Clinical Trials Directory

Trials / Completed

CompletedNCT00900250

Collecting and Storing Biological Samples From Young Patients With Hodgkin?s Lymphoma

Hodgkin Disease (HD) Banking Study

Status
Completed
Phase
Study type
Observational
Enrollment
1,271 (actual)
Sponsor
Children's Oncology Group · Network
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This laboratory study is collecting and storing samples of tissue and blood from young patients with Hodgkin's lymphoma. Collecting and storing samples of tumor tissue and blood from patients with cancer to study in the laboratory may help the study of cancer in the future.

Detailed description

OBJECTIVES: I. Establish a biologic specimen repository (of tumor tissue, tissue arrays, lymphoblastoid cell lines, host DNA, tumor and host RNA, serum, and plasma) and database linked to clinical features and outcomes from well-characterized cohorts of children and young adults with Hodgkin's lymphoma. II. Provide specimens from diagnosis, early response evaluation, completion of chemotherapy and radiotherapy, long-term follow up, and relapse to study prognostic factors for early response, relapse, long-term outcomes, and identification of new biological targets for therapy. OUTLINE: This is a multicenter study. Patients enrolled on Hodgkin's lymphoma (HL) therapeutic clinical trials undergo collection of tumor tissue samples at baseline and at relapse or disease progression. Serum and anticoagulated peripheral blood samples are collected at baseline, at week 1, on day 1 of course 2, after completion of chemotherapy, after completion of radiotherapy, at 1 year after diagnosis, and at relapse or disease progression. Patients with relapsed or progressive disease who plan to enroll on HL relapse/retrieval clinical trials undergo collection of tumor tissue, serum, and anticoagulated peripheral blood samples at relapse or disease progression. Patients enrolled more than 1 year after completion of treatment undergo collection of tumor specimens, serum, and anticoagulated peripheral blood samples at time of clinical evaluation.

Conditions

Interventions

TypeNameDescription
OTHERCytology Specimen Collection ProcedureCorrelative studies

Timeline

Start date
2006-10-23
Primary completion
2019-03-31
Completion
2019-03-31
First posted
2009-05-12
Last updated
2019-04-10

Locations

183 sites across 4 countries: United States, Australia, Canada, Switzerland

Source: ClinicalTrials.gov record NCT00900250. Inclusion in this directory is not an endorsement.