Prospective study of human papillomavirus and risk of cervical adenocarcinoma |
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Authors: | Lisen Arnheim Dahlström Nathalie Ylitalo Karin Sundström Juni Palmgren Alexander Ploner Sandra Eloranta Carani B. Sanjeevi Sonia Andersson Thomas Rohan Joakim Dillner Hans‐Olov Adami Pär Sparén |
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Affiliation: | 1. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden;2. Fax: +46 8 314975;3. Division of Clinical Cancer Epidemiology, Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden;4. Department of Mathematical Statistics, Stockholm University, Stockholm, Sweden;5. Department of Molecular Medicine and Surgery, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden;6. Department for Clinical Science, Intervention and Technology, Division of Obstetrics and Gynecology, Karolinska University Hospital Huddinge, Karolinska Institutet, Huddinge, Sweden;7. Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY;8. Department of Medical Microbiology, MAS University Hospital, Lund University, Malm?, Sweden;9. Department of Epidemiology, Harvard School of Public Health, Boston, MA |
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Abstract: | Human papillomaviruses (HPV) are established as a major cause of cervical carcinoma. However, causality inference is dependent on prospective evidence showing that exposure predicts risk for future disease. Such evidence is available for squamous cell carcinoma, but not for cervical adenocarcinoma. We followed a population‐based cohort of 994,120 women who participated in cytological screening in Sweden for a median of 6.7 years. Baseline smears from women who developed adenocarcinoma during follow‐up (118 women with in situ disease and 164 with invasive disease) and their individually matched controls (1,434 smears) were analyzed for HPV using PCR. Conditional logistic regression was used to estimate odds ratios (OR) of future adenocarcinoma with 95% confidence intervals (CI). Being positive for HPV 16 in the first cytologically normal smear was associated with increased risks for both future adenocarcinoma in situ (OR: 11.0, 95% CI: 2.6–46.8) and invasive adenocarcinoma (OR: 16.0, 95% CI: 3.8–66.7), compared to being negative for HPV 16. Similarly, an HPV 18 positive smear was associated with increased risks for adenocarcinoma in situ (OR: 26.0, 95% CI: 3.5–192) and invasive adenocarcinoma (OR: 28.0, 95% CI: 3.8–206), compared to an HPV 18 negative smear. Being positive for HPV 16/18 in 2 subsequent smears was associated with an infinite risk of both in situ and invasive adenocarcinoma. In conclusion, infections with HPV 16 and 18 are detectable up to at least 14 years before diagnosis of cervical adenocarcinoma. Our data provide prospective evidence that the association of HPV 16/18 with cervical adenocarcinoma is strong and causal. |
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Keywords: | adenocarcinoma adenocarcinoma in situ HPV cervical cancer prospective |
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