Long-term Use of CCB and Breast Cancer Risk

Sponsor
Curtin University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05972785
Collaborator
(none)
68,500
1
41
1669.3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
68500 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Association of Long-term Use of Calcium Channel Blockers (CCB) and Risk of Breast Cancer: A Retrospective Longitudinal Observational Study
Actual Study Start Date :
Jul 1, 2022
Anticipated Primary Completion Date :
Jun 30, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
No AHT

Women with HTN with no AHT use

Drug: None AHT
None AHT

AHT but non-CCB

Women with HTN exposed to other antihypertensive medicines but not exposed to calcium channel blockers

Drug: Beta blocker
Drugs with ATC code C07 will be categorised as beta-blockers.

Drug: Diuretic
Drugs with ATC code C03 will be categorised as diuretics.

Drug: RAS
Drugs with ATC code C09 will be categorised as RAS (agents acting on the renin angiotensin system).

Drug: Other AHT
Drugs with ATC code C02 will be categorised as other antihypertensives.

CCB only

Women with HTN exposed to calcium channel blockers but not exposed to other antihypertensive medicines

Drug: Calcium channel blocker
Drugs with ATC code C08 will be categorised as calcium channel blockers.

Both CCB and non-CCB

Women with HTN exposed to both calcium channel blockers and other antihypertensive medicines.

Drug: Calcium channel blocker
Drugs with ATC code C08 will be categorised as calcium channel blockers.

Drug: Beta blocker
Drugs with ATC code C07 will be categorised as beta-blockers.

Drug: Diuretic
Drugs with ATC code C03 will be categorised as diuretics.

Drug: RAS
Drugs with ATC code C09 will be categorised as RAS (agents acting on the renin angiotensin system).

Drug: Other AHT
Drugs with ATC code C02 will be categorised as other antihypertensives.

Outcome Measures

Primary Outcome Measures

  1. Incident rate of invasive breast cancer [From cohort entry until the earliest date of one of the following: a diagnosis of invasive breast cancer, bilateral mastectomy (without breast cancer) or death, assessed up to 14 years.]

    The outcome will be defined based on the ICD-10 code of C50.x (malignant neoplasm of breast).

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years and Older
Sexes Eligible for Study:
Female
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Curtin university Bentley Western Australia Australia 6102

Sponsors and Collaborators

  • Curtin University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rachael Moorin, Professor, Curtin University
ClinicalTrials.gov Identifier:
NCT05972785
Other Study ID Numbers:
  • 2014896
First Posted:
Aug 2, 2023
Last Update Posted:
Aug 2, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2023