Epidemiology of HPV 16 and cervical cancer in Finland and the potential impact of vaccination: Mathematical modelling analyses

被引:211
作者
Barnabas, Ruanne V. [1 ]
Laukkanen, Paivi
Koskela, Pentti
Kontula, Osmo
Lehtinen, Matti
Garnett, Geoff P.
机构
[1] Univ Oxford, Canc Epidemiol Unit, Oxford, England
[2] Imperial Coll, Dept Infect Dis Epidemiol, London, England
[3] Natl Publ Hlth Inst, Helsinki, Finland
[4] Finnish Canc Registry, Inst Stat & Epidemiol Canc Res, FIN-00170 Helsinki, Finland
[5] Family Federat Finland, Helsinki, Finland
[6] Univ Tampere, Sch Publ Hlth, FIN-33101 Tampere, Finland
关键词
D O I
10.1371/journal.pmed.0030138
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Candidate human papillomavirus (HPV) vaccines have demonstrated almost 90%-100% efficacy in preventing persistent, type-specific HPV infection over 18 mo in clinical trials. If these vaccines go on to demonstrate prevention of precancerous lesions in phase III clinical trials, they will be licensed for public use in the near future. How these vaccines will be used in countries with national cervical cancer screening programmes is an important question. Methods and Findings We developed a transmission model of HPV 16 infection and progression to cervical cancer and calibrated it to Finnish HPV 16 seroprevalence over time. The model was used to estimate the transmission probability of the virus, to look at the effect of changes in patterns of sexual behaviour and smoking on age-specific trends in cancer incidence, and to explore the impact of HPV 16 vaccination. We estimated a high per-partnership transmission probability of HPV 16, of 0.6. The modelling analyses showed that changes in sexual behaviour and smoking accounted, in part, for the increase seen in cervical cancer incidence in 35- to 39-y-old women from 1990 to 1999. At both low (10% in opportunistic immunisation) and high (90% in a national immunisation programme) coverage of the adolescent population, vaccinating women and men had little benefit over vaccinating women alone. We estimate that vaccinating 90% of young women before sexual debut has the potential to decrease HPV type-specific (e.g., type 16) cervical cancer incidence by 91%. If older women are more likely to have persistent infections and progress to cancer, then vaccination with a duration of protection of less than 15 y could result in an older susceptible cohort and no decrease in cancer incidence. While vaccination has the potential to significantly reduce type-specific cancer incidence, its combination with screening further improves cancer prevention. Conclusions HPV vaccination has the potential to significantly decrease HPV type-specific cervical cancer incidence. High vaccine coverage of women alone, sustained over many decades, with a long duration of vaccine-conferred protection, would have the greatest impact on type-specific cancer incidence. This level of coverage could be achieved through national coordinated programmes, with surveillance to detect cancers caused by nonvaccine oncogenic HPV types.
引用
收藏
页码:624 / 632
页数:9
相关论文
共 58 条
[1]   MODELING AGE-SPECIFIC AND TIME-SPECIFIC INCIDENCE FROM SEROPREVALENCE - TOXOPLASMOSIS [J].
ADES, AE ;
NOKES, DJ .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1993, 137 (09) :1022-1034
[2]  
af Geijersstam V, 1998, J INFECT DIS, V177, P1710, DOI 10.1086/517428
[3]  
Anttila A, 1999, INT J CANCER, V83, P59, DOI 10.1002/(SICI)1097-0215(19990924)83:1<59::AID-IJC12>3.0.CO
[4]  
2-N
[5]  
Barnabas RV, 2004, CLIN HDB HUMAN PAPIL
[6]   Estimating number of lifetime sexual partners: Men and women do it differently [J].
Brown, NR ;
Sinclair, RC .
JOURNAL OF SEX RESEARCH, 1999, 36 (03) :292-297
[7]  
Carter A, 2001, DANCE THEAT J, V16, P18
[8]   The natural history of human papillomavirus type 16 capsid antibodies among a cohort of university women [J].
Carter, JJ ;
Koutsky, LA ;
Wipf, GC ;
Christensen, ND ;
Lee, SK ;
Kuypers, J ;
Kiviat, N ;
Galloway, DA .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (05) :927-936
[9]   Comparison of human papillomavirus types 16, 18, and 6 capsid antibody responses following incident infection [J].
Carter, JJ ;
Koutsky, LA ;
Hughes, JP ;
Lee, SK ;
Kuypers, J ;
Kiviat, N ;
Galloway, DA .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (06) :1911-1919
[10]  
Castellsague Xavier, 2003, J Natl Cancer Inst Monogr, P20