Focus on skin cancer association and progression under TNF antagonist therapy

Claudine Piérard-Franchimont1, Gérald E Piérard, Pascale Quatresooz

  • 1University Hospital Sart Tilman, Department of Dermatopathology, CHU Sart Tilman, B-4000 Liège, Belgium. gerald.pierard@ulg.ac.be

Abstract

Insights

Tumor necrosis factor (TNF) antagonists may increase the risk of non-melanoma skin cancers (NMSC) and benign melanocytic tumors. Further research is needed to confirm these findings in human skin cancer patients.

Area of Science:

  • Dermatology
  • Oncology
  • Immunology

Background:

  • Basal cell carcinoma and squamous cell carcinoma are the most common human non-melanoma skin cancers (NMSC).
  • NMSC prevalence is higher in immunocompromised individuals.
  • Tumor necrosis factor (TNF) has demonstrated roles in both tumor promotion and apoptosis induction in animal models.

Purpose of the Study:

  • To investigate the potential association between TNF antagonist therapy and the development or progression of human skin cancers.
  • To review existing literature on the effects of TNF antagonists on non-melanoma skin cancers, melanoma, and benign melanocytic tumors.

Main Methods:

  • A review of peer-reviewed articles concerning human skin cancers potentially linked to TNF antagonists.
  • Analysis of reported cases of NMSC and other skin malignancies in patients undergoing TNF antagonist therapy.
  • Consideration of confounding factors such as cumulative co-exposures and other patient therapies.

Main Results:

  • Some patient reports suggest an increased occurrence and altered growth kinetics of NMSC in individuals treated with TNF antagonists.
  • There are suggestions of increased risk for other skin malignancies, including malignant melanoma, and benign melanocytic tumors.
  • Most current evidence consists of anecdotal case reports, necessitating cautious interpretation.

Conclusions:

  • Further research is essential to definitively establish and comprehend the risks associated with anti-TNF biologicals concerning human skin cancers.
  • Current observations suggest that NMSC progression may be enhanced in areas of skin field cancerization.
  • The development of benign melanocytic nevi is also a potential outcome observed during anti-TNF therapy.

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