Being enrolled in arm of th3resa trial that wasn't your "physician's choice", would your oncologist be willing to work with Genentech and FDA to see if drug, for which approval is expected to be applied based on Emilia's PFS data by mid-year, could be made available for time being as "compassionate use"?
http://www.fda.gov/ForConsumers/ByAu.../ucm176098.htm