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Trial Title:
Long-term Use of CCB and Breast Cancer Risk
NCT ID:
NCT05972785
Condition:
Hypertension,Essential
Breast Cancer
Conditions: Official terms:
Breast Neoplasms
Essential Hypertension
Calcium Channel Blockers
Calcium
Diuretics
Adrenergic beta-Antagonists
Study type:
Observational
Overall status:
Active, not recruiting
Study design:
Time perspective:
Retrospective
Intervention:
Intervention type:
Drug
Intervention name:
Calcium channel blocker
Description:
Drugs with ATC code C08 will be categorised as calcium channel blockers.
Arm group label:
Both CCB and non-CCB
Arm group label:
CCB only
Intervention type:
Drug
Intervention name:
Beta blocker
Description:
Drugs with ATC code C07 will be categorised as beta-blockers.
Arm group label:
AHT but non-CCB
Arm group label:
Both CCB and non-CCB
Intervention type:
Drug
Intervention name:
Diuretic
Description:
Drugs with ATC code C03 will be categorised as diuretics.
Arm group label:
AHT but non-CCB
Arm group label:
Both CCB and non-CCB
Intervention type:
Drug
Intervention name:
RAS
Description:
Drugs with ATC code C09 will be categorised as RAS (agents acting on the renin
angiotensin system).
Arm group label:
AHT but non-CCB
Arm group label:
Both CCB and non-CCB
Intervention type:
Drug
Intervention name:
Other AHT
Description:
Drugs with ATC code C02 will be categorised as other antihypertensives.
Arm group label:
AHT but non-CCB
Arm group label:
Both CCB and non-CCB
Intervention type:
Drug
Intervention name:
None AHT
Description:
None AHT
Arm group label:
No AHT
Summary:
The goal of this retrospective observational study is to examine whether long-term
calcium channel blocker (CCB) use is associated with the development of breast cancer
amongst women enrolled in three longitudinal cohort studies in Australia and the
Netherlands . The main questions it aims to answer are:
- Is long-term CCB use associated with the development of breast cancer amongst women
enrolled in three longitudinal cohort studies in Australia and the Netherlands and
what is the dose-response nature of this association.
- Does differences in the association between calcium channel blocker use and the
development of breast cancer exist between Australian and Dutch women.
The investigators will utilise data from the Australian Longitudinal Study on Women's
Health (ALSWH) , 45 and Up Study and Rotterdam study.
Detailed description:
Aims: To examine the association between long-term calcium channel blocker (CCB) use and
the development of breast cancer.
Data sources: the Australian Longitudinal Study on Women's Health , 45 and Up Study,
Rotterdam study and linked administrative data.
Study cohort: Women with self-reported hypertension (HTN) without prior breast cancer.
Harmonisation: Relevant variables will be checked for harmonisation in which variables
available in all three cohort will be used in the harmonised analysis. The variables will
be checked on the definition, measurement and harmonisation rules. Variables that cannot
be harmonised across the cohorts will be used in the cohort specific analyses.
Exposure measurement: The primary exposure is the use of CCB, which will be identified by
the anatomical therapeutic chemical code (C08) in the medicine data. Exposure to CCB as
well as other antihypertensive (AHT) medicines will be captured separately as the
cumulative dose-duration of exposure during follow up. Participants will be stratified in
four groups: women with HTN with no AHT use, women with HTN exposed to CCB only, women
with HTN exposed to non-CCB and women with HTN exposed to both CCB and non-CCB.
Outcome measurement: Data on a diagnosis of invasive breast cancer will be obtained from
cancer registries and hospital admission data using ICD-10 code of C50.x.
Potential confounders: age, education, marital status, socioeconomic status, body mass
index, diabetes, heart disease, stroke, age when had first child, parity, history of
hysterectomy or oophorectomy, use of hormonal contraception, use of hormonal replacement
therapy.
Statistical analysis: The association between CCB use and breast cancer risk will be
estimated by the Fine and Gray competing risk regression model in which a first diagnosis
of invasive breast cancer will be treated as the principle event and death and bilateral
mastectomy (without a diagnosis of breast cancer) will be competing risks. The nonlinear
threshold models will be used to capture any differential effect of the cumulative
dose-duration of CCB while simultaneously accounting for the cumulative dose-duration of
other AHT exposure on breast cancer risk. Other confounders will be accounted for in the
models using propensity scores.
Implications: Results from this study will contribute to addressing the concerns about
using CCB for hypertension treatment in women, particularly in those who have high risk
of breast cancer.
Criteria for eligibility:
Study pop:
The study will include eligible women enrolled in three longitudinal cohorts: ALSWH, 45
and Up Study and the Rotterdam study.
Sampling method:
Probability Sample
Criteria:
Inclusion criteria:
- Alive and still enrolled in the longitudinal cohort at the study entry (2004 to
2009)
- Self-reported/diagnosed hypertension at study entry.
Exclusion criteria:
- A history of breast cancer.
Gender:
Female
Minimum age:
45 Years
Maximum age:
N/A
Locations:
Facility:
Name:
Curtin university
Address:
City:
Bentley
Zip:
6102
Country:
Australia
Start date:
July 1, 2022
Completion date:
December 2025
Lead sponsor:
Agency:
Curtin University
Agency class:
Other
Source:
Curtin University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05972785