Her-2 and hormone therapy?
 

I am looking for feedback, or statistics from other “survivors” that are Her-2 positive that have done – Chemo, Herceptin and radiation …. And wondering how many of them have not developed cancer – without doing hormone therapy.

I am not convinced that hormone therapy will reduce my chances (as Her-2 positive) of getting cancer again. However, I have found it hard to find any hard statistics that are based on just HER-2 positive cancer and how it reacts to hormone therapy.

I keep reading this scary quote in so many of the clinical papers that says the “5 year survival rate”… ugh! I want to live more than 5 years!!! J Seems like the drug companies like to base everything on a 5 year life – and that is not acceptable – and I want to have quality of life --- not a life based around the hospital (like the last 6 months of my life!) and not taking more drugs….

Anyone have any feedback on this one? Thank you so much in advance!!!

Variations on a theme
 

Hi Karen,

It isn't the norm now, but in 2002 I did lumpectomy, CAFx6, rads, no trastuzumab, and 1 3/4 years of tamoxifen. I was offered Arimidex for 5 years and declined the Arimidex. I'm still in remission.

AlaskaAngel, 1.6 cm IDC (T1c), some DCIS, ER+, PR+, HER2+++

This is an interesting question. My first Onc did not want me on hormone therapy. So I asked Dr Burstein in Dana Farber. He answered that in his opinion, I should have it.
I had Arimidex and then Aromasin for 1,5 years with a lot of very bad side effects. I had to stop ( horrible joint pain, severe neuropathy and memory problems). I switched to Faslodex. These side effects almost disappeared. I have very bad mood swings, especially just after the monthly injection, throat pain, mild back pain, fatigue and a little neuropathy. I do not like taking it because I see my body getting old real fast. I want to be on the safe side so I continue anyway but in fact, it is not clear to me if this therapy works for HER2.
I do not know if there is any new information about this. Michka

Her-2 and Hormone therapy
 

I did a bunch of research today ... actually, and did find a lot of articles that say that being Her-2 + seems to make us resistant to hormone therapy. So.... guess that answered my question. There were a few articles that admitted there was still a debate going on it, however the first 8-10 I read - all but one said that they found that Her-2 didn't respond well to Hormone therapy. Enough for me to say no to it.... thank you for your responses. Hope this helps us all!
Oh, I searched plain old Google - for
"Her2neu and Hormone therapy"

Karen

things to consider
 

Hi,
I tried endocrine therapy a few times, but after much consideration decided to get off of it. It has been over 5 years and I'm NED. Such decisions are very difficult. If tamoxifen had not resulted in unwanted problems, I would have stayed on it. But I am doing well.
Best,
Monica

I was on hormone tx. with Herceptin for 5 years as a stage IV--just in the last year did we drop the hormone blockers and add chemo--so it proved effective for me.
Kathy T

I am at 4 years NED after mastectomy. The only defense is Femara against recurrence. I kept hoping this is the effective medication. Of course, many women don't have any treatment, no chemo, no radiation and no med and surgical removal of lesion is the only weapon. These are all stage 1 patients.

Ann

thank you -
 

Thank you for the feedback -

On my hormone %'s -
Est - 80%
Pro- 10%

Don't know what that means overall ... as my doctors here are still trying to explain in Italian and they stop with the argument that "I must" .... that I must trust them and I must do this therapy because they say. Because everyone does.

But, I'm still not sure if I want to subject my body to yet another drug .... I understand some people have little side effects, however it is the overall exposure to the drugs that I am against.

Thank you though - and if you, or anyone has feedback on the 80/10% - let me know ---

Karen

response to Debbie
 

One more thing ...

my Her-2 came back as 3+ ... so top of the scale....

this might make a difference too in how strong it is and leads me to think it might be more resistant to the hormone therapy.

K

I am Her2 (3+) ER was 50% and PR negative. I will be a 5 yr survivor in early September. I started with Tamoxifen for a few months but got my ovaries removed to take Arimidex which I have been on almost 4 yrs. I am doing well

Karen,

What endocrine therapy are they prescribing for you? Are you pre or post-menopause?

Hopeful

Hello just wanted to chime in. I have only 2% ER+. My original onc wanted me on Als I went for a secound oppinion and was told it was not nessasary. I should exercise and drop some weight and that would be very effective. I have chossen to do the latter. It is a tough desision because you apsolutly want to do the right thing. I think I am. I hope I am. The new donc said the herceptin is the key. As it coats the cancer cells and does not let them absorb anything. Thenit is viewed as a forign abject and discarded as waste. I like the sound of that. She also pointed out in the New Englan Journal Of Medician that we have a 91.7 chance of total cure if caught early and treated with chemo rads and herceptin. I liked the sound of that!!!!!!! I googled the artical and read it for myself.

Bold,

Can you please post a link to the article that talks about the 91.7% stat? I'm also 2% ER+ and HER2+ (3+).

Thanks!

I posted about this issue on another thread about Herceptin side effects - sorry.

I live in Canada and ER/PR is rated either +1, +2 or +3, 1 being weak and 3 strong. I am ER+1 (weakly positive) and PR-, and her2 pos +++.

My onc started me on Arimidex aromatase inhibitor in June. I finished the taxotere/carboplatin in March and have had no other chemo except 5.5 rounds of that, plus Herceptin from the beginning along with the TC, and continue Herceptin until Oct.

I didn't really get good answers as to why I should be on the AI Arimidex. She just said 'it'd be a shame after having done so much' blah blah blah. I argued with her and reluctantly began taking it the first of July. I began to notice nausea that would come in waves, and loss of appetite. Since it began about the same time as when I started Arimidex I blame it on that. I was expecting bone/muscle pain, if anything, not nausea. I stopped the Arimidex and have not taken any since Saturday a.m. Nausea is better!

I would like to read more about taking AI's if one is HER2 pos+++ and weakly ER+. So far I am not convinced that it works that well for my diagnosis.

Karen, I feel like you do....lots of frustration and fear about this 5 year survival stuff. One of the first things my oncologist said to me regarding NOT doing the chemo route was 'I think you'll be sorry you didn't in about 5 years'. Yeah? Will I be sorry anyway? I find it hard to get thru the day sometimes, the sorrow of it all overwhelms me......and I am angry that this had to happen to me! If Herceptin is so wonderful, why only a 5 yr survival rate? Where are the 10 years out from her2 positive women?

Stats
 

Bold,

I'd like to read those stats, too! 91% eh.....? Have not heard that before.

(Tapping foot, waiting.........)

I'm highly triple pos (3+) and have been taking arimidex since my ooph two years ago. I haven't heard this before and as I just celebrated four years out I've been thanking arimidex for that!
I still feel I prefer to take it than not, there's just too much not unknown on her2 for me to not do all I can to avoid a recurrance.

I was reading an article by Edith Perez on line yesterday (which, of course I now cannot find when I need it) but it gave the most precise breakdown I have seen for what AI's can do to help prognosis. The article addressed the different drugs individually. What was surprising to me was the stat for the benefit of Femara on recurrence risk: 60% overall relative reduction, but 14% relative reduction for distant recurrence. The main benefit of these drugs is preventing local recurrence or a new cancer from starting. While there is some protection against mets, it is nowhere near as strong. As I am considering stopping AI treatment early, this is an important consideration for me. I will continue to noodle around on line and will post a link to the article if I can find it again.

Hopeful

http://content.nejm.org/cgi/content/full/344/11/783

I am sorry it has taken me so long to get back. I have my computer getting de -wormed and I am at the mercy of my DH to borrow. I belive this is the article. I had to start over finding it so I am not 100% sure. I had it bookmarked on my computer.

2% is so nominal. I think that I have made the right choice. I think that sometimes we forget what a great drug herceptin is. It works very well to cure early stage cancers. Not to mention how it can put stage 4 into remmision for years.