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.


Journal

European journal of dermatology : EJD
ISSN: 1952-4013
Titre abrégé: Eur J Dermatol
Pays: France
ID NLM: 9206420

Informations de publication

Date de publication:
01 Jun 2023
Historique:
medline: 21 8 2023
pubmed: 18 8 2023
entrez: 18 8 2023
Statut: ppublish

Résumé

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. We evaluated the efficacy of sonidegib (200 mg daily) in laBCC patients on select concomitant medications. 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. 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. Administration of sonidegib with concomitant medications, excluding strong cytochrome P450 3A4/5 inhibitors/inducers, does not appear to alter its efficacy in laBCC patients.

Sections du résumé

BACKGROUND 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 OBJECTIVE
We evaluated the efficacy of sonidegib (200 mg daily) in laBCC patients on select concomitant medications.
MATERIALS & METHODS 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 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 CONCLUSIONS
Administration of sonidegib with concomitant medications, excluding strong cytochrome P450 3A4/5 inhibitors/inducers, does not appear to alter its efficacy in laBCC patients.

Identifiants

pubmed: 37594336
pii: ejd.2023.4498
doi: 10.1684/ejd.2023.4498
doi:

Substances chimiques

sonidegib 0RLU3VTK5M
Biphenyl Compounds 0
Pyridines 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

280-286

Auteurs

John T Lear (JT)

Manchester Academic Health Science Centre, University of Manchester, Manchester, UK, Salford Royal NHS Foundation Trust, Salford, UK.

Caroline Robert (C)

Department of Dermatology, Institut Gustave Roussy and Paris-Saclay University, Villejuif, France.

Jean-Jacques Grob (JJ)

Department of Dermatology and Oncology, University of Aix-Marseille, Timone Hospital, Marseille, France.

Reinhard Dummer (R)

Skin Cancer Center University Hospital, Zürich, Switzerland.

Alexander Guminski (A)

Department of Oncology, Royal North Shore Hospital, St Leonards, Australia, The University of Sydney, Sydney, Australia.

Nicholas Squittieri (N)

Medical Affairs Oncology, Sun Pharmaceutical Industries, Inc., Princeton, NJ, USA.

Michael 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.

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Classifications MeSH