A Study About How Blood Cell Growth Patterns Relate to Heart Health After Treatment for Hodgkin Lymphoma
Purpose
This study assesses how blood cell growth patterns (clonal hematopoiesis) relate to heart health or cardiovascular disease (CVD) after treatment in patients with Hodgkin lymphoma. In some patients, cancer treatment at a young age may lead to later complications, including problems with heart health. Checking for blood cell growth patterns called therapy-related clonal hematopoiesis (t-CH) can help predict who might be at risk for heart health problems after Hodgkin lymphoma treatment. If doctors know who may be at greater risk for developing later heart complications, then they can more closely monitor those patients to prevent or detect heart complications early.
Conditions
- Cardiovascular Disorder
- Classic Hodgkin Lymphoma
- Clonal Hematopoiesis
Eligibility
- Eligible Ages
- Over 7 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Patient must be >= 7 years of age at the time of enrollment (age to perform an MRI without sedation). - History of pathologically confirmed classical Hodgkin Lymphoma (cHL) initially diagnosed when the patient was >= 2 and < 22 years of age. - As part of frontline therapy for cHL, the patient must have received a cumulative doxorubicin equivalent anthracycline dose of ≥ 200 mg/m^2 as estimated in doxorubicin isotoxic equivalents dose conversion calculation. - Note: History of COG therapeutic trial participation is not required. Institutional records (e.g., clinic note, treatment summary, chemotherapy roadmap) can be used as reference documentation of receipt of anthracycline dose. - All systemic cancer treatment must have been completed ≥ 2 years prior to study enrollment. - Not known to have had a primary event (relapse/second malignancy/death). - Note: Subjects treated at another institution are eligible if they are now being followed at the current COG institution, if the study procedures can be performed and the data accessible by a COG institution where the study is open. - Patient must have access to cardiac MRI at the enrolling institution and must be able to complete cardiac MRI without sedation.
Exclusion Criteria
- Medical contraindication to undergoing a non-contrast cardiac MRI. - Patients with nodular lymphocyte-predominant HL. - Received cancer therapy in addition to that for primary Hodgkin Disease (e.g., for disease progression or recurrence, or subsequent malignant neoplasm). - History of CTCAE grade 3 or higher cardiovascular disease or condition known to exist prior to the patient's initial diagnosis of cHL. - Note: exceptions are made for congenital conditions considered fully resolved by surgery and chronic conditions such as hypertension or hypercholesterolemia that are managed with medical intervention. - History of an immunodeficiency that existed prior to cHL diagnosis, such as primary immunodeficiency syndromes, organ transplant recipients and conditions requiring systemic immunosuppressive agents.
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Other
- Time Perspective
- Other
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| Observational (blood samples, surveys, MRI, record review) | Patients undergo collection of blood samples, complete surveys, and undergo cardiac MRI on study. Patients also have their medical records reviewed and may have archived blood samples collected if available. |
|
Recruiting Locations
Mobile 4076598, Alabama 4829764 36604
Site Public Contact
800-388-8721
Phoenix 5308655, Arizona 5551752 85016
Site Public Contact
602-546-0920
New Haven 4839366, Connecticut 4831725 06520
Wilmington 4145381, Delaware 4142224 19803
Fort Myers 4155995, Florida 4155751 33908
Orlando 4167147, Florida 4155751 32806
Tampa 4174757, Florida 4155751 33607
Atlanta 4180439, Georgia 4197000 30329
Baltimore 4347778, Maryland 4361885 21201
Site Public Contact
800-888-8823
Ann Arbor 4984247, Michigan 5001836 48109
Site Public Contact
800-865-1125
Minneapolis 5037649, Minnesota 5037779 55404
St Louis 4407066, Missouri 4398678 63110
Hackensack 5098706, New Jersey 5101760 07601
Site Public Contact
551-996-2897
Albany 5106834, New York 5128638 12208
Site Public Contact
518-262-5513
Buffalo 5110629, New York 5128638 14263
Winston-Salem 4499612, North Carolina 4482348 27157
Site Public Contact
336-713-6771
Cincinnati 4508722, Ohio 5165418 45229
Columbus 4509177, Ohio 5165418 43205
Portland 5746545, Oregon 5744337 97239
Philadelphia 4560349, Pennsylvania 6254927 19104
Pittsburgh 5206379, Pennsylvania 6254927 15224
Knoxville 4634946, Tennessee 4662168 37916
Site Public Contact
865-541-8266
Fort Worth 4691930, Texas 4736286 76104
Houston 4699066, Texas 4736286 77030
San Antonio 4726206, Texas 4736286 78207
Charlottesville 4752031, Virginia 6254928 22908
Seattle 5809844, Washington 5815135 98105
Site Public Contact
866-987-2000
Madison 5261457, Wisconsin 5279468 53792
More Details
- NCT ID
- NCT05705531
- Status
- Recruiting
- Sponsor
- Children's Oncology Group
Detailed Description
PRIMARY OBJECTIVES: I. To assess the prevalence of therapy-related clonal hematopoiesis (t-CH) possessing somatic mutations associated with cardiovascular disease (CVD) in anthracycline exposed pediatric classical Hodgkin Lymphoma patients detected after front line Hodgkin Lymphoma therapy. II. To compare rates of t-CH possessing somatic mutations associated with CVD between anthracycline exposed pediatric classical Hodgkin Lymphoma patients with versus without objective signs of CVD according to cardiac magnetic resonance imaging (MRI). SECONDARY OBJECTIVES: I. To evaluate whether the incidence of t-CH possessing somatic mutations associated with CVD increases over time among pediatric classical Hodgkin Lymphoma patients previously treated with anthracyclines. II. To compare rates of objective findings of CVD between groups of anthracycline exposed pediatric classical Hodgkin Lymphoma patients with versus without clinical risk factors for CVD. EXPLORATORY OBJECTIVES: I. To compare the prevalence of t-CH with mutations associated with CVD between anthracycline exposed pediatric classical Hodgkin Lymphoma patients who received versus did not receive mediastinal radiation as part of their initial treatment. II. To assess whether specific patient characteristics and other treatment components (age, sex, race, dexrazoxane usage, etc.) are associated with an increased likelihood of t-CH with mutations associated with CVD. III. To evaluate the effect of t-CH with mutations associated with CVD on objective findings of CVD, as adjusted for or mediated by other factors such as patient characteristics and clinical conditions associated with an elevated risk for CVD. OUTLINE: This is an observational study. Patients undergo collection of blood samples, complete surveys, and undergo cardiac MRI on study. Patients also have their medical records reviewed and may have archived blood samples collected if available.