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Randomized Implementation of Primary HPV Testing in the Organized Screening for Cervical Cancer in Stockholm

Primary Purpose

High-grade Cervical Intraepithelial Neoplasia

Status
Active
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
HPV testing
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for High-grade Cervical Intraepithelial Neoplasia focused on measuring HPV testing, Primary screening, Cervical Cancer

Eligibility Criteria

30 Years - 64 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

Women between the age 30 and 64 years resident in the Stockholm-Gotland region. No exclusion criteria.

Sites / Locations

  • Karolinska University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

HPV testing

cytology

Arm Description

Women randomised to this arm get primary HPV testing

women included follow the standard procedure with primary cytology

Outcomes

Primary Outcome Measures

Cervical intraepithelial neoplasia 2+ (CIN2+)
The number of women with CIN2+ detected by primary HPV testing will be compared with the number of women with CIN2+ detected by primary cytology

Secondary Outcome Measures

Cost for the two different diagnostic procedures
The cost for the new procedure with HPV test in primary screening will be compared to the routine procedure with primary cytology

Full Information

First Posted
December 20, 2011
Last Updated
February 10, 2023
Sponsor
Karolinska Institutet
Collaborators
Region Stockholm
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1. Study Identification

Unique Protocol Identification Number
NCT01511328
Brief Title
Randomized Implementation of Primary HPV Testing in the Organized Screening for Cervical Cancer in Stockholm
Official Title
Randomized Implementation of Primary Human Papillomavirus (HPV) Testing in the Organized Screening for Cervical Cancer in Stockholm
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 1, 2012 (Actual)
Primary Completion Date
June 30, 2017 (Actual)
Study Completion Date
December 2031 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Region Stockholm

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose is to evaluate whether implementation of primary human papillomavirus (HPV) screening in the screening programme for cervical cancer improves the programme in terms of better cancer protection and better cost efficiency.
Detailed Description
Primary HPV screening is a method with higher sensitivity than cytology for detection of high-grade cervical intraepithelial neoplasia, which is the precursor of cervical cancer. In particular, HPV test is a better test for revealing adenocarcinomas, since these cancers often show a normal cytology. Cervical cancer screening at age 60: Cytology is less effective in older women, and screening with cytology in women over 60 has no documented effect. Today a large part of cervical cancer develop in women older than 60, to whom no screening is offered. The prevalence of HPV is around 4% in this age group. Since we know that testing negative for HPV gives a better long-term protection against cervical cancer compared to cytology, primary screening for HPV in 60-year old women would give a longer lasting protection in this high-risk group compared with today. Cervical cancer screening at age 30-40: HPV screening is most cost effective above 35 years of age. The reason for this is that HPV is less prevalent at age 35 than in younger women and also because cervical cancer seldom develops before this age. Since the HPV test has a negative predictive value (NPV) of almost 100% this could lead to longer screening intervals, which would be improve cost-effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
High-grade Cervical Intraepithelial Neoplasia
Keywords
HPV testing, Primary screening, Cervical Cancer

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
270000 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HPV testing
Arm Type
Experimental
Arm Description
Women randomised to this arm get primary HPV testing
Arm Title
cytology
Arm Type
No Intervention
Arm Description
women included follow the standard procedure with primary cytology
Intervention Type
Other
Intervention Name(s)
HPV testing
Intervention Description
Testing for Human Papilloma Virus
Primary Outcome Measure Information:
Title
Cervical intraepithelial neoplasia 2+ (CIN2+)
Description
The number of women with CIN2+ detected by primary HPV testing will be compared with the number of women with CIN2+ detected by primary cytology
Time Frame
first evaluation, the 1 of january 2013
Secondary Outcome Measure Information:
Title
Cost for the two different diagnostic procedures
Description
The cost for the new procedure with HPV test in primary screening will be compared to the routine procedure with primary cytology
Time Frame
first evaluation, 1 of January 2013

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women between the age 30 and 64 years resident in the Stockholm-Gotland region. No exclusion criteria.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joakim Dillner, MD, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
141 86
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
19796748
Citation
Arbyn M, Ronco G, Meijer CJ, Naucler P. Trials comparing cytology with human papillomavirus screening. Lancet Oncol. 2009 Oct;10(10):935-6. doi: 10.1016/S1470-2045(09)70296-7. No abstract available.
Results Reference
background
PubMed Identifier
19141778
Citation
Naucler P, Ryd W, Tornberg S, Strand A, Wadell G, Elfgren K, Radberg T, Strander B, Forslund O, Hansson BG, Hagmar B, Johansson B, Rylander E, Dillner J. Efficacy of HPV DNA testing with cytology triage and/or repeat HPV DNA testing in primary cervical cancer screening. J Natl Cancer Inst. 2009 Jan 21;101(2):88-99. doi: 10.1093/jnci/djn444. Epub 2009 Jan 13.
Results Reference
background
PubMed Identifier
28566363
Citation
Lamin H, Eklund C, Elfstrom KM, Carlsten-Thor A, Hortlund M, Elfgren K, Tornberg S, Dillner J. Randomised healthcare policy evaluation of organised primary human papillomavirus screening of women aged 56-60. BMJ Open. 2017 May 30;7(5):e014788. doi: 10.1136/bmjopen-2016-014788.
Results Reference
result
PubMed Identifier
34424907
Citation
Elfstrom KM, Eklund C, Lamin H, Ohman D, Hortlund M, Elfgren K, Sundstrom K, Dillner J. Organized primary human papillomavirus-based cervical screening: A randomized healthcare policy trial. PLoS Med. 2021 Aug 23;18(8):e1003748. doi: 10.1371/journal.pmed.1003748. eCollection 2021 Aug.
Results Reference
derived
PubMed Identifier
31585095
Citation
Sahlgren H, Elfstrom KM, Lamin H, Carlsten-Thor A, Eklund C, Dillner J, Elfgren K. Colposcopic and histopathologic evaluation of women with HPV persistence exiting an organized screening program. Am J Obstet Gynecol. 2020 Mar;222(3):253.e1-253.e8. doi: 10.1016/j.ajog.2019.09.039. Epub 2019 Oct 1.
Results Reference
derived

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Randomized Implementation of Primary HPV Testing in the Organized Screening for Cervical Cancer in Stockholm

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