Phase II, Single-Arm Trial of Induction and Concurrent Vismodegib With Curative-Intent Radiation Therapy for Locally Advanced, Unresectable Basal Cell Carcinoma

Author:

Barker Christopher A.1,Dufault Suzanne2ORCID,Arron Sarah T.3ORCID,Ho Alan L.4ORCID,Algazi Alain P.5ORCID,Dunn Lara A.4,Humphries Audrey A.6ORCID,Hultman Carter6,Lian Ming1,Knott P. Daniel7,Yom Sue S.67ORCID

Affiliation:

1. Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY

2. Department of Epidemiology & Biostatistics, University of California San Francisco, San Francisco, CA

3. Department of Dermatology, University of California San Francisco, San Francisco, CA

4. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

5. Department of Medicine, University of California San Francisco, San Francisco, CA

6. Department of Radiation Oncology, University of California San Francisco, San Francisco, CA

7. Department of Department of Otolaryngology—Head and Neck Surgery, University of California San Francisco, San Francisco, CA

Abstract

PURPOSE Locally advanced, unresectable basal cell carcinoma (LA BCC) can be treated with radiation therapy (RT), but locoregional control (LRC) rates are unsatisfactory. Vismodegib is a hedgehog pathway inhibitor (HPI) active in BCC that may radiosensitize BCC. We evaluated the combination of vismodegib and RT for patients with LA BCC. METHODS In this multicenter, single-arm, phase II study, patients with unresectable LA BCC received 12 weeks of induction vismodegib, followed by 7 weeks of concurrent vismodegib and RT. The primary end point was LRC rate at 1 year after the end of treatment. Secondary end points included objective response, progression-free survival (PFS), overall survival (OS), safety, and patient-reported quality of life (PRQOL). RESULTS Twenty-four patients received vismodegib; five were unable to complete 12 weeks of induction therapy. LRC was achieved in 91% (95% CI, 68 to 98) of patients at 1 year. The response rate was 63% (95% CI, 38 to 84) after induction vismodegib and 83% (95% CI, 59 to 96) after concurrent vismodegib and RT. With a median follow-up of 5.7 years, 1-year PFS and OS rates were 100% and 96%, and at 5 years PFS and OS rates were 78% and 83%, respectively. Distant metastasis or BCC-related death has not been observed. The most frequent treatment-related adverse events (AEs) were dysgeusia, fatigue, and myalgias occurring in 83%, 75%, and 75% of patients. No grade 4 to 5 treatment-related AEs occurred. PRQOL demonstrated clinically meaningful improvements in all subscales, with emotions and functioning improvements persisting for a year after the end of treatment. CONCLUSION In patients with unresectable LA BCC, the combination of vismodegib and RT yielded high rates of LRC and PFS and durable improvements in PRQOL.

Publisher

American Society of Clinical Oncology (ASCO)

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