Atrial Fibrillation Among Patients With Hematologic Malignancies on Tyrosine Kinase Inhibitor Therapy
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Time periods mentioned: 12 months
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Participants will wear a smartwatch and, later, a heart monitor patch to check for AF and other irregular heart rhythms over 12 months."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study looks at how often atrial fibrillation (AF), an irregular heartbeat, occurs in people with certain blood cancers who are starting treatment. It compares people starting a cancer drug called a Bruton's tyrosine kinase inhibitor (BTKI) with people not taking a BTKI. Over 12 months, participants will use a smartwatch and later a heart monitor patch to check their heart rhythm.
This study looks at how often atrial fibrillation (AF), an irregular heart rhythm, occurs in people with certain blood cancers who are starting a type of cancer medicine called a Bruton's tyrosine kinase inhibitor (BTKI). Researchers will follow 400 people starting BTKI therapy and compare them to 100 people with similar blood cancers who are not taking a BTKI. Participants will wear a smartwatch and, later, a heart monitor patch to check for AF and other irregular heart rhythms over 12 months. The study will also look at whether AF affects cancer treatment, such as needing to pause, lower the dose, or stop the BTKI, and whether it leads to other health problems such as bleeding, stroke, or heart-related hospital visits.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- You are older than 18.
- You have one of these blood cancers: chronic lymphocytic leukemia (CLL), Waldenstrom macroglobulinemia (WM), mantle cell lymphoma (MCL), or marginal zone lymphoma (MZL).
- You are starting a BTKI or another type of treatment for your blood cancer.
Who can't join
- You have taken a BTKI before.
- You have a history of persistent AF, an irregular heartbeat that stays rather than coming and going.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * Age greater than 18 years * Diagnosis of chronic lymphocytic leukemia (CLL), Waldenstrom macroglobulinemia (WM), mantle cell lymphoma (MCL), or marginal zone lymphoma (MZL) * New initiation of Bruton's tyrosine kinase inhibitor (BTKI) therapy or non-BTKI therapy (eg, venetoclax based) for management of hematologic malignancy Exclusion Criteria: * Prior exposure to BTKI therapy * History of persistent atrial fibrillation
Study sites (3)
CA
- City of Hope · Duarte, CA 91010Study Coordinator · Study contact · 800-826-4673 · jrhee@coh.orgJune-Wha Rhee, MD · Sub-investigatorMore trials in Duarte
- UC San Diego Health · San Diego, CA 92103Ruby Swaim · Study contact · 858-246-2510 · rswaim@health.ucsd.eduAnna Narezkina, MD · Sub-investigatorMore trials in San Diego
- Stanford Health Care · Stanford, CA 94305Daniel Gonzalez, MTM · Study contact · 707-628-2150 · danieljg@stanford.eduTina Baykaner, MD · Principal investigatorMore trials in Stanford