Hodgkin Lymphoma Clinical Trial
Official title:
Genetic Study of Families With High Frequency of Hodgkin Lymphoma
Hodgkin lymphoma (HL) is a relatively rare disorder with known familiar aggregation (i.e. HL
in more than one child, or parent and child). Because affected individuals in familial HL are
genetically related, the existence of such families has long been considered as evidence in
support of a genetic basis of HL susceptibility. However, it is largely unknown which genetic
variations are responsible for recurring HL in families. Because the effects of genetic
variants are likely to be strong in familial HL, identification of such variations will
potentially reveal biological pathways critical to the pathogenesis of HL.
PRIMARY OBJECTIVE:
- To perform genome-wide sequencing of families with recurring Hodgkin lymphoma cases
(affected as well as non-affected family members) to identify potential disease-causing
germline genetic variations.
SECONDARY OBJECTIVE:
- To describe demographic and clinical features of the affected families.
This study entails a clinical interview and submission of a peripheral blood or saliva sample
for non-tumor DNA. Participants diagnosed with HL at outside institutions will be requested
to sign a release form to allow the outside institution to send their pathology report
confirming their HL diagnosis. If available, previously banked tumor tissue samples will be
utilized to assess genetic alterations related to HL. Detailed history will be obtained
(e.g., demographics, environmental exposures, cancer risk factors, and family pedigree) to
facilitate the analysis of phenotype-genotype correlations, taking into account potential
confounding factors.
Investigators will examine the germline and possibly the tumor DNA of each individual
participant and use the data from all participants to determine if a gene change is related
to HL.
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