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Concomitant medication use does not appear to alter long-term efficacy of sonidegib for advanced basal cell carcinoma: a post hoc analysis based on the 42-month BOLT study.
Lear, John T; Robert, Caroline; Grob, Jean-Jacques; Dummer, Reinhard; Guminski, Alexander; Squittieri, Nicholas; Migden, Michael.
Afiliación
  • Lear JT; Manchester Academic Health Science Centre, University of Manchester, Manchester, UK, Salford Royal NHS Foundation Trust, Salford, UK.
  • Robert C; Department of Dermatology, Institut Gustave Roussy and Paris-Saclay University, Villejuif, France.
  • Grob JJ; Department of Dermatology and Oncology, University of Aix-Marseille, Timone Hospital, Marseille, France.
  • Dummer R; Skin Cancer Center University Hospital, Zürich, Switzerland.
  • Guminski A; Department of Oncology, Royal North Shore Hospital, St Leonards, Australia, The University of Sydney, Sydney, Australia.
  • Squittieri N; Medical Affairs Oncology, Sun Pharmaceutical Industries, Inc., Princeton, NJ, USA.
  • Migden M; University of Texas MD Anderson Cancer Center, Departments of Dermatology, Division of Internal Medicine, and Head and Neck Surgery, Division of Surgery, Houston, TX, USA.
Eur J Dermatol ; 33(3): 280-286, 2023 Jun 01.
Article en En | MEDLINE | ID: mdl-37594336
BACKGROUND: Sonidegib is approved to treat locally advanced basal cell carcinoma (laBCC) in patients not amenable to surgery or radiation. The BOLT trial demonstrated durable efficacy of sonidegib in laBCC patients over 42 months. BCC is most common in the elderly, who often take chronic medications. OBJECTIVES: We evaluated the efficacy of sonidegib (200 mg daily) in laBCC patients on select concomitant medications. MATERIALS & METHODS: In the Phase II BOLT study, laBCC patients were randomized 1:2 to sonidegib 200 mg:800 mg daily. The primary endpoint was objective response rate (ORR) per central review. Post hoc assessments included ORR and duration of response (DOR) per investigator review for patients on concomitant medications. RESULTS: At 42 months, ORR for laBCC patients taking sonidegib 200 mg daily (n=66) was 71.2% and DOR was 15.7 months according to investigator review. Patients on select concomitant medications (n=37) had an ORR of 73.0%; DOR was not estimable. CONCLUSION: Administration of sonidegib with concomitant medications, excluding strong cytochrome P450 3A4/5 inhibitors/inducers, does not appear to alter its efficacy in laBCC patients.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Carcinoma Basocelular Tipo de estudio: Clinical_trials Límite: Aged / Humans Idioma: En Revista: Eur J Dermatol Asunto de la revista: DERMATOLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Carcinoma Basocelular Tipo de estudio: Clinical_trials Límite: Aged / Humans Idioma: En Revista: Eur J Dermatol Asunto de la revista: DERMATOLOGIA Año: 2023 Tipo del documento: Article