<p>The CS-MATCH-0007 protocol is a collaboration between the Center for Cancer Genomics (CCG) and the Division of Cancer Treatment and Diagnosis (DCTD) to perform whole-exome sequencing and RNA sequencing using pre-and post-treatment tumor biopsy specimens from all patients enrolled on a treatment arm of the <a href="https://clinicaltrials.gov/ct2/show/NCT02465060?term=NCT02465060&#x26;rank=1"></a><a href="https://classic.clinicaltrials.gov/ct2/show/NCT02465060?term=NCT02465060&#x26;rank=1">NCI-MATCH Clinical Trial (EAY131)</a>. The goal of this study is to identify the molecular basis for response and resistance to targeted therapies that are matched to their corresponding genomic alterations. Arm H is one of the treatment sub-protocols within the <a href="https://clinicaltrials.gov/ct2/show/NCT02465060?term=NCT02465060&#x26;rank=1"></a><a href="https://classic.clinicaltrials.gov/ct2/show/NCT02465060?term=NCT02465060&#x26;rank=1">NCI-MATCH Clinical Trial (EAY131)</a> where patients with BRAF V600K/V600E mutations are treated with Dabrafenib and Trametinib. This subprotocol is one of the treatment arms in the EAY-131 trial included in the CS-MATCH-0007 protocol and will provide specimens for the program including DNA from tumor tissue and whole blood and RNA from tumor tissue. A fuller genomic landscape of tumors from these patients will enable discovery of potential molecular features correlated to clinical outcomes or lay the foundation for future studies leading to new and more effective treatments.</p>

Genomic Characterization CS-MATCH-0007 Arm H

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