Does a grade 3 tumor always mean IV chemo?
Hi all,
I'm wondering if grade 3 tumors are most often treated with IV chemo, or if there's a chance for the pill only? My surgeon told me I will definitely need chemo, but we will have to wait til after surgery and further tests to determine what kind of chemo. My tumor is ER+ (66%) PR- , HER2-. They also did a ki-67 test and that was 88%. By those scores, my tumor is definitely aggressive, so I'm wondering if there's any chance at all for pill form of chemo. I'll do whatever it takes, these are just things rolling around in my mind.
Comments
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Hello djm71,
So sorry to hear you are going through this difficult time. I was there less than a year ago and can understand... if it helps any I can say this website is full of wonderful women ready to help and support you. Hang in there, it will get better!
From what you tell us, this information is based on your biopsy, so some things , numbers, etc may change after surgery when they examine the whole tissue, they also may send it for an oncotype dx. And that number will help you and the doctors make the decision about chemotherapy. Generally chemo is done intravenously and the hormone therapy that likely will follow would be a pill.
I hope that helped some, go step by step.
One second at a time and Much love your way!
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Hi djm!
There are pill forms of chemo, but they're not used for early stage breast cancer. Maybe, you're thinking of hormonal therapy, which is a daily pill and is used to address ER+ cancer. Did your doctor order an Ocotype test? That is often used to determine whether or not chemo will be beneficial to the patient.
You might want to get a second opinion re: chemo; the size of your cancer is fairly small. Do you have an affected lymph nodes? That might swing your doctors behind chemo. Best wishes to you!
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He did order the oncotype test. And he is going to take out 1or 2 lymph nodes in surgery on June 30 and check them. He told me that I would need chemo for sure but that nowadays that could mean a pill for 5-10 years, or the IV kind. So he must have been referring to the hormone therapy. It's all so confusing. I guess I need to slow down and just take things as they come. Thanks so much for your help
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You and I have very similar diagnosis... Small tumor, ER+ PR+ HER-, grade 3. I had BMX in April with tissue expander placement. I just finished my second of 4 rounds of chemo (1 every 3 weeks) and will follow with radiation and hormone therapy. I had 1 node affected so they are being overly aggressive as my tumor was just barely 1/2cm and already in the node, so an agressive little sucker!
Anyways, wanted to reach out and let you know if you have any questions just ask!!
-Keely
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Do whatever it takes is my advice. Under treatment equals worry about the future, and who needs that?
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I will find out my oncotype score in about 1.5 hours at my oncologist appointment today. I DREAD chemo, radiation doesn't thrill me either, but chemo....that deflates me thinking of it. I am hoping my stage 1a, 1.7cm, grade 3, ER+/PR+, HER2- tumor can cooperate and score LOW. If it's close to the "maybe" midrange score level, I will do the chemo as much as I don't want to. I am 57 and want to live a few more decades...if this is my chance, I'll take it. I was bummed when the core biopsy resulted in a grade 2 and then the post lumpectomy pathology report upped it to a grade 3. I need a break here.
My 82 and 83 year old parents just moved in with my husband and I in March of this year. My mom has advanced gastric cancer (diagnosed in Dec. 2015). My dad is frail, they manage ok now since they no longer have to care for their own home and we do the cooking, cleaning, etc.. My mom was doing horribly after the radiation early this year and one round of chemo; when she moved in she needed quite a bit of care. She doing VERY well for now and is taking herceptin treatments as she is HER2 +.
The thought of her needing me if she has a set-back in the next few months makes me very anxious. I also work full time as an occupational health RN. My poor husband, our nephew, his sister's 46 year old son was diagnosed with ALS in February and is declining rapidly. We are heartbroken. WHY WHY WHY????? Between our nephew's ALS, my recent breast cancer diagnosis, my parents needs, selling their home for them, the depression my dad suffers from after losing his independence, and my mom's health....it's been a ROUGH YEAR!
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Voban
I am so sorry to hear all of that you are going through. I don't really know what to say, just that I really hope everything goes well for you and your family.
Hugs coming your way, and you will be in my prayers.
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djm71 - Whether or not it has spread to your lymph nodes will generally decide the issue of (IV) chemo. If one or more have been affected, they will probably recommend systematic treatment, ie chemo and hormonal treatment after chemo. If not and you have good margins with surgery, they will probably give you the option of hormone(pill) only.
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voban what a dreadful time for you, and the others, of course. Re the chemo. Everyone reacts differently, so don't go on what happens to others. The best advice I ever received was not to have preconceived notions about any stage of your treatments. My dread of chemo was unfounded, since they have excellent nausea drugs now. As for radiation, a breeze. You do need to put your medical needs to the head of the queue right now IMO. Good luck with your decisions.
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I am so sorry you have to be here. Treatment is difficult enough without the added stress of your responsibilities.
If chemo is recommended for you, know that chemo is MOST effective on faster dividing grade 3 cancer cells. It is less effective on grade 1. So it adds one more weapon to your arsenal, if needed. Chemo for you would likely be only 3-4 months.
The 5-10 year pill will be the anti-hormone therapy, another great weapon. Many at stage 4 achieve NED (no evidence of disease) with just the anti-hormone drugs. You may read that some have a difficult time tolerating this therapy due to side effects, but many do just fine. You won't know till you try it.
Good luck to you.
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when I found out that I needed chemo, I found it hard to wrap my head around it, mostly because I wasn't expecting it. Docs were saying I probably wouldn't need it until they discovered the positive node. I have to say that it was no picnic. But it wasn't as difficult as I imagined either. No nausea whatsoever, and except for being bald, I didn't look too bad either. With a wig on, most people couldn't tell. Hopefully you won't need it, but if you do, it's livable
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Well, I was grade 3 but very low Oncotype, so grade isn't the determining factor anymore. The Oncotype counselors on the phone told me 30% of grade 3's have low Oncotype. Your estrogen score is medium, from the biopsy. Ki67% is high, and that is a concern, but the Oncotype has 5 measures of proliferation and ki67% is only one of them: it can be unreliable.
I am surprised the Oncotype was ordered after the biopsy. Usually it is done on the surgical samples. This happened to me as well and I did not trust it, because the biopsy tests initially had me as Her2+ then another lab had me as negative. I had all tests repeated after surgery but it took some advocacy on my part and it was hard to summon the energy. I will say-to reassure- that my Oncotype after surgery was identical to the one on the biopsy samples.
Oncotype testing sometimes indicates no chemo for a positive lymph node, but a higher estrogen sensitivity would probably be a key factor.
It is hard to wait to get all the info in but once surgery is over, you will know everything. I watched a lot of movies and then did mad research once I got the results. Until then distraction was best. It sounds like you have a lot of negative distractions with a lot of troubles and hoping you can find some pleasant and relaxing ones too. Good luck with surgery!
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