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Updated: Oct 21, 2025

Cell Population Analyses During Skin Carcinogenesis
Published on: August 21, 2013
Key Clinical Adverse Events in Patients with Advanced Basal Cell Carcinoma Treated with Sonidegib or Vismodegib: A
Ralf Gutzmer1, Carmen Loquai2, Caroline Robert3
1Skin Cancer Center Minden, Department of Dermatology, Johannes-Wesling-Klinikum Minden/Ruhr-University Bochum, Minden, Germany. rgutzmer@gmx.de.
Introduction:
Sonidegib is approved to treat locally advanced basal cell carcinoma (laBCC) in the USA, EU, Switzerland, and Australia and metastatic basal cell carcinoma (mBCC) in Switzerland and Australia in patients not amenable to surgery or radiotherapy. Vismodegib is approved to treat patients with mBCC, recurrent laBCC, or those not candidates for surgery or radiation. There is no head-to-head trial comparing Hedgehog inhibitors. We describe time to onset and severity of adverse events (AEs) in two studies reporting cumulative AE incidence every treatment cycle: the sonidegib phase 2 BOLT study and the expanded-access, open-label vismodegib study.
Methods:
This analysis included patients with histologically confirmed laBCC or mBCC from BOLT who received sonidegib 200 mg once daily (QD) and patients from the vismodegib study who received vismodegib 150 mg QD. Cumulative occurrence of AEs and median time to AE onset were calculated on 30-day cycles for sonidegib and 28-day cycles for vismodegib. AEs were graded for severity using the Common Terminology Criteria for Adverse Events. Only common (at least 15% incidence) AEs were analyzed in this study.
Results:
Over 18 treatment cycles, the most common all-grade AEs for sonidegib and vismodegib were muscle spasm (54.4% vs 70.6%; P = 0.0236), alopecia (49.4% vs 58.0%; no significant difference [NS]), and dysgeusia (43.0% vs 70.6%; P = 0.0003); incidences of diarrhea, nausea, fatigue, and weight decrease were 31.6% vs 25.2% (NS), 39.2% vs 19.3% (P = 0.0032), 32.9% vs 19.3% (P = 0.0429), and 30.4% vs 16.0% (P = 0.0217), respectively. Sonidegib-treated patients had more delayed median time to onset for all AEs than vismodegib-treated patients, except fatigue and weight decrease (NS). Most AEs reported were grade ≤ 2.
Conclusion:
This post hoc analysis suggests lower overall incidence and slower onset of certain AEs in patients treated with sonidegib compared with vismodegib. In the absence of head-to-head comparisons, the relevance of these findings needs further studies to provide conclusive evidence.
Insights
Sonidegib may offer a better safety profile than vismodegib for advanced basal cell carcinoma patients, showing a lower incidence and slower onset of adverse events. Further head-to-head studies are needed for confirmation.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Sonidegib and vismodegib are Hedgehog pathway inhibitors used for advanced basal cell carcinoma (BCC).
- Current approvals vary by region and BCC subtype (locally advanced or metastatic).
- No direct head-to-head trials exist comparing these two agents.
Purpose of the Study:
- To compare the time to onset and severity of adverse events (AEs) between sonidegib and vismodegib.
- To analyze cumulative AE incidence in patients with locally advanced or metastatic BCC.
Main Methods:
- Post hoc analysis of two studies: sonidegib BOLT trial and vismodegib expanded-access study.
- Inclusion of patients with histologically confirmed laBCC or mBCC.
- Calculation of cumulative AE incidence and median time to onset per treatment cycle, focusing on common AEs (≥15% incidence).
Main Results:
- Sonidegib showed a lower incidence of muscle spasm and dysgeusia compared to vismodegib.
- Incidences of alopecia were similar between the two drugs.
- Sonidegib-treated patients experienced a delayed median time to onset for most AEs, except fatigue and weight decrease.
Conclusions:
- Sonidegib may be associated with a lower overall incidence and slower onset of certain adverse events compared to vismodegib.
- These findings suggest a potential safety advantage for sonidegib.
- Further head-to-head clinical trials are necessary to establish definitive conclusions.
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