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Published in: Cancer Causes & Control 9/2011

01-09-2011 | Original paper

An examination of male and female odds ratios by BMI, cigarette smoking, and alcohol consumption for cancers of the oral cavity, pharynx, and larynx in pooled data from 15 case–control studies

Authors: Jay H. Lubin, Joshua Muscat, Mia M. Gaudet, Andrew F. Olshan, Maria Paula Curado, Luigino Dal Maso, Victor Wünsch-Filho, Erich M. Sturgis, Neonilia Szeszenia-Dabrowska, Xavier Castellsague, Zuo-Feng Zhang, Elaine Smith, Leticia Fernandez, Elena Matos, Silvia Franceschi, Eleonora Fabianova, Peter Rudnai, Mark P. Purdue, Dana Mates, Qingyi Wei, Rolando Herrero, Karl Kelsey, Hal Morgenstern, Oxana Shangina, Sergio Koifman, Jolanta Lissowska, Fabio Levi, Alexander W. Daudt, Jose Eluf Neto, Chu Chen, Philip Lazarus, Deborah M. Winn, Stephen M. Schwartz, Paolo Boffetta, Paul Brennan, Ana Menezes, Carlo La Vecchia, Michael McClean, Renato Talamini, Thangarajan Rajkumar, Richard B. Hayes, Mia Hashibe

Published in: Cancer Causes & Control | Issue 9/2011

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Abstract

Background

Greater tobacco smoking and alcohol consumption and lower body mass index (BMI) increase odds ratios (OR) for oral cavity, oropharyngeal, hypopharyngeal, and laryngeal cancers; however, there are no comprehensive sex-specific comparisons of ORs for these factors.

Methods

We analyzed 2,441 oral cavity (925 women and 1,516 men), 2,297 oropharynx (564 women and 1,733 men), 508 hypopharynx (96 women and 412 men), and 1,740 larynx (237 women and 1,503 men) cases from the INHANCE consortium of 15 head and neck cancer case–control studies. Controls numbered from 7,604 to 13,829 subjects, depending on analysis. Analyses fitted linear-exponential excess ORs models.

Results

ORs were increased in underweight (<18.5 BMI) relative to normal weight (18.5–24.9) and reduced in overweight and obese categories (≥25 BMI) for all sites and were homogeneous by sex. ORs by smoking and drinking in women compared with men were significantly greater for oropharyngeal cancer (p < 0.01 for both factors), suggestive for hypopharyngeal cancer (p = 0.05 and p = 0.06, respectively), but homogeneous for oral cavity (p = 0.56 and p = 0.64) and laryngeal (p = 0.18 and p = 0.72) cancers.

Conclusions

The extent that OR modifications of smoking and drinking by sex for oropharyngeal and, possibly, hypopharyngeal cancers represent true associations, or derive from unmeasured confounders or unobserved sex-related disease subtypes (e.g., human papillomavirus–positive oropharyngeal cancer) remains to be clarified.
Appendix
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Literature
1.
go back to reference Gillison ML (2007) Current topics in the epidemiology of oral cavity and oropharyngeal cancers. Head Neck 29(8):779–792PubMedCrossRef Gillison ML (2007) Current topics in the epidemiology of oral cavity and oropharyngeal cancers. Head Neck 29(8):779–792PubMedCrossRef
2.
go back to reference Mayne AT, Morse DE, Winn DM (2006) Cancers of the oral cavity and pharynx. In: Schottenfeld D, Fraumeni JF Jr (eds) Cancer epidemiology and prevention. Oxford University Press Inc, New York, pp 674–696CrossRef Mayne AT, Morse DE, Winn DM (2006) Cancers of the oral cavity and pharynx. In: Schottenfeld D, Fraumeni JF Jr (eds) Cancer epidemiology and prevention. Oxford University Press Inc, New York, pp 674–696CrossRef
3.
go back to reference Olshan AF (2006) Cancer of the larynx. In: Schottenfeld D, Fraumeni JF Jr (eds) Cancer epidemiology and prevention. Oxford University Press Inc, New York, pp 627–637CrossRef Olshan AF (2006) Cancer of the larynx. In: Schottenfeld D, Fraumeni JF Jr (eds) Cancer epidemiology and prevention. Oxford University Press Inc, New York, pp 627–637CrossRef
4.
go back to reference Franceschi S, Bidoli E, Herrero R, Munoz N (2000) Comparison of cancers of the oral cavity and pharynx worldwide: etiological clues. Oral Oncol 36(1):106–115PubMedCrossRef Franceschi S, Bidoli E, Herrero R, Munoz N (2000) Comparison of cancers of the oral cavity and pharynx worldwide: etiological clues. Oral Oncol 36(1):106–115PubMedCrossRef
5.
go back to reference Hayes RB, Bravo-Otero E, Kleinman DV et al (1999) Tobacco and alcohol use and oral cancer in Puerto Rico. Cancer Causes Control 10(1):27–33PubMedCrossRef Hayes RB, Bravo-Otero E, Kleinman DV et al (1999) Tobacco and alcohol use and oral cancer in Puerto Rico. Cancer Causes Control 10(1):27–33PubMedCrossRef
6.
go back to reference Blot WJ, Mclaughlin JK, Winn DM et al (1988) Smoking and drinking in relation to oral and pharyngeal cancer. Cancer Res 48(11):3282–3287PubMed Blot WJ, Mclaughlin JK, Winn DM et al (1988) Smoking and drinking in relation to oral and pharyngeal cancer. Cancer Res 48(11):3282–3287PubMed
7.
go back to reference Muscat JE, Richie JP, Thompson S, Wynder EL (1996) Gender differences in smoking and risk for oral cancer. Cancer Res 56(22):5192–5197PubMed Muscat JE, Richie JP, Thompson S, Wynder EL (1996) Gender differences in smoking and risk for oral cancer. Cancer Res 56(22):5192–5197PubMed
8.
go back to reference Kabat GC, Chang CJ, Wynder EL (1994) The role of tobacco, alcohol-use, and body-mass index in oral and pharyngeal cancer. Int J Epidemiol 23(6):1137–1144PubMedCrossRef Kabat GC, Chang CJ, Wynder EL (1994) The role of tobacco, alcohol-use, and body-mass index in oral and pharyngeal cancer. Int J Epidemiol 23(6):1137–1144PubMedCrossRef
9.
go back to reference Freedman ND, Abnet CC, Leitzmann MF, Hollenbeck AR, Schatzkin A (2007) Prospective investigation of the cigarette smoking-head and neck cancer association by sex. Cancer 1101593–1101601 Freedman ND, Abnet CC, Leitzmann MF, Hollenbeck AR, Schatzkin A (2007) Prospective investigation of the cigarette smoking-head and neck cancer association by sex. Cancer 1101593–1101601
10.
go back to reference Ide R, Mizoue T, Fujino Y et al (2008) Cigarette smoking, alcohol drinking, and oral and pharyngeal cancer mortality in Japan. Oral Dis 14(4):314–319PubMedCrossRef Ide R, Mizoue T, Fujino Y et al (2008) Cigarette smoking, alcohol drinking, and oral and pharyngeal cancer mortality in Japan. Oral Dis 14(4):314–319PubMedCrossRef
11.
go back to reference Akiba S, Hirayama T (1990) Cigarette-smoking and cancer mortality risk in Japanese men and women—results from reanalysis of the 6-Prefecture Cohort Study Data. Environ Health Perspect 8719–8726 Akiba S, Hirayama T (1990) Cigarette-smoking and cancer mortality risk in Japanese men and women—results from reanalysis of the 6-Prefecture Cohort Study Data. Environ Health Perspect 8719–8726
12.
go back to reference Nilsson S, Carstensen JM, Pershagen G (2001) Mortality among male and female smokers in Sweden: a 33 year follow up. J Epidemiol Community Health 55(11):825–830PubMedCrossRef Nilsson S, Carstensen JM, Pershagen G (2001) Mortality among male and female smokers in Sweden: a 33 year follow up. J Epidemiol Community Health 55(11):825–830PubMedCrossRef
13.
go back to reference Freedman ND, Schatzkin A, Leitzmann MF, Hollenbeck AR, Abnet CC (2007) Alcohol and head and neck cancer risk in a prospective study. Br J Cancer 96(9):1469–1474PubMed Freedman ND, Schatzkin A, Leitzmann MF, Hollenbeck AR, Abnet CC (2007) Alcohol and head and neck cancer risk in a prospective study. Br J Cancer 96(9):1469–1474PubMed
14.
go back to reference Garavello W, Randi G, Bosetti C et al (2006) Body size and laryngeal cancer risk. Ann Oncol 17(9):1459–1463PubMedCrossRef Garavello W, Randi G, Bosetti C et al (2006) Body size and laryngeal cancer risk. Ann Oncol 17(9):1459–1463PubMedCrossRef
15.
go back to reference Franceschi S, Maso LD, Levi F, Conti E, Talamini R, La Vecchia C (2001) Leanness as early marker of cancer of the oral cavity and pharynx. Ann Oncol 12(3):331–336PubMedCrossRef Franceschi S, Maso LD, Levi F, Conti E, Talamini R, La Vecchia C (2001) Leanness as early marker of cancer of the oral cavity and pharynx. Ann Oncol 12(3):331–336PubMedCrossRef
16.
go back to reference Hashibe M, Brennan P, Benhamou S et al (2007) 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. J Natl Cancer Inst 99(10):777–789PubMedCrossRef Hashibe M, Brennan P, Benhamou S et al (2007) 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. J Natl Cancer Inst 99(10):777–789PubMedCrossRef
17.
go back to reference Purdue MP, Hashibe M, Berthiller J et al (2009) Type of alcoholic beverage and risk of head and neck cancer—a pooled analysis within the INHANCE consortium. Am J Epidemiol 169(2):132–142PubMedCrossRef Purdue MP, Hashibe M, Berthiller J et al (2009) Type of alcoholic beverage and risk of head and neck cancer—a pooled analysis within the INHANCE consortium. Am J Epidemiol 169(2):132–142PubMedCrossRef
18.
go back to reference Lubin JH, Purdue M, Kelsey KT et al (2009) Total exposure and exposure rate effects for alcohol and smoking and risk of head and neck cancer: a pooled analysis of case-control studies. Am J Epidemiol 170(8):937–947PubMedCrossRef Lubin JH, Purdue M, Kelsey KT et al (2009) Total exposure and exposure rate effects for alcohol and smoking and risk of head and neck cancer: a pooled analysis of case-control studies. Am J Epidemiol 170(8):937–947PubMedCrossRef
19.
go back to reference Gaudet MM, Olshan AF, Berthiller J et al (2010) Body mass index and risk of head and neck cancer in a pooled analysis of case-control studies in the International Head and Neck Cancer Epidemiology (INHANCE) Consortium. Int J Epidemiol 39(4):1091–1102PubMedCrossRef Gaudet MM, Olshan AF, Berthiller J et al (2010) Body mass index and risk of head and neck cancer in a pooled analysis of case-control studies in the International Head and Neck Cancer Epidemiology (INHANCE) Consortium. Int J Epidemiol 39(4):1091–1102PubMedCrossRef
20.
go back to reference Lubin JH, Gaudet MM, Olshan AF et al (2010) Body mass index, cigarette smoking and alcohol consumption and cancers of the oral cavity, pharynx and larynx: modeling odds ratios in pooled case-control data. Am J Epidemiol 171(12):1250–1261PubMedCrossRef Lubin JH, Gaudet MM, Olshan AF et al (2010) Body mass index, cigarette smoking and alcohol consumption and cancers of the oral cavity, pharynx and larynx: modeling odds ratios in pooled case-control data. Am J Epidemiol 171(12):1250–1261PubMedCrossRef
21.
22.
go back to reference Preston DL, Lubin JH, Pierce DA, McConney ME (2006) Epicure user’s guide. HiroSoft International Corporation, Seattle Preston DL, Lubin JH, Pierce DA, McConney ME (2006) Epicure user’s guide. HiroSoft International Corporation, Seattle
23.
go back to reference Olshan AF, Weissler MC, Watson MA, Bell DA (2000) GSTM1, GSTT1, GSTP1, CYP1A1, and NAT1 polymorphisms, tobacco use, and the risk of head and neck cancer. Cancer Epidemiol Biomarkers Prev 9(2):185–191PubMed Olshan AF, Weissler MC, Watson MA, Bell DA (2000) GSTM1, GSTT1, GSTP1, CYP1A1, and NAT1 polymorphisms, tobacco use, and the risk of head and neck cancer. Cancer Epidemiol Biomarkers Prev 9(2):185–191PubMed
24.
go back to reference Gallus S, Bosetti C, Franceschi S, Levi F, Negri E, La Vecchia C (2003) Laryngeal cancer in women: tobacco, alcohol, nutritional, and hormonal factors. Cancer Epidemiol Biomarkers Prev 12(6):514–517PubMed Gallus S, Bosetti C, Franceschi S, Levi F, Negri E, La Vecchia C (2003) Laryngeal cancer in women: tobacco, alcohol, nutritional, and hormonal factors. Cancer Epidemiol Biomarkers Prev 12(6):514–517PubMed
25.
go back to reference Altieri A, Bosetti C, Gallus S et al (2004) Wine, beer and spirits and risk of oral and pharyngeal cancer: a case-control study from Italy and Switzerland. Oral Oncol 40(9):904–909PubMedCrossRef Altieri A, Bosetti C, Gallus S et al (2004) Wine, beer and spirits and risk of oral and pharyngeal cancer: a case-control study from Italy and Switzerland. Oral Oncol 40(9):904–909PubMedCrossRef
26.
go back to reference D’Avanzo B, La Vecchia C, Talamini R, Franceschi S (1996) Anthropometric measures and risk of cancers of the upper digestive and respiratory tract. Nutr Cancer 26(2):219–227PubMedCrossRef D’Avanzo B, La Vecchia C, Talamini R, Franceschi S (1996) Anthropometric measures and risk of cancers of the upper digestive and respiratory tract. Nutr Cancer 26(2):219–227PubMedCrossRef
27.
go back to reference Nieto A, Sanchez MJ, Martinez C et al (2003) Lifetime body mass index and risk of oral cavity and oropharyngeal cancer by smoking and drinking habits. Br J Cancer 89(9):1667–1671PubMedCrossRef Nieto A, Sanchez MJ, Martinez C et al (2003) Lifetime body mass index and risk of oral cavity and oropharyngeal cancer by smoking and drinking habits. Br J Cancer 89(9):1667–1671PubMedCrossRef
28.
go back to reference Rajkumar T, Sridhar H, Balaram P et al (2003) Oral cancer in Southern India: the influence of body size, diet, infections and sexual practices. Eur J Cancer Prev 12(2):135–143PubMedCrossRef Rajkumar T, Sridhar H, Balaram P et al (2003) Oral cancer in Southern India: the influence of body size, diet, infections and sexual practices. Eur J Cancer Prev 12(2):135–143PubMedCrossRef
29.
go back to reference Kreimer AR, Randi G, Herrero R et al (2006) Diet and body mass, and oral and oropharyngeal squamous cell carcinomas: analysis from the IARC multinational case-control study. Int J Cancer 118(9):2293–2297PubMedCrossRef Kreimer AR, Randi G, Herrero R et al (2006) Diet and body mass, and oral and oropharyngeal squamous cell carcinomas: analysis from the IARC multinational case-control study. Int J Cancer 118(9):2293–2297PubMedCrossRef
30.
go back to reference Flegal KM, Graubard BI, Williamson DF, Cooper RS (2010) Reverse causation and illness-related weight loss in observational studies of body weight and mortality. Am J Epidemiol 173(1):1–9PubMedCrossRef Flegal KM, Graubard BI, Williamson DF, Cooper RS (2010) Reverse causation and illness-related weight loss in observational studies of body weight and mortality. Am J Epidemiol 173(1):1–9PubMedCrossRef
31.
go back to reference Hashibe M, Sankaranarayanan R, Thomas G et al (2000) Alcohol drinking, body mass index and the risk of oral leukoplakia in an Indian population. Int J Cancer 88(1):129–134PubMedCrossRef Hashibe M, Sankaranarayanan R, Thomas G et al (2000) Alcohol drinking, body mass index and the risk of oral leukoplakia in an Indian population. Int J Cancer 88(1):129–134PubMedCrossRef
32.
go back to reference Hashibe M, Sankaranarayanan R, Thomas G et al (2002) Body mass index, tobacco chewing, alcohol drinking and the risk of oral submucous fibrosis in Kerala, India. Cancer Causes Control 13(1):55–64PubMedCrossRef Hashibe M, Sankaranarayanan R, Thomas G et al (2002) Body mass index, tobacco chewing, alcohol drinking and the risk of oral submucous fibrosis in Kerala, India. Cancer Causes Control 13(1):55–64PubMedCrossRef
33.
go back to reference Freedman ND, Abnet CC, Leitzmann MF et al (2007) A prospective study of tobacco, alcohol, and the risk of esophageal and gastric cancer subtypes. Am J Epidemiol 165(12):1424–1433PubMedCrossRef Freedman ND, Abnet CC, Leitzmann MF et al (2007) A prospective study of tobacco, alcohol, and the risk of esophageal and gastric cancer subtypes. Am J Epidemiol 165(12):1424–1433PubMedCrossRef
34.
go back to reference Henschke CI, Miettinen OS (2004) Women’s susceptibility to tobacco carcinogens. Lung Cancer 43(1):1–5PubMedCrossRef Henschke CI, Miettinen OS (2004) Women’s susceptibility to tobacco carcinogens. Lung Cancer 43(1):1–5PubMedCrossRef
35.
go back to reference Risch HA, Miller AB (2002) Re: Sex, smoking, and cancer: a reappraisal. J Natl Cancer Inst 94(4):308PubMed Risch HA, Miller AB (2002) Re: Sex, smoking, and cancer: a reappraisal. J Natl Cancer Inst 94(4):308PubMed
36.
go back to reference Zang EA (2002) Re: Sex, smoking, and cancer: a reappraisal. J Natl Cancer Inst 94(4):308–309PubMed Zang EA (2002) Re: Sex, smoking, and cancer: a reappraisal. J Natl Cancer Inst 94(4):308–309PubMed
37.
38.
go back to reference Bain C, Feskanich D, Speizer FE et al (2004) Lung cancer rates in men and women with comparable histories of smoking. J Natl Cancer Inst 96(11):826–834PubMedCrossRef Bain C, Feskanich D, Speizer FE et al (2004) Lung cancer rates in men and women with comparable histories of smoking. J Natl Cancer Inst 96(11):826–834PubMedCrossRef
39.
go back to reference Bain C, Feskanich D, Speizer FE et al (2004) Erratum. J Natl Cancer Inst 96(23):1796–1797CrossRef Bain C, Feskanich D, Speizer FE et al (2004) Erratum. J Natl Cancer Inst 96(23):1796–1797CrossRef
40.
go back to reference Jemal A, Travis WD, Tarone RE, Travis L, Devesa SS (2003) Lung cancer rates convergence in young men and women in the United States: analysis by birth cohort and histologic type. Int J Cancer 105(1):101–107PubMedCrossRef Jemal A, Travis WD, Tarone RE, Travis L, Devesa SS (2003) Lung cancer rates convergence in young men and women in the United States: analysis by birth cohort and histologic type. Int J Cancer 105(1):101–107PubMedCrossRef
41.
go back to reference Karagas MR, Park S, Warren A et al (2005) Gender, smoking, glutathione-S-transferase variants and bladder cancer incidence: a population-based study. Cancer Lett 219(1):63–69PubMedCrossRef Karagas MR, Park S, Warren A et al (2005) Gender, smoking, glutathione-S-transferase variants and bladder cancer incidence: a population-based study. Cancer Lett 219(1):63–69PubMedCrossRef
42.
go back to reference Castelao JE, Yuan JM, Skipper PL et al (2001) Gender- and smoking-related bladder cancer risk. J Natl Cancer Inst 93(7):538–545PubMedCrossRef Castelao JE, Yuan JM, Skipper PL et al (2001) Gender- and smoking-related bladder cancer risk. J Natl Cancer Inst 93(7):538–545PubMedCrossRef
43.
go back to reference Puente D, Hartge P, Greiser E et al (2006) A pooled analysis of bladder cancer case-control studies evaluating smoking in men and women. Cancer Causes Control 17(1):71–79PubMedCrossRef Puente D, Hartge P, Greiser E et al (2006) A pooled analysis of bladder cancer case-control studies evaluating smoking in men and women. Cancer Causes Control 17(1):71–79PubMedCrossRef
44.
go back to reference Baris D, Karagas MR, Verrill C et al (2009) A case-control study of smoking and bladder cancer risk: emergent patterns over time. J Natl Cancer Inst 101(22):1553–1561PubMedCrossRef Baris D, Karagas MR, Verrill C et al (2009) A case-control study of smoking and bladder cancer risk: emergent patterns over time. J Natl Cancer Inst 101(22):1553–1561PubMedCrossRef
45.
go back to reference Silverman DT, Devesa SS, Moore LL, Rothman N (2006) Bladder cancer. In: Schottenfeld D, Fraumeni JF Jr (eds) Cancer epidemiology and prevention. Oxford University Press Inc, New York, pp 1101–1127CrossRef Silverman DT, Devesa SS, Moore LL, Rothman N (2006) Bladder cancer. In: Schottenfeld D, Fraumeni JF Jr (eds) Cancer epidemiology and prevention. Oxford University Press Inc, New York, pp 1101–1127CrossRef
46.
go back to reference Lynch SM, Vrieling A, Lubin JH et al (2009) Cigarette smoking and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium. Am J Epidemiol 170(4):403–413PubMedCrossRef Lynch SM, Vrieling A, Lubin JH et al (2009) Cigarette smoking and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium. Am J Epidemiol 170(4):403–413PubMedCrossRef
47.
go back to reference Axelson O (1978) Aspects on confounding in occupational-health epidemiology. Scand J Work Environ Health 4(1):98–102 Axelson O (1978) Aspects on confounding in occupational-health epidemiology. Scand J Work Environ Health 4(1):98–102
48.
go back to reference Markowitz LE, Sternberg M, Dunne EF, McQuillan G, Unger ER (2009) Seroprevalence of human papillomavirus types 6, 11, 16, and 18 in the United States: National Health and Nutrition Examination Survey 2003–2004. J Infect Dis 200(7):1059–1067PubMedCrossRef Markowitz LE, Sternberg M, Dunne EF, McQuillan G, Unger ER (2009) Seroprevalence of human papillomavirus types 6, 11, 16, and 18 in the United States: National Health and Nutrition Examination Survey 2003–2004. J Infect Dis 200(7):1059–1067PubMedCrossRef
49.
go back to reference Hobbs CGL, Sterne JAC, Bailey M, Heyderman RS, Birchall MA, Thomas SJ (2006) Human papillomavirus and head and neck cancer: a systematic review and meta-analysis. Clin Otolaryngol 31(4):259–266PubMedCrossRef Hobbs CGL, Sterne JAC, Bailey M, Heyderman RS, Birchall MA, Thomas SJ (2006) Human papillomavirus and head and neck cancer: a systematic review and meta-analysis. Clin Otolaryngol 31(4):259–266PubMedCrossRef
50.
go back to reference Stone KM, Karem KL, Sternberg MR et al (2002) Seroprevalence of human papillomavirus type 16 infection in the United States. J Infect Dis 186(10):1396–1402PubMedCrossRef Stone KM, Karem KL, Sternberg MR et al (2002) Seroprevalence of human papillomavirus type 16 infection in the United States. J Infect Dis 186(10):1396–1402PubMedCrossRef
51.
go back to reference Gillison ML, D’Souza G, Westra W et al (2008) Distinct risk factor profiles for human papillomavirus type 16-positive and human papillomavirus type 16-negative head and neck cancers. J Natl Cancer Inst 100(6):407–420PubMedCrossRef Gillison ML, D’Souza G, Westra W et al (2008) Distinct risk factor profiles for human papillomavirus type 16-positive and human papillomavirus type 16-negative head and neck cancers. J Natl Cancer Inst 100(6):407–420PubMedCrossRef
52.
go back to reference Herrero R, Castellsague X, Pawlita M et al (2003) Human papillomavirus and oral cancer: the International Agency for Research on Cancer Multicenter Study. J Natl Cancer Inst 95(23):1772–1783PubMed Herrero R, Castellsague X, Pawlita M et al (2003) Human papillomavirus and oral cancer: the International Agency for Research on Cancer Multicenter Study. J Natl Cancer Inst 95(23):1772–1783PubMed
53.
go back to reference Gail MH, Wacholder S, Lubin JH (1988) Indirect correction for confounding under multiplicative and additive risk models. Am J Ind Med 13119–13130 Gail MH, Wacholder S, Lubin JH (1988) Indirect correction for confounding under multiplicative and additive risk models. Am J Ind Med 13119–13130
54.
go back to reference Wacholder S, Lubin JH, Dosemeci M, Gail MH (1991) Bias despite masked assessment of clinical outcomes when an outcome is defined as one of several component events. Control Clin Trials 12(4):457–461PubMedCrossRef Wacholder S, Lubin JH, Dosemeci M, Gail MH (1991) Bias despite masked assessment of clinical outcomes when an outcome is defined as one of several component events. Control Clin Trials 12(4):457–461PubMedCrossRef
55.
go back to reference Ang KK, Harris J, Wheeler R et al (2010) Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med 363(1):24–35PubMedCrossRef Ang KK, Harris J, Wheeler R et al (2010) Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med 363(1):24–35PubMedCrossRef
56.
go back to reference Ritchie JM, Smith EM, Summersgill KF et al (2003) Human papillomavirus infection as a prognostic factor in carcinomas of the oral cavity and oropharynx. Int J Cancer 104(3):336–344PubMedCrossRef Ritchie JM, Smith EM, Summersgill KF et al (2003) Human papillomavirus infection as a prognostic factor in carcinomas of the oral cavity and oropharynx. Int J Cancer 104(3):336–344PubMedCrossRef
57.
go back to reference Jung AC, Briolat J, Millon R et al (2010) Biological and clinical relevance of transcriptionally active human papillomavirus (HPV) infection in oropharynx squamous cell carcinoma. Int J Cancer 126(8):1882–1894PubMed Jung AC, Briolat J, Millon R et al (2010) Biological and clinical relevance of transcriptionally active human papillomavirus (HPV) infection in oropharynx squamous cell carcinoma. Int J Cancer 126(8):1882–1894PubMed
58.
go back to reference Tachezy R, Klozar J, Salakova M et al (2005) HPV and other risk factors of oral cavity/oropharyngeal cancer in the Czech Republic. Oral Dis 11(3):181–185PubMedCrossRef Tachezy R, Klozar J, Salakova M et al (2005) HPV and other risk factors of oral cavity/oropharyngeal cancer in the Czech Republic. Oral Dis 11(3):181–185PubMedCrossRef
59.
go back to reference Ghosh A, Ghosh S, Maiti GP et al (2009) SH3GL2 and CDKN2A/2B loci are independently altered in early dysplastic lesions of head and neck: correlation with HPV infection and tobacco habit. J Pathol 217(3):408–419PubMedCrossRef Ghosh A, Ghosh S, Maiti GP et al (2009) SH3GL2 and CDKN2A/2B loci are independently altered in early dysplastic lesions of head and neck: correlation with HPV infection and tobacco habit. J Pathol 217(3):408–419PubMedCrossRef
60.
go back to reference Reimers N, Kasper HU, Weissenborn SJ et al (2007) Combined analysis of HPV-DNA, p16 and EGFR expression to predict prognosis in oropharyngeal cancer. Int J Cancer 120(8):1731–1738PubMedCrossRef Reimers N, Kasper HU, Weissenborn SJ et al (2007) Combined analysis of HPV-DNA, p16 and EGFR expression to predict prognosis in oropharyngeal cancer. Int J Cancer 120(8):1731–1738PubMedCrossRef
61.
go back to reference Schwartz SR, Yueh B, McDougall JK, Daling JR, Schwartz SM (2001) Human papillomavirus infection and survival in oral squamous cell cancer: a population-based study. Otolaryngol Head Neck Surg 125(1):1–9PubMedCrossRef Schwartz SR, Yueh B, McDougall JK, Daling JR, Schwartz SM (2001) Human papillomavirus infection and survival in oral squamous cell cancer: a population-based study. Otolaryngol Head Neck Surg 125(1):1–9PubMedCrossRef
62.
go back to reference Paz IB, Cook N, Odom-Maryon T, Xie Y, Wilczynski SP (1997) Human papillomavirus (HPV) in head and neck cancer—an association of HPV 16 with squamous cell carcinoma of Waldeyer’s tonsillar ring. Cancer 79(3):595–604PubMedCrossRef Paz IB, Cook N, Odom-Maryon T, Xie Y, Wilczynski SP (1997) Human papillomavirus (HPV) in head and neck cancer—an association of HPV 16 with squamous cell carcinoma of Waldeyer’s tonsillar ring. Cancer 79(3):595–604PubMedCrossRef
Metadata
Title
An examination of male and female odds ratios by BMI, cigarette smoking, and alcohol consumption for cancers of the oral cavity, pharynx, and larynx in pooled data from 15 case–control studies
Authors
Jay H. Lubin
Joshua Muscat
Mia M. Gaudet
Andrew F. Olshan
Maria Paula Curado
Luigino Dal Maso
Victor Wünsch-Filho
Erich M. Sturgis
Neonilia Szeszenia-Dabrowska
Xavier Castellsague
Zuo-Feng Zhang
Elaine Smith
Leticia Fernandez
Elena Matos
Silvia Franceschi
Eleonora Fabianova
Peter Rudnai
Mark P. Purdue
Dana Mates
Qingyi Wei
Rolando Herrero
Karl Kelsey
Hal Morgenstern
Oxana Shangina
Sergio Koifman
Jolanta Lissowska
Fabio Levi
Alexander W. Daudt
Jose Eluf Neto
Chu Chen
Philip Lazarus
Deborah M. Winn
Stephen M. Schwartz
Paolo Boffetta
Paul Brennan
Ana Menezes
Carlo La Vecchia
Michael McClean
Renato Talamini
Thangarajan Rajkumar
Richard B. Hayes
Mia Hashibe
Publication date
01-09-2011
Publisher
Springer Netherlands
Published in
Cancer Causes & Control / Issue 9/2011
Print ISSN: 0957-5243
Electronic ISSN: 1573-7225
DOI
https://doi.org/10.1007/s10552-011-9792-x

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Dr. Véronique Diéras
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