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Updated: Oct 15, 2025

Cell Population Analyses During Skin Carcinogenesis
Published on: August 21, 2013
Efficacy of sonic hedgehog inhibitors rechallenge, after initial complete response in recurrent advanced basal cell
A Bassompierre1, S Dalac2, B Dreno3
1Department of Dermatology, Lille University, CHU Lille, Lille, France.
Background:
Smoothened (SMO) inhibitors, blocking the sonic hedgehog pathway, have been approved for advanced basal cell carcinoma (aBCC). Safety analyses reveal a high rate of adverse events (AEs) and, most of the time, vismodegib is most commonly stopped when the best overall response is reached. The long-term evolution of aBCC after vismodegib discontinuation is poorly described. The aim of this study is to evaluate the efficacy and safety of the SMO inhibitors (SMOis) available (vismodegib and sonidegib) following rechallenge after complete response (CR) following an initial treatment by vismodegib.
Materials And Methods:
This real-life, retrospective, multicenter and descriptive study is based on an extraction from the CARADERM accredited database, including 40 French regional hospitals, of patients requiring BCC systemic treatment.
Results:
Of 303 patients treated with vismodegib, 110 achieved an initial CR. The vast majority of these patients (98.2%) stopped vismodegib, notably due to poorly tolerated AEs. The CARADERM database provided a median follow-up of 21 months (13.5-36.0 months) after CR. Of the 110 patients, 48.1% relapsed after a median relapse-free survival of 24 months (13.0-38.0 months). Among them, 35 patients were retreated by an SMOi and the overall response rate was 65.7% (34.3% of CR and 31.4% of partial response). The median duration of retreatment was 6.0 months (4.0-9.5 months).
Conclusion:
Our real-life study, carried out on patients with complex clinical pictures, shows that after treatment discontinuation, 48.1% of patients achieved CR relapse within an average of 24 months (13.0-38.0 months). It emphasized that even though rechallenge can be considered as a therapeutic option, efficacy seems to decrease, suggesting the development of resistance mechanisms.
Insights
Smoothened (SMO) inhibitors effectively treat advanced basal cell carcinoma but are often discontinued due to side effects. Rechallenge with SMO inhibitors after initial response shows reduced efficacy, suggesting resistance may develop.
Area of Science:
- Oncology
- Dermatology
Background:
- Smoothened (SMO) inhibitors are approved for advanced basal cell carcinoma (aBCC).
- High adverse event rates frequently lead to treatment discontinuation, even after achieving a complete response (CR).
- Long-term outcomes after discontinuing SMO inhibitors for aBCC are not well-documented.
Purpose of the Study:
- To evaluate the efficacy and safety of SMO inhibitors (vismodegib and sonidegib) in patients rechallenged after initial complete response to vismodegib.
- To analyze the long-term evolution of advanced basal cell carcinoma following SMO inhibitor treatment discontinuation.
Main Methods:
- Retrospective, multicenter, descriptive study using the CARADERM database from 40 French hospitals.
- Inclusion of patients with advanced basal cell carcinoma requiring systemic treatment.
- Analysis of data from patients treated with vismodegib, focusing on those achieving CR and subsequent outcomes.
Main Results:
- Of 303 patients treated with vismodegib, 110 achieved CR and discontinued treatment, primarily due to adverse events.
- 48.1% of these patients relapsed after a median of 24 months.
- Among relapsed patients, 35 were retreated with an SMO inhibitor, achieving an overall response rate of 65.7% (34.3% CR, 31.4% partial response).
Conclusions:
- Relapse after discontinuing SMO inhibitors for advanced basal cell carcinoma occurs in nearly half of patients within approximately 24 months.
- Rechallenge with SMO inhibitors is a viable therapeutic option, but efficacy may be reduced, potentially due to resistance mechanisms.
- Further research is needed to understand and overcome resistance to SMO inhibitors in advanced basal cell carcinoma.
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