WASHINGTON (AP) — The Food and Drug Administration expanded approval of a Pfizer drug to treat a small subset of lung cancer patients with a rare mutation.
The agency says Xalkori capsules are now approved for patients with the ROS-1 gene mutation, who make up about 1 percent of U.S. patients with non-small cell lung cancer, the most common form of the disease.
The twice-a-day drug is part of a new wave of medications that fight disease by targeting specific genes found in certain patients. It was initially approved in 2011 for another subset of lung cancer patients who have a gene that stimulates tumor growth.
The drug blocks certain proteins found in tumors with genetic mutations, with the aim of slowing cancer spread.
Xalkori posted sales of $438 million in 2014.





![[object Object]](https://img.manufacturing.net/files/base/indm/all/image/2016/03/mnet_66736_echo_voyager_boeing.png?auto=format%2Ccompress&fit=crop&h=167&q=70&w=250)

![[object Object]](https://img.manufacturing.net/files/base/indm/all/image/2016/03/mnet_66726_nuclear_plant_ap.png?auto=format%2Ccompress&fit=crop&h=167&q=70&w=250)














