Welcome to NGC. Skip directly to: Search Box, Navigation, Content.


Brief Summary

GUIDELINE TITLE

American Cancer Society guideline for human papillomavirus (HPV) vaccine use to prevent cervical cancer and its precursors.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

The table below summarizes the American Cancer Society (ACS) recommendations for human papillomavirus (HPV) vaccines.

Summary of ACS Recommendations for HPV Vaccine Use to Prevent Cervical Cancer and Its Precursors

  • Routine HPV vaccination is recommended for females aged 11 to 12 years.
  • Females as young as age 9 years may receive HPV vaccination.
  • HPV vaccination is also recommended for females aged 13 to 18 years to catch up missed vaccine or complete the vaccination series.
  • There are currently insufficient data* to recommend for or against universal vaccination of females aged 19 to 26 years in the general population. A decision about whether a woman aged 19 to 26 years should receive the vaccine should be based on an informed discussion between the woman and her health care provider regarding her risk of previous HPV exposure and potential benefit from vaccination. Ideally the vaccine should be administered prior to potential exposure to genital HPV through sexual intercourse because the potential benefit is likely to diminish with increasing number of lifetime sexual partners.
  • HPV vaccination is not currently recommended for women over age 26 years or for males.
  • Screening for cervical intraepithelial neoplasia and cancer should continue in both vaccinated and unvaccinated women according to current ACS early detection guidelines.

*Insufficient evidence of benefit in women aged 19 to 26 years refers to (1) clinical trial data in women with an average of 2, and not more than 4, lifetime sexual partners, indicating a limited reduction in the overall incidence of cervical intraepithelial neoplasia (CIN)2/3; (2) the absence of efficacy data for the prevention of HPV16/18-related CIN2/3 in women who have had more than 4 lifetime sexual partners; and (3) the lack of cost-effectiveness analyses for vaccination in this age group.

To attain the greatest impact on cervical cancer prevention, the ACS provides the following supporting recommendations:

Screening

  • It is critical that women, whether vaccinated or not, continue screening according to current ACS early detection guidelines.
  • A preventive health care visit in which vaccination is discussed or offered represents an appropriate opportunity to offer Pap screening to sexually active patients.
  • HPV testing before initiating vaccination is not recommended.

Vaccine Implementation and Utilization

  • Public health and policy efforts are needed to ensure access and encourage high HPV vaccine coverage for all racial, ethnic, and socioeconomic groups, particularly for females of color, immigrants, those living in rural areas, low-income and uninsured females, and others who have limited access to health care services.
  • Strategies should be implemented to maximize adherence to vaccination recommendations, including coadministration with other recommended adolescent vaccines, once sufficient safety data are available.
  • The use of noncomprehensive visits (e.g., minor illness visits, camp/sports physical visits) and alternative vaccination sites for adolescents unable to access comprehensive preventive care is encouraged.

Education

  • There is a critical need for education of providers, policy-makers, parents, adolescents, and young women about cervical cancer prevention and early detection, including the need for regular screening even after vaccination.

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is not specifically stated for each recommendation.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2007 Jan

GUIDELINE DEVELOPER(S)

American Cancer Society - Disease Specific Society

SOURCE(S) OF FUNDING

American Cancer Society

GUIDELINE COMMITTEE

American Cancer Society Guideline Panel

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Panel Members: Debbie Saslow, PhD; Philip E. Castle, PhD, MPH; J. Thomas Cox, MD; Diane D. Davey, MD; Mark H. Einstein, MD, MS; Daron G. Ferris, MD; Sue J. Goldie, MD, MPH; Diane M. Harper, MD, MPH, MS; Walter Kinney, MD; Anna-Barbara Moscicki, MD; Kenneth L. Noller, MD; Cosette M. Wheeler, PhD; Terri Ades, RN, MS, AOCN; Kimberly S. Andrews; Mary K. Doroshenk, MA; Kelly Green Kahn; Christy Schmidt; Omar Shafey, PhD, MPH; Robert A. Smith, PhD; Edward E. Partridge, MD (for the Gynecologic Cancer Advisory Group); Francisco Garcia, MD, MPH

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Workgroup members were asked to disclose relationships, including potential financial conflicts of interest, with vaccine manufacturers or trials. The following was disclosed: F. Garcia participated in an expert panel for GlaxoSmithKline (GSK) for an unrelated immune therapeutic class of agents; C. Cohen is a paid speaker for Merck; T. Cox is a paid member of the Merck Data Safety and Monitoring Committee and received an honorarium for serving on one management advisory board for GSK; D. Davey serves on the working group of the NCI-sponsored trial of GSK vaccine in Costa Rica; M. Einstein has received research support from GSK for a nonvaccine-related activity and serves on the speaker's bureau for Merck, but receives no salary support or honorarium; D. Ferris receives research support for vaccine trials from Merck and GSK and serves as a colposcopy quality control consultant to both Merck and GSK and on the Merck medical advisory board; D. Harper serves on the study planning committee for Merck and GSK and is a clinical site PI for GSK; A. Moscicki serves on Merck's speaker's bureau and adolescent advisory board and is a local PI on the GSK vaccine trial; E. Partridge received an honorarium for a one-day advisory meeting for Merck and is a PI for a clinical study site for Merck; C. Wheeler receives research support for vaccine trials from Merck and GSK; D. Solomon is a medical monitor for the NCI-sponsored trial of GSK vaccine in Costa Rica.

GUIDELINE STATUS

This is the current release of the guideline.

GUIDELINE AVAILABILITY

Electronic copies: Available from the American Cancer Society Web site.

Print copies: Available from the American Cancer Society, 250 Williams St., Suite 600, Atlanta, GA 30303; Web site: www.cancer.org.

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

The following are available:

Also available by calling 1-800-ACS-2345.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This NGC summary was completed by ECRI Institute on January 31, 2008. The information was verified by the guideline developer on February 29, 2008.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

DISCLAIMER

NGC DISCLAIMER

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.

All guidelines summarized by NGC and hosted on our site are produced under the auspices of medical specialty societies, relevant professional associations, public or private organizations, other government agencies, health care organizations or plans, and similar entities.

Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

NGC, AHRQ, and its contractor ECRI Institute make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI Institute, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.

Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
DHHS Logo