The Lymphoma Epidemiology of Outcomes (LEO) Cohort Study
Status: | Recruiting |
---|---|
Conditions: | Lymphoma, Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 6/16/2018 |
Start Date: | July 2015 |
End Date: | June 2020 |
Contact: | Julianne Lunde |
Email: | lunde.julianne@mayo.edu |
Phone: | 507-266-2657 |
The goal of this infrastructure grant is to establish and maintain a cohort of over 12,000
non-Hodgkin lymphoma (NHL) patients to support broad and cutting-edge research that
identifies clinical (including co-morbid diseases), epidemiologic (including lifestyle and
other exposures), host genetic, tumor, and treatment factors, as well as the interaction
among these factors, on short and long-term outcomes. These efforts will identify new
approaches to improve the survival and well-being of NHL patients.
non-Hodgkin lymphoma (NHL) patients to support broad and cutting-edge research that
identifies clinical (including co-morbid diseases), epidemiologic (including lifestyle and
other exposures), host genetic, tumor, and treatment factors, as well as the interaction
among these factors, on short and long-term outcomes. These efforts will identify new
approaches to improve the survival and well-being of NHL patients.
Newly diagnosed non-Hodgkin lymphoma (NHL) patients will be recruited from each center
participating in the LEO cohort. At time of consent, participants will be asked to completed
several questionnaires collecting health history, current medical and quality of life
questions. Patients will also provide a baseline blood sample that will processed locally and
stored centrally for future research use. Additionally, consent is given for use of excess
clinical tumor tissue for research use.
participating in the LEO cohort. At time of consent, participants will be asked to completed
several questionnaires collecting health history, current medical and quality of life
questions. Patients will also provide a baseline blood sample that will processed locally and
stored centrally for future research use. Additionally, consent is given for use of excess
clinical tumor tissue for research use.
Inclusion Criteria:
- Newly diagnosed non-Hodgkin Lymphoma (NHL), within 183 days of enrollment
- Patients may have been treated as long as initial NHL diagnosis is within 6 months of
enrollment
- 18 years of age or older
Exclusion Criteria:
- Lymphoma diagnosis greater than 184 days from date of consent
We found this trial at
8
sites
New York, New York 10021
Principal Investigator: Peter Martin, MD
Phone: 212-746-2190
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201 Dowman Dr
Atlanta, Georgia 30303
Atlanta, Georgia 30303
(404) 727-6123
Principal Investigator: Christopher Flowers, MD
Phone: 404-778-3942
Emory University Emory University, recognized internationally for its outstanding liberal artscolleges, graduate and professional schools,...
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101 Jessup Hall
Iowa City, Iowa 52242
Iowa City, Iowa 52242
(319) 335-3500
Principal Investigator: Brian Link, MD
Phone: 319-467-5839
University of Iowa With just over 30,000 students, the University of Iowa is one of...
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Miami, Florida 33124
(305) 284-2211
Principal Investigator: Izidore Lossos, MD
Phone: 305-243-2712
University of Miami A private research university with more than 15,000 students from around the...
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60 Crittenden Blvd # 70
Rochester, New York 14642
Rochester, New York 14642
(585) 275-2121
Principal Investigator: Johnathan Friedberg, MD
University of Rochester The University of Rochester is one of the country's top-tier research universities....
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Houston, Texas 77030
Principal Investigator: Loretta Nastoupil, MD
Phone: 832-750-1554
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Rochester, Minnesota 55905
Principal Investigator: James Cerhan, MD, PhD
Phone: 507-266-2657
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Saint Louis, Missouri 63110
Principal Investigator: Brad Kahl, MD
Phone: 314-747-7638
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