Datar Cancer Genetics Launches Breakthrough Blood Test for Early Detection of 15 Cancers

Early detection of cancer has been the Holy Grail for scientists all over the world. Late stage detection is one of the primary reasons for death in cancer patients. Datar Cancer Genetics has developed a simple non-invasive blood test to detect the presence of cancer in seemingly healthy persons, using advanced molecular analysis of nano particles released by cancer cells. The pattern of various genes expressed in the cancer cells is captured in these nano particles known as ‘exosomes’. This breakthrough technology has been developed in India using latest Artificial Intelligence techniques and is based upon the study of more than 3000 samples from cancer patients. The test analyzes all 22000 protein-coding genes in the human genome and is able to detect the presence of breast, cervices, ovary, endometrium, lung, colon, sarcoma and many more cancers with an accuracy of better than 95%.
 
The test is available in all cities in India and the company has made arrangements for collection of the blood sample from home/office. The test can be availed by any person above the age of 35 and who has no previous known history of having any cancer.
 
Speaking at the launch, Dr. D. Akolkar, Director of Research and Innovation said that it is a proud moment not only for the company but also for the country as the test has given a pole vault position in cancer research. He also said that the company, working with a frugal budget has beaten the worldwide competition which is funded with billions of dollars and government support. Dr. Akolkar said that research in cancer is an imperative of recent times and Datar Cancer Genetics has committed significant resources not only for early detection of cancer but towards making the treatment of stage IV patients more effective and possibly curative.
 
Datar Cancer Genetics Limited has been accredited by NABL and TUV for ISO 9001:2008 for medical reporting and has a modern, differential pressure molecular oncology facility in Nasik, India. With the launch of the Early Warning Test, the company has entered into a USD 20 billion market worldwide.

Source:http://businesswireindia.com/news/fulldetails/datar-cancer-genetics-launches-breakthrough-blood-test-early-detection-15-cancers/55351

Comments

Post a Comment

Popular posts from this blog

EMA validates Incyte’s MAA for retifanlimab to treat metastatic squamous cell anal carcinoma

Incyte, global biopharmaceutical company, announced the validation of the Company’s Marketing Authorization Application (MAA) for retifanlimab, an intravenous PD-1 inhibitor, as a potential treatment for adult patients with locally advanced or metastatic squamous cell anal carcinoma (SCAC) who have progressed on, or who are intolerant of, platinum-based chemotherapy. The European Medicines Agency’s (EMA) validation of the MAA confirms that the submission is sufficiently complete to begin the formal review process. “While the incidence of SCAC is increasing in Europe, treatment options for advanced disease are limited in their effectiveness, and there are no approved options once patients have progressed on standard therapy,” said Lance Leopold, M.D., Group vice president, Immuno-Oncology Clinical Development, Incyte. “The EMA validation of the MAA for retifanlimab – which follows the recent US Food & Drug Administration acceptance of our Biologics License Application for Priority R...
Read more

Tumour-targeting drug paves way for bone cancer treatment

 The treatment of osteosarcoma, the most common tumour of bone, is challenging, but a new study is offering hope to the patients with this disease. The study led by The University of  Texas MD Anderson Cancer Centre  found that a drug, known as bone metastasis-targeting peptidomimetic (BMTP-11), has potential as a new therapeutic strategy for this devastating illness. Results from the preclinical study looked at BMTP-11 alone and in combination with the chemotherapy agent gemcitabine. Although osteosarcoma is a relatively rare cancer, it is a leading disease-related cause of death in children and young adults ages 10 to 20. However, over the last 25 years, the five-year survival rate has remained unchanged, and the treatment options for these patients are few. In addition, the side effects of available treatment options often are significant and cumulative, and may cause other health problems and damage to major organs. "What's novel about this treatment is that...
Read more

Merck’s Keytruda plus platinum- and fluoropyrimidine-based chemotherapy receives US FDA nod to treat certain patients with locally advanced/metastatic esophageal or GEJ carcinoma

Merck, known as MSD outside the United States and Canada, announced that the US Food and Drug Administration (FDA) has approved Keytruda, Merck’s anti-PD-1 therapy, for the treatment of patients with locally advanced or metastatic esophageal or gastroesophageal junction (GEJ) (tumors with epicenter 1 to 5 centimeters above the GEJ) carcinoma that is not amenable to surgical resection or definitive chemoradiation in combination with platinum- and fluoropyrimidine-based chemotherapy. The approval is based on results from the phase 3 KEYNOTE-590 trial, which demonstrated significant improvements in overall survival (OS), progression-free survival (PFS) and objective response rate (ORR) for Keytruda plus fluorouracil (FU) and cisplatin versus FU and cisplatin alone, regardless of histology or PD-L1 expression status. For OS and PFS, Keytruda plus FU and cisplatin reduced the risk of death by 27% (HR=0.73 [95% CI, 0.62-0.86]; p<0.0001) and reduced the risk of disease progression or death...
Read more