Recurrent Melanoma Clinical Trial
Official title:
Stand Up to Cancer Consortium Genomics-Enabled Medicine for Melanoma (G.E.M.M.): Using Molecularly-Guided Therapy for Patients With BRAF Wild-Type (BRAFwt) Metastatic Melanoma
This phase II trial studies how well molecularly targeted therapy works in treating patients with melanoma that has spread to other parts of the body. Patients must have received or do not qualify for prior immunotherapy. Targeted therapy is a type of treatment that uses drugs or other substances to identify and attack specific types of cancer cells with less harm to normal cells. Molecularly targeted therapy works by treating patients with substances that kill cancer cells by targeting key molecules involved in cancer cell growth.
PRIMARY OBJECTIVES:
I. To determine the difference in best overall response rate (BORR) between patients treated
with MEK162 following personalized molecularly guided assignment vs. a historical BORR of 7%
in this patient population.
SECONDARY OBJECTIVES:
I. To evaluate the safety of performing individualized drug therapy (including novel agents
and commercially-available agents) in the context of a personalized medicine clinical trial.
II. To define the difference in progression free survival (PFS) between patients treated with
MEK162 following personalized molecularly guided assignment vs. a historical PFS rate of 2
months in this patient population.
III. To continually assess data in real time so as to iteratively refine and standardize a
set of statistical and informatics methodologies for matching treatments to the patient's
tumor, based on the molecular profile.
OUTLINE:
Patients undergo collection of tissue and blood samples for deoxyribonucleic acid (DNA) and
ribonucleic acid (RNA) analysis via sequencing. Based on the results of the DNA and RNA
analysis, patients receive molecularly targeted therapy. Treatment continues in the absence
of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up for 30 days.
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