Ian Krop, MD, PhD, principal investigator of the study, reports that the hybrid agent, called T-DM1, shrank tumors by 30 percent or more in 40 percent of women with confirmed HER2-positive cancers.
Another 13 percent had stable disease for at least six months, for a total clinical benefit rate of approximately 53 percent.
The median time before the disease progressed was 7.3 months, including both responders and non-responders. Patients received T-DM1 as long as it was effective and well-tolerated. A total of 110 women were enrolled in the study.
T-DM1 is comprised of the cell-killing drug DM1 and is chemically linked to trastuzumab, a monoclonal antibody. Trastuzumab selectively binds to the HER2 growth signal receptor, which is highly overexpressed in HER2-positive breast tumors. Approximately 20 percent of breast cancers are HER2-postive.
Trastuzumab, developed by Genentech and sold under the name Herceptin, has markedly improved the treatment of HER2-positive cancer, but resistance to trastuzumab is a significant problem.
“The antibody binds to the HER2 protein on tumor cells and delivers the drug (DM1) selectively to them — but not to normal cells,” Krop explained.
“This allows us to deliver high doses of the chemotherapy directly to tumor cells. And at the same time, the antibody continues to block the HER2 growth signals.”
Krop said that one of the unique features of the study is that it is the first to address a population of women with metastatic HER2-positive breast cancer whose disease had progressed despite treatm