Immunotherapy and Its Timing in Advanced Basal Cell Carcinoma Treatment.

Dermatol Pract Concept

Skin Cancer and Melanoma Unit, 1st Department of Dermatology-Venereology, National and Kapodistrian University of Athens, Andreas Sygros Hospital, Athens, Greece.

Published: October 2023

AI Article Synopsis

  • Advanced basal cell carcinoma (BCC) patients, particularly those not eligible for surgery or radiotherapy, can use hedgehog pathway inhibitors (HHI) like vismodegib and sonidegib as first-line treatments, though high discontinuation rates exist (88-92%).
  • Factors influencing treatment discontinuation include how well the tumor responds, side effects, and the patient's choice, with many stopping after 8 to 12 months.
  • The review discusses the possibility of switching to immunotherapy (e.g., cemiplimab) after HHI treatment, covering its effectiveness and safety as a secondary option or in combination with other therapies.

Article Abstract

For patients with advanced basal cell carcinoma (BCC), including locally advanced or metastatic BCC not amenable to curative surgery or radiotherapy, hedgehog pathway inhibitors (HHI) vismodegib and sonidegib are approved as first-line systemic treatment. Results from clinical trials highlight that the overall discontinuation rate of HHI treatment varies from 88% to 92% with vismodegib and is approximately 92% with sonidegib, and half of patients will discontinue HHI after approximately 8 to 12 months. The main factors weighing in on the decision to discontinue HHI include efficacy (tumor response), adverse events and patient decision. In clinical practice, some of the patients that stop HHI may be re-evaluated if the tumor becomes amenable to surgery, or restart HHI at a later time, while others will need to switch to immunotherapy, depending on the reasons for HHI discontinuation. In this review, we revisit the therapeutic decisions considering a switch from HHI to immunotherapy with anti-PD-1 agent cemiplimab and we highlight the place of cemiplimab in the therapeutic ladder for patients with advanced BCC. We discuss the evidence on the efficacy and safety of anti-PD-1 agents as second-line systemic monotherapy, or in combination with other treatments, and the emergence of checkpoint immunotherapy as a neoadjuvant treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656142PMC
http://dx.doi.org/10.5826/dpc.1304a252DOI Listing

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