The latest generation of genomic tests for breast cancer can improve physicians' ability to diagnose the disease and more precisely tailor each patient's treatment, according to a study being presented at the 2012 CTRC-AACR San Antonio Breast Cancer Symposium (SABCS). The study examined the first commercially available genomic tests to determine the molecular subtype of a breast cancer tumor.
Researchers concluded that these relatively new genomic tests can more accurately classify breast cancer tumors. That in turn can help doctors better predict what type of treatment is best for that cancer subtype.
Genomic testing is part of the revolution in personalized medicine. It uses a patient's tumor genomic profile and other information to individualize treatment with the goal of better clinical results and overall cost savings. Genomic tests examine tumor tissue and the activity of groups of genes within the tumor, to provide a more comprehensive view of the cancer and treatment options.
The study findings also suggest that some breast cancer patients who are currently prescribed chemotherapy after surgery may be able to avoid that therapy and its risks.
"We now have a better tool for determining which patients do not need to undergo treatments such as chemotherapy, when that treatment would be expensive and would not be useful to that particular patient," said medical oncologist Massimo Cristofanilli, M.D., FACP, lead author of the study and chief of the breast service line at Fox Chase Cancer Center, in Philadelphia.