Crizotinib approved for ROS1 + lung cancer

On March 11 the FDA approved the selling of Crizotinib for patients with ROS1 mutations in lung cancer. The ORR was 66% and the median DOR was 18.3 months. Safety profile was similar to that in ALK + patients.

http://www.businesswire.com/news/home/20160311005839/en/XALKORI%C2%AE-crizotinib-Approved-U.S.-FDA-Treatment-Patients

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