I reside in Canada where axillary
dissectionAortic dissection is still the norm. I have a 1.1cm X .8cm infiltrating duct carcinoma at 3o'clock on my left breast. It was discovered on an ultrasound (negative on mammogram) and follow-up core biopsy. I have had a MRI which clarified that this is the only
lumpLumps in the breasts.
I will be having a lumpectamy on Tuesday. My doctor asked me to participate in the B32, randomized Phase 3 clinical trial. I am concerned about the after-effects of the more intrusive, Axillary
dissectionAortic dissection and since the study only gives me a 50% chance of having a Sentinel
nodeLymph node biopsy
Swollen glands
Swollen lymph nodes in the groin
Swollen lymph nodes under arm dissectionAortic dissection, I have opted out of the study and requested a Sentinel
nodeLymph node biopsy
Swollen glands
Swollen lymph nodes in the groin
Swollen lymph nodes under arm dissection. My surgeon has agreed to this, but is somewhat reluctant, as this method of treating cancer is still not the standard in Canada.
I weighed my decision based on the following: I was asked to be in the study, therefore, I must be at a lower risk; there is a 3 - 5% chance of a false negative (my greatest concern, although I don't really comprehend the implication of this); I have a fear of the intrusiveness of axillary dissection and the possibility of lymphademia. How do I know whether I have made the right decision? What risks should I weigh? Have I considered the right decision making criteria in my decision? What else should I consider? Sentinal node dissection appears to be more common in the US. What has led to the trust in this approach?
Many thanks!