Skip to main content
OpenTrials
Completed

NCT Number: NCT02178579

Prospective Observation of Cardiac Safety With Proteasome Inhibition

The purpose of this study is to better define and understand potential cardiac toxicities of proteasome inhibitors and to understand optimal management strategies to treat and prevent cardiovascular events.

Completed

Looking for future studies?

Notify Me

Key information

About this study

Cancer treatments, using proteasome inhibitors, have the potential in induce cardiac toxicities including heart failure (HF), hypertension, arrhythmias and ischemic heart disease. While the presence of cardiac events may be a class effect of proteasome inhibitors (PI), the effect may be more profound with the irreversible inhibition of carfilzomib compared with reversible inhibition with bortezomib. Data available from currently published clinical trials may be inadequate to fully understand the incidence and severity of cardiac injury in patients treated with proteasome inhibitors because the trials were not designed to fully assess cardiac events. The purpose of this study is to better define and understand potential cardiac toxicity and begin to understand optimal management strategies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Relapsed multiple myeloma at any time-point in treatment course and planning to start a proteasome inhibitor-based therapy as part of standard care
  • Received at least one prior line of therapy for multiple myeloma (induction therapy followed by stem cell transplant and consolidation/maintenance therapy will be considered as one line of therapy)
  • Males and females ≥ 18 years of age
  • Able to provide written informed consent in accordance with federal, local, and institutional guidelines

Exclusion criteria

  • POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes)
  • Known or suspected AL amyloidosis, secondary amyloidosis or cardiac amyloidosis
  • Plasma cell leukemia (> 2.0 × 109/L circulating plasma cells by standard differential)
  • Waldenström Macroglobulinemia
  • Myelodysplastic syndrome
  • History of MI within the last 3 months
  • Symptomatic unstable cardiac arrhythmia requiring treatment in the past 3 months
  • Class 3 or 4 New York Heart Association Heart Failure in the past 3 months
  • Any other clinically significant medical disease or condition that, in the investigator's opinion, may interfere with protocol adherence or a subject's ability to give informed consent

Treatment and study plan

Primary outcomes

  1. Frequency of cardiac events of patients receiving PIs for MM.

    Time frame: 18 months

Sponsors and collaborators

Lead sponsor

Vanderbilt University Medical Center

Other

Collaborators

  • Takeda

Registry information

Acronym: PROTECT

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Jul 1, 2014
Registry last updated
Sep 14, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.