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Response to Alpelisib in Clinically Distinct Pediatric Patients With PIK3CA -related Disorders.
Kolitz, Elysha; Fernandes, Neil J; Agim, Nnenna G; Ludwigl, Kathleen.
Afiliação
  • Kolitz E; University of Texas Southwestern Medical School, University of Texas Southwestern Medical Center.
  • Fernandes NJ; Division of Pediatric Radiology, Department of Radiology.
  • Agim NG; Division of Pediatric Dermatology, Department of Dermatology.
  • Ludwigl K; Department of Pediatric Hematology/Oncology, University of Texas Southwestern Medical Center, Children's Health Dallas, Dallas, TX.
J Pediatr Hematol Oncol ; 44(8): 482-485, 2022 11 01.
Article em En | MEDLINE | ID: mdl-35129141
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Tiazóis Aspecto: Patient_preference Limite: Child / Humans Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Tiazóis Aspecto: Patient_preference Limite: Child / Humans Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article País de publicação: Estados Unidos