Diagnosed with invasive ductal Carcinoma 2.2mm. Er/HER2 +3 positive
I was originally diagnosed with DCIS in two ducts. After lumpechtomy, the pathology report showed a 2.2mm tumor attached in one duct. It was diagnosed as invasive ductal Carcinoma-Estrogen positive, progesterone positive but weak & HER2 positive at a +3. All was removed and have clear margins. Had 2 lymph nodes removed, all negative. However, because of the tumor being HER2 positive and grade 3. The Oncologist is stating that I should consider chemotherapy for 3 months & then HER2 inhibitor infusions 1 year to increase the probability of the cancer returning. I am scared to death of chemo. He said if I chose not to have it, research shows a 80% life expectancy at 15 years. With chemo and the inhibitor it increases to 97% at 8 years. I want to give my self the best outcome but chemotherapy has so many bad side effects. Please I need advice from experienced survivors.
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That's great, good for you! Excellent results. Can you hear when you have the cap on? I've been told my first treatment is at least 4 hrs infusion plus at least extra 3 hours in cap. Also did you wear a scarf or something? my hair with no blow drying or products of any kind for I guess 6 months? is not a good look for my job. Thank you for replying!
Not really, pretty much anecdotal. I couldn’t tolerate the cold last session, so this might not work for me.
Thanks I will definitely try the cold cap.
Thanks so much. It gives me alot to discuss with my oncologist. All the replies have helped me so much to better understand what I am in for. I am now leaning toward having the chemo & the Her2 inhibitor to better my chance for no recurrance.
I am glad you are planning for chemo. I am really glad you found Mayo connect! Aren’t these girls all pretty great. I had a similar diagnosis as you but not the same chemo protocol since herceptin was not approved for frontline use yet. I took a 3 drug regimen for 6 treatments. Being very young, in my 30’s I wanted to reduce my risk as much as possible.
While it certainly was not easy, it was worth it! Today the regimens are a little easier to tolerate and more targeted. The side effects controls are better than ever. I would do it again if it meant I could have another 20 years like the 20 I have had since then.
I know this is a long term perspective, but isn’t that what we are all hoping for.
Do you have a start date for chemo yet?
At your age, I would definitely give that regimen a try. I am going through it now, but at age 81, otherwise healthy. Had DCIS stage 0 at age 67, now IDC stage 1, lymph nodes negative, but HER2+, contralateral breast. I’ve only had two treatments so far, fingers crossed that I can tolerate it. If not, how many years do I have left anyway? I don’t care about the hair loss, but I would have at age 61. Wishing you wisdom in making your choice, and a good outcome with treatment! ❤️
Thanks for the info and encouragement. I really need it. I see the oncologist again on 4/30. He wanted to present my case to the board of oncologists since my tumor id so small, to get their perspective.
My family wanted me to get a second opinion on the treatment plan suggestion. I told him I will let him know at our next appointment, my decision on the chemo after I did my own reaearch.
Sounds like everyone is on agreement. I have decided to give it a try, especially since it seems that once you have been diagnosed and it's removed, you need to worry for the rest of your life that it will recur. As I told my family, I have a lot of living to do at least 40 more years, if have something to say about it. Ha! Ha! I just want to give myself the best chance to make it as close to thst number as possible.
There must be research on this. Peripheral neuropathy caused by chemo is not only unpleasant if not painful - it makes you much more at risk of falling. Your brain and your feet no longer communicate properly. Even worse if you have vision problems.
My oncologist said there is some evidence to support cryotherapy to prevent PN, but I don’t have the specifics.