Invitrogen gets breast cancer test approval

Invitrogen has won FDA approval of a test that can determine whether a woman with breast cancer will benefit from Genentech's Herceptin. The SPOT-Light test, as it is known, uses a DNA probe for the HER2 gene, which is amplified in 18 to 30 percent of breast cancers and can predict whether a patient will benefit from Herceptin. While a test is already available for Herceptin, many smaller hospitals don't have the resources to process the tests. Invitrogen's SPOT-Light doesn't require specialized equipment and can be processed in most hospital labs. 

"Given the emerging potential use of trastuzumab (Herceptin) in the adjuvant setting, the need to accurately determine the front-line HER2 status in breast cancer has never been more critical," said Jeffrey Ross, M.D., of Albany Medical College. Invitrogen's test is yet another step in the direciton of personalized medicine. Such tests allow physicians to choose the right treatment for patients and save money by not giving the expensive drug to patients who won't benefit from it.

- check out Invitrogen's release
- read the Sign on San Diego article for more

Suggested Articles

Novartis unveiled more data showing how its asthma combo QMF149 fared against the standard of care: a combination of the same types of drugs.

Johns Hopkins researchers developed a biodegradable polymer to transport large therapies into cells—including genes and even CRISPR.

UCB’s bispecific antibody recently beat Johnson & Johnson’s Stelara at clearing psoriasis symptoms, and now it has bested AbbVie’s Humira, too.