Abstract
Background: One of the most common cancers is squamous cell carcinoma of the head and neck which is a serious health challenge worldwide. Considering the importance of knowledge of incidence, death and risk factors in prevention programs, this study was conducted to investigate the incidence, mortality and risk factors for oral cavity and lip cancer in the world.
Methods: A search was performed in Web of Science, PubMed and Scopus. The search keywords included: oral cavity or lip cancer, epidemiology, incidence, mortality, risk factors, and a combination of these terms. Studies that referred to epidemiological aspects of oral cavity and lip cancer epidemiology and risk factors were included in the review.
Results: The five countries with the highest number of cancer of the oral cavity and lip included India, the United States, China, Pakistan and Bangladesh. The standard incidence of these cancers in the world was 4 per 100,000 people (in men versus women, 5.5 and 2.5 per hundred thousand, respectively). The five countries with the highest number of deaths from oral cavity cancer were India, China, Pakistan, Bangladesh and Russia. In 2012, the standardized death rate for this type of cancer was 1.9 per 100,000 people in the world (2.7 vs. 1.2 in every 100,000 of men vs. women, respectively). The most important risk factors for oral and lip cancer include tobacco smoke, alcohol drinking, viral infections, exposure to sunlight, and socioeconomic status.
Conclusion: In order to reduce the burden of this cancer, there are the strategies for preventing risk factors such as tobacco and alcohol control, and vaccination against HPV infection to prevent oral cancers. Also, early detection by screening high-risk populations for oral cancer as well as risk reduction through training programs for physician and patients are effective.
Introduction
Squamous cell carcinoma of the head and neck belong to a non-homogeneous group of cancers that are located at various places in the body1 and are one of the most common cancers in the world with more than 450,000 new cases and 350,000 deaths annually2. Squamous cell carcinoma consists of oral cavity, oropharynx, nasal cavity, para nasal sinus, nasopharynx, hypopharynx, larynx, tongue, tonsils, parotid glands, salivary glands3, and lip4. Each of the head and neck cancers is associated with various risk factors and prognosis5. The oral cavity is the most common cancer in the head and neck region2, with an annual incidence of 300,373 and a mortality rate of 145,3535. Cancer of the lip is a typical malignant tumor that consists of 25 – 30 % of all cancers in the mouth6. Oral and lip cancer is a serious health challenge worldwide4. The incidence and mortality of this cancer is very different in various parts of the world and has a wide geographical variation. On the other hand, there is no comprehensive estimate of the incidence and mortality of this cancer. Considering the importance of being informed about the incidence, death and risk factors in prevention programs, this study aimed to determine the incidence, mortality and risk factors for oral cavity and lip cancer worldwide.
Methods
A search was performed in Web of Science, PubMed and Scopus. The search keywords included: oral cavity or lip cancer, epidemiology, incidence, mortality, risk factors, and a combination of these terms. Studies that referred to epidemiological aspects of oral cavity and lip cancer epidemiology and risk factors were included in the review.
Results
Incidence and mortality
Regarding the incidence and mortality rate of oral cavity cancer in the world, in 2012, there were a total of 300,373 cases of this cancer worldwide, of which 1989,755 were males and 101,398 were females4. The 5 countries with the highest number of this cancer were India (with 77,003 cases), the United States (with 26,064 cases), China (with 21,413 cases), Pakistan (with 12,761 cases), and Bangladesh (with 10,550 cases)4. The standard incidence of oral cavity cancer in the world was 4 in every 3,000 people, 5.5 in men and 2.5 in women per 100,000 people4. In 2012, the global age-standardized rate (ASR) for lip cancer was 0.3 per 100,000 (0.4 in men and 0.2 in women)7. In terms of the number of new cases worldwide, most of the lip cancer cases (19.2 %) occurred in Central and Eastern Europe. At the national level, both Papua New Guinea and Australia had the highest ASR of this cancer, which was 8.9 and 2.6, respectively, per 100,000 people. Globally, Central and Eastern European countries such as Serbia and Ukraine ranked 4th and 5th highest, respectively, for lip cancer. The regions with the lowest incidence were in Eastern/ South-eastern Asia and sub-Saharan Africa. The incidence of lip cancer was higher among men than women, and this rate was 2.5 for men compared to women. Lip cancer in men and women older than 60 years old were 63.2 % and 69.9 %, respectively7. In 2012, the ASR for oral cavity cancer was 2.7 per 100,000 (3.7 in men and 1.8 in women per 100,000). New Zealand's Papua New Guinea had the highest ASR of oral cavity cancer, with 10.6 new cases per 100,000. However, the 2nd, 3rd and 4th countries with the highest ASR for oral cavity cancer were Maldives, Sri Lanka and Pakistan (predominantly South Asian regions). The lowest incidence was observed in Oceania (for men) and in East/ South-east Asia (for women)7.
In 2012, there was 145,353 mortalities from oral cavity and lip cancer worldwide, of which 97,940 were men and 47,413 were women. The five countries with the highest number of deaths from oral cavity cancer were India (with 52,067 deaths), China (with 11,333 deaths), Pakistan (with 7,266 deaths), Bangladesh (with 6,071 deaths), and Russia (with 5,658 deaths). In 2012, the standardized death rate for this cancer in the world was 1.9 per 100,000 people (2.7 in men and 1.2 in women for every 100,000)4. In 2012, cancer of the oral cavity and lip was the 12th most common cancer in Asia and was the 8th highest among cancers in men. Lip and oral cavity malignancy is the 2nd most common cancer among men in South Asia. In fact, in 2012, Sri Lanka had the highest ASR of South Asia; this cancer was the most common among men in this country8. In Australia, lip and oral cavity ranked as the 9th most common cancer among men with a standardized incidence age of 8.8%, while in New Zealand, it ranked as the 14th most common cancer among men with an ASR of 5.5 per 100,000. Papua New Guinea and Solomon Islands reported a high incidence rate of oral cancer due to tobacco and paan, while Vanuatu Island showed lower incidence8, 9.
Risk factors for oral cavity cancer
Tobacco
Excessive use of tobacco (both smoked and chewable) is a potential risk factor for oral cavity cancer10. The onset of consumption, duration and frequency of chewing of bidis or smoked cigarettes on a daily basis are strongly linked to oral cancer11.
Smoked tobacco
Smoked tobacco is a risk factor for the upper respiratory tract12, and there is a positive relationship between the risk of using tobacco smoke and oral cavity cancer13, 14. This relationship has been confirmed in several studies15, 16, 17. The risk for oral cavity cancer in people who use tobacco is 1.4 – 1.7 times higher than those who do not consume tobacco15, 16, 17, 18. Several case-control studies have reported that the lower the age of tobacco consumption onset, the higher the risk for oral cavity cancer19, 20. A study in India illustrated that the risk of oral cavity cancer in traditional tobacco (bidi, chutta and cheroot) users is twice as high as industrial tobacco users because traditional tobacco has a higher alkalinity and carcinogenicity21.
Smoke-free tobacco
Toxicants in smoke-free tobacco appear to increase the risk of oral cavity cancer12. The risk of oral cavity cancer depends on the length of time22, duration of use12, and onset in the early age22.
Exposure to tobacco smoke
Studies of the association between the effects of environmental exposure and tobacco smoke and the risk of oral cancer cavity are scarce12. In a study conducted on the relationship between tobacco smoke in the home or workplace with oral and pharyngeal cancers, it was found that the risk of oral cavity cancer was lower than that of pharyngeal cancer (not significant), and that the unauthorized use of tobacco for more than 15 years had no risk for oral cavity at home or in the workplace23.
Marijuana smoke
Marijuana increases the risk of oral and lip cancer24. Marijuana is mostly smoked with carcinogenic smoke included aromatic multi-ring hydrocarbons, which can be higher than those in tobacco smoke25. Generally, marijuana consumers are tobacco or alcohol consumers26.
Alcohol consumption
The risk of oral cavity malignancy is increased by drinking alcohol; the higher the daily intake and duration of use, the higher the risk of oral cavity cancer12. Alcohol consumption of more than 150 g per day extends the risk of oral cavity cancer27. On the other hand, studies conducted on the relationship of age of onset of alcohol consumption and the risk of oral cavity cancer have shown that the risk of this cancer is elevated if the age of alcohol consumption begins in the teenage years22, 28.
Paan (betel quid chewing)
Paan consumption also increases the risk of oral cavity cancer. Paan contains arecanut, betel leaves, slaked lime (which may include tobacco); other ingredients (such as spices, sweets and essence) may be added to the paan, according to taste29. The use of paan and gutkha is abundant in most countries and is difficult to control it despite that fact that excessive use of both causes cancer 30. In Asia, taking paan with or without tobacco is a stronger risk factor than tobacco or alcohol31, 32. In fact, the risk of oral cavity cancer in people who consume paan is about 1.5 -3 times greater than that of tobacco consumption and about 2-11 times greater than that of alcohol consumption31, 32, 33. Due to the lack of awareness and education, people who generally use paan and gutkha are not aware of their harmful effects. Generally, they believe that these products are used to clean the mouth (like mouthwash), help digestion, aid germ astringency, and boost or relieve the mood34.
Diet
It seems that inequality in the diet (or its misuse) is responsible for 11-15% of oral cavity and larynx cancers12. Low consumption of vegetables and fruits increases the risk of oral cavity malignancy35, 36. As well, red meat consumption of greater than once a week elevates the risk of oral malignancy compared to white meats like chicken and fish10. Moreover, the use of hot drinks such as tea can increase the risk of oral cancer, which may be due to repeated heat damage due to mucosal contraction of the oral cavity10, 37. Regarding the consumption of coffee, the results of the studies have been contradictory12.
Body Mass Index (BMI)
In some studies, weight gain has been reported as a protective factor, but weight loss has been reported as a potential risk factor for oral cavity cancer38.
Human papillomavirus and sexual behaviors
Viral papillomavirus infection is one of the most principal causes of squamous cell carcinoma of the head and neck39, 40. The apparent increase in the incidence of oral HPV in the general population has been observed, which has led to an increase in concerns about human papillomavirus (HPV) infection and the risk of oral cavity cancer41, 42. The number of sexual partners plays a main role in the transmission of the HPV virus, which can increase the risk of oral cancer43. About 25 % of cases of oral cavity cancer are related to HPV44, 45. Given the recent global trend of oral HPV infections, the incidence of oral cancer is expected to increase in the coming decades46.
Family history of cancer
Family history of oral malignancy in different populations may depend on various environmental and genetic factors, including the prevalence of genetic dissimilarity in genes and exposure to diverse environmental factors47. This variation is more dependent on differences in exposure to tobacco and alcohol, which are very significant factors for oral cavity cancer48. Furthermore, genetic polymorphisms can expand the sensitivity of oral carcinoma through interactions with alcohol, tobacco and possibly diet components47. Besides, the use of these can be the reason for oral cavity carcinoma49. These finding indicate genetic instability is a risk factor for oral carcinoma49.
Oral and dental health
Oral health behaviors are a risk factor for oral cavity cancer10. Various factors have been used to assess oral and dental health; these include daily brushing, used materials, number of teeth lost, number of filled or damaged teeth, frequency of check-ups, gingival bleeding, and overall teeth status12. Missing more than five teeth is considered as an indicator of increased risk for oral malignancy10. Effective brushing eliminates dental plaques and subsequently improves oral and dental health; therefore, it reduces the risk of cancer of the head and neck region50. Dental plaque is a reservoir for the growth of pathogens and the production of nitrosamines that help to increase inflammation of the mouth10. Regular brushing can eliminate dental plaque, alcohol, nicotine, fungi, nitrosamines, and other toxic toxins, thereby delaying or preventing carcinogenesis10.
Use of mouthwash
The relationship between alcohol mouthwash and oral cancer growth over the past decade has been the topic of debate12. Some studies have confirmed a positive relationship between mouthwash and oral malignancy12. However, the concentration of alcohol in the mouthwash has not been sufficiently evaluated12.
Oral mucus diseases
Potentially malignant oral disorders such as leukoplakia, submucous erythroplasia T fibrosis, lichen planus, and chronic oral candidiasis may increase the risk of squamous cell carcinoma51, 52. Some systemic diseases can have an effect on oral health, leading to malignancy or even cancer of the mouth12. Although most oral lesions are benign, many of them may appear with potential abnormalities in the mouth46. One of the most common oral lesions is squamous cell papilloma - a malignant, neuromuscular lesion that is swollen and usually has a monopoly of small white or red designs on the surface53. Also, lesions of the oral cavity of leukoplakia are also white plaques that can be considered as potential lesions46.
Social inequality
According to the study, the risk of oral cavity cancer is higher in the lower classes12.
Occupational exposure
In many occupations and industries, the risk of this cancer has been observed. The relationship between exposure to perchlorethylene (organic solvents used in cleaning laundry) and oral cavity cancer has been demonstrated12. An increased risk of this cancer in India has been confirmed among male farmers and industrial laborers12. Also, in one study, an elevated risk of this cancer was observed among male workers who worked at a cane factory in Puerto Rico12.
Risk factors for lip cancer
Exposure to sunlight
Exposure to sunlight is a principal risk factor for lip cancer54; it increases the incidence of illness in people who are working outdoors or live in the countryside55. In particular, UV — especially UVB (wavelengths of 320 – 900 nm) — is considered as the most salient environmental factor. UVA (wavelength 320-400 nm) may also play a role in carcinogenesis56. Evidence related to the association between exposure to sunlight and lip cancer has been shown through examinations of changes in lip cancer that are associated with sun rays and ethnic characteristics55.
Tobacco smoke
Smoking is a principal risk factor for lip cancer, which can affect both lips equally57. Malignant lesions typically occur in a place where the cigar or pipe cigar is placed58. Traditional tobacco smoking, especially pipe smoking, is related with lip cancer. The nitrosamines found in tobacco are one of the main carcinogenic agents for cancer induction56.
Viral infection
Viruses are one of the most important features in the development of this cancer57. The relationship between this cancer and herpes labialis infection has been observed. Herpes simplex virus type 1 and also HPV (especially HPV-16) have the potential for carcinogenicity56. The most common pathogenesis of lip cancer is the recurrence of herpes virus57.
Race
People with bright eyes, hair and skin are at high risk of lip cancer56, 57; about half of cancers occur in the North European countries59. Lip cancer is negligible in people with darker skin and among blacks and Eastern folks56, 57. This variation is due to the natural pigmentation of the natural melanin at the vermilion border, which is found in non-white races and creates a protection against sunlight56.
Familial and genetic factors
Genetic or familial factors are one of the factors which contribute to the development of lip cancer57. Different diseases are more common among relatives than ordinary people59 and it has been proven that there is an inherited basis for lip cancer. Also, the exposure to common risk factors, such as environmental exposure, increases the risk of inheritance and family life56.
Immunosuppression and immunodeficiency
An increase in the prevalence of various malignancies has been reported in transplant recipients56. Kidney transplant patients in immuno-suppressive states have reported the most prevalence of obstructive and malignant lip lesions among renal transplant patients57; indeed, the risk of lip cancer increases with long-term treatment of immunosuppression56.
Occupation
Exposure to sunlight, especially outdoor activity, is a risk factor for lip cancer60. Fishing, agriculture, forestry and agriculture, creosote exposure, and work in the greenhouse are linked to lip cancer56, 57. The number of cases of lip cancer in men is greater than that of women, which may be related to occupation and behavioral differences between the sexes since a high percentage of men work outdoors58. Some researchers believe that using lipstick could act as a protective agent, contributing to the observed gender differences61.
Residential area
Lip cancer is more common in people living in rural areas than those living in urban areas, and the most likely cause is exposure to sunlight62.
Socioeconomic status
Low socioeconomic status is strongly related to the high risk of lip cancer. However, the correlation between socioeconomic status and other risk factors (such as high smoking, rural and occupational status) may increase the risk of lip cancer56, 57.
Conclusion
The aim of this study was to determine the epidemiological aspects and risk factors of oral cavity and lip cancer in the world. Findings of the study showed that the five countries with the highest number of oral cavity and lip cancers were India, the United States, China, Pakistan and Bangladesh. The standard incidence of these cancers in the world was 4 per 100,000 people (in men 5.5 and 2.5 in women per every 100,000). The five countries with the highest number of deaths from oral and lip cancer were India, China, Pakistan, Bangladesh and Russia. In 2012, the standardized death rate for oral and lip cancer in the world was 1.9 per 100,000 people (2.7 in men and 1.2 in women per every 100,000). Excessive use of tobacco (both smoked and chewable), marijuana smoke, alcohol consumption, diet, and body mass index are all risk factors for oral cancer. It seems that other factors, including HPV infection, genetic or family factors, oral health behaviors, systemic diseases, social inequalities and occupational exposures, are all considered as risk factors for oral cavity cancer. Exposure to sunlight, tobacco smoke, viruses, and racial variations play an important role in the progress of lip cancer. Also, genetic or family factors, immunosuppressive regimens, occupation, place of residence, and socioeconomic status are the most salient factors contributing to the development of lip cancer. In general, in order to reduce the burden of this cancer, strategies for preventing risk factors, including through controlling tobacco and alcohol use, vaccination against HPV infection to prevent oral cancer, early detection of screening of high-risk populations, and risk reduction through training programs for physician and patients, can all be effective.
Abbreviations
ASR: Age-standardized rate
BMI: Body Mass Index
HPV: Human papillomavirus virus
Acknowledgments
Not applicable.
Author’s contributions
All authors equally contributed to this article. All authors read and approved the final manuscript.
Funding
Not applicable.
Availability of data and materials
Not applicable.
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
References
-
Yete
S.,
D'Souza
W.,
Saranath
D.,
High-Risk Human Papillomavirus in Oral Cancer: Clinical Implications. Oncology.
2018;
94
(3)
:
133-141
.
View Article PubMed Google Scholar -
Abreu
P.M.,
Có
A.C.G.,
Azevedo
P.L.,
Valle
I.B.,
Frequency of HPV in oral cavity squamous cell carcinoma. BMC cancer.
2018;
18
(1)
:
324
.
View Article PubMed Google Scholar -
Argiris
A.,
Karamouzis
M.V.,
Raben
D.,
Ferris
R.L.,
Head and neck cancer. The Lancet.
2008;
371
(9625)
:
1695-709
.
View Article Google Scholar -
Siakholak
F.R.,
Ghoncheh
M.,
Pakzad
R.,
Gandomani
H.S.,
Ghorat
F.,
Salehiniya
H.,
Epidemiology, incidence and mortality of oral cavity and lips cancer and their relationship with the human development index in the world. Biomedical Research and Therapy.
2016;
3
(10)
:
872-888
.
View Article Google Scholar -
Ferlay
J.,
Soerjomataram
I.,
Dikshit
R.,
Eser
S.,
Mathers
C.,
Rebelo
M.,
Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. International journal of cancer.
2015;
136
(5)
:
E359-E386
.
View Article PubMed Google Scholar -
Maruccia
M.,
Onesti
M.G.,
Parisi
P.,
Cigna
E.,
Scuderi
N.,
Lip cancer: a 10-year retrospective epidemiological study. Anticancer research.
2012;
32
(4)
:
1543-1546
.
-
Shield
K.D.,
Ferlay
J.,
Jemal
A.,
Sankaranarayanan
R.,
Chaturvedi
A.K.,
Bray
F.,
The global incidence of lip, oral cavity, and pharyngeal cancers by subsite in 2012. CA: a cancer journal for clinicians.
2017;
67
(1)
:
51-64
.
View Article PubMed Google Scholar -
Gupta
N.,
Gupta
R.,
Changing Trends in oral cancer-a global scenario. Nepal journal of epidemiology.
2016;
6
(4)
:
613
.
View Article PubMed Google Scholar -
Lumukana
R.,
King
T.,
Smoking and chewing habits of oral cancer patients in the Solomon Islands. Pacific health dialog.
2003;
10
(1)
:
41-44
.
-
Gupta
B.,
Bray
F.,
Kumar
N.,
Johnson
N.W.,
Associations between oral hygiene habits, diet, tobacco and alcohol and risk of oral cancer: A case-control study from India. Cancer epidemiology. 2017;51:7-14. PMid:28968558.
.
View Article Google Scholar -
Gupta
B.,
Kumar
N.,
Johnson
N.W.,
Relationship of lifetime exposure to tobacco, alcohol and second hand tobacco smoke with upper aero-digestive tract cancers in India: a case-control study with a life-course perspective. Asian Pacific journal of cancer prevention: APJCP.
2017;
18
(2)
:
347
.
-
Radoï
L.,
Luce
D.,
A review of risk factors for oral cavity cancer: the importance of a standardized case definition. Community dentistry and oral epidemiology.
2013;
41
(2)
:
97-109
.
View Article PubMed Google Scholar -
Lubin
J.H.,
Purdue
M.,
Kelsey
K.,
Zhang
Z.F.,
Winn
D.,
Wei
Q.,
Total exposure and exposure rate effects for alcohol and smoking and risk of head and neck cancer: a pooled analysis of case-control studies. American journal of epidemiology.
2009;
170
(8)
:
937-947
.
View Article PubMed Google Scholar -
Polesel
J.,
Talamini
R.,
Vecchia
C.,
Tobacco smoking and the risk of upper aero‐digestive tract cancers: A reanalysis of case-control studies using spline models. International journal of cancer.
2008;
122
(10)
:
2398-2402
.
View Article PubMed Google Scholar -
Hashibe
M.,
Brennan
P.,
Benhamou
S.,
Castellsague
X.,
Chen
C.,
Alcohol drinking in never users of tobacco, cigarette smoking in never drinkers, and the risk of head and neck cancer: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. Journal of the National Cancer Institute.
2007;
99
:
777-789
.
View Article PubMed Google Scholar -
Znaor
A.,
Brennan
P.,
Independent and combined effects of tobacco smoking, chewing and alcohol drinking on the risk of oral, pharyngeal and esophageal cancers in Indian men. International journal of cancer.
2003;
105
(5)
:
681-686
.
View Article PubMed Google Scholar -
Winn
D.M.,
Blot
W.J.,
Pickle
L.W.,
Toledo
A.,
Fraumeni
J.F.,
Snuff dipping and oral cancer among women in the southern United States. New England Journal of Medicine.
1981;
304
(13)
:
745-749
.
View Article PubMed Google Scholar -
Hashibe
M.,
Brennan
P.,
Interaction between tobacco and alcohol use and the risk of head and neck cancer: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. Cancer Epidemiology and Prevention Biomarkers.
2009;
18
(2)
:
541-550
.
View Article PubMed Google Scholar -
Franceschi
S.,
Barra
S.,
Vecchia
C.,
Bidoli
E.,
Negri
E.,
Talamini
R.,
Risk factors for cancer of the tongue and the mouth. A case‐control study from northern Italy. Cancer.
1992;
70
(9)
:
2227-2233
.
View Article Google Scholar -
Sankaranarayanan
R.,
Duffy
S.W.,
Day
N.E.,
Nair
M.K.,
Padmakumary
G.,
A case‐control investigation of cancer of the oral tongue and the floor of the mouth in Southern India. International Journal of Cancer.
1989;
44
(4)
:
617-621
.
View Article PubMed Google Scholar -
Gupta
P.C.,
Murti
P.,
Bhonsle
R.,
Epidemiology of cancer by tobacco products and the significance of TSNA. Critical reviews in toxicology.
1996;
26
(2)
:
183-198
.
View Article PubMed Google Scholar -
Sankaranarayanan
R.,
Duffy
S.W.,
Padmakumary
G.,
Day
N.E.,
Nair
M.K.,
Risk factors for cancer of the buccal and labial mucosa in Kerala, southern India. Journal of Epidemiology & Community Health.
1990;
44
(4)
:
286-292
.
View Article PubMed Google Scholar -
Lee
Y.C.A.,
Boffetta
P.,
Sturgis
E.M.,
Wei
Q.,
Zhang
Z.F.,
Muscat
J.,
Involuntary smoking and head and neck cancer risk: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. Cancer Epidemiology and Prevention Biomarkers.
2008;
17
(8)
:
1974-1981
.
View Article PubMed Google Scholar -
Rosenblatt
K.A.,
Daling
J.R.,
Chen
C.,
Sherman
K.J.,
Schwartz
S.M.,
Marijuana use and risk of oral squamous cell carcinoma. Cancer Research.
2004;
64
(11)
:
4049-4054
.
View Article PubMed Google Scholar -
Moir
D.,
Rickert
W.S.,
A comparison of mainstream and sidestream marijuana and tobacco cigarette smoke produced under two machine smoking conditions. Chemical research in toxicology.
2007;
21
(2)
:
494-502
.
View Article PubMed Google Scholar -
Lee
Y.C.,
Boffetta
P.,
Involuntary smoking and the risk of head and neck cancer: Pooled analysis in the INHANCE consortium. AACR.
2008
.
-
Polesel
J.,
Maso
L.,
Estimating dose‐response relationship between ethanol and risk of cancer using regression spline models. International journal of cancer.
2005;
114
(5)
:
836-841
.
View Article PubMed Google Scholar -
Zheng
T.,
Boyle
P.,
Tobacco smoking, alcohol consumption, and risk of oral cancer: a case-control study in Beijing, People's Republic of China. Cancer Causes & Control.
1990;
1
(2)
:
173-179
.
View Article PubMed Google Scholar -
Humans IWGotEoCRt, Organization WH, Cancer IAfRo. Betel-quid and areca-nut chewing and some areca-nut-derived nitrosamines. IARC.
2004
.
-
G. Shah,
P. Chaturvedi,
S. Vaishampayan,
Arecanut as an emerging etiology of oral cancers in India. Indian journal of medical and paediatric oncology: official journal of Indian Society of Medical & Paediatric Oncology. 2012;
33
(2)
:
71
.
View Article PubMed Google Scholar -
Merchant
A.,
Husain
S.S.,
M. Hosain,
Paan without tobacco: an independent risk factor for oral cancer. International journal of cancer.
2000;
86
(1)
:
128-131
.
View Article Google Scholar -
Muwonge
R.,
Ramadas
K.,
Role of tobacco smoking, chewing and alcohol drinking in the risk of oral cancer in Trivandrum, India: a nested case-control design using incident cancer cases. Oral oncology.
2008;
44
(5)
:
446-454
.
View Article PubMed Google Scholar -
Balaram
P.,
Sridhar
H.,
Oral cancer in southern India: The influence of smoking, drinking, paan‐chewing and oral hygiene. International journal of cancer.
2002;
98
(3)
:
440-445
.
View Article PubMed Google Scholar -
Banerjee
S.C.,
Gutka and Tambaku Paan use among South Asian immigrants: a focus group study. Journal of immigrant and minority health.
2014;
16
(3)
:
531-539
.
View Article PubMed Google Scholar -
Freedman
N.D.,
Fruit and vegetable intake and head and neck cancer risk in a large United States prospective cohort study. International Journal of Cancer.
2008;
122
(10)
:
2330-2336
.
View Article PubMed Google Scholar -
Franceschi
S.,
Food groups, oils and butter, and cancer of the oral cavity and pharynx. British Journal of cancer.
1999;
80
(3-4)
:
614
.
View Article PubMed Google Scholar -
Bravi
F.,
Foods, nutrients and the risk of oral and pharyngeal cancer. British journal of cancer.
2013;
109
(11)
:
2904
.
View Article PubMed Google Scholar -
Hashibe
M.,
Alcohol drinking, body mass index and the risk of oral leukoplakia in an Indian population. International journal of cancer.
2000;
88
(1)
:
129-134
.
View Article Google Scholar -
D'souza
G.,
Case-control study of human papillomavirus and oropharyngeal cancer. New England Journal of Medicine.
2007;
356
(19)
:
1944-1956
.
View Article PubMed Google Scholar -
Gillison
M.L.,
Distinct risk factor profiles for human papillomavirus type 16-positive and human papillomavirus type 16-negative head and neck cancers. Journal of the National Cancer Institute.
2008;
100
(6)
:
407-420
.
View Article PubMed Google Scholar -
Muñoz
N.,
Epidemiologic classification of human papillomavirus types associated with cervical cancer. New England Journal of Medicine.
2003;
348
(6)
:
518-527
.
View Article PubMed Google Scholar -
Ikuta
K.,
Satoh
Y.,
Hoshikawa
Y.,
Sairenji
T.,
Detection of Epstein-Barr virus in salivas and throat washings in healthy adults and children. Microbes and infection.
2000;
2
(2)
:
115-120
.
View Article Google Scholar -
D'Souza
G.,
Oral sexual behaviors associated with prevalent oral human papillomavirus infection. The Journal of infectious diseases.
2009;
199
(9)
:
1263-1269
.
View Article PubMed Google Scholar -
Lingen
M.W.,
Low etiologic fraction for high-risk human papillomavirus in oral cavity squamous cell carcinomas. Oral oncology.
2013;
49
(1)
:
1-8
.
View Article PubMed Google Scholar -
Walline
H.M.,
High-risk human papillomavirus detection in oropharyngeal, nasopharyngeal, and oral cavity cancers: comparison of multiple methods. JAMA otolaryngology-head & neck surgery.
2013;
139
(12)
:
1320-1327
.
View Article PubMed Google Scholar -
Pierangeli
A.,
Frequent detection of high human papillomavirus DNA loads in oral potentially malignant disorders. Clinical Microbiology and Infection.
2016;
22
(1)
:
e9-e15
.
View Article PubMed Google Scholar -
Garavello
W.,
Family history and the risk of oral and pharyngeal cancer. International journal of cancer.
2008;
122
(8)
:
1827-1831
.
View Article PubMed Google Scholar -
Vecchia
C.,
F.Lucchini,
F.Negri,
F. Levi,
Trends in oral cancer mortality in Europe. Oral oncology.
2004;
40
(4)
:
433-439
.
View Article PubMed Google Scholar -
Morris
B. L.,
Family cancer history and susceptibility to oral carcinoma in Puerto Rico. Cancer.
2001;
92
(8)
:
2102-2108
.
View Article Google Scholar -
Zeng
X.T.,
Meta-analysis on the association between toothbrushing and head and neck cancer. Oral oncology.
2015;
51
(5)
:
446-451
.
View Article PubMed Google Scholar -
Ho
P.S.,
Malignant transformation of oral potentially malignant disorders in males: a retrospective cohort study. Bmc Cancer.
2009;
9
(1)
:
260
.
View Article PubMed Google Scholar -
Lee
J.J.,
Carcinoma and dysplasia in oral leukoplakias in Taiwan: prevalence and risk factors. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology.
2006;
101
(4)
:
472-480
.
View Article PubMed Google Scholar -
Waal
V.D.,
Potentially malignant disorders of the oral and oropharyngeal mucosa; terminology, classification and present concepts of management. Oral oncology.
2009;
45
(4-5))
:
317-323
.
View Article PubMed Google Scholar -
Ribeiro
I.L.A.,
L.V. Rodrigues,
A.M.G. Valença,
L. Neto,
E. Andrade,
Factors associated with lip and oral cavity cancer. Revista Brasileira de Epidemiologia.
2015;
18
:
618-629
.
View Article PubMed Google Scholar -
Visscher
J.,
Schaapveld
M.,
Otter
R.,
Visser
O.,
Waal
W.I.,
Epidemiology of cancer of the lip in the Netherlands. Oral oncology.
1998;
34
(5)
:
421-426
.
View Article Google Scholar -
Visscher
J.,
Van
D.W.I.,
Etiology of cancer of the lip: A review. International journal of oral and maxillofacial surgery.
1998;
;27
(3)
:
199-203
.
View Article Google Scholar -
Moore
S.R.,
Johnson
N.,
Pierce
A.M.,
Wilson
D.F.,
The epidemiology of lip cancer: a review of global incidence and aetiology. Oral diseases.
1999;
5
(3)
:
185-195
.
View Article PubMed Google Scholar -
Czerninski
R.,
Zini
A.,
Sgan‐Cohen
H.,
Lip cancer: incidence, trends, histology and survival: 1970-2006. British Journal of Dermatology.
2010;
162
(5)
:
1103-1109
.
View Article PubMed Google Scholar -
Lindqvist
C.,
Teppo
L.,
Epidemiological evaluation of sunlight as a risk factor of lip cancer. British journal of cancer.
1978;
37
(6)
:
983
.
View Article PubMed Google Scholar -
Keller
A.Z.,
Cellular types, survival, race, nativity, occupations, habits and associated diseases in the pathogenesis of lip cancers. American journal of epidemiology.
1970;
91
(5)
:
486-499
.
View Article PubMed Google Scholar -
Abreu
L.,
Kruger
E.,
Tennant
M.,
Lip cancer in Western Australia, 1982-2006: a 25‐year retrospective epidemiological study. Australian dental journal.
2009;
54
(2)
:
130-135
.
View Article PubMed Google Scholar -
Doll
R.,
Urban and rural factors in the aetiology of cancer. International journal of cancer.
1991;
47
(6)
:
803-810
.
View Article PubMed Google Scholar
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Volume & Issue : Vol 7 No 8 (2020)
Page No.: 3898-3905
Published on: 2020-08-25
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