Lumpectomy or Mastectomy with Reconstruction?
I'm very newly clinically diagnosed (I'm 36) and I met with the bs yesterday. Right now (MRI is on Friday) she recommends lumpectomy with radiation, but says that a mastectomy is a good route too - it's just about personal preference, but she has set me up with a consult with a plastic surgeon (that's later this morning). I know I will be armed with a bit information after the consult and MRI results (and I will get a 2nd or 3rd opinion), but I wanted to know how some of my fellow younger women made the decision to go one way or the other. It looks like a lot of people go with the lumpectomy and later go with the mastectomy (either a unilateral or prophylactic bmx). I like the option of one and done and with the possibility of avoiding radiation, but it is a major surgery (and I have no idea if it's fully covered by my insurance). Ugh!
Comments
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Because of your age they will probably do genetic testing on you, and that will help you decide. I'm 37 and that was the reason why insurance company covered the testing. You can always have a mastectomy later , but you will never get back what you cut off. Since you want to have children would you also want to breastfeed? Even a prophylactic surgery will be covered by insurance, and the reconstruction or breast lift for the healthy breast is also covered. You will be able to make up your mind once you speak with the plastic surgeon. -
Grace, here is Beesie's very informative post from another thread:
I didn't have a choice - I had so much DCIS in a small breast that the only way to remove it all was with a MX. But given a choice, I would gladly have gone with a lumpectomy + rads. Like Annette, I had no risk factors that would have made rads more difficult or risky for me and I simply was more concerned about the side effects from the MX than from the rads. Today, having lived 7 years with my MX, I would still say the same thing - for me, I'd pick a lumpectomy + rads over a MX if I had a choice.
Since I didn't have a choice, I had a single MX. I'm glad I made that decision. My PS explained that the idea that a BMX is going to provide a better cosmetic result is simply untrue. A good PS should be able to achieve reasonable symmetry with a single MX. And a BMX by no means ensures that the results will be better or more symmetrical. Plus there is so much more to this decision - and living with a MX and reconstruction - than just the cosmetic appearance.
What I've learned from having my MX is that a MX affects you for your lifetime. I'm more than 7 years out and there are days when the affect of my MX and reconstruction is still very noticeable to me - muscle aches, sore ribs, etc.. There are activities that I no longer do, or try to avoid, because of the reconstruction. How I felt about my MX and reconstruction when I first had my surgery (elated!), how I felt about it two years later (surprisingly disappointed), 5 years later (it is what it is) and now 7 years later (occasionally frustrated) has continued to change and evolve. I think that's important to understand because so much of what you read on this board is from people who have just completed the process, or who are still in the middle of the process. Whether they feel good about it or bad about it at this point in time could easily change as time goes on.
Sometime ago I created a list of considerations for those making the lumpectomy vs mastectomy vs. bilateral mastectomy decision. I've reposted this many times now, and I've added input from many other women. Going through this list might help you come to terms with how you will deal with either of these options and what the best decision is for you:- Do you want to avoid radiation? If your DCIS isn't near the chest wall, 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 DCIS is found near the chest wall. Radiation might also be recommended if it turns out that you have a large area of invasive cancer in addition to the DCIS and/or if it turns out that you are node positive (which is only possible if you have invasive cancer).
- Do you want to avoid Tamoxifen? For those who are ER positive who have DCIS, this may be possible if you have a mastectomy and particularly if you have a bilateral mastectomy. Tamoxifen provides 3 benefits: 1) It reduces the risk of local recurrence; 2) it reduces the risk of the development of a new breast cancer in either breast; and 3) it reduces the risk of a distant recurrence. For most women, a mastectomy will reduce the first risk to a low enough level that the benefit from Tamox will be minimal. For most women, a bilateral mastectomy will reduce the second risk to a low enough level that the benefit from Tamox will be minimal. The third benefit, protection against a distant recurrence (i.e. mets), isn’t a factor for women who have DCIS, since by definition DCIS cannot move beyond the breast. However for those who have invasive cancer, this is a crucial benefit and is not affected at all by the type of surgery. So if you have an invasive tumor that is ER+, usually Tamoxifen (or an AI) will be recommended whether you have a lumpectomy, mastectomy or a BMX. However if you have DCIS (and therefore face virtually no risk of mets) or a very small non-aggressive invasive tumor (and therefore face only a very small risk of mets), it may be possible to pass on Tamox with little change in your long-term prognosis.
- 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 do you feel about going through a longer surgery and a longer, more restricted recovery period?
- If you have a lumpectomy, 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.
- If you have a mastectomy, do you plan to have reconstruction? 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. Are you prepared for this?
- 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 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?
- If you have MX or BMX, how you do feel about your body image and how will this be affected by a mastectomy? 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 mastectomy, 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 DCIS 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 nipple(s)? Are your nipples important to you sexually? A mastectomy 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 (and except with a new untested reconstruction procedure) 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. Keep in mind as well that most women are pleased with their decision to have a mastectomy or bilateral when it's first done - they are relieved that the cancer is gone and the surgery is over and in most cases it wasn't nearly as bad as they feared. For women who are affected by the loss, the real impact usually doesn't hit until many months or even years later. That’s why trying to think ahead to a time when this diagnosis is long behind you is important.
- If you have a MX or BMX, 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?
- 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.
- Do you know what your doctors estimate your recurrence risk will be if you have a lumpectomy and radiation? Is this risk level one that you can live with or one that scares you? Will you live in constant fear or will you be satisfied that you've reduced your risk sufficiently and not worry about it except when you have your 6 month or annual screenings? If you will always worry, then having a mastectomy might be a better option for you; many women get peace of mind by having a mastectomy. Be aware however that while a mastectomy will likely significantly reduce your local (in the breast area) recurrence risk, a recurrence or the development of a new BC is still possible after a mastectomy. Lots to consider.
- Do you know your risk to get BC in your other (the non-cancer) breast? Is this a risk level that scares you? Or is this a risk level that you can live with? Keep in mind that DCIS cannot recur 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 and this may be compounded if you have other risk factors. Find out your risk level from your oncologist. When you talk to him or her, determine if BRCA 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). Those who are BRCA positive are very high risk to get BC and for many women, a positive BRCA test result is a compelling reason to have a bilateral mastectomy. On the other hand, for many women a negative BRCA test result helps with the decision to have a lumpectomy or single mastectomy rather than a bilateral. Talk to your oncologist. 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 single MX 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?
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I hope that this list is helpful. The thing to remember is that everyone's experience with surgery is different, everyone's pro vs. con list is different and everyone's emotions are different. Additionally, there is so much in this situation that you can't control..... how you feel about your breasts after reconstruction..... whether you have pain from your mastectomy or reconstruction or not... whether the fears you have now, just after you've been diagnosed, will still be as strong in 6 months or 2 years..., etc.. So don't make your decision based on what someone else did or the experience that someone else had or how someone else felt. Make the decision based on knowing yourself. Do what's best for you. Good luck with the decision! -
inks - thanks so much for that information. Yes, I'm going to see the genetic counselor on Monday (does it really take 2 weeks to get the results?). I have BCBS and have been on the phone with them trying to obtain a point-of-contact person. Apparently,my plan does provide a case manager, but they hey just need to find who that person is. I will be sure to ask him or her about all these coverage questions. It's good to know that insurance (in general) covers these procedures.
I met with the PS today. He was okay personality wise (if a bit aloof) but was very thorough and was patient with all of my questions. I hadn't even gotten around to reading up on the two common procedures. The DIEP seems very intense to me, and TE with implants seem scary due to infection/rejection risk. I'm glad I spent the time getting all the information from him, but I'm still waiting on the MRI (and, I guess, the genetic information). Anyway, thank you for your input. And I hope all went well with your surgery and that your chemo treatment is going ok.
Melissa - Thank you so, so much for posting this! This is so very helpful! -
I have BCBS also and they got the clearance for genetic testing and the MRI within two days, they had to work with my primary care office. My genetic test result took about 3 weeks. This will give you lots of time to make good decisions, in hospitals that specialize in breast cancer the outcomes are the same with lumpectomy and radiation as is with MX. My surgeon here in Rochester speaks very highly about MSKCC, he has seen the lectures by those doctors, most up to date treatments. The hospital or breast center that has managed your care so far may have Navigators who can help you with arranging all things and your insurance. -
I started with a plan for a lumpectomy, and due to a second spot they found later, went with a mastectomy. I think that a lot of people choose a mastectomy, especially at our age, because we don't want to go through this again. I didn't want to have a lumpectomy, and then have to go back for a mastectomy if they didn't get it all (or found something else). I am happy with my choice, for 2 independent spots of cancer, a mastectomy was the best choice, and it gave me the option to skip radiation. There is too much to think about, and a lot of choices. Find the things that are most important to you in the decision, and make your choice based on that. -
Ladies - there are so many reasons why you should or shouldn't have a mastectomy, and most are intensely personal.
But please don't make that decision based on the fact that a mastectomy will definitely let you skip radiation. There are no guarantees.
Like Beesie mentioned in her post above, your tumor may be close to the chest wall, or there may be other factors that warrant radiation in addition to a mastectomy. Sometimes you just won't know until that final pathology report. -
I think the choice involves many factors - overall health, lifestyle, emotional factors, etc....
For me the BMX was the obvious choice. I didn't want to go through this again (hopefully). I wanted to be aggressive. My mammogram didn't find my lump so why would I want to do that again??? I had a clean mammogram a few months before I found the 1 cm lump myself. I didn't trust that in the future anything growing would be found with tests. I wanted to do DIEP but I was too thin to be a candidate. I met with two PS's before I did anything and both said the same thing. Neither one would do any muscle involved reconstruction on me either because I am into fitness and teach aerobics. They both indicated that using muscle would probably compromise my quality of life since I am so active. They both recommended TE's and implants. That is what I had done. I am very happy with the results. They look very real and even when I teach my aerobics class in my tight fitting fitness clothes, I look completely normal...you would never know I had reconstruction. I was fortunate to not really have any issues with reconstruction. I know most women do well, but others have had some problems. I also know that if I had done a lumpectomy I would have worried too much about it and wonder if I had made the right decision. That is just my personality type....knowing this further confirmed it was best for me to have a BMX. It is such a personal choice. There is not one right answer...only the right answer for you personally. Make a decision you feel most comfortable with. Good luck!
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mdg - did you do the lumpectomy first for diagnosis reasons or did you have a choice at the time to do a mastectomy? I seem to have a choice to go either way. -
GraceBer -- I had a choice initially -- went for a lumpectomy because I wanted the cancer out and hadn't had enough time to figure out what I wanted to do for reconstruction. As it turns out, my surgical pathology came back complicated and my team subsequently recommended a mastectomy. I also just found out I have DCIS in the other side. So I'm having a bi-lat mastectomy and DIEP recon in December. My rad onc did mention to me that it would be nice to avoid radiation if I could given I'm youngish (in my forties). Having a mastectomy does not always guarantee no radiation, but I had no cancer in my lymph nodes and the cancer was not close to my chest wall, so I was told if I had a mastectomy, I wouldn't need radiation.Good luck with your decision.
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I had a choice and chose lx with reduction on other side, as they thought there was only 1 spot of dcis on the right. The would have gone for rads. After that procedure they found ilc/idc in another spot on right, and a tubular invasive in the tissue taken off the left side. So went back for bmx 10 days later. Tho I could probably have had a one sided mx, I didnt want to wait thru life for the left side shoe to drop, so was glad to have them both off. -
I’m 36. When I first got diagnosed 8.1.2013 I thought I did not have a choice and prepared myself for the double mastectomy. It wasn’t the mastectomy or radiation that scared me, it was the chemo. I went through the whole I will be losing my breast. I had a love/hate relationship with them because they are big and I’m a petite girl who is shy. My mother got BC at 33 was the first case study in our state and had to do double mastectomy with chemo/rads.. My grandmother at 60 and did left breast mastectomy with chemo/rads, and two first cousin who did mastectomy with chemo/rads and both died from BC.
I was shocked when I was given a choice. I did the genetic testing took two weeks for the results my BRCA came back negative, so insurance would only pay for one side mastectomy with reconstruction and reduction in the other side. Insurance is paying for my Oophorectomy. In order for me to see a plastic surgeon it was a week wait. I was still in shock with the BRCA being negative. This changed what I was thinking about now regarding taking the boobs. I opted for a lumpectomy, because I wanted Felix gone. I’m doing chemotherapy now and I might have to go back for a mas/with reduction afterward. My tumor, Felix, is close to the chest wall and right over my heart, so the radiologist do not want to give me boost, so I will be doing 7 weeks of rads after chemo. Of course this could all change after chemotherapy, but right now I’m content of lumpectomy. I didn’t want to spend time in the hospital.
You will need to do some research and talk things through. I kept a journal and made tons of list as to pros and cons. I did a lot of second guessing, especially with chemo. I ran an oncotype test which I should have done the mammaprint test first given my age. They both had conflicting information and it delayed my treatment. I was anger with myself of awhile. One thing a good BC survivor told me is once you make a decision don’t second guess it. She told me that whatever choice I make that is my road, I won’t know what the “other me” path would be like, so let it go. Make your list and try to make peace with the choice. The answer will come to you. -
I had a lumpectomy when I was 20 yrs old and when I had a 6mths mammogram checkup they found more in both breasts so I opted for a bilateral double mastectomy w/ nipple sparring when I was 22. I'm now 23.
There's definitely pros/cons for either option, mostly for the double mastectomy.
eg) Like no more nerve sensation, can no longer breast feed, etc.Personally I think it's up to your own preference and what you are comfortable with.
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