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Specialist Recommendation on FBC (Familial Breast Cancer) Chemoprevention Prescribing

Impact of Familial Cancer Specialist Recommendation on Chemoprevention Prescribing for Familial Breast Cancer (FBC) Risk in Primary Care: Short Survey and Interrupted Time Series Analysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04058418
Acronym
FBC
Enrollment
50
Registered
2019-08-15
Start date
2019-07-22
Completion date
2019-12-31
Last updated
2023-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Familial Breast Cancer

Brief summary

Some women are more likely to get breast cancer as it runs in their family, they are at risk of familial breast cancer. There are medications, called chemoprevention, which may lower their risk of developing breast cancer by a third. However chemoprevention can also cause serious side effects, like womb cancer and blood clots. This makes decision to start them difficult. Researchers found that not all women who can have these medications are on them. The investigators want to ask familial breast cancer specialists whether they recommend general practitioners (GP) to prescribe chemoprevention, by sending them a short survey. These specialists look after women where breast cancer runs in the family. The specialists assess a women's chance of getting breast cancer and advice those with increased risk what can be done to prevent breast cancer. The investigators will then look at whether specialist recommendation makes a difference to whether GPs prescribe chemoprevention medication. This will be done by linking the specialists' survey response to information on GP prescribing that the government regularly publishes. This may help the investigators understand why chemoprevention is not used as often as it potentially can be.

Detailed description

Phase I: Short survey of lead clinicians of familial cancer services, descriptive analysis of recommendations by areas of the country Phase II: Prescribing data analysis (using OpenPrescribing) comprising: 1. t-test to compare the chemoprevention prescribing rate in general practices where chemoprevention is recommended versus not recommended; 2. interrupted times series analysis to assess the change in the chemoprevention prescribing after recommendation from specialist compared with changes occurring in practices where chemoprevention is not recommended and 3. panel regression across all practices, in order to distinguish the relative impacts of national versus local recommendation, and the change over time.

Interventions

OTHERSurvey Administration

Completion of a short survey.

Sponsors

University of Oxford
CollaboratorOTHER
University of Nottingham
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Lead clinicians of NHS familial cancer services across England * Standard general practices (classed as type 4 by NHS Digital, to exclude walk-in centres, prisons, care homes, etc.) with prescribing data for chemoprevention available on OpenPrescribing

Exclusion criteria

* General practices with less than 10 female patients aged 35 to 44 registered * General practices which cannot be linked to any familial cancer service from survey responses

Design outcomes

Primary

MeasureTime frameDescription
Proportion of specialist service that recommends chemoprevention prescribing by areas in England2019Proportion of specialist service that recommends chemoprevention prescribing by areas in England, measured using survey questionnaire
Chemoprevention medication prescribing rates in primary care by area in Englandpost specialist recommendation over 24 months2.1. The chemoprevention prescribing rate in general practices where chemoprevention is recommended versus not recommended. The rate will be measured as the number of average daily quantities (ADQs) of chemoprevention prescribed per 1000 registered female patients aged between 35 and 74 per practice. For our primary outcome we will measure only tamoxifen items, and assess other therapies used in chemoprevention in supplementary analyses. 2.2. The change in chemoprevention prescribing rate (described in outcome 2.1) in general practices after recommendation from local specialist, compared with changes occurring in practices where chemoprevention is not recommended. 2.3. The relative change in the chemoprevention prescribing rate (described in outcome 2.1) in general practice in response to local recommendation, compared with change occurring in response to national recommendation.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026