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Old 10-01-2008, 03:06 AM   #1
Alice
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Hi,
I don't know if I have too much info for you but I just want you to know that we have all felt what you are feeling now.
There is strong evidence that herceptin works well in her2+ casses. If you feel put off by your onc you may want to get a second opinion. Even if the second opinion is the same as the first, you may feel more of a connection with a different doctor.
I know all of these decisions are difficult and them throwing numbers at you doesn't help. I hope more respond to your post that maybe can help you better than I.
Herceptin seems to be the mirical that us her2+ patients have been hoping for. It is very tollerable and well worth the benefits. As far as the being grade 3 being equal to having pos nodes, I think that herceptin has put us back to 0. My tumor was also grade 3 and I never heard that from my onc.
Alice

Last edited by Alice; 10-01-2008 at 03:09 AM..
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Old 10-01-2008, 04:44 AM   #2
Jackie07
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DianneS,

When a tumor is classified as Grade III, it is very aggresive - growing super fast (think about the cells growing exponentially from 1, 2, 4, 16, 256, 256x256....) Once the tumor grows to a certain size, some of the cells start to peel away and 'invade' the surrounding tissues, possibly enter the lymph system...

With mastectomy, you are pretty safe as far as the breasts are concerned, but only a systemic approach (chemo and Herceptin - miracle drug for Her-2 positive breast cancer) can give you protection against having cancer sprouting in other parts of your body.

My tumor was not cut completely, so I had 'local' recurrence. The cancer had spread to my underarm lymphnodes, so it was considered 'regional'. Thus I had local regional recurrence. Because it was a chunk of tumor left to grow, chemo was not able to kill all the cancer cells.

And because it was mistaken as scar tissue, my recurrence was not found until it was quite big and with two lymph nodes involvement.

I wished my surgeon would had taken the more aggressive apprach and let me have the double mastectomy the first time around. I think your doctor (and most doctors now) understands the aggressiveness of HER-2 +++ breast cancer. It is doable. Many of us on this board have had chemo + Herceptin. Just like my heart condition was caught before I even had symptoms, I am sure all the side effects you are worried about will be detected before there's any visible damage.

If your doctor thinks you are in good enough shape to have the treatment, I (personally) think you should heed their advice and give it a try.
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http://www.kevinmd.com/blog/2011/06/doctors-letter-patient-newly-diagnosed-cancer.html
http://www.asco.org/ASCOv2/MultiMedi...=114&trackID=2

NICU 4.4 LB
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3 Infertility tmts 99 > 3 u. fibroids > Pills
CN 3 GKRS 52301
IDC 1.2 cm Her2 +++ ER 5% R. Lmptmy SLNB+1 71703 6 FEC 33 R Tamoxifen
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Old 10-01-2008, 06:50 AM   #3
Jean
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Hi Diane,
Welcome to our very special site and I am sorry that you have been dx with bc....and yes we all understand your feelings and concerns.

What Jackie has mentioned about the size of your tumor and grade is all true. While we certainly do not want to put drugs into our bodies you must consider all your options to fight this disease.

Also stats are great when they are in your favor!

You did not mention the type of chemo your dr. wants to treat with...it sounds like A/C and taxol herceptin.

First of all let me share this....my tumor was grade 1,
small tumor...6MM - at the time of my dx. I was told no chemo/herceptin since the SIZE of my tumor was so tiny. When you think about considering treatment based on size - doesn't it sound silly? The cells in my tiny tumor were very aggressive...so does it sound wise to base your treatment decisions based on size... how about the character of your tumor. I had to fight hard to get treatment of herceptin off label since it had not be approved by our FDA at the time, unless you were a stage IV and your cancer had spread....very upsetting to digest this information. Yes, we do KNOW that herceptin works, for some it doesn't but there are other meds to work with if that should be your case.
But we do know thorugh the studies that herceptin is saving lives.

Now, if you are concerned about A/C chemo you could ask your dr. about TCH treatment which is showing through data to be just as effective without the risk of heart damage and the worry of leukemia.

But I doubt he will want to use TCH since you are weakly ER and maybe (we don't know) your PR status maybe negative also. If you were strongly ER positive that would change the treatment. I believe your dr. is concerned and treating with A/C and taxol for the best results for your treatment.

You were aggresive with your surgery by removing both breast. You must have the herceptin without a doubt,
of course I am of the mind that the chemo is also
important at this time. Years ago onc. would treat based on node status, that has changed also. We now know that cells can travel through the blood system without showing the node invasion. Your tumor was a good size....I had asked my dr. how many cells in a tumor of 6MM (my size) his answer was MILLIONS...
that was enough for me. Diane consider this...your lympth node is much like a catch basket in the kitchen sink...now consider a small tiny tomato seed that can easily pass through the basket and not be detected.

The odds are there with millions of cells that can get out into our systems. Her2 likes to travel...

Hopefully our future will be when we do not need these strong chemo drugs and we can use drugs like herceptin which only goes after HER2 and does not destory our good cells.

I am sure many other sisters will respond to your post and offer some information to help you thorugh your decision for treatment.

Please know we are all here to answer any questions and you are not alone...we are here to support you.

Wishing you all the best.
Jean
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Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006

Last edited by Jean; 10-01-2008 at 06:54 AM..
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Old 10-01-2008, 06:55 AM   #4
DonnaD
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Dianne,
Welcome to our home. I hope you to will join our family. We are here for you, with knowledge, support and understanding.

Jackie07 and Jean have already given you great info. I am sure more will also respond . I did not use stats in making my decision. I wanted to be as aggressive as possible so I could to beat this disease. Chemo was a scary thought for all of us. But you can get thought it, and we are here to help!

Herceptin is our miracle drug. Many on this site who were not able to get it when they were first diagnosed are convinced they would not have had a reoccurrence if they had Herceptin. I am so thankful it was available to me.

Have you ever thought of getting a second opinion? If you go ahead with treatment you are going to be seeing your onc for 15 months and then years after that. Being up on the latest treatment and trials is very important but..... You need someone you feel comfortable with, who will encourage you, be supportive and answer your questions and phone calls. It is so much easier if it is a good fit.

If you have a chance pull up the post "All those Dancing with NED." NED means no evidence of disease. Their posts should offer you much hope. Be sure and read their signatures, so you can see the treatment they rec'd.

Decisions on treatments are very hard, especially at first when you are new to this disease and learning daily. But there are many around to help. Just ask your sisters.

Keep us informed.
Donna
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Donna
Crystal Lake, IL
Diagnosed 8/4/06 at age 54
Lumpectomy 8/30/06
Stage llA, grade 3, ER/PR-, Her2++
1.7 cm tumor, 1+ lymph node out of 9
Completed 4 A/C, & 4 Taxol with Herceptin
36 rads completed 5/16/07
Mammograms, 7/07 clear
fractured ribs in radiated area 10/07
Finished Herceptin 12/27/07
Mammogram,CT,tumor markers 1/08 - small lung nodules in radiated area, repeated tests 3/08 stable
Mammogram,CT ,tumor markers 6/08 stable
NED 2 years!!
3 years !!!
4years!!!!
4 years, 10 months and 8 day NED, calling it 5 years!!!
Official 5 years 8/30/2011
8/31/ 2012 - 6 years!!!!!!

Last edited by DonnaD; 10-01-2008 at 07:01 AM..
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Old 10-01-2008, 07:13 AM   #5
Jean
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Diane,
you asked what to expect....

1. yes, you will feel like you have a flu...achy etc.
tired... those type of reactions. But know your dr. will give you meds to stop the nausea. Many of us worked while on Chemo...while others could not...we are all different in our reactions to chemo.
But for the most part the meds that are given help greatly.

2. You will lose your hair. Of course it will grow back.
For me that was not a dramatic event...I was more concerned with staying cancer free and if having to lose my hair ...I really did not care.

I did not have Taxol but other taxane called taxatore, which is another drug in the taxane family. This work well with herceptin. I am sure others on the site will give you details on Taxol. I did have a small amount of
neuropathy in my toes...after 6 months it become less,
and after a full year there was still some left over numbness...but slight. There are meds to help with this and Vit. B6 is a great supplement.

I think it is wise of you to get all the information you can gather before making decisions. This will empower to make the best decsion for you...just make your decsion based on knowledge and NOT FEAR....

All best wishes to you,
Kind Regards
jean
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Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006
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Old 10-01-2008, 07:40 AM   #6
Colleens_Husband
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Diane:

Welcome to the forums. I am glad you found us and I am sad that you ever had to learn about HER2 cancer. Please understand that my wife is the one who endured the chemo, and I just observed, so my answers to your question may be a little odd to others here. But it is a different perspective and getting as many different ways of looking at a problem may be helpful.

Is the chemo worth it? Absolutely. You are playing math games when you make medical decisions. You need to increase your chances of survival every way you can. You have already made a difficult survival choice in having a double mastectomy. The chemo is the same exact choice you made earlier only instead you are trading long-term survival and health versus short-term discomfort.

And what are you going to get out of the chemo? Peace of mind. In the end, you will know you did everything you could to beat cancer and you took no easy ways out. There is no way of knowing you beat cancer for sure, and if you read this forum long enough, you will see hundreds of posts of people wondering if they are NED (no evidence of disease).

I know chemo is no fun. Colleen had TAC and that was a fresh slice of hell. Days 7 through 10 were awful. She also had TCH and that was much more tolerable. She only missed one day of work per cycle with that combination. She said TCH was like having a mild flu for a week.

Diane, you will be in our hearts and prayers,

Lee
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This happened to Colleen:

Diagnosed in September 2007
ER-/PR-/HER2 Neu+++ 2.1 cm x .9 cm spicluted tumor with three fingers, Stage 2B
Sentinal node biopsy and lymph node removal with 3/18 positive in October 2007
4 TAC infusions
lumpectomy March 2008, bad margins
Re-excision on June 3rd, 2008 with clean margins
Fitted for compression sleeve July 16, 2008
Started the first of two TCH infusions August 14, 2008
Done with chemo and now a member of the blue dot club 9/17/08
Starting radiation October 1, 2008
life is still on hold
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Old 10-01-2008, 11:28 AM   #7
WomanofSteel
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I am one of those people that Lee speaks of. Although because of my age and my daughter, I opted for the recommended chemo my onc suggested because of the agressiveness of my cancer, I did not get Herceptin. I wonder everyday if this would have made a difference for me with my reoccurence. My personal feeling is that you should be agressive as possible with what treatment is offered you early on. The side effects are certainly worth the increase in percentages or years if you look at it that way.
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dx aug 03
invasive dcis 1 cm
er/pr/her2+
bcs 8/4/03
bcs 8/21/03 0/16 nodes
tx 4x ca 36 rad tam
postmenopausal 06 aromasin
sept 07 biopsy node in neck
muga/pet/cat/bone mets to lungs nodes and liver stage iv
tx hki-272
tx not working switched to taxol herceptin
Taxol not working switched to navelbine
navelbine is causing bad neuropathy
starting gemzar
gemzar quit on me now on Ixempra due to increasing number and size of liver mets
another progression starting tykerb/xeloda
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Old 10-01-2008, 04:21 PM   #8
Louise O'Brien
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Dianne:

I see you're from Canada - so the treatment is relatively standard from province to province.

I was exactly where you are now - two years ago. Your discussion with the oncologist sounds exactly like the discussion I had with mine two years ago.

Under our health care system - Herceptin is combined with chemo. It was the chemo that horrified me. Like you - I considered walking away from the whole thing.

I can only tell you now - two years later - I am so thankful I did not. I chose full treatment and I know now I will never have to second guess myself wondering ... did I do enough... what if.... what if?? I feel I did everything I could, in my power to try to stop this thing.

Her2 is an aggressive little devil and no one knows how it is going to react. And Herceptin has had dramatic results.

If I had a friend who was Her2 positive I would do everything in my power to convince her to take Herceptin. The more research you do - the more you will find this out.

As for chemo - it's doable. Everyone says that but it's true. You have decisions to make and this is a stressful time but I'll step out on a limb here to urge you - don't walk away from Herceptin.
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