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Journal of the National Cancer Institute Advance Access originally published online on November 11, 2008
JNCI Journal of the National Cancer Institute 2008 100(22):1654; doi:10.1093/jnci/djn367
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© The Author 2008. Published by Oxford University Press.

CORRESPONDENCE

Re: Cost-Effectiveness of Cervical Cancer Screening With Human Papillomavirus DNA Testing and HPV-16,18 Vaccination

Paolo Giorgi Rossi, Marco Zappa

Affiliations of authors: Agency for Public Health, Lazio Region, Rome, Italy (PGR); Clinical and Descriptive Epidemiology Unit, ISPO, Cancer Prevention Research Institute of the Tuscany Region, Florence, Italy (MZ)

Correspondence to: Paolo Giorgi Rossi, PhD, Agency for Public Health, Lazio Region, via di S. Costanza, 53, 00198 Rome, Italy (e-mail: giorgirossi{at}asplazio.it).

Goldhaber-Fiebert et al. (1) presented a convincing model for the natural history of cervical cancer. The results of this study should be considered by all policy makers in taking decisions about the preventive strategies for cervical cancer.

The evaluation of this model was made by comparing the observed incidence curve by age of cervical cancer onset with the predicted incidence curve. In industrialized countries, this incidence curve is the result of a complex interaction involving the clinical history of the disease, sexual behaviors, and the screening habits of the different cohorts of women. The model reproduces the observed curve perfectly, and this reproduction is the result of a mixture of five populations with different cervical cancer screening behaviors and age distributions. The sum of these five populations produces the observed figures of screening behaviors by age in the United States and the number of invasive cancers that occurred (2).

The preventive strategies proposed are based mainly on two interventions: vaccination and screening. Both of these interventions have two main factors that determine their effectiveness: the technical characteristics of vaccine and screening test (ie, the protection against infection and the types of human papillomaviruses that the vaccine is directed against and the sensitivity and specificity of the test) and the compliance of the population (ie, the vaccine coverage and test uptake).

To better understand the role that each factor plays in determining effectiveness and also to have a valid target that is sensitive to the model characteristics, we believe that the proportion of cancer occurring in screened women, in unscreened people, and in vaccinated and unvaccinated women should be one of the most important outcomes to be presented for validation of a model for the natural history of cervical cancer. Given the structure of the model, it should be very easy to provide this output. Unfortunately, for the United States, there are few data on screening history for invasive cervical cancers (3,4) that could be used to validate the model; however, these data are available for other countries (57).

All of these studies conclude that lack of participation in screening is still a major risk factor for invasive cancer in industrialized countries. Will lack of participation still be the major failure for the future preventive programs?

NOTES

The Agency for Public Health received a grant from Sanofi Pasteur MSD for a study on the "Burden of HPV Disease in Italy." P. G. Rossi received travel reimbursement from Sanofi Pasteur MSD to present the results of the study at two international conferences.

REFERENCES

1. Goldhaber-Fiebert JD, Stout NK, Salomon JA, Kuntz KM, Goldie SJ. Cost-effectiveness of cervical cancer screening with human papillomavirus DNA testing and HPV-16,18 vaccination. J Natl Cancer Inst (2008) 100(5):308–320.[Abstract/Free Full Text]

2. Goldhaber-Fiebert JD, Stout NK, Ortendahl J, Kuntz KM, Goldie SJ, Salomon JA. Modeling human papillomavirus and cervical cancer in the United States for analyses of screening and vaccination. Popul Health Metr (2007) 5:11.[CrossRef][Medline]

3. Leyden WA, Manos MM, Geiger AM, et al. Cervical cancer in women with comprehensive health care access: attributable factors in the screening process. J Natl Cancer Inst (2005) 97(9):675–683.[Abstract/Free Full Text]

4. Sung HY, Kearney KA, Miller M, Kinney W, Sawaya GF, Hiatt RA. Papanicolaou smear history and diagnosis of invasive cervical carcinoma among members of a large prepaid health plan. Cancer (2000) 88(10):2283–2289.[CrossRef][Web of Science][Medline]

5. Bos AB, Rebolj M, Habbema JD, van Ballegooijen M. Nonattendance is still the main limitation for the effectiveness of screening for cervical cancer in the Netherlands. Int J Cancer (2006) 119(10):2372–2375.[CrossRef][Web of Science][Medline]

6. Ingemann-Hansen O, Lidang M, Niemann I, et al. Screening history of women with cervical cancer: a 6-year study in Aarhus, Denmark. Br J Cancer (2008) 98(7):1292–1294.[CrossRef][Web of Science][Medline]

7. Morrell S, Taylor R, Wain G. A study of Pap test history and histologically determined cervical cancer in NSW women, 1997–2003. J Med Screen (2005) 12(4):190–196.[Abstract/Free Full Text]


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This Article
Right arrow Extract Freely available
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100/22/1654    most recent
djn367v1
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