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Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy (PRADA)

Primary Purpose

Breast Cancer, Heart Failure

Status
Completed
Phase
Phase 2
Locations
Norway
Study Type
Interventional
Intervention
Metoprolol
Placebo
Candesartan
Placebo
Sponsored by
University Hospital, Akershus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Breast Cancer focused on measuring Anthracyclines, Trastuzumab

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women aged 18-70 years
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  • Serum creatinine < 140 μmol/L or estimated creatinine clearance > 60 ml/min (using the modification of diet and renal disease (MDRD) formula)
  • Systolic blood pressure >= 110 mgHg and < 170 mmHg
  • LVEF >= 50%

Exclusion Criteria:

  • Hypotension, defined as systolic blood pressure < 110 mmHg
  • Bradycardia, defined as heart rate < 50 b.p.m.
  • Prior anthracycline chemotherapy regimen
  • Prior malignancy requiring chemotherapy or radiotherapy
  • Symptomatic heart failure
  • Systolic dysfunction (LVEF < 50%)
  • Clinically significant coronary artery disease, valvular heart disease, significant arrhythmias, or conduction delays.
  • Uncontrolled arterial hypertension defined as systolic blood pressure > 170 mm Hg
  • Treatment with ACEI, ARB or beta-blocker within the last 4 weeks prior to study start
  • Intolerance to ACEI, ARB or beta-blocker
  • Uncontrolled concomitant serious illness
  • Pregnancy or breastfeeding
  • Active abuse of drugs or alcohol
  • Suspected poor compliance
  • Inability to tolerate the MRI scanning protocol

Sites / Locations

  • Akershus University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

Metoprolol

Placebo for Metoprolol

Candesartan

Placebo for Candesartan

Arm Description

Tablet, target dose 100 mg once daily

Tablet, target dose 100 mg once daily

Tablet, target dose 32 mg once daily

Tablet, target dose 32 mg once daily

Outcomes

Primary Outcome Measures

Change in left ventricular ejection fraction, as assessed by cardiac MRI

Secondary Outcome Measures

Change in contrast enhancement by MRI
Change in left 2D global strain, as assessed by echocardiography
Incidence of clinical of heart failure or objective left ventricular dysfunction
Left ventricular dysfunction defined as ejection fraction < 55% by cardiac MRI
Change in biochemical markers of cardiac injury, i.e. hs-cTnT
Change in left ventricular diastolic function, as assessed by echocardiography
Diastolic function assessed by e/e'
Change in biochemical markers of cardiac function, i.e. NT-proBNP
Change in contrast enhancement, as assessed by cardiac MRI

Full Information

First Posted
September 5, 2011
Last Updated
October 21, 2014
Sponsor
University Hospital, Akershus
Collaborators
University of Oslo, Norwegian Cancer Society, AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT01434134
Brief Title
Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy
Acronym
PRADA
Official Title
Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy: A Randomized, Placebo-controlled, 2x2 Factorial, Double Blind Trial of Candesartan and Metoprolol
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
September 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Akershus
Collaborators
University of Oslo, Norwegian Cancer Society, AstraZeneca

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Women treated for breast cancer are at increased risk for cardiovascular disease, including heart failure. In this study, by using magnetic resonance imaging (MRI), the investigators want to assess if heart failure medications such as beta blockers and angiotensin receptor blockers can prevent cardiac dysfunction during early breast cancer therapy.
Detailed Description
Breast cancer is one of the most common malignancies in women. Recent progress in the detection and treatment of breast cancer has resulted in survival gains, but a consequence of therapeutic advances is an increasing number of long-term survivors who may be at risk for development of cardiovascular disease. Several studies suggest that women treated for breast cancer may be at increased risk for cardiovascular disease, the probable causes being multi-factorial. Importantly, therapies for breast cancer, including radiotherapy, anti-HER-2 regimens and certain chemotherapeutic regimens, may increase the risk of subsequent cardiovascular disease, including atherosclerotic disease, left ventricular dysfunction, and heart failure. In the current study we propose to undertake a randomized, placebo-controlled, 2x2 factorial, double-blind trial to assess whether left ventricular dysfunction and/or injury is preventable, completely or partly, by the concomitant administration of the angiotensin receptor blocker (ARB), candesartan, and the beta blocker, metoprolol, during postoperative chemotherapy and radiotherapy. The proposed study addresses an important clinical problem in a large patient group. Thus, the possibility of preventing cardiovascular side effects of contemporary therapy for breast cancer is important both clinically and scientifically.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Heart Failure
Keywords
Anthracyclines, Trastuzumab

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
130 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metoprolol
Arm Type
Experimental
Arm Description
Tablet, target dose 100 mg once daily
Arm Title
Placebo for Metoprolol
Arm Type
Placebo Comparator
Arm Description
Tablet, target dose 100 mg once daily
Arm Title
Candesartan
Arm Type
Experimental
Arm Description
Tablet, target dose 32 mg once daily
Arm Title
Placebo for Candesartan
Arm Type
Placebo Comparator
Arm Description
Tablet, target dose 32 mg once daily
Intervention Type
Drug
Intervention Name(s)
Metoprolol
Intervention Description
Tablet, target dose 100 mg once daily
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Tablet, target dose 100 mg once daily
Intervention Type
Drug
Intervention Name(s)
Candesartan
Intervention Description
Tablet, target dose 32 mg once daily
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Tablet, 32 mg once daily
Primary Outcome Measure Information:
Title
Change in left ventricular ejection fraction, as assessed by cardiac MRI
Time Frame
Baseline and end of study (up to 72 weeks)
Secondary Outcome Measure Information:
Title
Change in contrast enhancement by MRI
Time Frame
Baseline and approximately 4 weeks
Title
Change in left 2D global strain, as assessed by echocardiography
Time Frame
Baseline and end of study (up to 72 weeks)
Title
Incidence of clinical of heart failure or objective left ventricular dysfunction
Description
Left ventricular dysfunction defined as ejection fraction < 55% by cardiac MRI
Time Frame
Up to 72 weeks
Title
Change in biochemical markers of cardiac injury, i.e. hs-cTnT
Time Frame
Baseline and end of study (up to 72 weeks)
Title
Change in left ventricular diastolic function, as assessed by echocardiography
Description
Diastolic function assessed by e/e'
Time Frame
Baseline and end of study (up to 72 weeks)
Title
Change in biochemical markers of cardiac function, i.e. NT-proBNP
Time Frame
Baseline and end of study (up to 72 weeks)
Title
Change in contrast enhancement, as assessed by cardiac MRI
Time Frame
Baseline and end of study (up to 72 weeks)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women aged 18-70 years Eastern Cooperative Oncology Group (ECOG) performance status 0-1 Serum creatinine < 140 μmol/L or estimated creatinine clearance > 60 ml/min (using the modification of diet and renal disease (MDRD) formula) Systolic blood pressure >= 110 mgHg and < 170 mmHg LVEF >= 50% Exclusion Criteria: Hypotension, defined as systolic blood pressure < 110 mmHg Bradycardia, defined as heart rate < 50 b.p.m. Prior anthracycline chemotherapy regimen Prior malignancy requiring chemotherapy or radiotherapy Symptomatic heart failure Systolic dysfunction (LVEF < 50%) Clinically significant coronary artery disease, valvular heart disease, significant arrhythmias, or conduction delays. Uncontrolled arterial hypertension defined as systolic blood pressure > 170 mm Hg Treatment with ACEI, ARB or beta-blocker within the last 4 weeks prior to study start Intolerance to ACEI, ARB or beta-blocker Uncontrolled concomitant serious illness Pregnancy or breastfeeding Active abuse of drugs or alcohol Suspected poor compliance Inability to tolerate the MRI scanning protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stein Vaaler
Organizational Affiliation
University Hospital, Akershus
Official's Role
Study Director
Facility Information:
Facility Name
Akershus University Hospital
City
Lørenskog
ZIP/Postal Code
1478
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
33993702
Citation
Heck SL, Mecinaj A, Ree AH, Hoffmann P, Schulz-Menger J, Fagerland MW, Gravdehaug B, Rosjo H, Steine K, Geisler J, Gulati G, Omland T. Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy (PRADA): Extended Follow-Up of a 2x2 Factorial, Randomized, Placebo-Controlled, Double-Blind Clinical Trial of Candesartan and Metoprolol. Circulation. 2021 Jun 22;143(25):2431-2440. doi: 10.1161/CIRCULATIONAHA.121.054698. Epub 2021 May 16.
Results Reference
derived
PubMed Identifier
29118031
Citation
Gulati G, Heck SL, Rosjo H, Ree AH, Hoffmann P, Hagve TA, Norseth J, Gravdehaug B, Steine K, Geisler J, Omland T. Neurohormonal Blockade and Circulating Cardiovascular Biomarkers During Anthracycline Therapy in Breast Cancer Patients: Results From the PRADA (Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy) Study. J Am Heart Assoc. 2017 Nov 8;6(11):e006513. doi: 10.1161/JAHA.117.006513.
Results Reference
derived
PubMed Identifier
23207160
Citation
Heck SL, Gulati G, Ree AH, Schulz-Menger J, Gravdehaug B, Rosjo H, Steine K, Bratland A, Hoffmann P, Geisler J, Omland T. Rationale and design of the prevention of cardiac dysfunction during an Adjuvant Breast Cancer Therapy (PRADA) Trial. Cardiology. 2012;123(4):240-7. doi: 10.1159/000343622. Epub 2012 Nov 30.
Results Reference
derived

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Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy

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