View Full Version : more response to the historic FDA approval of neoadjuvant perjeta
http://2013researchtopractice.createsend1.com/t/ViewEmail/y/19EDD2979CADDDCC/9FE6FF52FCD6984446778398EADC2510
'lizbeth
10-05-2013, 09:20 AM
Lani, this is a treasure trove of information.
I find this comment intriguing - what does Dr. O’Shaughnessy know that the rest do not seem to be clued into?
I would use it most of the time in combination with trastuzumab/chemotherapy. The pCR rates are of high importance in ER-negative, HER2-positive disease, and pertuzumab clearly increases the rate for these patients. Patients with luminal B HER2-positive breast cancer also have improved outcomes when they achieve pCR, so pertuzumab will be of benefit to those patients also. Joyce O’Shaughnessy, MD Co-Director
Breast Cancer Research Program
Baylor-Charles A Sammons
Cancer Center
Texas Oncology
US Oncology
Dallas, Texas
This lady is sharp . . . and on the ball!
Also, the randomized TRYPHAENA trial showed similar pCR rates of about 60% to 70% when patients were assigned preoperatively to TCH with pertuzumab versus FEC followed by taxane/trastuzumab/pertuzumab. TCH/pertuzumab may become the standard toward the end of the year.
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