Emerging Nonsurgical Therapies for Locally Advanced and Metastatic Nonmelanoma Skin Cancer

Leon Chen, Alexander B. Aria, Sirunya Silapunt, Michael R. Migden

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

BACKGROUND Locally advanced and metastatic nonmelanoma skin cancer (NMSC) not amenable to surgical resection requires a different approach to therapy.OBJECTIVETo review the efficacy and adverse effects of emerging treatment options for locally advanced and metastatic NMSC.MATERIALS AND METHODSA comprehensive search on PubMed was conducted to identify relevant literature investigating the role of program cell death 1 (PD-1) inhibitor, cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) inhibitor, epidermal growth factor receptor (EGFR) inhibitor, and Hedgehog pathway inhibitors in the treatment of NMSC.RESULTSPD-1 inhibitor and CTLA-4 inhibitor have shown promising efficacy with tolerable side-effect profiles in the treatment of NMSC, although the number of cases reported is limited. Currently, 3 larger-scale clinical trials are investigating PD-1 inhibitor therapy for NMSC. Similarly, EGFR inhibitor demonstrated marginal success in unresectable cutaneous squamous cell carcinomas. Hedgehog pathway inhibitors were approved by the US FDA for treatment of locally advanced and metastatic basal cell carcinomas and have shown favorable efficacy. Common adverse effects included muscle spasm, alopecia, and dysgeusia.CONCLUSIONSystemic therapies including PD-1 inhibitors and CTLA-4 inhibitors have demonstrated early promising results for difficult-to-treat NMSC. Future studies are necessary to optimize treatment outcome.

Original languageEnglish (US)
Pages (from-to)1-16
Number of pages16
JournalDermatologic Surgery
Volume45
Issue number1
DOIs
StatePublished - Jan 1 2019

ASJC Scopus subject areas

  • Surgery
  • Dermatology

Fingerprint

Dive into the research topics of 'Emerging Nonsurgical Therapies for Locally Advanced and Metastatic Nonmelanoma Skin Cancer'. Together they form a unique fingerprint.

Cite this