Identification of Genomic Lesions Promoting Nodal Metastasis in Malignant Melanoma
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Melanoma (Skin)
- Sponsor
- Case Comprehensive Cancer Center
- Enrollment
- 5
- Locations
- 1
- Primary Endpoint
- Comparison of genetic profile of patients with primary melanomas with and without synchronous regional nodal involvement
- Status
- Terminated
- Last Updated
- 9 years ago
Overview
Brief Summary
RATIONALE: Studying the genes expressed in samples of tumor tissue from patients with cancer may help doctors identify biomarkers related to cancer.
PURPOSE: This research study is looking at tumor tissue samples from patients with stage I, stage II, or stage III malignant melanoma.
Detailed Description
OBJECTIVES: * Determine the genetic profile of primary melanomas with and without synchronous regional nodal involvement by examining for 1) activating mutations B-Raf and N-Ras associated with melanoma development, and 2) allelic imbalances across the genome. * Compare the genetic profile of primary melanomas from patients with and without lymph node involvement. * Determine the combinations of genetic lesions that correlate with nodal metastasis by adopting a statistical machine learning approach to build a lesion-based classifier for nodal metastasis. OUTLINE: Laser capture microdissection is performed on the archived tissue samples to isolate melanoma cells. DNA is then purified from the samples and amplified using PCR. Matrix-assisted laser desorption/ionization (MALDI)-time of flight mass spectrometry technology is used to detect mutations of B-Raf and N-Ras. Single nucleotide polymorphism arrays are also performed. Information about the patient's demographics (e.g., TNM staging, sex, age, and tissue collection dates) will be gathered by chart review or from the Multidisciplinary Melanoma Conference at University Hospitals tumor conference report in order to match cases.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Node positive Group (experimental group)
- •Primary melanoma \> 2 mm in depth
- •Metastasis must be \> 0.1 mm and detectable by IHC or hematoxylin and eosin (H\&E) to be considered node positive
- •Slides and block for primary and node must be archived in UH dermatopathology
- •Node Negative Group (control group)
- •Primary melanoma \> 2 mm in depth
- •A negative sentinel lymph node must be negative by IHC and H\&E
- •No stage IV disease
- •No acral and mucosal histology
- •No history of prior invasive melanoma
Exclusion Criteria
- •Acral and mucosal histology
- •Previous diagnosis of invasive melanoma
- •previous chemotherapy or immunotherapy
- •patients who are found to have stage IV disease during workup
Outcomes
Primary Outcomes
Comparison of genetic profile of patients with primary melanomas with and without synchronous regional nodal involvement
Time Frame: at the time of presentation
Genetic profile of patients with primary melanomas with and without synchronous regional nodal involvement
Time Frame: at the time of presentation
Combinations of genetic lesions that correlate with nodal metastasis
Time Frame: at the time of presentation