Mastecomy/Lumpectomy no longer and option/priority - stage IV
I was told by my MO that at the present time surgery was no longer a priority. There are studies that indicate that by removing the main breast tumor, it frees up the free flowing estrogen's, proteins etc to all the mets so they can then feed easier. Meaning ,we give the mets a larger amount of foods they like. The main breast cancer helps to keep absorbing all the goodies these mets want .
I hope that makes some sense. My MO did say maybe in the future I could have surgery for cosmetic reasons. I have googled some and there are studies that support this.
Just wanted to know if this is pretty common and what any other thoughts you all have?
Comments
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Freygea,
Sorry that you are joining us. I have no hard and fast numbers for you, but I know there are others who have not had surgery, if they are stage IV at the outset. On the other hand, some have had surgery as it is thought that reducing the tumor load may be helpful. "Free flowing" estrogen would only be an issue for those who are ER+, though I have not heard of this. I had a bmx, only to discover, 6 weeks later, that I had a bone met. I have been NED since initial tx, on AI's only (rads to bone met). I often wonder what the course of tx would have been if the bone met had been found before surgery.
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Hi Freygea,
I'm so sorry to hear of your stage IV dx. Your head must still be reeling as I saw in another post you were just diagnosed in May. I hope you will find both good information and support on this forum.
For what it is worth, you may count it as a blessing that you did not undergo lumpectomy/mastectomy before learning you were stage IV. It went the other way for me. I had a lumpectomy with sentinel node biopsy and learned I had mets to bone afterward. I have always wished I could have been spared the disfigurement and nerve pain caused by the lumpectomy. The surgical site still bothers me, even a year later. And I have been fortunate in never having edema.
More generally speaking, it seems there are 2 schools of thought regarding tumor removal at stage IV. Some believe lessening the tumor burden or load helps the body to fight the remaining cancer, others seem to think it is unimportant to remove the original tumor after metatases. Like most everything else with mbc, I don't think anyone really knows for sure.
I see you are triple positive, ER/PR+ and HER+ so you and your doctors will have a lot of treatments to choose from. Wishing you great results with minimal side effects.
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Freygea-I just found this post after seeing your post in the Herceptin/Perjeta forum. I'm sorry you find yourself here. I too was dx Stage IV from the start, so I know how ovewhelming it can all be. The ladies on this site are wonderful and have a wealth of knowledge about treatment and managing side effects.
My doctor did not recommend surgery either, using the "the horse is already out of the gate" analogy, and I'm ok with that decision. I had extensive bone mets at dx, but the most troublesome were two in my spine wich I had radiation for because they were concerned with spinal cord compression. After radiation I started Taxotere, Herceptin, Perjeta and xgeva. The first round was the hardest as I was still in a lot of pain, but once the tumors started to shrink I was able to do day to day activities much easier. I continued to work 40 hours, although my job allows me to work from home when needed and they were very kind and flexible with my schedule.
Now I am on Herceptin, Perjeta, xgeva and Tamoxifen and I feel pretty darn good! I still have a lump in my breast that I can feel, but I do believe it is slowly shrinking. My bones will always show "evidence of disease" on a CT scan as my dr says, but he says it is probably scar tissue. I still get twinges and muscle spasms if I overdo it, but I'm learning my new limits. My scans have been extended from every 3 months to every 6. I still get a 3 month echocardiogram because Herceptin can be toxic to the heart. So far so good!
I wish you the best with your treatment. Feel free to throw out any questions you may have...someone will always have an answer!
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Thank you all! I am still really scattered so my posts tend to be short and well..scattered..lol. I have been reading all of your posts in the various threads and they are very inspiring. It is great to see we can and are living with stage IV and that it is not the end all.
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Freygea, welcome. There are different schools of thought about breast surgery for stage IV, and decisions have to be individualized. Here is what my MO said about why she did not recommend surgery for the breast tumor that was found at the same time as liver mets:
1. Anesthesia and surgery cause reactions in the body, at the cellular level, that can promote the spread of the cancer.
2. The breast tumor is a useful way to monitor how effective treatment is. (Indeed, during taxol we could feel it shrinking, as my tumor markers dropped. It seems to be gone now, according to exams and scans.)
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I too was stage IV from the start. Diagnosed in January 2015, and I just finished up 8 rounds of chemo. PET and MRI says all the cancer they saw on previous scans is dead so the doctor says he now wants to do surgery. He agreed there is some thought that there is no point to doing the surgery after it's spread but believes it is for the best. His simplified explanation was that without the mother ship (the breast tumor), the mets do not do as well. He said there was some study started at MD Anderson to compare stage IV patients (he said just like me so I assume he meant stage IV from the start) with surgery vs without but said they stopped the study because the patients without surgery were having re-occurrences much sooner.
I haven't done extensive reading up on the issue but from what I've read here, that MD Anderson story appears to be untrue but I'm ok with doing the surgery. I think I would ok with not doing it too.
Another note, he did mention that the size of the breast tumor hasn't changed (originally about 5cm) but it shows no metabolic activity. I find that puzzling since his description of other spots on previous scan are now completely gone. My lymph nodes for example, they show no metabolic activity and are no longer enlarged.
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Hi Bama - Just wondering - Is your doctor recommending a lumpectomy or a mastectomy?
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He didn't mention either. I meet with the surgeon on Thursday. I assume she will be the one to made the recommendation?
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My situation is similar to bama351. Was diagnosed as Stage IV November 2014. Started neo-adjuvant chemo in December 2014, 6 rounds of Herceptin/Perjeta/Taxotere and finished March 31. Had PET and full body bone scan (had 3 small bones mets) and both scans showed NED. My tumor in the right breast was 5.3 cm and is now 2 cm, just dead tissue. Originally I was told that due to my Stage IV status I would not get a masectomy after chemo but would continue with Herceptin/Perjeta infusions every 3 weeks indefinately. Then when I saw him last month he said my case went in front of the tumor board and they said because I responded very well to the chemo treatments and was NED they strongly recommended I have the masectomy. My Onc said that I not only had a large tumor in the breast but several smaller ones also and that there is a chance of recurrence in the affected breast and it may not respond as well. The tumor board also stated that most of the cancer was localized in the breast with only 3 small bone mets which are now gone so for those two reasons they changed and approved the surgery. Met with the BS last week and have masectomy scheduled for July 7. I have not decided if I will have reconstruction or not. Will decide after the masectomy and consult with PS.
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BG I would love to be added to the FB group. I'm on there most of the day for my work. My FB name is Amy Ebert Haggerty
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Amy,
This thread has been inactive for over a year. So as not to leave you hanging, perhaps you could pm the person who posted about a FB group or one of the other women who responded to this thread. Take care
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I am also on taxatere herceptin and perjeta and have been told no to surgery, I have to do taxatere 8 treatments and then herceptin and perjeta indefinitely, I was D.C. With stage 3 breast ca, but after same day pet scan stage 4 liver and bone mets 15 mm in liver, devastated to find out that I had stage 4 and I am also her+ I would like people to help me if they can give me some feedback on what to do thx al
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Hey Jc free did you ever have that mastectomy?
How did it all turn out
Curious, Paula
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Hi Paula, I was DX stage 4 on 3/13/2015. I too was told no to any surgery. In a way I'm glad I didn't have to put my body thru that on top of everything else. Many people don't seem to understand this when it comes to breast cancer. I do get upset when I have to come right out and explain that I am inoperable!! I hope you don't have to face any of those strange looks...it's hard enough for people to understand metastatic breast cancer. You are in my thoughts and prayers.
Keep shining bright
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nan812,
Thank you for the kind words and yes I feel those weed looks but it's ok. Just am tired and live alone, kids gone and I am divorced I find myself lonely slit even though I am working 3 part time jobs, I also have to push myself to get out,
Again thank you for the kind words and best of luck
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Paula - MBC is lonely even for those in the middle of a family. I hope you get more involved here. Start by filling out your diagnosis and treatment in your BCO profile and then making it public in the settings area. Send me a message through BCO if you need help.
Then poke around in the threads where people with similar diagnosis or on similar treatments are posting.
Everyone belongs on the Stage V Fitness thread. Exercise is a great way to feel better, improve your outcome and generally get your behind out the door.
>Z<
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