The US Food and Drug Administration (FDA) has approved GE Healthcare’s Cysview to detect non-muscle-invasive papillary bladder cancer in patients with known or suspected bladder cancer.
The optical imaging agent, which has a blue as well as a white light setting, demonstrated an improved rate of detection of non-muscle-invasive papillary cancer compared to standard white light cystoscopy alone, according to Phase III clinical data.
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According to the National Cancer Institute, over 70,000 people in the US were diagnosed with cancer of the bladder in 2009, with an estimated 14,000 deaths.
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