Utility of Novel BRAF Test for Melanoma

Sponsor
Massachusetts General Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT01840527
Collaborator
(none)
220
3
112
73.3
0.7

Study Details

Study Description

Brief Summary

This primary purpose of this study is to obtain blood samples from participants with both early and later stages of melanoma (Stage II/III and Stage IV). The researchers hope to better understand an abnormal protein found in many melanoma tumors called the BRAFV600 mutation.

There will be two separate cohorts (groups) of participants on this study. You will be placed in one of the Groups.

Group 1-For participants with advanced melanoma: Your existing tumor tissue sample will be compared to the blood samples given in order to further analyze and to understand the BRAFV600E gene mutation.

Group 2-For participants with stage II/III melanoma: Following surgery, blood samples will be collected and analyzed.

Understanding the BRAFV600E gene mutation in melanoma will help the researchers better understand the disease, and help plan treatment options for people with melanoma of all stages in the future.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    There will be no extra clinic visits for this study. These research blood samples will be drawn at the same time as your regularly scheduled blood draws that are part of standard care for melanoma.

    About 2 to 4 teaspoons of blood will be drawn for each research sample.

    Depending on which group you are in, you will have either a one time blood draw or ongoing blood work for 1-2 years.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    220 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Exploring the Utility of a Novel BRAF Test in Patients With Melanoma
    Study Start Date :
    May 1, 2013
    Actual Primary Completion Date :
    Mar 29, 2017
    Anticipated Study Completion Date :
    Sep 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Group 1

    Advanced Melanoma

    Group 2

    Stage II/III Melanoma

    Outcome Measures

    Primary Outcome Measures

    1. Determine Specificity and Sensitivity of Blood Based Assay [2 years]

      To determine the specificity and sensitivity of the blood based assay vis-a-vis tissue based BRAF analysis in patients with advanced and high-risk melanoma

    Secondary Outcome Measures

    1. Explore Pharmacodynamic Effects of MAPK Pathway Inhibitors [2 years]

      To explore the pharmacodynamic effects of MAPK pathway inhibitors (including selective BRAF inhibitors, MEK inhibitors, and ERK inhibitors) utilizing pre-and on-treatment peripheral blood BRAFV600E mutational testing in patients with advanced melanoma, (non-resectable Stage III or Stage IV)

    2. Define Prognostic Value of Peripheral Blood BRAFV600 Testing in Melanoma [2 years]

      To define the prognostic value of peripheral blood BRAFV600 mutational testing in patients with Stage II and resectable Stage III melanoma

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Biopsy proven advanced (unresectable stage IIIC or stage IV)or high risk (stage II or stage III) malignant melanoma
    Exclusion Criteria:
    • History of a different malignancy except for the following circumstances: disease-free for at least 2 years and deemed by the investigator to be at low risk for recurrence; or non-metastatic prostate cancer, cervical cancer in situ and basal cell or squamous cell carcinoma

    • Known history of a different BRAF mutant malignancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Massachusetts General Hospital Boston Massachusetts United States 02114
    2 Beth Israel Deaconess Medical Center Boston Massachusetts United States 02215
    3 Dana-Farber Cancer Institute Boston Massachusetts United States 02215

    Sponsors and Collaborators

    • Massachusetts General Hospital

    Investigators

    • Principal Investigator: Ryan Sullivan, MD, Massachusetts General Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ryan Sullivan, M.D., Principal Investigator, Massachusetts General Hospital
    ClinicalTrials.gov Identifier:
    NCT01840527
    Other Study ID Numbers:
    • 12-488
    First Posted:
    Apr 25, 2013
    Last Update Posted:
    Oct 29, 2021
    Last Verified:
    Oct 1, 2021
    Keywords provided by Ryan Sullivan, M.D., Principal Investigator, Massachusetts General Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 29, 2021