> Over 370,000 patients in India develop solid tumor based cancers annually and are in need of more comprehensive genomic profiling
> The NGS panel assesses mutations across 50 actionable and clinically validated oncogenes and tumor suppressor genes with a higher level of sensitivity and specificity than existing methods
> Cancer Genetics will create a genomic database and information exchange of cancer hotspots that will help clinicians and researchers personalize and improve patient outcomes throughout India and Asia
RUTHERFORD, N.J. and HYDERABAD, India, April 21, 2015 (GLOBE NEWSWIRE) -- Cancer Genetics Inc. (Nasdaq:CGIX) ("CGI" or "the Company") announced today that Cancer Genetics India (CG India) has launched a Next-Generation Sequencing (NGS) based panel targeting the five most common solid tumors: breast, colorectal, lung, skin, and ovarian cancer for the Indian and broader Asian markets. The NGS-based panel provides a comprehensive genomic assessment of cancer mutations, with dramatically increased sensitivity compared to other testing methodologies, and can be applied to over 370,000 patients annually in India alone. The NGS panel covers over 2,800 clinically validated, common cancer mutations and can be used from as little as 10 nanograms of DNA from a variety of sample types, including fresh frozen or formalin-fixed paraffin-embedded (FFPE) tissue.
With more than 1 million new cases of cancer diagnosed in India each year, there is a significant need for NGS based comprehensive testing that provides both cost-savings and increased accuracy over other technologies by assessing a comprehensive number of genetic mutations in a single test. The tests will also help CG India in its strategic initiative to generate a library of critical, actionable genomic data that can be used by clinicians for improved patient management and by researchers in India and worldwide to develop more targeted therapeutics. The International Agency for Research on Cancer (IARC) based in France predicts that the number of new annual cancer cases in India will double in the next 20 years only heightening the need for improved technology to help diagnose and manage cancers earlier and more comprehensively.
"Cancer Genetics India's NGS tumor hotspot panel will allow clinicians in India the capability to access the genomic information necessary to improve the diagnosis and management of patients with common cancers," said Dr. Vidudala Prasad, Ph.D., Head of Research and Development at Indo American Cancer Hospital in Hyderabad, India. "It also offers valuable genomic insights for investigators working on oncology-focused clinical trials."
CG India is now one of few companies in India that is making this NGS technology and mutation hotspot panel available for use by oncologists, biopharmaceutical companies, and research organizations. Panna Sharma, CEO of Cancer Genetics, Inc. commented: "There is a critical need in India and Asia for high-quality assessment of cancer that is comprehensive, genomically-guided and supported with state of the art bioinformatics. The clinical and research community will find tremendous value in both the NGS panel and in our genomic database which we expect will be an invaluable tool in the improvement of cancer outcomes for patients and in the acceleration of novel discoveries into the marketplace."
CG India is also in discussions with a number of biopharma and research companies in the formation of strategic collaborations and partnerships to use the NGS hotspot technology for discovery and accelerated research. The NGS panel addresses a significant, underserved and growing market, and is expected to contribute to CG India's overall growth.
The use of the NGS hotspot panel will enable the collection of a large library of genomic data that can be used to improve the quality and accuracy of clinical research and discovery efforts. Mr. Sharma added: "CG India is among the first companies to launch NGS testing in India. This new panel further establishes us as a leader in DNA based diagnostics in India. With the launch of this new panel, we are in a unique position to deepen our collaborations and partnerships with major cancer centers, academic government institutions, and biopharma companies focused on oncology research."
About Cancer Genetics
Cancer Genetics, Inc. is an emerging leader in DNA-based cancer diagnostics, servicing some of the most prestigious medical institutions in the world. Our tests target cancers that are difficult to diagnose and predict treatment outcomes. These cancers include hematological, urogenital and HPV-associated cancers. We also offer a comprehensive range of non-proprietary oncology-focused tests and laboratory services that provide critical genomic information to healthcare professionals, as well as biopharma and biotech companies. Our state-of-the-art reference labs are focused entirely on maintaining clinical excellence and are both CLIA certified and CAP accredited and have licensure from several states including New York State. We have established strong research collaborations with major cancer centers such as Memorial Sloan-Kettering, The Cleveland Clinic, Mayo Clinic and the National Cancer Institute.
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Forward Looking Statements: This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements pertaining to future financial and/or operating results, future developments in research, technology, clinical development and potential opportunities for Cancer Genetics, Inc. tests and services, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements. Any statements that are not historical fact (including, but not limited to, statements that contain words such as "will," "believes," "plans," "anticipates," "expects," "estimates") should also be considered to be forward-looking statements. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential products, risks of cancellation of customer contracts or discontinuance of trials, uncertainty in the results of clinical trials or regulatory approvals, need and ability to obtain future capital, maintenance of intellectual property rights and other risks discussed in the Company's Form 10-K for the year ended December 31, 2014 along with other filings with the Securities and Exchange Commission. These forward-looking statements speak only as of the date hereof. Cancer Genetics disclaims any obligation to update these forward-looking statements.