http://theoncologist.alphamedpress.o.../full/13/6/620
Taken from the above referenced article:
Another concern regarding the use of trastuzumab has been the association of its use with the development of metastatic CNS disease. A higher incidence of progression in the CNS has been observed in several retrospective studies of patients with HER-2–positive metastatic breast cancer treated with trastuzumab [
43–
45]. Our analysis demonstrated a higher incidence of CNS metastasis as the first recurrence event among patients treated with trastuzumab, which nonetheless was outweighed by the overall lower risk for distant recurrence (non-CNS visceral disease) and the impressive benefits in survival. The exact reasons for this phenomenon are unclear, but the etiology is probably multifactorial, involving a lower bioavailability of trastuzumab in the CNS because of poor blood–brain barrier penetration and its high effectiveness in preventing the development of non-CNS visceral disease. Although some investigators have suggested that HER-2–positive disease may preferentially involve the CNS, evidence from large retrospective datasets of nontrastuzumab-treated patients is inconclusive [
46,
47].
So, do I show this to my onc to get her to order an MRI?
__________________
Gerri
Dx: 11/23/05, Lumpectomy 12/12/05
Tumor 2.2 cm, Stage II, Grade 3, Sentinel Node biopsy negative
ER+ (30%) /PR+ (50%), HER2+++
AC X 4 dose dense, Taxol X 4 dose dense
Herceptin started with 2nd Taxol, given weekly until chemo done
then given every 3 weeks for one year ending on March 16, 2007
Radiation 30 treatments
Tamoxifen - 2 yrs (pre-menopausal)
May 2008 - Feb 2012 Femara
Aug 2008 - Feb 2012 Zometa every 6 months
March 2012 - Stop Femara, now Evista for bone strengthening
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Enjoy the little things, for one day you may look
back and realize they were the big things.
- Robert Brault