Secondary Prevention of Cervical Cancer: ASCO Resource–Stratified Guideline Update

Author:

Shastri Surendra S.1,Temin Sarah2ORCID,Almonte Maribel3ORCID,Basu Partha3ORCID,Campos Nicole G.4ORCID,Gravitt Patty E.5,Gupta Vandana6,Lombe Dorothy C.7ORCID,Murillo Rául8ORCID,Nakisige Carolyn9,Ogilvie Gina10,Pinder Leeya F.11,Poli Usha R.12ORCID,Qiao Youlin13ORCID,Woo Yin Ling14ORCID,Jeronimo Jose5

Affiliation:

1. The University of Texas, MD Anderson Cancer Center, Houston, TX

2. American Society of Clinical Oncology, Alexandria, VA

3. IARC, Lyon, France

4. Harvard University T.H. Chan School of Public Health, Boston, MA

5. National Cancer Institute, Bethesda, MD

6. V Care Foundation, Mumbai, India

7. Regional Cancer Treatment Services, MidCentral District Health Board, Palmerston North, New Zealand

8. Centro Javeriano de Oncología, Bogota, Colombia

9. Mulago Hospital, Kampala, Uganda

10. BC Women's Hospital, Vancouver, BC, Canada

11. University of Washington, Seattle, WA

12. India Institute of Public Health, Hyderabad, India

13. Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

14. University of Malaya, Kuala Lumpur, Malaysia

Abstract

PURPOSE To update resource-stratified, evidence-based recommendations on secondary prevention of cervical cancer globally. METHODS American Society of Clinical Oncology convened a multidisciplinary, multinational Expert Panel to produce recommendations reflecting four resource-tiered settings. A review of existing guidelines, formal consensus-based process, and modified ADAPTE process to adapt existing guidelines was conducted. Other experts participated in formal consensus. RESULTS This guideline update reflects changes in evidence since the previous update. Five existing guidelines were identified and reviewed, and adapted recommendations form the evidence base. Cost-effectiveness analyses provided indirect evidence to inform consensus, which resulted in ≥ 75% agreement. RECOMMENDATIONS Human papillomavirus (HPV) DNA testing is recommended in all resource settings; visual inspection with acetic acid may be used in basic settings. Recommended age ranges and frequencies vary by the following setting: maximal: age 25-65 years, every 5 years; enhanced: age 30-65 years, if two consecutive negative tests at 5-year intervals, then every 10 years; limited: age 30-49 years, every 10 years; basic: age 30-49 years, one to three times per lifetime. For basic settings, visual assessment is used to determine treatment eligibility; in other settings, genotyping with cytology or cytology alone is used to determine treatment. For basic settings, treatment is recommended if abnormal triage results are obtained; in other settings, abnormal triage results followed by colposcopy is recommended. For basic settings, treatment options are thermal ablation or loop electrosurgical excision procedure; for other settings, loop electrosurgical excision procedure or ablation is recommended; with a 12-month follow-up in all settings. Women who are HIV-positive should be screened with HPV testing after diagnosis, twice as many times per lifetime as the general population. Screening is recommended at 6 weeks postpartum in basic settings; in other settings, screening is recommended at 6 months. In basic settings without mass screening, infrastructure for HPV testing, diagnosis, and treatment should be developed. Additional information is available at www.asco.org/resource-stratified-guidelines .

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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