Development of a Tumor Molecular Analyses Program and Its Use to Support Treatment Decisions

UNC Lineberger Comprehensive Cancer Center

Status: Completed

Conditions: Neoplasm

Treatments: Diagnostic Test: Tumor Genetic Sequencing

Study type: Interventional

Funder types: Other

Identifiers

NCT01457196

LCCC1108

Details and patient eligibility

About

The primary objective of this specimen correlative study is two-fold: to provide a mechanism for the association of known molecular alterations with clinical outcomes, and to provide rapid genetic profiling of alterations with known clinical utility using tumor and germline specimens to support treatment decisions.

Enrollment: 2,798 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Current or prospective cancer patients; current cancer patients must have histologically or cytologically confirmed diagnosis of cancer

2. Tumor tissue available and suitable for molecular analyses from at least one of the following sources:

   • Tissue previously stored in UNC's Tissue Procurement Facility (TPF)
   • Tissue previous stored at an institution other than UNC-CH, provided investigators can determine that the tumors were sampled and stored under appropriate conditions for inclusion in the study
   • Patient undergoing tissue collection as per clinical standard of care and willing to allow specimens from surplus tissue to be diverted for research purposes
   • Patient undergoing tissue collection as per clinical standard of care and willing to have additional specimens taken for research
   • Patient willing to undergo biopsy for purpose of research only

3. The following inclusion criteria apply only to patients undergoing biopsy for research purposes only under this protocol:

   • ≥18 years of age
   • Treatment options offer no expectation of cure, e.g., advanced solid tumor patients with metastatic disease. NOTE: This restriction applies to biopsy of vital organs only, e.g., lung, liver, etc.
   • Appropriate candidate for research biopsy based on institutional standards for target biopsy site

Exclusion criteria

1. Any condition that would make participation in the protocol unreasonably hazardous for the patient in the opinion of the treating physician
2. Dementia, altered mental status, or any psychiatric condition or co-morbid condition that would prohibit the understanding or rendering of informed consent.
3. The following exclusion criteria apply only to enrolled patients undergoing biopsy for research purposes only:
4. History of serious or life-threatening allergic reaction to local anesthetics (i.e. lidocaine, xylocaine) or any medications used for conscious sedation (if applicable).
5. Requires general anesthesia for collection of biopsy
6. Pregnant or lactating women
7. Active cardiac disease
8. Patients receiving bevacizumab less than 6 weeks prior to enrollment into this study should not undergo research core biopsies because of the concern for potential increased bleeding risk and delayed healing. (NOTE: Patients receiving bevacizumab who are undergoing a research biopsy of accessible organs (e.g. breast, lymph node, skin etc.) must be two weeks from the last dose of the angiogenesis inhibitor).

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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2,798 participants in 1 patient group

Sequencing Arm

Other group

Treatment:

Diagnostic Test: Tumor Genetic Sequencing