A Review of Hedgehog Inhibitors Sonidegib and Vismodegib for Treatment of Advanced Basal Cell Carcinoma

J Drugs Dermatol. 2021 Feb 1;20(2):156-165. doi: 10.36849/JDD.5657.

Abstract

Basal cell carcinoma (BCC) is the most common malignancy in fair-skinned populations. Most cases are successfully treated with surgery, but in advanced BCC—including locally advanced BCC and metastatic BCC—surgery is likely to result in substantial morbidity or unlikely to be effective. In those patients, the systemic Hedgehog inhibitors (HHIs) sonidegib and vismodegib are the only approved pharmacologic treatment option. Although a number of clinical studies highlight the similarities and differences between the two HHIs, no head-to-head clinical comparison is available. Results from the pivotal BOLT and ERIVANCE clinical studies for sonidegib and vismodegib, respectively, demonstrate similar efficacy measured by objective response rate, complete response rate, and histologic tumor subtype. Safety results for both studies are comparable with similar common adverse events reported for muscle spasms, alopecia, and dysgeusia. A notable difference between sonidegib and vismodegib is their respective pharmacokinetic profiles with sonidegib reaching peak concentration in plasma within 2–4 hours of dosing and steady state in plasma achieved by week 17 of treatment, while vismodegib reaches peak plasma concentration approximately 2 days after a single dose and steady state within 21 days of repeated dosing. This review compares efficacy, safety, and pharmacokinetics of sonidegib and vismodegib based on published literature to date. J Drugs Dermatol. 2021;20(2):156-165. doi:10.36849/JDD.5657 THIS ARTICLE HAD BEEN MADE AVAILABLE FREE OF CHARGE. PLEASE SCROLL DOWN TO ACCESS THE FULL TEXT OF THIS ARTICLE WITHOUT LOGGING IN. NO PURCHASE NECESSARY. PLEASE CONTACT THE PUBLISHER WITH ANY QUESTIONS.

Publication types

  • Review

MeSH terms

  • Alopecia / chemically induced
  • Alopecia / epidemiology
  • Anilides / administration & dosage*
  • Anilides / adverse effects
  • Anilides / pharmacokinetics
  • Biphenyl Compounds / administration & dosage*
  • Biphenyl Compounds / adverse effects
  • Biphenyl Compounds / pharmacokinetics
  • Carcinoma, Basal Cell / blood
  • Carcinoma, Basal Cell / drug therapy*
  • Carcinoma, Basal Cell / mortality
  • Carcinoma, Basal Cell / pathology
  • Clinical Trials, Phase II as Topic
  • Dysgeusia / chemically induced
  • Dysgeusia / epidemiology
  • Hedgehog Proteins / antagonists & inhibitors*
  • Hedgehog Proteins / metabolism
  • Humans
  • Multicenter Studies as Topic
  • Progression-Free Survival
  • Pyridines / administration & dosage*
  • Pyridines / adverse effects
  • Pyridines / pharmacokinetics
  • Randomized Controlled Trials as Topic
  • Signal Transduction / drug effects
  • Skin Neoplasms / blood
  • Skin Neoplasms / drug therapy*
  • Skin Neoplasms / mortality
  • Skin Neoplasms / pathology
  • Spasm / chemically induced
  • Spasm / epidemiology

Substances

  • Anilides
  • Biphenyl Compounds
  • Hedgehog Proteins
  • HhAntag691
  • Pyridines
  • sonidegib