I'm just now returning from the International Association for the Study of Lung Cancer's "12th Annual Targeted Therapies in Lung Cancer Conference", which consisted of about 170 very brief talks about several classes of agents, as I described in my last post.  Some of these are likely to emerge as viable, truly beneficial therapies for patients; many others will fall by the wayside.

After the last several posts have discussed our friend and lung cancer expert Dr. Ross Camidge, we'll turn to the related topic of ROS mutations, which have been the subject of research by Dr. Ross Camidge (though apparently not named for him) and also researchers at Massachusetts General Hospital. This is a gene for a DNA repair protein, and the tyrosine kinase binding portion (the part that gets turned on to set off a cascade of downstream intracellular events) for ROS1 is very similar to that for ALK.