Response to Alpelisib in Clinically Distinct Pediatric Patients With PIK3CA -related Disorders

J Pediatr Hematol Oncol. 2022 Nov 1;44(8):482-485. doi: 10.1097/MPH.0000000000002418. Epub 2022 Feb 4.

Abstract

PIK3CA -related disorders include vascular malformations, potential overgrowth of various tissues, limb abnormalities, disordered soft tissue, and/or fatty hyperplasia that often leads to significant morbidity. Alpelisib, a targeted inhibitor of p110α, an enzyme encoded by the PIK3CA gene, has demonstrated success in a cohort of patients with PIK3CA -driven overgrowth syndromes. We describe the clinical course of 2 pediatric patients treated with alpelisib under the Novartis Managed Access Program. Both patients, though clinically distinct, demonstrate improvements in overgrowth volumes/extent, function of their affected limb, and quality of life, without significant adverse effects after prolonged treatment.

MeSH terms

  • Child
  • Class I Phosphatidylinositol 3-Kinases / genetics
  • Humans
  • Mutation
  • Quality of Life*
  • Thiazoles* / adverse effects

Substances

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