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Reduction in HPV 16/18-associated high grade cervical lesions following HPV vaccine introduction in the United States - 2008-2012
. 2015 Mar 24;33(13):1608-13. doi: 10.1016/j.vaccine.2015.01.084. Epub 2015 Feb 11. Reduction in HPV 16/18-associated high grade cervical lesions following HPV vaccine introduction in the United States - 2008-2012 Nancy M Bennett 2 , Linda M Niccolai 3 , Sean Schafer 4 , Ina U Park 5 , Karen C Bloch 6 , Elizabeth R Unger 7 , Erin Whitney 8 , Pamela Julian 9 , Mary W Scahill 10 , Nasreen Abdullah 11 , Diane Levine 12 , Michelle L Johnson 13 , Martin Steinau 14 , Lauri E Markowitz 15 ; HPV-IMPACT Working Group
Collaborators, Affiliations
Collaborators
- HPV-IMPACT Working Group:
Affiliations
- 1 Division of STD Prevention, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-E02, Atlanta, GA 30333, USA. Electronic address: shariri@cdc.gov.
- 2 Center for Community Health and Department of Medicine, University of Rochester School of Medicine and Dentistry, 46 Prince Street, Rochester, NY 14607, USA. Electronic address: nancy_bennett@urmc.rochester.edu.
- 3 Division of Epidemiology of Microbial Diseases, Yale School of Public Health, 60 College Street, P.O. Box 208034, New Haven, CT 06520, USA. Electronic address: linda.niccolai@yale.edu.
- 4 HIV/STD/TB Program, Center for Public Health Practice, Oregon Public Health Division, 800 NE Oregon Street, Suite 1130, Portland, OR 97232, USA. Electronic address: sean.schafer@state.or.us.
- 5 STD Control Branch, California Department of Public Health, 850 Marina Bay Parkway, Bldg P, 2nd Floor, Richmond, CA 94804, USA. Electronic address: ina.park@cdph.ca.gov.
- 6 Departments of Internal Medicine, Vanderbilt University Medical Center, A-2200 MCN, Nashville, TN 37232, USA. Electronic address: karen.bloch@vanderbilt.edu.
- 7 Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-G41, Atlanta, GA 30333, USA. Electronic address: eunger@cdc.gov.
- 8 STD Control Branch, California Department of Public Health, 850 Marina Bay Parkway, Bldg P, 2nd Floor, Richmond, CA 94804, USA. Electronic address: erin.whitney@cdph.ca.gov.
- 9 Division of Epidemiology of Microbial Diseases, Yale School of Public Health, 60 College Street, P.O. Box 208034, New Haven, CT 06520, USA. Electronic address: pamela.julian@yale.edu.
- 10 Center for Community Health and Department of Medicine, University of Rochester School of Medicine and Dentistry, 46 Prince Street, Rochester, NY 14607, USA. Electronic address: maryw_scahill@urmc.rocheter.edu.
- 11 HIV/STD/TB Program, Center for Public Health Practice, Oregon Public Health Division, 800 NE Oregon Street, Suite 1130, Portland, OR 97232, USA. Electronic address: nasreen.abdullah@state.or.us.
- 12 Departments of Internal Medicine, Vanderbilt University Medical Center, A-2200 MCN, Nashville, TN 37232, USA. Electronic address: diane.levine@vanderbilt.edu.
- 13 Division of STD Prevention, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-E02, Atlanta, GA 30333, USA. Electronic address: huk3@cdc.gov.
- 14 Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-G41, Atlanta, GA 30333, USA. Electronic address: msteinau@cdc.gov.
- 15 Division of STD Prevention, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-E02, Atlanta, GA 30333, USA. Electronic address: lmarkowitz@cdc.gov.
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Reduction in HPV 16/18-associated high grade cervical lesions following HPV vaccine introduction in the United States - 2008-2012
Susan Hariri et al. Vaccine. 2015.
. 2015 Mar 24;33(13):1608-13. doi: 10.1016/j.vaccine.2015.01.084. Epub 2015 Feb 11. Authors Susan Hariri 1 , Nancy M Bennett 2 , Linda M Niccolai 3 , Sean Schafer 4 , Ina U Park 5 , Karen C Bloch 6 , Elizabeth R Unger 7 , Erin Whitney 8 , Pamela Julian 9 , Mary W Scahill 10 , Nasreen Abdullah 11 , Diane Levine 12 , Michelle L Johnson 13 , Martin Steinau 14 , Lauri E Markowitz 15 ; HPV-IMPACT Working Group Collaborators
- HPV-IMPACT Working Group:
Affiliations
- 1 Division of STD Prevention, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-E02, Atlanta, GA 30333, USA. Electronic address: shariri@cdc.gov.
- 2 Center for Community Health and Department of Medicine, University of Rochester School of Medicine and Dentistry, 46 Prince Street, Rochester, NY 14607, USA. Electronic address: nancy_bennett@urmc.rochester.edu.
- 3 Division of Epidemiology of Microbial Diseases, Yale School of Public Health, 60 College Street, P.O. Box 208034, New Haven, CT 06520, USA. Electronic address: linda.niccolai@yale.edu.
- 4 HIV/STD/TB Program, Center for Public Health Practice, Oregon Public Health Division, 800 NE Oregon Street, Suite 1130, Portland, OR 97232, USA. Electronic address: sean.schafer@state.or.us.
- 5 STD Control Branch, California Department of Public Health, 850 Marina Bay Parkway, Bldg P, 2nd Floor, Richmond, CA 94804, USA. Electronic address: ina.park@cdph.ca.gov.
- 6 Departments of Internal Medicine, Vanderbilt University Medical Center, A-2200 MCN, Nashville, TN 37232, USA. Electronic address: karen.bloch@vanderbilt.edu.
- 7 Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-G41, Atlanta, GA 30333, USA. Electronic address: eunger@cdc.gov.
- 8 STD Control Branch, California Department of Public Health, 850 Marina Bay Parkway, Bldg P, 2nd Floor, Richmond, CA 94804, USA. Electronic address: erin.whitney@cdph.ca.gov.
- 9 Division of Epidemiology of Microbial Diseases, Yale School of Public Health, 60 College Street, P.O. Box 208034, New Haven, CT 06520, USA. Electronic address: pamela.julian@yale.edu.
- 10 Center for Community Health and Department of Medicine, University of Rochester School of Medicine and Dentistry, 46 Prince Street, Rochester, NY 14607, USA. Electronic address: maryw_scahill@urmc.rocheter.edu.
- 11 HIV/STD/TB Program, Center for Public Health Practice, Oregon Public Health Division, 800 NE Oregon Street, Suite 1130, Portland, OR 97232, USA. Electronic address: nasreen.abdullah@state.or.us.
- 12 Departments of Internal Medicine, Vanderbilt University Medical Center, A-2200 MCN, Nashville, TN 37232, USA. Electronic address: diane.levine@vanderbilt.edu.
- 13 Division of STD Prevention, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-E02, Atlanta, GA 30333, USA. Electronic address: huk3@cdc.gov.
- 14 Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-G41, Atlanta, GA 30333, USA. Electronic address: msteinau@cdc.gov.
- 15 Division of STD Prevention, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road, NE MS-E02, Atlanta, GA 30333, USA. Electronic address: lmarkowitz@cdc.gov.
Item in Clipboard
Abstract
Background: Prevention of pre-invasive cervical lesions is an important benefit of HPV vaccines, but demonstrating impact on these lesions is impeded by changes in cervical cancer screening. Monitoring vaccine-types associated with lesions can help distinguish vaccine impact from screening effects. We examined trends in prevalence of HPV 16/18 types detected in cervical intraepithelial neoplasia 2, 3, and adenocarcinoma in situ (CIN2+) among women diagnosed with CIN2+ from 2008 to 2012 by vaccination status. We estimated vaccine effectiveness against HPV 16/18-attributable CIN2+ among women who received ≥1 dose by increasing time intervals between date of first vaccination and the screening test that led to detection of CIN2+ lesion.
Methods: Data are from a population-based sentinel surveillance system to monitor HPV vaccine impact on type-specific CIN2+ among adult female residents of five catchment areas in California, Connecticut, New York, Oregon, and Tennessee. Vaccination and cervical cancer screening information was retrieved. Archived diagnostic specimens were obtained from reporting laboratories for HPV DNA typing.
Results: From 2008 to 2012, prevalence of HPV 16/18 in CIN2+ lesions statistically significantly decreased from 53.6% to 28.4% among women who received at least one dose (Ptrend<.001) but not among unvaccinated women (57.1% vs 52.5%; Ptrend=.08) or women with unknown vaccination status (55.0% vs 50.5%; Ptrend=.71). Estimated vaccine effectiveness for prevention of HPV 16/18-attributable CIN2+ was 21% (95% CI: 1-37), 49% (95% CI: 28-64), and 72% (95% CI: 45-86) in women who initiated vaccination 25-36 months, 37-48 months, and >48 months prior to the screening test that led to CIN2+ diagnosis.
Conclusions: Population-based data from the United States indicate significant reductions in CIN2+ lesions attributable to types targeted by the vaccines and increasing HPV vaccine effectiveness with increasing interval between first vaccination and earliest detection of cervical disease.
Keywords: CIN; Cervical intraepithelial neoplasia; HPV; High grade cervical lesion; Human papillomavirus; Vaccine.
Published by Elsevier Ltd.
PubMed Disclaimer
Conflict of interest statement
Conflict of interest
L. Niccolai was a consultant/advisory board member for Merck. All other authors declare no conflict of interest.
Figures
Fig. 1.
Flow chart of women studied…
Fig. 1.
Flow chart of women studied from the HPV-IMPACT project.
Fig. 1.
Flow chart of women studied from the HPV-IMPACT project.
Fig. 2.
HPV 16/18 attribution to CIN2+…
Fig. 2.
HPV 16/18 attribution to CIN2+ lesions among women age-eligible for vaccination, by year…
Fig. 2.
HPV 16/18 attribution to CIN2+ lesions among women age-eligible for vaccination, by year and vaccination status. Abbreviations: CIN2+; cervical intraepithelial neoplasia grades 2; 3 and adenocarcinoma in situ (AIS). aVaccinated includes women vaccinated >30 days before trigger test (screening test that led to CIN2+ diagnosis).
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