Combination of an EGFR blocker and a COX-2 inhibitor for the treatment of advanced cutaneous squamous cell carcinoma

J Dtsch Dermatol Ges. 2008 Dec;6(12):1066-9. doi: 10.1111/j.1610-0387.2008.06861.x.
[Article in English, German]

Abstract

Cutaneous squamous cell carcinoma (SCC) is one of the most common cancers worldwide. Epidermal growth factor receptor (EGFR) is expressed at the cell surface by more than 90% of SCCs and its activation is responsible for cell cycle progression, proliferation, survival, angiogenesis and metastasis. Cyclooxygenase-2 (COX-2) is an enzyme up-regulated through EGFR signaling and responsible for some of the EGFR-dependent biological effects. An 88-year-old man presented with a recurrent, locoregionally meta-static SCC of the right parietal region, which was resistant to radiotherapy. With a combination therapy of an EGFR blocker (cetuximab) and a COX-2 inhibitor (celecoxib), the tumor regressed partially and the patient's Karnofsky index improved. We speculate that the combined use of cetuximab and COX-2 inhibitors can be a new and effective therapy for advanced and recurrent cutaneous SCCs.

Publication types

  • Case Reports

MeSH terms

  • Aged, 80 and over
  • Antibodies, Monoclonal / administration & dosage*
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Carcinoma, Squamous Cell / diagnosis
  • Carcinoma, Squamous Cell / drug therapy*
  • Celecoxib
  • Cetuximab
  • Cyclooxygenase 2 Inhibitors / administration & dosage*
  • Cyclooxygenase Inhibitors / administration & dosage
  • ErbB Receptors / antagonists & inhibitors*
  • Humans
  • Male
  • Pyrazoles / administration & dosage*
  • Skin Neoplasms / diagnosis
  • Skin Neoplasms / drug therapy*
  • Sulfonamides / administration & dosage*
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Pyrazoles
  • Sulfonamides
  • EGFR protein, human
  • ErbB Receptors
  • Celecoxib
  • Cetuximab