A Multi-Centre Non-Inferiority Randomized Controlled Trial of STOPping Cardiac MEDications in Patients With Normalized Cancer Therapy Related Cardiac Dysfunction: The STOP-MED CTRCD Trial

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Cancer therapy-related cardiac dysfunction (CTRCD) is when the heart's ability to pump oxygenated blood to the body is compromised. It is a side effect of cancer therapy which can occur as commonly as in 1 in 5 patients. When this occurs, heart failure medications are started to protect the heart from progressing to heart failure. With early detection and treatment, heart function recovers to normal in \>80% of patients. Unfortunately, heart failure medications are associated with an undesirable long-term pill burden, financial costs, and side-effects (e.g., dizziness and fatigue). As a result, cancer survivors frequently ask if they can safely stop their heart failure medications once their heart function has returned to normal. Currently there is no scientific evidence in this area of Cardio-Oncology. To address this knowledge gap, the investigators have designed a randomized control trial to assess the safety of stopping heart failure medication in patients with CTRCD and recovered heart function. The investigators will enrol patients who have completed their cancer therapy and are on heart medications for their CTRCD, which has now normalized. The investigators will randomize patients with no other reasons to continue heart failure medications (e.g., kidney disease) to continuing or stopping their heart medications safely. All patients will undergo a cardiac MRI at baseline, 1 and 5 years with safety assessments at 6-8 weeks, 6 months and 3 and 5 years. The investigators will determine if stopping medications is non-inferior to continuing medications by counting the numbers of patients who develop heart dysfunction by 1 year in each group.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adult patients (age ≥18 years) with cancer therapy completed more than 6 months prior (other than hormonal therapy) and no plan for further cancer treatments with potential risk for CTRCD.

• Prior cancer therapy with anthracyclines and/ or HER2-targeted therapy.

• Prior asymptomatic, moderate to severe CTRCD, defined using the ESC/ICOS criteria (MODERATE: ≥10% drop in LVEF from baseline to 40% to 49.9% OR \<10% drop to 40-49.9% with a reduction in GLS by \>15% or new abnormal Troponin I/T or NT-proBNP or SEVERE: new LVEF reduction to \<40% from normal baseline LVEF), diagnosed within 1 year of completing potentially cardiotoxic cancer therapy.

• Current use of ≥1 HF medication started for CTRCD for at least 6 months with LVEF ≥55% by recently performed (≤6 months) echocardiogram, normal sex and age adjusted NT-proBNP or BNP ≤97.5th Centile, and no symptoms attributable to HF.

• Reference ranges for NT-proBNP and BNP by age and sex:

⁃ \<30 years: Female: NT-proBNP ≤196 pg/ml, BNP ≤55 pg/ml Male: NT-proBNP ≤104 pg/ml, BNP ≤29 pg/ml

• Confirmation of LVEF ≥55% and normal volumes at baseline CMR (i.e., some patients recruited based on echocardiography, may be excluded if baseline CMR LVEF/volumes are not normal). This is included given that the primary outcome includes the use of CMR LVEF.

Locations
United States
Massachusetts
Brigham and Women's Hospital
RECRUITING
Boston
Other Locations
Australia
Baker Heart and Diabetes Institute
RECRUITING
Melbourne
Canada
Foothills Medical Centre
NOT_YET_RECRUITING
Calgary
Edmonton Clinic Health Academy
NOT_YET_RECRUITING
Edmonton
Hamilton General Hospital
NOT_YET_RECRUITING
Hamilton
University of Ottawa Heart Institute
NOT_YET_RECRUITING
Ottawa
St Michael's Hospital
NOT_YET_RECRUITING
Toronto
University Health Network
RECRUITING
Toronto
St. Boniface Hospital
NOT_YET_RECRUITING
Winnipeg
United Kingdom
Barts Health NHS Trust, University College London
NOT_YET_RECRUITING
London
Contact Information
Primary
Paaladinesh Thavendiranathan, MD
dinesh.thavendiranathan@uhn.ca
416-340-5326
Time Frame
Start Date: 2024-03-04
Estimated Completion Date: 2031-12
Participants
Target number of participants: 335
Treatments
Experimental: Stop Group
This group will stop their heart failure medication(s) under the supervision of the study team. The investigators expect most participants in the STOP group to only be on beta-blockers (BB) and/or angiotensin-converting-enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARB). The ACEi or ARB will be stopped first. The ACEi or ARB will be reduced by 50% every 7 days and stopped 7 days after 25% of maximal recommended dose for HF is reached. At this point (or at baseline if only on BB), the BB dose will be reduced by 50% every 7 days then stopped once 25% of the maximal dose is reached. Participants on 75% of the maximal dose will be reduced to 50% of the maximal dose before reducing by 50% every 7 days. Other HF medications will be stopped as follows: MRA: reduce by 50% every 7 days then stop once 50% of maximal dose is reached; SGLT2i: stopped without titration, ARNi: reduce by 50% every 7 days then stop once 25% of the maximal dose.
No_intervention: Standard of Care Group
This group with continue with their heart failure medication(s) for at least 1 year.
Related Therapeutic Areas
Sponsors
Collaborators: St. Boniface Hospital, Brigham and Women's Hospital, Alberta Health Services, Calgary, Hamilton Health Sciences Corporation, Unity Health Toronto, Ottawa Heart Institute Research Corporation, University College London Hospitals, Baker Heart and Diabetes Institute
Leads: University Health Network, Toronto

This content was sourced from clinicaltrials.gov