I'm writing on behalf of my wife, she is 32 yrs. old, premenopausal, and being treated (lumpectomy and
radiationCystitis - noninfectious
Radiation therapy to come) for
invasiveGestational trophoblastic disease
Invasive
Minimally invasive heart surgery
Noninvasive
Noninvasive test
Squamous cell carcinoma - invasive ductal carcinoma, she is
nodeLymph node biopsy
Swollen glands
Swollen lymph nodes in the groin
Swollen lymph nodes under arm negative, 1.5 mm tumour, low/moderate grade tumour, er+, pr+, no
familyBirth control and family planning
Choosing a primary care provider
Ewing’s sarcoma
Family troubles - resources history of breast/ovarian cancer but a personal history of thyroid cancer. Although our oncologist generally treats young
womenWomen's way more aggressively my wife's tumour is so small he has recommended no further
systemicSystemic lupus erythematosus
Systemic lupus erythematosus rash on the face treatment and believes her risk for recurrence to be about 5%. We understand that in the context of risk vs benefit chemotherapy in my wife's case doesn't make sense, but he doesn't really recommend tamoxifen either. Most of the benefit she would derive would be from a reduction of risk of contralateral disease, and tamoxifen as prevention seems a little more complicated. How long do you take it, more than 5 years? When do you stop receiving a benefit? If you only take it for 5 years, which 5 years do you choose, the riskiest ones (later on in life)? Do you add medication to suppress ovarian function? Is it possible to spawn a tamoxifen "resistance", so that if a recurrence or new primary came up it would be er-? If tamoxifen is not recommended for my wife, and she is at a high risk for contralateral disease, whom would it be recommended for? What are your thoughts on tamoxifen for reducing risk in someone like my wife? Any insight would be of great help to us at this anxious time.