search
Back to results

Extending the National Health Service (NHS) Breast Screening Age Range (AgeX)

Primary Purpose

Breast Cancer Mortality

Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Invitation for breast screening
Sponsored by
University of Oxford
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Breast Cancer Mortality focused on measuring Breast cancer, Breast screening, Mammography, Routine screening programme

Eligibility Criteria

47 Years - 73 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Female, and
  • Aged 47-49 years or 71-73 years, and
  • In a Breast Screening Unit participating in the study. (All Breast Screening Units in England are expected to participate in the study with the exception of a few that use non-standard methods for creating screening batches).

Exclusion Criteria:

  • Anyone not satisfying the inclusion criteria

Sites / Locations

  • Cancer Epidemiology Unit, Richard Doll Building, University of Oxford, Roosevelt Drive

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Women aged 47-49 invited for breast screening

Women aged 71-73 invited for breast screening

Arm Description

Outcomes

Primary Outcome Measures

Breast cancer mortality

Secondary Outcome Measures

Breast cancer incidence, up to the same date that the primary outcome (breast cancer mortality) is reported
Hospital admissions for mastectomy and lumpectomy, up to the same date that the primary outcome (breast cancer mortality) is reported
All-cause mortality, up to the same date that the primary outcome (breast cancer mortality) is reported

Full Information

First Posted
March 3, 2010
Last Updated
January 5, 2023
Sponsor
University of Oxford
Collaborators
Public Health England, Cancer Research UK
search

1. Study Identification

Unique Protocol Identification Number
NCT01081288
Brief Title
Extending the National Health Service (NHS) Breast Screening Age Range
Acronym
AgeX
Official Title
Nationwide Cluster-randomised Trial of Extending the NHS Breast Screening Age Range in England
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 2009 (undefined)
Primary Completion Date
December 31, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oxford
Collaborators
Public Health England, Cancer Research UK

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Nationwide cluster-randomised trial of extending the NHS breast screening age range in England
Detailed Description
In 1988, the national Breast Screening Programme (BSP) began offering women aged 50-64 years triennial mammographic screening and full national coverage was achieved by the mid-1990s. In 2003, the age range for triennial screening was extended from 50-64 to 50-70 years; proposals from committees in the Department of Health to randomise this age extension and thereby to obtain reliable information on both the risks and benefits of additional screening at ages 65-70 were not adopted. Currently, 80 breast screening units cover all of England, each responsible for a defined area, and each year they invite about 2.8 million women aged 50-70, with 2.0 million accepting. The BSP sets standards for the screening units and monitors performance through its national quality assurance network. In 2007, the Prime Minister announced plans for eventual extension to the range 47-73 years. This offered another opportunity to obtain reliable evidence about the effects of extending the age range of triennial screening. Hence, a trial of this age extension has begun, in which only half are offered extra screening, with the effects monitored through routinely collected NHS statistics. Following a 2009-10 pilot study of the acceptability of cluster-randomisation of additional screening at ages 47-49 and 71-73 in 5 breast screening units, the AgeX trial extended recruitment to about five-sixths of the breast screening clinics in England, and this cluster-randomisation continues. In 2011, the Government deferred the earliest possible date when screening would be extended to all women aged 47-73. Later, Public Health England (PHE, which is responsible for government screening programmes) stated that final decisions about extension of the age range would await the emergence of reliable evidence of its effects. The AgeX trial will eventually provide this. In 2012, an independent panel set up by the Department of Health and the charity Cancer Research UK reported "The UK breast screening programmes [at ages 50-70] confer significant benefit and should continue…. The impact of breast screening outside the ages 50-69 years is very uncertain. The Panel supports the principle of the ongoing trial in the UK [AgeX] for randomising women under age 50 and above age 70 to be invited for breast screening". Meanwhile, as female life expectancy is increasing, interest has grown in the possible advantages of continuing to screen women not just in their early 70s but throughout their 70s. The advantages and the disadvantages of continuing triennial screening after age 70 would be seen more clearly in a trial of 2 or 3 additional invitations (covering ages 71-76 or 71-79) than in a trial of just one. In 2013 the All-Party Parliamentary Group on Breast Cancer in Older Women (APPG) said "Women are not routinely invited for breast screening past the age of 70 … the current 'age extension trial' [of screening past age 70] … should be extended past 73 to 76, and, if appropriate … further extended". In a separate report in 2015 the APPG reiterated this conclusion. Although AgeX began as a trial of additional screening at ages 47-49 and at ages 71-73, it has therefore become a trial in which the older women allocated additional screening can, where resources are available, continue be invited triennially at ages 71-76 or at ages 71-79, thereby assessing the effects of continuing triennial screening for several years after age 70.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Mortality
Keywords
Breast cancer, Breast screening, Mammography, Routine screening programme

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4000000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Women aged 47-49 invited for breast screening
Arm Type
Active Comparator
Arm Title
Women aged 71-73 invited for breast screening
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Invitation for breast screening
Intervention Description
Invitation for breast screening to women in different age groups
Primary Outcome Measure Information:
Title
Breast cancer mortality
Time Frame
17 years
Secondary Outcome Measure Information:
Title
Breast cancer incidence, up to the same date that the primary outcome (breast cancer mortality) is reported
Time Frame
17 years
Title
Hospital admissions for mastectomy and lumpectomy, up to the same date that the primary outcome (breast cancer mortality) is reported
Time Frame
17 years
Title
All-cause mortality, up to the same date that the primary outcome (breast cancer mortality) is reported
Time Frame
17 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
47 Years
Maximum Age & Unit of Time
73 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Female, and Aged 47-49 years or 71-73 years, and In a Breast Screening Unit participating in the study. (All Breast Screening Units in England are expected to participate in the study with the exception of a few that use non-standard methods for creating screening batches). Exclusion Criteria: Anyone not satisfying the inclusion criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julietta Patnick, BA
Organizational Affiliation
University of Oxford
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cancer Epidemiology Unit, Richard Doll Building, University of Oxford, Roosevelt Drive
City
Oxford
ZIP/Postal Code
OX3 7LF
Country
United Kingdom

12. IPD Sharing Statement

Links:
URL
http://www.agex.uk/
Description
Breast Screening Programme Age Extension Trial

Learn more about this trial

Extending the National Health Service (NHS) Breast Screening Age Range

We'll reach out to this number within 24 hrs