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Clinical Trial Summary

The purpose of this study is to investigate possible genetic factors that contribute to the development of lymphomas. The databank will be used to determine whether familial lymphomas have unique genetic characteristics different from sporadic lymphomas and to attempt to identify a gene that confers an increased risk of lymphoma.


Clinical Trial Description

- Patients who participate will be asked to complete detailed family and medical history questionnaires initially, with a follow-up questionnaire every year. - Patients will be asked to supply a blood sample and possibly a mouthwash sample, both of which can be done by mail. - Patients will be asked to consent to the release of their lymphoma tissue block for the purposes of the study. - Patients will be given letters of invitation for their affected relatives to invite them to participate. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00131014
Study type Observational
Source Dana-Farber Cancer Institute
Contact Celeste Carey, MS
Phone 857-215-1646
Email celeste_carey@dfci.harvard.edu
Status Recruiting
Phase
Start date August 9, 2004
Completion date January 2033

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