Annual Report on Celera (Quest) License
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|Monday, 05 March 2012 10:45 (UTC + 1)|
Sydney, Australia, March 5, 2012 / B3C newswire / - Cellmid Limited (ASX: CDY) has received its second annual report from Celera-Quest Diagnostics in relation to its lung cancer diagnostic licence (details of the license are included at the end of this announcement). The report confirmed that midkine is one of the six biomarkers on Celera’s lung cancer diagnostic panel.
Results of a recent study have also been provided by Celera-Quest Diagnostics demonstrating that the six marker lung cancer panel showed 94% specificity (at 70% sensitivity) in accurately classifying non-malignant nodules identified during CT (computed tomography) scanning of a high risk smoker population.
Even though the rate of smoking is declining there are an estimated 94 million current and past smokers in the United States who are at risk of contracting lung cancer. Of this group those aged over 55 are at greatest risk. Mortality caused by lung cancer can be markedly reduced if cancerous nodules are detected and removed very early; however it is usually the case that once patients are symptomatic, the cancer has already spread from its initial site, thereby reducing the chances of successful treatment.
Population screening of at-risk groups using imaging such as CT scanning has been proposed as one way to reduce lung cancer mortality. This proposal was recently tested by the US National Institute of Health (NIH) in a large-scale study of 53,454 current and ex- smokers aged 55-74, which found that screening by CT scanning reduced mortality by 20% in 6 years 1 .
While this is some good news for the seven million American smokers over 55, the low specificity of CT scanning is still a concern as the same study showed that 25% of the solitary nodules identified by CT scan proved to be non-cancerous after lung biopsy (75% specificity).
Unnecessary biopsy of otherwise benign nodules creates additional costs and significant morbidity for this already very large patient group. Celera-Quest Diagnostics’ six marker lung cancer panel with its 94% specificity may therefore become a useful adjunct to imaging. It may assist in further clarifying the diagnosis in patients who have tested positive during their CT screening (estimated to be 1.7 million in the highest risk group).
In order to commercialize the lung cancer panel the assay is currently being transferred to a multiplex format. With Quest Diagnostics’ extensive distribution capabilities it will most likely be sold as a Lab Developed Test (LDT). In addition to the specific application for high risk screening, Celera-Quest Diagnostics has confirmed that it continues with the development of additional lung cancer tests using midkine.
License between Cellmid Limited and Celera-Quest Diagnostics for lung cancer In October 2009
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