimus measured by tandem mass spectrometry were tracked through 12 months of age, and clinical outcomes (seizure characteristics and developmental profiles) were tracked through 24 months of age. Results There were 92 AEs, with 34 possibly, probably, or definitely related to treatment. Of those, only two were grade 3 (both elevated lipids) and all AEs were resolved by the age of 24 months. During the trial, 94% of blood sirolimus trough levels were in the target range (5–15 ng/mL). Treatment was well tolerated, with less than 8% of doses held because of an AE (241 of 2941). Of the five patients, three developed seizures (but were well controlled on medications) at 24 months of age. Of the five patients, four had normal cognitive development for age. One was diagnosed with possible autism spectrum disorder. Interpretation These results suggest that sirolimus is both safe and well tolerated by infants with TSC in the first year of life. Additionally, the preliminary work suggests a favorable efficacy profile compared with previous TSC cohorts not exposed to early sirolimus treatment. Results support sirolimus being studied as preventive treatment in TSC, which is now underway in a prospective phase 2 clinical trial (TSC‐STEPS).