Significant research results announced during the recent San Antonio Breast Cancer Symposium (SABCS) (December 2011) showed that adding a new targeted medicine, pertuzumab, to a combination of trastuzumab (Herceptin) and docetaxel chemotherapy extended progression-free survival by a median of 6.1 months in patients with advanced HER2-positive breast cancer compared with patients who received the combination therapy with placebo.
Researchers conducted an international phase 3, double-blind, randomized trial, known as CLEOPATRA (CLinical Evaluation Of Pertuzumab And TRAstuzumab), in which they randomly assigned 808 patients to receive trastuzumab and docetaxel chemotherapy with pertuzumab or placebo. Progression-free survival (PFS) was 18.5 months for patients who received pertuzumab compared with 12.4 months for patients who received placebo — a 38 percent reduction in risk for progression.
The findings represent a significant advance in the treatment of this advanced breast cancer, said senior researcher José Baselga, M.D., Ph.D., professor in the department of medicine at Harvard Medical School, associate director of the Massachusetts General Hospital Cancer Center and chief of hematology/oncology at Massachusetts General Hospital.
“Most metastatic patients with HER2-positive breast cancer eventually stop responding to trastuzumab, so the fact that we now have an agent that can be added to current treatment to delay progression is very exciting. With the advent of trastuzumab and now pertuzumab, we have come a very long way in treating a type of breast cancer that once had a very poor prognosis.”
The three-drug combination also appears to be remarkably safe and well tolerated, with only minimal side effects seen with the addition of pertuzumab. In particular, no additional cardiac toxicity was seen.
Pertuzumab is designed to work in combination with trastuzumab as a dual blockade of the HER2 growth factor, which fuels about one third of all breast tumors. Both drugs are monoclonal antibodies that bind to the HER2 receptor protein in different locations. Pertuzumab’s role is to prevent the receptor from linking to HER3 and therefore forming a “dimer” that further signals tumor growth — making pertuzumab the first in a new class of drugs called “dimerization inhibitors,” Baselga said. “These two agents offer a dual HER2 blockade, shutting down different mechanisms responsible for HER2 signaling.”
While not enough time has passed for a valid statistical analysis of survival outcomes, the interim results also showed a positive trend in the Pertuzumab group. Researchers reported 69 deaths among the 402 patients treated with the three-drug combination and 96 deaths among the 406 patients who received two drugs.
Enrollment is already under way in a new double-blind, randomized clinical trial, APHINITY, to test the use of pertuzumab as adjuvant treatment for early-stage HER2-positive breast cancer.
The results were published in the New England Journal of Medicine.
