Is she for real!! After Treatments
Just got out of my oncologist office for a three month check up after starting Tamoxifen and to my great surprise I was given information that I never expected!!! and was wondering if someone could tell me if they were told the same thing...
My oncologist told me that I would not be having follow up scans because if "my cancer comes back it would be a non curable cancer and there would be nothing they could do beyond that" Is she for real?? is this normal proceedures?? I can't believe that I will only be having one Mammo every year and even that shouldn't it be every 6 months? I though it was regular practice to have a yearly scan?
If someone has answers for me I would greatly apreciate them
(Sorry for the grammar and spelling, I am french)
Thanks
Jo
Comments
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Perhaps the protocol is different in France, if that's where you're being treated. I've never heard of any oncologist in the U.S., Canada, or the U.K. saying that if the cancer came back there would be nothing to be done. Just check on the boards here and you'll find many, many women being treated for metastatic cancer, and doing very well.
In most cancer centers, whether scans are recommended depends on the seriousness of the breast cancer. And the frequency of checkups also relates to the seriousness of the original diagnosis. I had a Stage 1a breast cancer, very early, so only needed mammograms once a year and saw my oncologist every six months for the first few years. I never had any scans. But I know that most women with more advanced cancers are seen every few months and do have regular scans and more frequent mammos. If scans show any spread of the cancer, aggressive treatment is usually initiated immediately.
Perhaps you should seek a second opinion.
Barbara
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Jo, I don't have any routine scans. My docs told me that the survival rate in the case of recurrence doesn't change whether you find something on a scan or it shows up clinically. That does not mean that there is nothing they can do to treat you.
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Hi Jo,
I don't know what kind of bc you were dx with, but I was dx with stage 2 DCIS 0/4 nodes and I also am on tamoxifen ...but I was told that I would be followed very closely for a few years. I recently had pap smear and ultrasound because I had a bit of vaginal bleeding...my doctor said it was nothing but better to be save than sorry. I also will be having mammograms on my left breast every 3mths and every 6mths both breasts. I'm in Canada and that is the routine follow up here...I can't say for Europe, but if you are questioning it I would get another opinion. It is your health and you have the right to know.
Good luck
Lucy
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Jo,
I too had Stage I and have never had a scan. In the first year, I had appointments every 3 months with my oncologist and almost as many with my breast surgeon. As of July (a year and 3 months after mastectomy) I was "graduated" to every 6 months. I have mammo and ultrasound once a year on my remaining breast, and MRI of both breasts once a year halfway in between mammos.
The U.S. National Comprehensive Cancer Network (NCCN) Guidelines for treatment of breast cancer say that CT and PET scans are not routinely recommended in early stage cancer -- only if "symptoms or other findings suggest that cancer may have spread to other organs." Also, "PET scans may be used to initially evaluate patients with metastatic or recurrent [their emphasis] breast cancer, or... if results of other tests do not clearly show whether the cancer has spread beyond the breast to other areas of the body."
A small study reported last November strongly supports combined CT/PET scan followup for women who have had inflammatory breast cancer (IBC).
But in general, for early stage breast cancer, the radiation exposure and costs of CT/PET scans are not warranted for routine follow-up when there is no other suggestion of recurrence or mets.
I hope what your onc MEANT (but obviously failed!) to communicate is what Tina/abbadoodles said: that the treatment and survival rate are the same if recurrence/mets is discovered by symptoms, or earlier on a scan. It's certainly not true that "nothing can be done" -- there are treatments that can be given.
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Hi, Jo. I had IDC, Stage II, no nodes involved, ER/PR+. I'm on Arimidex.
Once a year, I get:
1. mammo and ultrasound
2. MRI of the breasts due to my breasts having dense tissue.
3. bone density (because of the Arimidex)
My onc sees me every 6 months and that is because I'm on Arimidex. My breast surgeon told me she would see me once a year for the rest of my life. My breast surgeon usually does her own ultrasound of my breasts when I'm in there as well, in addition to the one they do at the time of my mammogram.
I have never been given a PET scan and probably would not unless I had a complaint.
Good luck to you!
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I had all the tests right after diagnoses. I had a CT scan of chest and abdomen, bone scan (different than bone density), MUGA (to see if my heart was strong enough for chemo). Then when the CT scan came back it showed something on my liver. I then had a CT/PET scan..it was nothing. After chemo, mast and rads and more chemo I haven't had anymore scans. Only have mammo once a year. I did not have reconstruction. I go to a well known hospital, Duke, and they don't do MRIs even though my breast is dense. I would only get scans if symptoms occur. I had 5 positive nodes out of 7 with extranodal extension (means cancer escaped the nodes). For me, I don't want routine scans. It would cause more anxiety for me. I'm hoping you misunderstood your oncologist. There is many things to do if one gets metastasis. You either need her to clarify what she meant, or seek another opinion.
Shirley
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Everyone here has clarified it pretty much. Just to go a step further...
Studies were done on women after tx. Some women were regularly scanned, the other group was not. The women that had regular scans actually had shorter life spans, due to the anxiety and stress that comes along with testing.
As the girls above have said, I think your oncologist was trying to say that whether you found a bone met through a scan, or found it by breaking a bone, it wouldn't change your statistics for survival.
And we all know that statistics, are just numbers. Most of which are outdated.
A good rule of thumb is the two week rule. If you have a pain that is constant for two weeks, then you should call your oncologist.
As far as mammo's every 6 months or every one year, you can alternate those appts with seeing your breast surgeon for an ultrasound, that way, you're covered throughout the year.
There is a good thread, treatment is over, now what? info... you may want to read it.
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Hi Jo and everyone,
I am really glad to see this post and maybe someone else can benefit too by bumping it up.
Earlier this week, I cancelled a bone scan that my oncologist ordered simply because I cannot handle the stress of it right now (I flatly refused a CT scan). I feel absolutely fine and have no symptoms-- he just all of a sudden ordered it in December, after I had been told several times that I would not be having post-treatment CT or bone scans. I suffered a lot of anxiety because of this sudden about-face at the cancer center, and I was not given a reason why. (no complaints about symptoms, no red flags, etc.) I have to wonder what kind of $$$ the cancer center gets for the scans, even though they are done off-site at a radiology center across town... plus, just prior to that, my state insurance announced they would probably be broke at the end of the year... hmm, strange coincidence!
Thanks for listening and best wishes to all!
Mary Jo
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Jo,
My onc. says the same thing that Abbadoodles dr. said: that he doesn't do regular scans, as the survival rate is the same if a recurrence is found based on scans or if it's found based on any se's we have... example, if I have a pain, and have a test which confirms a recurrence.
Mary Jo,
Hmm... that sounds suspicious to me, too! If your onc. said that they won't do scans, unless you were having any se's, I would be inclined to refuse the scans, too. We don't need any more stress, and worrying about test results causes me way too much stress! Good to hear from you, glad that you are doing great!!
Hugs
Harley
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Hi Harley!
I'm so glad to hear from you and you look absolutely great!! I bet it is gorgeous today down in your area of NC-- it is a sunny 66 degrees here today, and would you believe it was a freaky awful 4 degrees this past Tuesday morning!
Thanks for your encouragement-- this is one time that I have gone with my gut feeling, instead of second-guessing myself. And you are so right about our stress level! I have also thought about the stress level of my husband, kids, and parents-- they don't need it either, because they've all been right here with me thru it all. The additional radiation and radioactive junk they put in the body concerns me too.
This may sound nutty, but I would be very interested to hear from someone in-the-know as to if and how doctors and cancer centers benefit financially from ordering scans from a separate facility...
Hugs back to you!
Mary Jo
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Erica-
I got to a Breast Center at one of the oldest, premier teaching hospitals in Chicago, ranked consistently in the top10. I was dx'd 10/2006 w/lumpectomy followed by ACT-H and rads. Have finished all as of Mar. 2008. Was told I will have mamms 6 mos., then possibly dropping to every 12 mos. Onc. appointments @ 3 months now, will drop to 6 mos. THAT'S IT. No counting, scanning, etc. Just "call us if you have symptoms that persist for more than 2 weeks." At first it bothered me, but I think now that that continuous stress of testing may be something I really won't miss.
Dona Nobis Pacem,
Beth
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My onc told me the same thing -- no scans unless a symptom presents.
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