al from Canada
05-04-2007, 09:01 AM
I know I havn't posted for a while but ran across this.
Al
April 2007 • Volume 16 Number 4
Focus on Breast Cancer
Trastuzumab Plus Bevacizumab Promising in Metastatic Ca</B>
SAN ANTONIO—The combination of trastuzumab (Herceptin) and bevacizumab (Avastin) as first-line treatment of metastatic breast cancer showed promising results in the first phase II study to evaluate this regimen. Mark Pegram, MD, and colleagues from the UCLA School of Medicine reported the findings at the 29th Annual San Antonio Breast Cancer Symposium (abstract 301).
There is strong rationale for this combination, Dr. Pegram said. Overexpression of HER2 is associated with upregulation of vascular endothelial growth factor (VEGF) in breast cancer cells; there is a strong association between HER2 and VEGF, which predicts clinical outcome in primary breast tumors; and in xenograft models, the combination produces superior outcomes, compared with either agent used alone.
The phase II study included 37 patients with HER2-positive metastatic breast cancer and no prior chemotherapy for this stage. All patients received trastuzumab as a 4 mg/kg loading dose, then 2 mg/kg weekly, plus bevacizumab 10 mg/kg on day 7, then every 2 weeks.
Interim efficacy data found an overall response rate of 54.1%, Dr. Pegram reported. Only 16.2% of patients progressed while on the combination (see Table).
http://i.cmpnet.com/cancernetwork/journals/oncnews/200704/ONI_April07_p12.gif
Stringent cardiac safety surveillance was part of the amended protocol in 13 patients: Grade 1 cardiac toxicity was noted in seven patients, grade 2 in five patients, and grade 4 in one patient. Mean left ventricular fraction was significantly lower after treatment: 63.42% pretreatment vs 60.24% post-treatment (P = .02), Dr. Pegram said. Other adverse events were mild and manageable, although 15 patients developed hypertension (8 grade 1-2, and 7 grade 3).
"Bevacizumab and trastuzumab is a clinically feasible and active combination in HER2-amplified recurrent or metastatic breast cancer. Our data support the use of therapies directed against both the HER2 and VEGF targets in these patients," Dr. Pegram concluded.
Al
April 2007 • Volume 16 Number 4
Focus on Breast Cancer
Trastuzumab Plus Bevacizumab Promising in Metastatic Ca</B>
SAN ANTONIO—The combination of trastuzumab (Herceptin) and bevacizumab (Avastin) as first-line treatment of metastatic breast cancer showed promising results in the first phase II study to evaluate this regimen. Mark Pegram, MD, and colleagues from the UCLA School of Medicine reported the findings at the 29th Annual San Antonio Breast Cancer Symposium (abstract 301).
There is strong rationale for this combination, Dr. Pegram said. Overexpression of HER2 is associated with upregulation of vascular endothelial growth factor (VEGF) in breast cancer cells; there is a strong association between HER2 and VEGF, which predicts clinical outcome in primary breast tumors; and in xenograft models, the combination produces superior outcomes, compared with either agent used alone.
The phase II study included 37 patients with HER2-positive metastatic breast cancer and no prior chemotherapy for this stage. All patients received trastuzumab as a 4 mg/kg loading dose, then 2 mg/kg weekly, plus bevacizumab 10 mg/kg on day 7, then every 2 weeks.
Interim efficacy data found an overall response rate of 54.1%, Dr. Pegram reported. Only 16.2% of patients progressed while on the combination (see Table).
http://i.cmpnet.com/cancernetwork/journals/oncnews/200704/ONI_April07_p12.gif
Stringent cardiac safety surveillance was part of the amended protocol in 13 patients: Grade 1 cardiac toxicity was noted in seven patients, grade 2 in five patients, and grade 4 in one patient. Mean left ventricular fraction was significantly lower after treatment: 63.42% pretreatment vs 60.24% post-treatment (P = .02), Dr. Pegram said. Other adverse events were mild and manageable, although 15 patients developed hypertension (8 grade 1-2, and 7 grade 3).
"Bevacizumab and trastuzumab is a clinically feasible and active combination in HER2-amplified recurrent or metastatic breast cancer. Our data support the use of therapies directed against both the HER2 and VEGF targets in these patients," Dr. Pegram concluded.