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Clinical Trials/NCT01567722
NCT01567722
Terminated
Not Applicable

Tissue Acquisition for Analysis of Prognostic Factors, Immunology, and Genetic Progression of HIV-1 Associated Malignancies

AIDS Malignancy Consortium14 sites in 1 country114 target enrollmentJanuary 2, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
AIDS Malignancy Consortium
Enrollment
114
Locations
14
Primary Endpoint
Collection of Tissue Specimen From Study Participants
Status
Terminated
Last Updated
3 years ago

Overview

Brief Summary

RATIONALE: Collecting and studying tissue samples from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer.

PURPOSE: This research trial studies collecting tissue samples from patients with HIV-related malignancies.

Detailed Description

OBJECTIVES: * To obtain high-quality, clinically annotated tissue from patients with human immunodeficiency virus (HIV)-1 malignancy. * To study clinical, genetic, and immunologic parameters that have prognostic significance and/or are involved in the initiation and progression of HIV-1 malignancies, including complete genomic sequence determination of HIV-associated diffuse large B-cell lymphomas, lung cancer, anal cancer, and cervical cancer. OUTLINE: This is a multicenter study. Patients undergo tumor, lymph node, bone marrow, or skin biopsy, and peripheral blood mononuclear cells collection. Samples are submitted to the AIDS Malignancy Consortium (AMC) Biorepository and transferred to the AIDS and Cancer Specimen Resource (ACSR). Samples are then analyzed by the Genome Science Center of British Columbia (GSC-BC) and the HIV+ Tumor Molecular Characterization Project (HTMCP) for full genomic sequencing analysis that may include, but are not limited to, array-based gene expression profiling, comparative genome hybridization, and single nucleotide polymorphism studies by flow cytometry, cytogenetics, and molecular studies. Patients' clinical data, demographics, and treatment given are also collected prospectively in order to record treatment outcome and toxicity. Patients are followed up at 6 months, 1 year, and 2 years for data-reporting purposes.

Registry
clinicaltrials.gov
Start Date
January 2, 2013
End Date
January 14, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
AIDS Malignancy Consortium
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Collection of Tissue Specimen From Study Participants

Time Frame: Study entry (prior to chemotherapy initiation)

Summary of the specimens available by study arm

Study Sites (14)

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