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Targeted Therapy for Oral Cavity and Oropharyngeal Cancer
Targeted therapy can be used to treat oral cavity and oropharyngeal cancers by destroying cancer cells or slowing their growth.
Targeted therapy is the use of medicines that target, or are directed at, proteins on cancer cells that help them grow, spread, and live longer. The side effects are different from chemotherapy, sometimes less severe.
Targeting oral cavity and oropharyngeal cancer cells with EGFR changes
Epidermal growth factor receptor (EGFR) is a protein found on the surface of certain cancer cells that helps those cells grow and divide. Oral cavity and oropharyngeal cancer cells sometimes have higher than normal amounts of EGFR. Blocking this protein can help slow or stop cancer cell growth.
Cetuximab (Erbitux)
Cetuximab (Erbitux) is a drug that targets EGFR and can be used to treat some oral cavity and oropharyngeal cancers.
This drug is a monoclonal antibody, which is a man-made version of an immune system protein. By blocking EGFR, cetuximab can help slow or stop cancer cell growth.
Cetuximab can be combined with radiation therapy for some earlier stage cancers. For more advanced cancers, it may be combined with standard chemo drugs such as cisplatin, combined with immunotherapy, or used by itself.
Cetuximab is given by infusion into a vein (IV), either once a week or every other week.
Possible side effects of targeted therapy
Common side effects of cetuximab include:
- Skin problems such as an acne-like rash on the face and chest
- Skin sensitivity to the sun
- Headache
- Tiredness
- Fever
- Diarrhea
An allergic reaction during the first infusion is a rare but serious side effect of cetuximab. This could cause breathing problems and low blood pressure. You will be given medicine before treatment to help prevent this.
More information about targeted therapy
To learn more about how targeted drugs are used to treat cancer, see Targeted Cancer Therapy.
To learn about some of the side effects listed here and how to manage them, see Managing Cancer-related Side Effects.
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- References
Developed by the American Cancer Society medical and editorial content team with medical review and contribution by the American Society of Clinical Oncology (ASCO).
Burtness B, Goldwasser MA, Flood W, Mattar B, Forastiere AA; Eastern Cooperative Oncology Group. Phase III randomized trial of cisplatin plus placebo compared with cisplatin plus cetuximab in metastatic/recurrent head and neck cancer: an Eastern Cooperative Oncology Group study. J Clin Oncol. 2005 Dec 1;23(34):8646-54.
Chung CH, Li J, Steuer CE, Bhateja P, Johnson M, Masannat J, Poole MI, Song F, Hernandez-Prera JC, Molina H, Wenig BM, Kumar S, Kuperwasser C, Stephens PJ, Farinhas JM, Shin DM, Kish JA, Muzaffar J, Kirtane K, Rocco JW, Schell MJ, Saba NF, Bonomi M. Phase II Multi-institutional Clinical Trial Result of Concurrent Cetuximab and Nivolumab in Recurrent and/or Metastatic Head and Neck Squamous Cell Carcinoma. Clin Cancer Res. 2022 Jun 1;28(11):2329-2338.
Fury MG, Sherman E, Lisa D, Agarwal N, Algazy K, Brockstein B, Langer C, Lim D, Mehra R, Rajan SK, Korte S, Lipson B, Yunus F, Tanvetyanon T, Smith-Marrone S, Ng K, Xiao H, Haque S, Pfister DG. A randomized phase II study of cetuximab every 2 weeks at either 500 or 750 mg/m2 for patients with recurrent or metastatic head and neck squamous cell cancer. J Natl Compr Canc Netw. 2012 Nov 1;10(11):1391-8.
National Comprehensive Cancer Network. Clinical Practice Guidelines in Oncology (NCCN Guidelines), Head and Neck Cancers, V.1.2026. Accessed at www.nccn.org/professionals/physician_gls/pdf/head-and-neck.pdf on February 3, 2026.
Sacco AG, Chen R, Worden FP, Wong DJL, Adkins D, Swiecicki P, Chai-Ho W, Oppelt P, Ghosh D, Bykowski J, Molinolo A, Pittman E, Estrada MV, Gold K, Daniels G, Lippman SM, Natsuhara A, Messer K, Cohen EEW. Pembrolizumab plus cetuximab in patients with recurrent or metastatic head and neck squamous cell carcinoma: an open-label, multi-arm, non-randomised, multicentre, phase 2 trial. Lancet Oncol. 2021 Jun;22(6):883-892.
Last Revised: March 23, 2026
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