Abstract

BackgroundWith rapid advances in genomic medicine, the complexity of delivering precision medicine to oncology patients across a university health system demanded the creation of a Molecular Tumor Board (MTB) for patient selection and assessment of treatment options. The objective of this report is to analyze our progress to date and discuss the importance of the MTB in the implementation of personalized medicine.Materials and MethodsPatients were reviewed in the MTB for appropriateness for comprehensive next generation sequencing (NGS) cancer gene set testing based on set criteria that were in place. Because profiling of stage IV lung cancer, colon cancer, and melanoma cancers were standard of care, these cancer types were excluded from this process. We subsequently analyzed the types of cases referred for testing and approved with regards to their results.Results191 cases were discussed at the MTB and 132 cases were approved for testing. Forty-six cases (34.8%) had driver mutations that were associated with an active targeted therapeutic agent, including BRAF, PIK3CA, IDH1, KRAS, and BRCA1. An additional 56 cases (42.4%) had driver mutations previously reported in some type of cancer. Twenty-two cases (16.7%) did not have any clinically significant mutations. Eight cases did not yield adequate DNA. 15 cases were considered for targeted therapy, 13 of which received targeted therapy. One patient experienced a near complete response. Seven of 13 had stable disease or a partial response.ConclusionsMTB at University of Alabama-Birmingham is unique because it reviews the appropriateness of NGS testing for patients with recurrent cancer and serves as a forum to educate our physicians about the pathways of precision medicine. Our results suggest that our detection of actionable mutations may be higher due to our careful selection. The application of precision medicine and molecular genetic testing for cancer patients remains a continuous educational process for physicians.

Highlights

  • Genomic medicine has been advancing rapidly since the introduction of massive parallel sequencing/ generation sequencing (NGS) technologies

  • Materials and Methods: Patients were reviewed in the Molecular Tumor Board (MTB) for appropriateness for comprehensive generation sequencing (NGS) cancer gene set testing based on set criteria that were in place

  • 191 cases were discussed at the MTB and 132 cases were approved for testing

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Summary

Introduction

Genomic medicine has been advancing rapidly since the introduction of massive parallel sequencing/ generation sequencing (NGS) technologies. Finding a driver gene mutation can lead to specific targeted therapies, which forms the basis for personalized / precision medicine [2, 3]. NGS is a powerful tool and while the cost associated with the assay is declining, NGS still requires extensive informatics support for data analysis. The integration of these test results into clinical care has been largely left up to the treating physician [4]. With rapid advances in genomic medicine, the complexity of delivering precision medicine to oncology patients across a university health system demanded the creation of a Molecular Tumor Board (MTB) for patient selection and assessment of treatment options. The objective of this report is to analyze our progress to date and discuss the importance of the MTB in the implementation of personalized medicine

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