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Final Recommendation Statement

Oral Cancer: Screening, 1996

January 01, 1996

Recommendations made by the USPSTF are independent of the U.S. government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.

This Recommendation is out of date

It has been replaced by the following: Oral Cancer: Screening (2013)

Recommendation Summary

Population Recommendation Grade
Asymptomatic persons There is insufficient evidence to recommend for or against routine screening of asymptomatic persons for oral cancer by primary care clinicians . C

Recommendation Information

Full Recommendation:

Recommendations made by the USPSTF are independent of the U.S. government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.

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The term "oral cancer" includes a diverse group of tumors arising from the oral cavity. Usually included are cancers of the lip, tongue, pharynx, and oral cavity. The annual incidence of oral cancer in the U.S. is about 11/100,000 population, with a male/female ratio greater than 2:1.1 Oral cancer is responsible for 2% of all cancer deaths in the U.S., and it is projected to account for over 28,000 new cases and about 8,400 deaths in 1995.2

Fifty-three percent of oral cancers have spread to regional or distant structures at the time of diagnosis.1 Overall 5-year survival is 52%, but it ranges from 79% for localized disease to 19% if distant metastases are present.1 The natural history of each type of cancer can be quite different. Cancer of the lip accounts for 11% of new cases of oral cancer but only 1% of deaths. In contrast, cancer of the pharynx accounts for 31% of new cases of oral cancer but 50% of deaths.1 The median age at diagnosis of oral cancers is 64 years, and 95% occur in persons over age 40. About half of all oropharyngeal cancers and the majority of deaths from this disease occur in persons over age 65.1

Use of tobacco in all forms and, to a lesser extent, alcohol abuse are the major risk factors for the development of oral cancer.3 The risk of oral cancer is increased 6-28 times in current smokers,4 and the effects of tobacco and alcohol account for 90% of oral cancer in the U.S. 5 In parts of India and Asia where chewing tobacco or betel nut is very common, the incidence of oral cancer is 3 times higher than in the U.S.5 In several areas of India, oral cancer accounts for 40% of all female cancer deaths.5 Other risk factors for oral cancer include occupational exposures, solar radiation (for cancer of the lip), and the presence of premalignant lesions such as leukoplakia or erythroplakia.3 Depending on the degree of histologic abnormality, up to 18% of cases of leukoplakia may develop into invasive cancers over long-term follow-up.5 Patients infected with human immunodeficiency virus are at increased risk of oral cancers, most commonly Kaposi's sarcoma and non-Hodgkin's lymphoma.6 

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The principal screening test for oropharyngeal cancer in asymptomatic persons is inspection and palpation of the oral cavity. Studies indicate that many oral cancers occur on the floor of the mouth, the ventral and lateral regions of the tongue, and the soft palate, anatomic sites that may be inaccessible to routine visual inspection.7 The recommended examination technique involves a careful visual examination of the oral cavity and extraoral areas using a dental mirror, retracting the tongue with a gauze pad to visualize hard-to-see areas. It also includes digital palpation with a gloved hand for masses. Complete descriptions of the recommended techniques have been published.8 There is little information, however, on the sensitivity of this procedure in detecting oral cancer or on the frequency of false-positive results when a lesion is found. The abbreviated oral inspection that is more typical of the routine physical examination is also of unknown accuracy and predictive value. Studies in India and Sri Lanka have shown that nonphysician basic health care workers, given a short course on screening for oral cancer, can identify oral cancers and their precursors.9,10 Mehta found a 59% sensitivity and 98% specificity for lesions appropriately referred to dentists by the basic health care workers.9 No outcome data were reported in these studies, and it is unclear how these findings relate to the very different, lower prevalence population of the United States.

Some studies suggest that dentists are more effective than are physicians in routinely performing a complete mouth examination and detecting early-stage oral cancer.11 Older Americans, the population at greatest risk for oral cancer, visit the dentist infrequently, however physician visits are much more frequent in older persons.12 No studies of the sensitivity and specificity of screening for oral cancer by dentists have been reported.

Alternative screening tests for oral cancer have been proposed, such as tolonium chloride rinses to stain suspicious lesions,13,14 but further research is needed to evaluate the accuracy and acceptability of these techniques before routine use in the general population can be considered. 

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No controlled trials of screening for oral cancer that include data on clinical outcomes have been reported. There is consistent evidence that persons with early-stage oral cancer have a better prognosis than those diagnosed with more advanced disease.1,2 Because of the possible effects of lead-time and length bias, however, these observational data are not sufficient to prove that screening and earlier detection improve the prognosis in patients with oral cancer. Some authors have questioned the effectiveness of early detection in improving prognosis.15 Prospective trials of screening for oral cancer, although difficult and expensive to conduct in the general population, might be feasible in high-risk populations in which the incidence of oral cancer is substantially greater.

Several studies have examined treatment of oral leukoplakia, a form of premalignancy, as a means of preventing oral cancer. Primary treatment of oral leukoplakia and prevention of second primary lesions in patients with treated oral cancer have been studied in several randomized, placebo-controlled chemoprevention trials of high-dose isotretinoin (13-cis-retinoic acid).16-18 These studies demonstrated that isotretinoin was effective in promoting remission of leukoplakia and preventing the occurrence of second primary oral cancers.17 Leukoplakia relapsed in a majority of cases within 3-6 months after discontinuation of therapy, however, and the rate of toxicity of treatment was high (mild to moderate side effects in up to 79% of patients). A trial of alternate maintenance therapies after isotretinoin induction for leukoplakia suggested that low-dose isotretinoin was more effective in maintaining remissions than beta-carotene and caused fewer side effects than high-dose therapy: 12% of participants experienced severe toxicity and 42% had moderate toxicity from low-dose isotretinoin, including dry skin, cheilitis, and conjunctivitis.18

Uncontrolled trials using beta-carotene demonstrated variable reductions (up to 71%) in the occurrence of oral leukoplakia and mucosal dysplasia.19-21 In a randomized trial, however, the majority of patients with leukoplakia progressed during beta-carotene treatment.18 Although side effects of beta-carotene are minimal, older male smokers who took beta-carotene for 5-8 years experienced slightly higher rates of lung cancer and overall mortality in a recently completed trial in Finland.22 

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The American Cancer Society recommends a cancer checkup that includes oral examination every 3 years for persons over age 20 and annually for those over age 40.24 The Canadian Task Force on the Periodic Health Examination concluded that there was insufficient evidence to include or exclude screening for oral cancer in the periodic health examination of persons in the general population, but suggested that annual oral examination by a physician or dentist should be considered for persons over 60 with risk factors for oral cancer (e.g., smokers and regular drinkers).25 Although the National Institutes of Health no longer issue specific clinical guidelines regarding screening for oral cancer, both the National Cancer Institute and the National Institute of Dental Research support efforts to promote the early detection of oral cancers during routine dental examinations.8,26

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Primary prevention strategies, such as counseling patients regarding the use of tobacco and alcohol, may have a greater impact on the morbidity and mortality associated with oral cancer than measures aimed at early detection. There is good evidence that tobacco use and excessive consumption of alcohol are both independent and synergistic risk factors for oral cancer.3 Over 90% of oropharyngeal cancer deaths are associated with smoking.5 In addition to smoking and alcohol, oral cancer is also associated with the use of snuff and chewing tobacco.27

Oral cancer is a relatively uncommon cancer in the United States. Even among high-risk groups such as smokers, oral cancer accounts for a relatively small proportion (<2%) of all deaths.4 Available screening tests for oral cancer are limited to the physical examination of the mouth, a test of undetermined sensitivity, specificity, and positive predictive value. Despite the strong association between stage at diagnosis and survival, there are few controlled data to determine whether routine screening in the primary care setting leads to earlier diagnosis or reduced mortality from oral cancer. Given the significant morbidity and mortality associated with advanced oral cancer and its treatment, clinicians may wish to include careful examinations for oral cancer in asymptomatic persons at significantly increased risk for the disease (see Clinical Intervention) direct evidence of a benefit of screening in any group, however, is lacking. It is also appropriate to refer patients for regular visits to a dentist, for whom complete examination of the oral cavity is often more feasible (see Chapter 61).

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There is insufficient evidence to recommend for or against routine screening of asymptomatic persons for oral cancer by primary care clinicians ("C" recommendation). Although direct evidence of a benefit is lacking, clinicians may wish to include an examination for cancerous and precancerous lesions of the oral cavity in the periodic health examination of persons who chew or smoke tobacco (or did so previously), older persons who drink regularly, and anyone with suspicious symptoms or lesions detected through self-examination. All patients, especially those at increased risk, should be advised to receive a complete dental examination on a regular basis (see Chapter 61). All adolescent and adult patients should be asked to describe their use of tobacco (Chapter 54) and alcohol (Chapter 52). Appropriate counseling should be offered to those persons who smoke cigarettes, pipes, or cigars, those who use chewing tobacco or snuff, and those who have evidence of alcohol abuse. Persons with increased exposure to sunlight should be advised to take protective measures when outdoors to protect their lips and skin from the harmful effects of ultraviolet rays (see Chapter 12).

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The draft update of this chapter was prepared for the U.S. Preventive Services Task Force by Paul S. Frame, MD, based on materials prepared for the Canadian Task Force on the Periodic Health Examination by Carl Rosati, MD, FRCSC.

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1. Ries LAG, Miller BA, Hankey BF, et al, eds. SEER cancer statistics review, 1973-1991: tables and graphs. Bethesda: National Cancer Institute. 1994;(NIH Publication no. 94-2789.)
2. Wingo PA, Tong T, Bolden S. Cancer statistics, 1995. CA Cancer J Clin. 1995;45:8–30. [PubMed]
3. Vokes EE, Weichselbaum RR, Lippman SM, et al. Head and neck cancer. N Engl J Med. 1993;328:184–194. [PubMed]
4. Centers for Disease Control and Prevention. Cigarette smoking—attributable mortality and years of potential life lost — United States, 1990. MMWR. 1993;42:645–649. [PubMed]
5. Silverman S Jr. Oral cancer. Atlanta: American Cancer Society, 1990. 
6. Epstein JB, Silverman S. Head and neck malignancies associated with HIV infection. Oral Surg Oral Med Oral Pathol. 1992;73:193–200. [PubMed]
7. Mashberg A, Meyers H. Anatomical site and size of 222 early asymptomatic oral squamous [cell] carcinomas: [a continuing prospective study of oral cancer. II.] Cancer. 1976;37:2149–2157. [PubMed]
8. Department of Health and Human Services, National Cancer Institute. Tobacco effects in the mouth. Bethesda: Public Health Service. 1992;(DHHS Publication no. (NCI) 92-3330.)
9. Mehta FS, [Gupta PC,] Bhonsle RB, [Murti PR,] Daftary DK, et al. Detection of oral cancer using basic health workers in an area of high oral cancer incidence in India. Cancer Detect Prev. 1986;9:219–225. [PubMed]
10. Warnakulasuriya KAAS, Nanayakkara BG. Reproducibility of an oral cancer and precancer detection program using a primary health care model in Sri Lanka. Cancer Detect Prev. 1991;15:331–334. [PubMed]
11. Elwood JM, Gallagher RP. Factors influencing early diagnosis of cancer of the oral cavity. Can Med Assoc J. 1985;133:651–656. [PMC free article] [PubMed]
12. Fedele DJ, Jones JA, Niessen LC. Oral cancer screening in the elderly. J Am Geriatr Soc. 1991;39:920–925. [PubMed]
13. Mashberg A. Final evaluation of tolonium chloride rinse for screening of high-risk patients with asymptomatic squamous carcinoma. J Am Dent Assoc. 1983;106:319–323. [PubMed]
14. Rosenberg D, Cretin S.. Use of meta-analysis to evaluate tolonium chloride in oral cancer screening. Oral Surg Oral Med Oral Pathol. 1989;67:621–627. [PubMed]
15. Williams RG The early diagnosis of carcinoma of the mouth. Ann R Coll Surg Engl. 1981;63:423–425. [PMC free article] [PubMed]
16. Hong WK, Endicott J, Itri LM, et al. 13-cis-retinoic acid in the treatment of oral leukoplakia. N Engl J Med. 1986;315:1501–1505. [PubMed]
17. Hong WK, Lippman SM, Itri LM, et al. Prevention of second primary tumors with isotretinoin in squamous cell carcinoma of the head and neck. N Engl J Med. 1990;323:795–801. [PubMed]
18. Lippman SM, Batsakis JG, Toth BB, et al. Comparison of low dose isotretinoin with beta carotene to prevent oral carcinogenesis. N Engl J Med. 1993;328:15–20. [PubMed]
19. Malaker K, Anderson BJ, Beecroft WA, et al. Management of oral mucosal dysplasia with beta -carotene retinoic acid: a pilot crossover study. Cancer Detect Prev. 1991;15:335–340. [PubMed]
20. Garewal HS. Potential role of beta-carotene in prevention of oral cancer. Am J Clin Nutr. 1991;53:294S–297S. [PubMed]
21. Stich HF, Mathew B, Sankaranarayanan R, et al. Remission of precancerous lesions in the oral cavity of tobacco chewers and maintenance of the protective effect of beta -carotene or vitamin A. Am J Clin Nutr. 1991;53:298S–304S. [PubMed]
22. The Alpha-tocopherol, Beta Carotene Cancer Prevention Study Group. The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. N Engl J Med. 1994;330:1029–1035. [PubMed]
23. Benner SE, Winn RJ, Lippman SM, et al. Regression of oral leukoplakia with alpha-tocopherol: a Community Clinical Oncology Program chemoprevention study. J Natl Cancer Inst. 1993;85:44–47. [PubMed]
24. American Cancer Society. Guidelines for the cancer-related checkup: an update. Atlanta: American Cancer Society, 1993. [PubMed]
25. Canadian Task Force on the Periodic Health Examination. Canadian guide to clinical preventive health care. Ottawa: Canada Communication Group. 1994:838–847.
26. National Institute of Dental Research. Detecting oral cancer: a guide for dentists. Bethesda: National Institute of Dental Research, 1994.
27. Connolly GN, Winn DM, Hecht SS, et al. The reemergence of smokeless tobacco. N Engl J Med. 1986;314:1020–1027. [PubMed]

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