Lumpectomy vs mastectomy
What are the pros and cons of lumpectomy vs mastectomy? How was a decision made?
Comments
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Hi there. That is a tough one, with lots of factors. Do you have a copy of a biopsy report yet? In my own case the tumor was small, no nodes were involved, and I have no family history of cancer. So I opted for a lumpectomy followed by three weeks of radiation then a tamoxifen pill every day.
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What is your DX?
There are so many variables. (For some a LX is not a possibility.).
The type of BC - DCIS (Ductal Carcinoma In Sittu), IDC (Invasive Ductal Carcinoma), ILC (Invasive Lobular Carcinoma) IBC (Inflammatory Breast Cancer) . The Stage and grade. The ER/PR and HER2 status. These all come into play when looking at options.
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I've found it useful, on this great forum, to read about other's decision-making with treatment. So here is mine! It is just to illustrate that the decision needs to be influenced, as a prior poster said, by the nature of the BC variant that has been diagnosed, and that it is helpful to have a clear sense of what your priorities are. As such, these are really individual decisions
I had two types of tumor (double trouble!), an IDC (Grade 1) sitting above an ILC (Grade 2). All surrounded by DCIS/LCIS/ADH. A seething cauldron of cellular trouble! The two tumors and DCIS etc were all identified in imaging prior to surgery.
Initially, I had a lumpectomy and SND, as the imaged tumors and problematic areas were small enough to indicate this could be done. Pathology after the lumpectomy found another 3 tiny spots of ILC in addition to the area already identified, all of which were too small to image against my dense breast tissue, and one was right on the margin.
So the choice was then resection to get clean margins, then proceed to radio, or a UMX. The BS explained that with ILC, getting clean margins in a resection did not guarantee that there were no other small areas of disease in that breast which we didn't know about, and could not see, however these would be dealt with by radio.
I was keen to avoid radiotherapy if possible, as the radiation oncologist had explained that there are side effects with radio that generally show up 20-25 years after treatment. That's prob not something to worry about if you are older, but is more of a concern if you're younger. With the UMX, I would only need radiotherapy if tumor cells were found close to the chest wall.
I chose to go with UMX.
-I felt that I had a higher risk of recurrence because I'm younger, 44yo, so apart from anything I have more years for a recurrence occur; and it seemed to me that seething cauldron of trouble would just keep cooking things up!
-being younger also meant there were more years (I hope!) for SE from radio to emerge
- the pathology of the disease, ILC, which can be difficult to detect plus dense breasts making imaging very challenging
-the possibility that I'd have to have a UMX anyway if they could not get clear margins on the resection (I really dislike surgery recovery, I will happily try to avoid it!)
-I decided not to have recon. I was not very concerned about having to use a prosthesis and felt that I would cope OK emotionally with losing a breast (and that my partner would cope OK with it too!). I also did not want an implant to affect my ability to take part in the activities that are crucial for my quality of life (ocean swimming, in particular)
Pathology after the UMX showed no further areas of disease- so I could have gone with the further lumpectomy and radio safely. However, I am very happy not to have radio.
In terms of the two operations, I would say my recovery from the UMX has actually been better. I developed a hematoma after the lumpectomy, which delayed healing. I'm counting down the days until I can get back in the water...
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Because of the location of my tumors (all by the nipple), I am going to lose the nipple on that side no matter what, and I had already had a scare earlier this year on the other one, so it was a no brainer for me to get a double mastectomy rather than just the one sided lumpectomy. I wanted to avoid having to have several surgeries, and worrying about it coming back all the time. Plus I feel like I will get a better outcome visually if they are reconstructing both at the same time.
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Thank you so much for this detailed response. I greatly appreciate all the detailed explanation.
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mybctc - here is a previous list of pros and cons created by the member Beesie. This post has been edited to remove the DCIS version and add the invasive version.
Some time ago I put together a list of considerations for someone who was making the surgical choice between a lumpectomy, mastectomy and bilateral mastectomy. I've posted this many times now and have continued to refine it and add to it, thanks to great input from many others. Some women have gone through the list and decided to have a lumpectomy, others have chosen a single mastectomy and others have opted for a bilateral mastectomy. So the purpose is simply to help women figure out what's right for them - both in the short term but more importantly, over the long term. Please note that this list is written for women who have invasive cancer (Stage I or above). Some of the decision factors are different for women who have pure DCIS (Stage 0). A different version of this list, written specifically for women with DCIS, is available in my post on the first page of this discussion thread in the DCIS Forum: 'Topic: lumpectomy vs mastectomy - why did you choose your route?'.
Before getting to that list, here is some research that compares long-term recurrence and survival results. I'm including this because sometimes women choose to have a MX because they believe that it's a more aggressive approach. If that's a big part of someone's rationale for having an MX or BMX, it's important to look at the research to see if it's really true. What the research has generally shown is that long-term survival is the same regardless of the type of surgery one has. The reason that the choice of surgery doesn't affect survival is largely because it's not the breast cancer in the breast that affects survival, but it's the breast cancer that's left the breast that is the concern. The risk is that some BC might have moved beyond the breast prior to surgery. So the type of surgery one has, whether it's a lumpectomy or a MX or a BMX, doesn't generally affect survival rates. There have been a few more recent studies that have however shown different results. A couple of studies have shown that survival might actually be higher for those who have a lumpectomy, possibly because these women usually also have radiation, whereas women who have a MX don't usually get rads. But another recent study suggested that younger women may benefit, in terms of long term survival, from a MX.
Here are a number of the studies that compare the different surgical approaches: (Note that a number of these articles are from Medscape, and you will have to register with them to be able to view the articles.)
April 2016 Is breast conserving therapy or mastectomy better for early breast cancer? and
August 2016 (this is another write-up of the same study as above) Young Patients With Early Breast Cancer Live Longer With Mastectomy
December 2015 Ten-Year Data: Lumpectomy and Radiotherapy Trump Mastectomy
December 2014 No Survival Benefit for Increasingly Used Bilateral Mastectomy
January 2013 Lumpectomy May Have Better Survival Than Mastectomy
Now, on to my list of the considerations:
- Do you want to avoid radiation?
If your cancer isn't near the chest wall and if your nodes are clear, then it may be possible to avoid radiation if you have a mastectomy. This is a big selling point for many women who choose to have mastectomies. However you should be aware that there is no guarantee that radiation may not be necessary even if you have a mastectomy, if some cancer cells are found near the chest wall, or if the area of invasive cancer is very large and/or if it turns out that you are node positive (particularly several nodes).
- Do you want to avoid hormone therapy (Tamoxifen or an AI) or Herceptin or chemo?
It is very important to understand that your choice of surgery – lumpectomy, mastectomy or bilateral mastectomy – will not change the recommendation as to whether or not you should have chemo, Herceptin (if HER2+) or endocrine (hormone) therapy (if ER+). So you can't avoid any of these treatments - if your MO believes they are necessary - by opting to have a MX or BMX. (Note that the exception is women with DCIS or possibly very early Stage I invasive cancer, who may be able to avoid Tamoxifen by having a mastectomy or a BMX.)
- Does the length of the surgery and the length of the recovery period matter to you?
For most women, a lumpectomy is a relatively easy surgery and recovery. After a lumpectomy, radiation usually is given for 6 weeks. A mastectomy is a longer, more complex surgery and the recovery period is longer.
- How will you deal with the side effects from Rads?
For most patients the side effects of rads are not as difficult as they expected, but most women do experience some side effects. You should be prepared for some temporary discomfort, fatigue and skin irritation, particularly towards the end of your rads cycle. Most side effects go away a few weeks after treatment ends but if you have other health problems, particularly heart or lung problems, you may be at risk for more serious side effects. This can be an important consideration and should be discussed with your doctor.
- Do you plan to have reconstruction if you have a MX or BMX?
If so, be aware that reconstruction, even "immediate" reconstruction, is usually a long process - many months - and most often requires more than one surgery. Some women have little discomfort during the reconstruction process but other women find the process to be very difficult - there is no way to know until you are going through it.
- If you have a MX or BMX, how will you deal with possible complications with reconstruction?
Some lucky women breeze through reconstruction but unfortunately, many have complications. These may be short-term and/or fixable or they may be long-term and difficult to fix. Common problems include ripples and indentations and unevenness. You may have lingering side effects (muscle pain, spasms, itching, etc.) on one side or both (if you have a BMX). If you don't end up with symmetry (symmetry is not a sure thing by any means, even if you have a bilateral mastectomy with reconstruction done on both sides at the same time), will you regret the decision to remove your breasts or your healthy breast? Are you prepared for the possibility of revision surgery?
- How you do feel about your body image and how will this be affected by a mastectomy or BMX?
A reconstructed breast is not the same as a real breast. Some women love their reconstructed breasts while some women hate them. Most probably fall in-between. Reconstructed breasts usually looks fine in clothing but may not appear natural when naked. They may not feel natural or move naturally, particularly if you have implant reconstruction. If you do choose to have a MX or BMX, one option that will help you get a more natural appearance is a nipple sparing mastectomy (NSM). Not all breast surgeons are trained to do NSMs so your surgeon might not present this option to you. Ask your surgeon about it if you are interested and if he/she doesn't do nipple sparing mastectomies, it may be worth the effort to find a surgeon who does do NSMs in order to see if this option is available for you (your area of cancer can't be right up near the nipple).
- If you have a MX or BMX, how do you feel about losing the natural feeling in your breast(s) and your nipple(s)?
Are your breasts and nipples important to you sexually? A MX or BMX will change your body for the rest of your life and you have to be prepared for that. Keep in mind as well that even if you have a nipple sparing mastectomy, except in rare cases, the most feeling that can be retained in your nipples is about 20% - the nerves that affect 80% of nipple sensation are by necessity cut during the surgery and cannot be reconnected. Any breast/nipple feeling you regain will be surface feeling only (or phantom sensations, which are actually quite common and feel very real); there will be no feeling inside your breast, instead your breast will feel numb. For some, loss of breast/nipple sensation is a small price to pay; for others, it has a huge impact on their lives.
- If you have a MX or BMX, how will you deal emotionally with the loss of your breast(s)?
Some women are glad that their breast(s) is gone because it was the source of the cancer, but others become angry that cancer forced them to lose their breast(s). How do you think you will feel? Don't just consider how you feel now, as you are facing the breast cancer diagnosis, but try to think about how you will feel in a year and in a few years, once this diagnosis, and the fear, is well behind you.
- If you have a lumpectomy, how will you deal emotionally with your 6 month or annual mammos and/or MRIs?
For the first year or two after diagnosis, most women get very stressed when they have to go for their screenings. The good news is that usually this fear fades over time. However some women choose to have a BMX in order to avoid the anxiety of these checks.
- Will removal of your breast(s) help you move on from having had cancer or will it hamper your ability to move on?
Will you feel that the cancer is gone because your breast(s) is gone? Or will the loss of your breast(s) be a constant reminder that you had breast cancer?
- Appearance issues aside, before making this decision you should find out what your doctors estimate your recurrence risk will be if you have a lumpectomy and radiation vs. what it will be if you have a MX.
Is the risk level you will face after a lumpectomy + rads one that you can live with or one that scares you? Will you live in constant fear or will you be comfortable that you've reduced your risk sufficiently and not worry except when you have your 6 month or annual screenings? If you'll always worry, then having a mastectomy might be a better option; many women get peace of mind by having a mastectomy. But keep in mind that a MX or BMX does not mean that you no longer need to remain vigilant; you must continue to be checked for breast cancer. Although for most women the recurrence risk after a MX is low, anyone can still be diagnosed with a recurrence or a new primary breast cancer even after a MX or BMX. This is because it is impossible for the surgeon to remove every cell of breast tissue; some breast tissue always remains even after a MX or BMX, around the edges of the breast, or just a few cells against the chest well or the skin. Be aware too that while a mastectomy may significantly reduce your local (in the breast area) recurrence risk, it has no impact whatsoever on your risk of distant recurrence (i.e. mets).
- Do you know your risk to get BC again, in either breast (if you have a lumpectomy) or your non-cancer breast (if you have a MX)?
Is this a risk level that scares you? Or is this a risk level that you can live with? Keep in mind that breast cancer very rarely recurs in the contralateral breast so your current diagnosis doesn't impact your other breast. However, anyone who's been diagnosed with BC one time is at higher risk to be diagnosed again with a new primary breast cancer (i.e. a cancer unrelated to the original diagnosis) and this may be compounded if you have other risk factors. Find out your risk level from your oncologist. When you talk to your oncologist, determine if genetic testing might be appropriate for you based on your family history of cancer and/or your age and/or your ethnicity (those of Ashkenazi Jewish descent are at higher risk for BRCA mutations). Those who are found to have a genetic mutation may be at very high risk to get BC again and for many women, a positive genetic test result is a compelling reason to have a bilateral mastectomy. On the other hand, for many women a negative genetic test result helps with the decision to have a lumpectomy or single mastectomy rather than a bilateral. Talk to your oncologist and determine if you should see a genetic counselor. Don't assume that you know what your risk is; you may be surprised to find that it's much higher than you think or much lower than you think (my risk was much less than I would ever have thought).
- How will you feel if you have a lumpectomy or UMX and at some point in the future (maybe in 2 years or maybe in 30 years) you get BC again, either a recurrence in the same breast or a new BC in either breast?
Will you regret your decision and wish that you'd had a bilateral mastectomy? Or will you be grateful for the extra time that you had with your breasts, knowing that you made the best decision at the time with the information that you had?
- How will you feel if you have a bilateral mastectomy and no cancer or high risk conditions are found in the other breast?
Will you question (either immediately or years in the future) why you made the decision to have the bilateral? Or will you be satisfied that you made the best decision with the information you had? Consider as well how you might feel if your reconstruction is difficult and the results not to your expectations.
I hope that this helps. And remember.... this is your decision. How someone else feels about it and the experience that someone else had might be very different than how you will feel about it and the experience that you will have. So try to figure out what's best for you, or at least, the option that you think you can live with most easily, given all the risks associated with all of the options. Good luck with your decision!
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This is so helpful for me too. Thanks for posting! I'm struggling with this as well and this helps
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This is extremely helpful information. Thank you so much!! Michela Riccio
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Thanks! I am struggling with this too, but am leaning towards mastectomy with immediate reconstruction. I’m only 33, so have a hopefully very long time to live with this decision. I’m hoping to avoid rads. My tumor abuts my chest wall but no known wall involvement and my BS thinks he can get clear margins. Fingers crossed!!!
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Thanks so much for your response. And so sorry for my delay in responding. I will see my B's Wednesday and will hear his recommendation s. My breasts are large,the original tumor was 4cm and I have been on tchp everythree weeks forsix treatments. Just completed treatment 5 December 18.o e more to go January 8. 65 years old . Hoping for lumpectomy. Will keep u posted good luck to you!!
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I decided on nipple sparing mastectomy with immediate reconstruction and I want the other one done too. They won’t do them at the same time since they want to treat the cancer first.
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I was offered a lumpectomy with rads, or a mastectomy. Due to previous biopsies on the non-cancer breast, figured that one would sooner or later turn up something, being small breasted, not wanting to deal with the anxiety of the 6mth surveillance, my sis having had breast ca, (no on else though in the family history), I chose to do a double, nipple sparing mastectomy with direct implants. I did not have enough fat to use for DIEP. I walked out of the hospital the next day. I have no regrets and though not pretty with the scars at this time still, I have no regrets and having two nice rounded foobs, I can deal with it.
It is a tough decision for some, and others know right away. I knew right away what i would do. Good luck
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Would appreciate any experiences thoughts and opinions about complete pathologcal response on tchp or lack thereof? Can a lumpectomy be performed on a 2.4 tumor?
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how are you doing today?
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I had a lumpectomy on Tuesday Feb 6. I had been diagnosed with IDC. The path report came back great. in terms of showing a complete pathological response.
H iowever they had wanted to retest the tissue for Hormone Positivity because when I was first biopsied they told me Weak Projesterone Positive and estrgen negative and HER 2 Positive.
But I was told this is an extremely unlikely finding; very rare; thus they wanted to retest it upon surgery. Breast Surgeon gave me report yesterday and the report mentioned Lubular Cancer in Situ and I think it was mentioned in the context of this no longer being present; however since Diagnosis July 2017 i was always told i had Invasive Ductal Carcinoma. Thats mentioned as well.
Here's what the relevant portion of the report says:
Breast, Left, Lumpectomy:
Breast Tissue with focal in situ carcinoma., consistent with Lobular Carcinmoa in Situ.
no in situ or invasive ductal carcinoma demonstrated.
Foci of Fbriosis; Scarring and Old Hemorrhage.
Does anyone know what these words mean? Wont be going over this report for another two weeks but was given in the paper report yesterday and wondered if anyone knows how to interpret any of this?
Was told I had a complete pathologic response and was on TCHP from Sept 18- Dec 18.
I will get radiation next month and continue for one year on Herceptin. Would appreciate any input/feedback or response.
THANKS!
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I thought I would share too. I had a lumpectomy on Feb 7th. and never really considered anything more. My Mom was diagnosed at 70 and had a lumpectomy and brachytherapy radiation only. For a few years she went through the constant imaging, watching and some additional biopsies. At her age she figured she was done with her breasts anyway so she opted for a double mastectomy. Several years later, surprisingly, she was diagnosed with a distant recurrence in her liver. She is 81 now, 3 years on constant chemo pills - with very little side effects! She was very happy with her decision and of course sorry I am heading down a similar path.
For me, I was not ready to remove my breasts and my tumor was small, grade 2 and at least pre surgery looks like no nodes. March 1st is my follow up appointment and I will soon know whether I will have radiation, chemo, hormone therapy etc. So I will have some decisions at that point. I am 57 so I do want a good 20-25 years healthy and will do whatever I need to.
It is a very personal decision and there is no right or wrong answer so you need to do your research and trust that your decision is right for you. One thing I have learned is not to listen too much to what others think I should do (maybe with the exception of the doctors I trust). You need to live with your decision - they do not.
Trust yourself and I hope you do well whichever path you follow!
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ToughCookie...So did you get those clean margins? I hope so. 33 is so young! Wish I (at 63) were 33 again, even if it meant having breast cancer! LOL! Hope you had clear margins and the Lumpectomy worked out fine.
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Thany so much for this response! I was wondering if you are receiving radiation as I am and how things are going for you and your Mom? So sorry for the delayed response. All has gone well for me so far and hope the same for you and your Mom.
Michela
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Hi, ladies
Looking for your input and perspective on my dilemma.
Had a lumpectomy back in Jan. currently going thru chemo. Met with Radiologist the first time, she think my margins are too small, 0.5mm in two places, she wants minimum 2mm. I asked her whether I should get a mastectomy, she said she doesn't think so. but if I go for mastectomy, I will no longer need radiation.
So my options are: Recision + radiation (left breast) or mastectomy.
What I am not understanding is why radiologist didn't think mastectomy was necessary? wouldn't it outweigh the risk of radiation? Especially considering I have multi focal IDC, found 6 tumors from lumpectomy.
Your thoughts and experiences are greatly appreciated. Thanks
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I'm not sure why a radiologist is weighing in on the margins. Or why they would be consulted about type of surgery. I would discuss these concerns with your surgeon.
With multi-focal BC - I'd be worried about keeping the breast unless maybe the tumors were all in a small area.
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Notverybrave:
Thanks for your post. I feel the same way once i found out about the multifocal. I asked my surgeon how do we know there is no residual satilite tumors else where given the multifocal. She said we never can know anything for sure. Huh.
In BC, Canada, I just told by oncology team (not MO, she works for MO) that margins are decisions discuss between Surgeon and Radiation Oncologist. My current assumption is they both deal with local area of issue, MO deal with the whole body?
I am getting a 2nd opinion from a different surgeon. But getting bounce between surgeon and radiation oncologist is not great. My GP said i should listen to Oncologist since they are the expert on Cancer. It makes sense.
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