TY - JOUR
T1 - Timing, number, and type of sexual partners associated with risk of oropharyngeal cancer
AU - Drake, Virginia E.
AU - Fakhry, Carole
AU - Windon, Melina J.
AU - Stewart, C. Matthew
AU - Akst, Lee
AU - Hillel, Alexander
AU - Chien, Wade
AU - Ha, Patrick
AU - Miles, Brett
AU - Gourin, Christine G.
AU - Mandal, Rajarsi
AU - Mydlarz, Wojciech K.
AU - Rooper, Lisa
AU - Troy, Tanya
AU - Yavvari, Siddhartha
AU - Waterboer, Tim
AU - Brenner, Nicole
AU - Eisele, David W.
AU - D’Souza, Gypsyamber
N1 - Funding Information:
Alexander Hillel has received grant support from Medtronic and personal fees from Ambu. Patrick Ha has received personal fees from Rakuten Medical. Tim Waterboer serves on advisory boards for Merck Sharp & Dohme. The other authors made no disclosures.
Funding Information:
This study was supported by the National Institute of Dental and Craniofacial Research (grant P50 DE019032) and the National Institute on Deafness and Other Communication Disorders (grant 1K23DC014758).
Publisher Copyright:
© 2021 American Cancer Society
PY - 2021/4/1
Y1 - 2021/4/1
N2 - Background: Case-control studies from the early 2000s demonstrated that human papillomavirus–related oropharyngeal cancer (HPV-OPC) is a distinct entity associated with number of oral sex partners. Using contemporary data, we investigated novel risk factors (sexual debut behaviors, exposure intensity, and relationship dynamics) and serological markers on odds of HPV-OPC. Methods: HPV-OPC patients and frequency-matched controls were enrolled in a multicenter study from 2013 to 2018. Participants completed a behavioral survey. Characteristics were compared using a chi-square test for categorical variables and a t test for continuous variables. Adjusted odds ratios (aOR) were calculated using logistic regression. Results: A total of 163 HPV-OPC patients and 345 controls were included. Lifetime number of oral sex partners was associated with significantly increased odds of HPV-OPC (>10 partners: odds ratio [OR], 4.3 [95% CI, 2.8-6.7]). After adjustment for number of oral sex partners and smoking, younger age at first oral sex (<18 vs >20 years: aOR, 1.8 [95% CI, 1.1-3.2]) and oral sex intensity (>5 sex-years: aOR, 2.8 [95% CI, 1.1-7.5]) remained associated with significantly increased odds of HPV-OPC. Type of sexual partner such as older partners when a case was younger (OR, 1.7 [95% CI, 1.1-2.6]) or having a partner who had extramarital sex (OR, 1.6 [95% CI, 1.1-2.4]) was associated with HPV-OPC. Seropositivity for antibodies to HPV16 E6 (OR, 286 [95% CI, 122-670]) and any HPV16 E protein (E1, E2, E6, E7; OR, 163 [95% CI, 70-378]) was associated with increased odds of HPV-OPC. Conclusion: Number of oral sex partners remains a strong risk factor for HPV-OPC; however, timing and intensity of oral sex are novel independent risk factors. These behaviors suggest additional nuances of how and why some individuals develop HPV-OPC.
AB - Background: Case-control studies from the early 2000s demonstrated that human papillomavirus–related oropharyngeal cancer (HPV-OPC) is a distinct entity associated with number of oral sex partners. Using contemporary data, we investigated novel risk factors (sexual debut behaviors, exposure intensity, and relationship dynamics) and serological markers on odds of HPV-OPC. Methods: HPV-OPC patients and frequency-matched controls were enrolled in a multicenter study from 2013 to 2018. Participants completed a behavioral survey. Characteristics were compared using a chi-square test for categorical variables and a t test for continuous variables. Adjusted odds ratios (aOR) were calculated using logistic regression. Results: A total of 163 HPV-OPC patients and 345 controls were included. Lifetime number of oral sex partners was associated with significantly increased odds of HPV-OPC (>10 partners: odds ratio [OR], 4.3 [95% CI, 2.8-6.7]). After adjustment for number of oral sex partners and smoking, younger age at first oral sex (<18 vs >20 years: aOR, 1.8 [95% CI, 1.1-3.2]) and oral sex intensity (>5 sex-years: aOR, 2.8 [95% CI, 1.1-7.5]) remained associated with significantly increased odds of HPV-OPC. Type of sexual partner such as older partners when a case was younger (OR, 1.7 [95% CI, 1.1-2.6]) or having a partner who had extramarital sex (OR, 1.6 [95% CI, 1.1-2.4]) was associated with HPV-OPC. Seropositivity for antibodies to HPV16 E6 (OR, 286 [95% CI, 122-670]) and any HPV16 E protein (E1, E2, E6, E7; OR, 163 [95% CI, 70-378]) was associated with increased odds of HPV-OPC. Conclusion: Number of oral sex partners remains a strong risk factor for HPV-OPC; however, timing and intensity of oral sex are novel independent risk factors. These behaviors suggest additional nuances of how and why some individuals develop HPV-OPC.
KW - head and neck cancer
KW - oropharyngeal neoplasms
KW - papillomaviridae
KW - risk factors
KW - sexual behavior
UR - http://www.scopus.com/inward/record.url?scp=85099080426&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85099080426&partnerID=8YFLogxK
U2 - 10.1002/cncr.33346
DO - 10.1002/cncr.33346
M3 - Article
C2 - 33426652
AN - SCOPUS:85099080426
SN - 0008-543X
VL - 127
SP - 1029
EP - 1038
JO - Cancer
JF - Cancer
IS - 7
ER -