Survival after definitive treatment for oropharyngeal carcinoma depends principally on the stage of disease and ability to undergo standard treatment. Patients who are positive for high-risk human papillomavirus (HPV) have a better survival.[7]Fakhry C, Westra W, Li S, et al. Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trial. J Natl Cancer Inst. 2008 Feb 20;100(4):261-9.
https://academic.oup.com/jnci/article/100/4/261/908311
http://www.ncbi.nlm.nih.gov/pubmed/18270337?tool=bestpractice.com
[80]Nichols AC, Faquin WC, Westra WH, et al. HPV-16 infection predicts treatment outcome in oropharyngeal squamous cell carcinoma. Otolaryngol Head Neck Surg. 2009 Feb;140(2):228-34.
http://www.ncbi.nlm.nih.gov/pubmed/19201294?tool=bestpractice.com
[81]Lassen P, Eriksen JG, Hamilton-Dutoit S, et al. Effect of HPV-associated p16INK4A expression on response to radiotherapy and survival in squamous cell carcinoma of the head and neck. J Clin Oncol. 2009 Apr 20;27(12):1992-8.
http://www.ncbi.nlm.nih.gov/pubmed/19289615?tool=bestpractice.com
[119]Rischin D, Young RJ, Fisher R, et al. Prognostic significance of p16INK4A and human papillomavirus in patients with oropharyngeal cancer treated on TROG 02.02 phase III trial. J Clin Oncol. 2010 Sep 20;28(27):4142-8.
http://www.ncbi.nlm.nih.gov/pubmed/20697079?tool=bestpractice.com
[120]Ang KK, Harris J, Wheeler R, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med. 2010 Jul 1;363(1):24-35.
https://www.nejm.org/doi/10.1056/NEJMoa0912217
http://www.ncbi.nlm.nih.gov/pubmed/20530316?tool=bestpractice.com
Young age (<50 years) is also associated with a better cancer-specific survival compared with older age (>50 years) for tonsillar carcinoma. It is unclear whether the benefit associated with young age is related to a high prevalence of HPV-16 in this patient population or better tolerance to treatment.[121]Nguyen NP, Ly BH, Betz M, et al. Importance of age as a prognostic factor fortonsillar carcinoma. Ann Surg Oncol. 2010 Oct;17(10):2570-7.
http://www.ncbi.nlm.nih.gov/pubmed/20559738?tool=bestpractice.com
Survival for early stage oropharyngeal cancer is excellent, ranging from 80% to 90% at 5 years.[75]Cosmidis A, Rame JP, Dassonville O, et al; Groupement d'Etudes des Tumeurs de la Tête et du Cou (GETTEC). T1-T2 N0 oropharyngeal cancers treated with surgery alone: a GETTEC study. Eur Arch Otorhinolaryngol. 2004 May;261(5):276-81.
http://www.ncbi.nlm.nih.gov/pubmed/14551793?tool=bestpractice.com
[76]Parsons JT, Mendenhall WM, Stringer SP, et al. Squamous cell carcinoma of the oropharynx: surgery, radiotherapy, or both. Cancer. 2002 Jun 1;94(11):2967-80.
https://onlinelibrary.wiley.com/doi/full/10.1002/cncr.10567
http://www.ncbi.nlm.nih.gov/pubmed/12115386?tool=bestpractice.com
[122]Le Scodan R, Pommier P, Ardiet JM, et al. Exclusive brachytherapy for T1 and T2 squamous cell carcinomas of the velotonsillar area: results in 44 patients. Int J Radiat Oncol Biol Phys. 2005 Oct 1;63(2):441-8.
http://www.ncbi.nlm.nih.gov/pubmed/16168837?tool=bestpractice.com
[123]Levendag P, Nijdam W, Noever I, et al. Brachytherapy versus surgery in carcinoma of tonsillar fossa and/or soft palate: late adverse sequelae and performance status: can we be more selective and obtain better tissue sparing? Int J Radiat Oncol Biol Phys. 2004 Jul 1;59(3):713-24.
http://www.ncbi.nlm.nih.gov/pubmed/15183475?tool=bestpractice.com
Morbidity and mortality of treatment is the major selecting factor between surgery and radiation. For locally advanced resectable disease, survival ranges from 60% to 70% at 3 years.[88]Adelstein DJ, Saxton JP, Lavertu P, et al. A phase III randomized trial comparing concurrent chemotherapy and radiotherapy with radiotherapy alone in resectable stage III and IV squamous cell head and neck cancer: preliminary results. Head Neck. 1997 Oct;19(7):567-75.
http://www.ncbi.nlm.nih.gov/pubmed/9323144?tool=bestpractice.com
[124]Bernier J, Domenge C, Ozsahin M, et al; European Organization for Research and Treatment of Cancer Trial 22931. Postoperative irradiation with or without concomitant chemotherapy for locally advanced head and neck cancer. N Engl J Med. 2004 May 6;350(19):1945-52.
https://www.nejm.org/doi/full/10.1056/NEJMoa032641
http://www.ncbi.nlm.nih.gov/pubmed/15128894?tool=bestpractice.com
For locally unresectable disease, 3-year survival ranges from 40% to 55%.[91]Budach V, Stuschke M, Budach W, et al. Hyperfractionated accelerated chemoradiation with concurrent fluorouracil-mitomycin is more effective than dose-escalated hyperfractionated accelerated radiation therapy alone in locally advanced head and neck cancer: final results of the Radiotherapy Cooperative Clinical Trials Group of the German Cancer Society 95-06 Prospective Randomized Trial. J Clin Oncol. 2005 Feb 20;23(6):1125-35.
https://ascopubs.org/doi/full/10.1200/jco.2005.07.010
http://www.ncbi.nlm.nih.gov/pubmed/15718308?tool=bestpractice.com
[92]Bensadoun RJ, Benezery K, Dassonville O, et al. French multicenter phase III randomized study testing concurrent twice-a-day radiotherapy and cisplatin/5-fluorouracil chemotherapy (BiRCF) in unresectable pharyngeal carcinoma: results at 2 years (FNCLCC-GORTEC). Int J Radiat Oncol Biol Phys. 2006 Mar 15;64(4):983-94.
http://www.ncbi.nlm.nih.gov/pubmed/16376489?tool=bestpractice.com
[93]Staar S, Rudat V, Stuetzer H, et al. Intensified hyperfractionated accelerated radiotherapy limits the additional benefit of simultaneous chemotherapy: results of a multicentric randomized German trial in advanced head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2001 Aug 1;50(5):1161-71. [Erratum in: Int J Radiat Oncol Biol Phys 2001 Oct 1;51(2):569.]
http://www.ncbi.nlm.nih.gov/pubmed/11483325?tool=bestpractice.com
[94]Semrau R, Mueller RP, Stuetzer H, et al. Efficacy of intensified hyperfractionated and accelerated radiotherapy and concurrent chemotherapy with carboplatin and 5-fluorouracil: updated results of a randomized multicentric trial in advanced head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2006 Apr 1;64(5):1308-16.
http://www.ncbi.nlm.nih.gov/pubmed/16464538?tool=bestpractice.com
[95]Denis F, Garaud P, Bardet E, et al. Final results of the 94-01 French Head and Neck Oncology and Radiotherapy Group randomized trial comparing radiotherapy alone with concomitant chemoradiotherapy in advanced-stage oropharynx carcinoma. J Clin Oncol. 2004 Jan 1;22(1):69-76.
https://ascopubs.org/doi/full/10.1200/jco.2004.08.021
http://www.ncbi.nlm.nih.gov/pubmed/14657228?tool=bestpractice.com
[96]Calais G, Alfonsi M, Bardet E, et al. Randomized trial of radiation therapy versus concomitant chemotherapy and radiation therapy for advanced-stage oropharynx carcinoma. J Natl Cancer Inst. 1999 Dec 15;91(24):2081-6.
https://academic.oup.com/jnci/article/91/24/2081/2964959
http://www.ncbi.nlm.nih.gov/pubmed/10601378?tool=bestpractice.com
[97]Brizel DM, Albers ME, Fisher SR, et al. Hyperfractionated irradiation with or without concurrent chemotherapy for locally advanced head and neck cancer. N Engl J Med. 1998 Jun 18;338(25):1798-804.
https://www.nejm.org/doi/full/10.1056/NEJM199806183382503
http://www.ncbi.nlm.nih.gov/pubmed/9632446?tool=bestpractice.com
Patients with metastatic disease have a poor prognosis with median survival of about 10 months.[125]Pisani P, Airoldi M, Allais A, et al. Metastatic disease in head & neck oncology. Acta Otorhinolaryngol Ital. 2020 Apr;40(suppl. 1):S1-86.
https://old.actaitalica.it/article/view/874
http://www.ncbi.nlm.nih.gov/pubmed/32469009?tool=bestpractice.com
New radiation therapy techniques, such as intensity-modulated radiation therapy (IMRT), have the potential to improve patient quality of life because of their sparing effects on normal tissue. The National Comprehensive Cancer Network (NCCN) recommends IMRT to minimize damage to critical structures.[2]National Comprehensive Cancer Network. NCCN clinical practice guidelines in oncology: head and neck cancers [internet publication].
https://www.nccn.org/professionals/physician_gls/default.aspx
Lower rates of xerostomia have been reported when patients with head and neck cancers were treated with IMRT, without compromise on local disease control or survival. The incidence of dysphagia and aspiration may also be reduced due to its sparing effects on the pharyngeal muscles.[126]Guha S, Kelly CG, Guha R, et al. Intensity modulated radiation therapy (IMRT) in the treatment of squamous carcinoma of the oropharynx: an overview. J Cancer Sci Ther. 2012;4(4):77-83.
https://www.omicsonline.org/intensity-modulated-radiation-therapy-imrt-in-the-treatment-of-squamous-carcinoma-of-the-oropharynx-1948-5956.1000115.php?aid=5968
The patient's current and previous smoking status, including number of packs/day, at the time of diagnosis impact the survival rate of patients with oropharyngeal squamous cell carcinoma, independent of HPV negative status.[127]Grønhøj C, Jensen JS, Wagner S, et al. Impact on survival of tobacco smoking for cases with oropharyngeal squamous cell carcinoma and known human papillomavirus and p16-status: a multicenter retrospective study. Oncotarget. 2019 Jul 23;10(45):4655-63.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659794
http://www.ncbi.nlm.nih.gov/pubmed/31384393?tool=bestpractice.com
In addition, tobacco exposure can eliminate any survival benefit associated with HPV positive status in patients with oropharyngeal squamous cell carcinoma.[128]Elhalawani H, Mohamed ASR, Elgohari B, et al. Tobacco exposure as a major modifier of oncologic outcomes in human papillomavirus (HPV) associated oropharyngeal squamous cell carcinoma. BMC Cancer. 2020 Sep 23;20(1):912.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513300
http://www.ncbi.nlm.nih.gov/pubmed/32967643?tool=bestpractice.com