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Mol Oncol. 2014 Jul;8(5):859-73. doi: 10.1016/j.molonc.2014.03.021. Epub 2014 Apr 4.

Standardized decision support in next generation sequencing reports of somatic cancer variants.

Author information

1
Massachusetts General Hospital and Harvard Medical School, Molecular Pathology Lab, USA. Electronic address: rodrigo.dienstmann@sagebase.org.
2
Massachusetts General Hospital and Harvard Medical School, Molecular Pathology Lab, USA.
3
Massachusetts General Hospital Cancer Center and Harvard Medical School, 55 Fruit St GRJ, Boston, MA 02114, USA.

Abstract

Of hundreds to thousands of somatic mutations that exist in each cancer genome, a large number are unique and non-recurrent variants. Prioritizing genetic variants identified via next generation sequencing technologies remains a major challenge. Many such variants occur in tumor genes that have well-established biological and clinical relevance and are putative targets of molecular therapy, however, most variants are still of unknown significance. With large amounts of data being generated as high throughput sequencing assays enter the clinical realm, there is a growing need to better communicate relevant findings in a timely manner while remaining cognizant of the potential consequences of misuse or overinterpretation of genomic information. Herein we describe a systematic framework for variant annotation and prioritization, and we propose a structured molecular pathology report using standardized terminology in order to best inform oncology clinical practice. We hope that our experience developing a comprehensive knowledge database of emerging predictive markers matched to targeted therapies will help other institutions implement similar programs.

KEYWORDS:

Cancer; Genomics; Next-generation sequencing; Report; Variant annotation

PMID:
24768039
DOI:
10.1016/j.molonc.2014.03.021
[Indexed for MEDLINE]
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