Prospective study of human papillomavirus and risk of cervical adenocarcinoma

被引:52
作者
Dahlstrom, Lisen Arnheim [1 ]
Ylitalo, Nathalie [1 ,2 ]
Sundstrom, Karin [1 ]
Palmgren, Juni [1 ,3 ]
Ploner, Alexander [1 ]
Eloranta, Sandra [1 ]
Sanjeevi, Carani B. [4 ]
Andersson, Sonia [5 ]
Rohan, Thomas [6 ]
Dillner, Joakim [1 ,7 ]
Adami, Hans-Olov [1 ,8 ]
Sparen, Par [1 ]
机构
[1] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[2] Sahlgrens Univ Hosp, Dept Oncol, Div Clin Canc Epidemiol, Gothenburg, Sweden
[3] Stockholm Univ, Dept Math Stat, S-10691 Stockholm, Sweden
[4] Karolinska Inst, Dept Mol Med & Surg, Karolinska Univ Hosp, Stockholm, Sweden
[5] Karolinska Inst, Div Obstet & Gynecol, Karolinska Univ Hosp Huddinge, Dept Clin Sci Intervent & Technol, Huddinge, Sweden
[6] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[7] Lund Univ, MAS Univ Hosp, Dept Med Microbiol, Malmo, Sweden
[8] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
adenocarcinoma; adenocarcinoma in situ; HPV; cervical cancer; prospective; INTERNATIONAL TRENDS; IN-SITU; CANCER; HUMAN-PAPILLOMAVIRUS-16; PREVALENCE; INFECTION; CARCINOMA; WORLDWIDE;
D O I
10.1002/ijc.25408
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1923 / 1930
页数:8
相关论文
共 29 条
[1]   The role of human papillomavirus in cervical adenocarcinoma carcinogenesis [J].
Andersson, S ;
Rylander, E ;
Larsson, B ;
Strand, A ;
Silfversvärd, C ;
Wilander, E .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (02) :246-250
[2]   Screening-preventable cervical cancer risks:: Evidence from a nationwide audit in Sweden [J].
Andrae, Bengt ;
Kemetli, Levent ;
Sparen, Par ;
Silfverdal, Lena ;
Strander, Bjorn ;
Ryd, Walter ;
Dillner, Joakim ;
Tornberg, Sven .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (09) :622-629
[3]  
[Anonymous], 2008, LANG ENV STAT COMP
[4]   Trends in cancer of the cervix uteri in Sweden following cytological screening [J].
Bergström, R ;
Sparén, P ;
Adami, HO .
BRITISH JOURNAL OF CANCER, 1999, 81 (01) :159-166
[5]   Incidence trends of adenocarcinoma of the cervix in 13 European countries [J].
Bray, F ;
Carstensen, B ;
Moller, H ;
Zappa, M ;
Zakelj, MP ;
Lawrence, G ;
Hakama, M ;
Weiderpass, E .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2005, 14 (09) :2191-2199
[6]   Preferential risk of HPV16 for squamous cell carcinoma and of HPV18 for adenocarcinoma of the cervix compared to women with normal cytology in The Netherlands [J].
Bulk, S ;
Berkhof, J ;
Bulkmans, NWJ ;
Zielinski, GD ;
Rozendaal, L ;
van Kemenade, FJ ;
Snijders, PJF ;
Meijer, CJLM .
BRITISH JOURNAL OF CANCER, 2006, 94 (01) :171-175
[7]  
*CANC, 2008, CANC INC SWED 2007 O
[8]   Worldwide human papillomavirus etiology of cervical adenocarcinoma and its cofactors:: Implications for screening and prevention [J].
Castellsagué, X ;
Díaz, M ;
de Sanjosé, S ;
Muñoz, N ;
Herrero, R ;
Franceschi, S ;
Peeling, RW ;
Ashley, R ;
Smith, JS ;
Snijders, PJF ;
Meijer, CJLM ;
Bosch, FX .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (05) :303-315
[9]   Human papillomavirus 16 infection in adenocarcinoma of the cervix [J].
Chew, GK ;
Cruickshank, ME ;
Rooney, PH ;
Miller, ID ;
Parkin, DE ;
Murray, GI .
BRITISH JOURNAL OF CANCER, 2005, 93 (11) :1301-1304
[10]  
CHUA KL, 1995, ANAL QUANT CYTOL, V17, P221