A phase II double-blind multicentre, placebo-controlled trial to assess the efficacy and safety of alpelisib (BYL719) in paediatric and adult patients with Megalencephaly-CApillary malformation Polymicrogyria syndrome (MCAP): the SESAM study protocol

BMJ Open. 2024 Dec 20;14(12):e084614. doi: 10.1136/bmjopen-2024-084614.

Abstract

Introduction: The megalencephaly capillary malformation polymicrogyria (MCAP syndrome) results from mosaic gain-of-function PIK3CA variants. The main clinical features are macrocephaly, somatic overgrowth, neurodevelopmental delay and brain anomalies. Alpelisib (Vijoice) is a recently FDA-approved PI3Kα-specific inhibitor for patients with PIK3CA-related overgrowth spectrum (PROS). During its development, in patients with the MCAP subgroup of PROS, there was no specific, standardised evaluation of the effect on neuro-cognitive functioning. Moreover, it remains unknown if the molecule crosses the blood-brain barrier. Our objective is to evaluate the efficacy of a 24 month treatment with alpelisib on adaptive behaviour in patients with MCAP syndrome.

Methods and analysis: SESAM is an industry-sponsored two-period multicentre French academic phase II trial, with a 6-month double-blind, placebo-controlled period followed by an open-label period. The primary endpoint is a ≥4-point improvement in the Vineland II Adaptive Behaviour Scale (VABS), 24 months after treatment initiation. Secondary objectives are safety, VABS improvement at 6 months, impact on the quality of life, epilepsy and hypotonia. 20 patients aged 2 to 40 years with an MCAP diagnosis and neurodevelopmental disorders of various degrees, will be followed monthly in local centres, centrally assessed (clinical, biological, neuropsychological and functional evaluation) at baseline and every 6 months. Patients will be evaluated by volumetric MRI at baseline and at 24 months. An optional lumbar puncture will be performed to investigate blood-brain barrier crossing. Inclusions were completed by April 2024, with the end of follow-up in November 2026.Given the efficacy of alpelisib in patients with PROS, if the drug crosses the blood-brain barrier, we can expect a clinical benefit for patients with neurocognitive disorders.

Ethics and dissemination: Ethical approval was given by CPP Sud-Ouest et Outre-Mer I (reference: 2022-500197-34-01). Findings from this study will be disseminated via publication, reports and conference presentations.

Trial registration number: NCT05577754.

Keywords: Clinical trials; Developmental neurology & neurodisability; Neurogenetics; Paediatric clinical genetics & dysmorphology.

Publication types

  • Clinical Trial Protocol
  • Clinical Trial, Phase II
  • Multicenter Study

MeSH terms

  • Abnormalities, Multiple
  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Class I Phosphatidylinositol 3-Kinases / genetics
  • Clinical Trials, Phase II as Topic
  • Double-Blind Method
  • Female
  • Humans
  • Male
  • Megalencephaly* / drug therapy
  • Multicenter Studies as Topic
  • Port-Wine Stain / drug therapy
  • Quality of Life
  • Skin Diseases, Vascular
  • Telangiectasis / congenital
  • Treatment Outcome
  • Vascular Malformations / drug therapy
  • Young Adult

Substances

  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CA protein, human

Supplementary concepts

  • Megalencephaly cutis marmorata telangiectatica congenita

Associated data

  • ClinicalTrials.gov/NCT05577754