According to results from the BETH study presented at the San Antonio Breast Cancer Symposium(SABCS), held December 10?14, 2013 in San Antonio, Texas, combining the chemotherapy drugs docetaxel (Taxotere?; Sanofi) and carboplatin with the humanized monoclonal antibody (mAb) trastuzumab (Herceptin?; Genentech/Roche) was identified to be an ideal post-surgery treatment option for patients with HER2-positive breast cancer, regardless of tumor size and whether or not disease has spread to the lymph nodes.
?Worldwide, anthracyclines such as doxorubicin (Adriamycin) and epirubicin have dominated breast cancer treatment for decades because of a perceived incremental benefit of 3 to 5% in disease-free survival and overall survival that was observed in meta-analysis overview studies that viewed breast cancer as a single disease,? said Dennis J. Slamon, M.D., Ph.D., director of clinical/translational research at the University of California, Los Angeles (UCLA) Jonsson Comprehensive Cancer Center, and professor of medicine and chief of the Division of Hematology/Oncology at the UCLA Department of Medicine.
Dramatically improving outcomes
?It turns out that anthracyclines were particularly active in the treatment of HER2-positive disease once we applied molecular subtype analyses to breast cancers. These data were derived from treatments used before the development of trastuzumab. In HER2-positive breast cancers, anthracyclines improved outcomes dramatically while adding little or no incremental benefit to the other subtypes that represent 75 to 80% of the disease. Unfortunately, the long-term side effects of anthracyclines in all groups include congestive heart failure and leukemia. We and others have previously shown that adding trastuzumab to anthracycline-based therapy in adjuvant disease increases this cardiac toxicity between three- to fivefold.
New results have surpassed expectations and show that it really is not necessary to include an anthracycline as part of the treatment regimen to obtain really ideal results for patients with HER2-positive breast cancer…
?Our new results, which surpassed our expectations, show that it really is not necessary to include an anthracycline as part of the treatment regimen to obtain really ideal results for patients with HER2-positive breast cancer, even if they have a large tumor or have node-positive disease,? added Slamon, who is also a leader of a Stand Up To Cancer Dream Team. ?The importance of the results lies in the fact that the TCH [docetaxel, carboplatin, and trastuzumab] combination has a much better safety profile than anthracycline and trastuzumab combinations and is now equally effective.?
Slamon and colleagues designed a large, randomized, phase III clinical trial to evaluate whether adding a therapy called bevacizumab to postsurgery chemotherapy plus trastuzumab improved outcomes for patients with HER2-positive breast cancer that had spread to the lymph nodes or was highly likely to recur. They called their trial “BETH” or ?bevacizumab and trastuzumab adjuvant therapy in HER2-positive breast cancer,” and enrolled a total of 3,509 patients. The majority of these patients, 3,231, were in cohort 1 and randomly assigned to either TCH or TCH with bevacizumab. Cohort 2 was much smaller, with 278 patients randomly assigned by physicians who elected to use anthracycline-based therapy in addition to trastuzumab, using the anthracycline epirubicin, with or without bevacizumab.
The researchers found that disease-free survival after a median of 38 months follow-up was 92% for both arms of the TCH cohort. ?These are among the best results we have seen to date in the adjuvant treatment of HER2-positive breast cancer,? said Slamon. Disease-free survival in the control arm of cohort 2, patients randomly assigned to the anthracycline-containing chemotherapy and trastuzumab regimen, was slightly less, at 89%. Slamon noted that this was not a statistically significant difference and was based on a very small number of cases for comparison with the nonanthracycline TCH arm.
?In addition, the results of the trial are negative for any benefit from adding bevacizumab to adjuvant therapy for HER2-positive breast cancer. It does not appear to improve outcomes,? said Slamon. ?But this may be because 92% of patients in the TCH control arm remain disease-free after a median follow-up of 38 months. It is going to be difficult to develop treatment regimens that have even better response rates than that. While there is some small room for improvement, we now need to further concentrate on improving the safety of adjuvant treatment regimens.?
The researchers are continuing to follow patients to determine whether outcomes remain similar between the two arms of each of the cohorts in the long term. ?But my feeling is that the TCH regimen is driving the very positive responses we are seeing and I doubt that bevacizumab will make a significant difference, even after longer follow-up posttreatment,? Slamon added.
This study was supported by funds from Roche/Genentech. Slamon has served as an adviser to both companies in the past several years, including the time during which the study was conducted.
For more information:
 NCT00625898 – BETH Study: Treatment of HER2 Positive Breast Cancer With Chemotherapy Plus Trastuzumab vs Chemotherapy Plus Trastuzumab Plus Bevacizumab. [Study Record Detail]
 Slamon DJ, Swain SM, Buyse M, Martin M, Geyer CE, Im YH, Pienkowski T, et al.Primary results from BETH, a phase 3 controlled study of adjuvant chemotherapy and trastuzumab ? bevacizumab in patients with HER2-positive, node-positive or high risk node-negative breast cancer. Publication Number: S1-03. Presented: Dennis J. Slamon, M.D., Ph.D.
 Highlights from the 36th SABCS, San Antonio, Texas, USA – December 10 – 14, 2013 [Conference Overview]
Photo: Dennis J. Slamon, M.D., Ph.D. Photo Courtesy: The Cancer Therapy & Research Center (CTRC) at The University of Texas Health Science Center at San Antonio, the American Association for Cancer Research (AACR), and Baylor College of Medicine are joint sponsors of the San Antonio Breast Cancer Symposium.
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