If you are not Stage IV but have questions, you may post here

Options
1154155157159160171

Comments

  • Bcky
    Bcky Member Posts: 167
    edited July 2019

    ok thanks Chrissy B

  • Houston2016
    Houston2016 Member Posts: 317
    edited July 2019

    Hi everyone, can anyone tell me if weight loss a sign or symptom of recurrence? I recently lost like 5-10 lbs in a couple of months. I recently joined a gym and work out five days a week. However I think it's a short time to lose weight. I don't have any other symptoms. Thank you.

  • Artista964
    Artista964 Member Posts: 530
    edited July 2019

    If it was in a week, I'd be alarmed. Congrats on the weight loss.

  • Anotherone
    Anotherone Member Posts: 633
    edited July 2019

    It is. But as we well know it is a common occurrence unrelated to cancer as well. I think there may be a subtle difference in a weight loss - according to the scales I lost at most 1 kg while many people commented on my weight loss. So the metastatic weight loss is more related to how one looks than objective weight loss. I did not have any other defined symptoms until a month ago either - there were some fleeting ones that now in hindsight make sense.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited July 2019

    Normal weight loss with diet and exercise is one to two pounds per week. Working out five days a week certainly could be the cause.

  • MountainMia
    MountainMia Member Posts: 1,307
    edited July 2019

    This has probably been asked and answered many times in the thousands of comments in this thread, but my big question is, how was your mets found? If not de novo, was it in your normal follow-up screening? Did you have symptoms that led to scans? Is there a difference if it is organ-based mets vs bone mets? Thanks for any help understanding the process.

  • Anotherone
    Anotherone Member Posts: 633
    edited July 2019

    I had symptoms- shortness of breath on exertion, tachycardia and unproductive cough. I started having symptoms very late, my lungs and mediastinum were riddled with large and multiple ones.

  • BevJen
    BevJen Member Posts: 2,523
    edited July 2019

    I had no symptoms and actually felt great both times they found mets (first in 2006, second time in May 2019). First time gynecologist was doing a routine annual exam, and found a polyp on my cervix. She sent it out for pathology, and it was mets. Second time,my tumor markers (CA 27-29) kept going up over the course of about a year, but all scans were negative until a year out. Then they found mets in my liver. I think metastatic breast cancer can present in many different ways.


  • Anotherone
    Anotherone Member Posts: 633
    edited July 2019

    indeed, all depends where and how big

    BevJen , did they do PET scan and did not find liver metastasis during that year?

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited July 2019

    MountainMia, tho the question has been raised before, I always find the answers interesting on how someone's mets were found. I am a de novo gal. I found a lump in left breast six days after my annual mammogram. A biopsy ruled it malignant, then I had a series of dr. appts. to determine course of treatment. Prior to beginning chemo, my onc ordered a bone scan for what she said was a baseline. When that showed suspicious activity, I had a pet scan which reveals bone metastases to rib, scapula and hip

    . I didn't really have any kind of symptoms that shouted “something’s not right!” I was somewhat more tired and took long naps, but I’d always been a napper and I chalked it up to middle age. I also had mild soreness in my hip but also attributed that to age.




  • MountainMia
    MountainMia Member Posts: 1,307
    edited July 2019

    Anotherone, BevJen, and DivineMrsM, thank you for your answers. Even with only 3 of you (so far,) it's interesting and kind of frightening the range of possibilities. I'm not yet done with my (first?) treatment and don't know yet what follow-up will be involved, whether tumor markers will be tracked, MRIs will be ordered based on my dense breasts, or what. My docs seem to be minimalists so I don't have a clue what is their standard plan, or what I should push for. Thanks again.

  • Spoonie77
    Spoonie77 Member Posts: 925
    edited July 2019

    Did anyone experience unexplained weight loss?

    I've been emotional eating due to scanxiety and lymph/neck swelling for the past two weeks, yet in the past week I've now lost 7 pounds.

    Weight loss for me has always been a struggle and I'm definitely not exercising any more than just walking my dog around the block twice a day. In fact, yesterday I ate 4 pop tarts. Yet somehow between yesterday morning and today, I lost 2 more pounds. (total of 7)

    If I lose at this rate I will hit the 6% body weight loss in another week....more than half way to that 12 pound number.

    Color me worried. :/


  • Simone80
    Simone80 Member Posts: 988
    edited July 2019

    MountainMia,

    I found a enlarged lymph node in my neck during a self exam. I had no pain and was quite surprised when they told me it was also in my hip, ribs, and lower back.

  • Simone80
    Simone80 Member Posts: 988
    edited July 2019

    MountainMia,

    I found a enlarged lymph node in my neck during a self exam. I had no pain and was quite surprised when they told me it was also in my hip, ribs, and lower back.

  • BevJen
    BevJen Member Posts: 2,523
    edited July 2019

    MountainMia,

    In response to your question, this was the sequence. May 2018 CA 27-29 up to around 55; had CT and nuclear bone scan -- nothing showed. October 2018, CA 27-29 up to 94. CT and nuclear bone scan -- zippo. Asked for a breast MRI in case it was a local recurrence (although I had a bilateral mastectomy). Nothing. Wrote an email to Dr. Hortabagyi at MD Anderson asking what he would do (although I don't know him at all). He said if it was him, he'd have a PET/CT. Had PET/CT in Nov. 2018 -- nothing. Jan. 2019 tumor markers now at 181. Had consult at Hopkins in February -- everyone said they don't treat on markers -- rescan in spring. May 2019, a "wrinkle" appeared in the CT scan, nothing on nuclear bone scan. PET scan verified the wrinkle, although no one knew what it was. MRI of the abdomen followed -- oops, there it is. One liver met about 2 cm (and it didn't even show up before this???!!!) and maybe about 5 more teeny ones in both lobes of the liver. Liver biopsy also in May of the 2 cm lesion -- ILC, same as diagnosis in 2003!!!!

    Bev

  • Anotherone
    Anotherone Member Posts: 633
    edited July 2019

    Mia , may be markers and full body MRI every 2 years?

    In practice I do not think this regimen will be approved and I am not sure it will be worth for you to spend your money on it.

    Why don't you read "50 things one should do when diagnosed with breast cancer"( the title may be not exact but if you Google it will come up) and just live your life according to it ? I am sure it will beat early detection of metastasis since I believe studies did not show improved survival with early detection

  • MountainMia
    MountainMia Member Posts: 1,307
    edited July 2019

    Thanks, Anotherone. I was just curious about how mets presents itself, and apparently the answer is that it presents in many many different ways.

  • Artista964
    Artista964 Member Posts: 530
    edited July 2019

    The symptomless is scary.

  • BevJen
    BevJen Member Posts: 2,523
    edited July 2019

    Anotherone,

    I've heard that same comment about how it doesn't matter if it's found early. I don't know how much stock I put in that. That assumes that we all have the same end point once metastasis is found. That may have been true at one time when there were very limited treatment options, but I'm not so sure it's true now necessarily. I realize that the American Society of Clinical Oncologists keep repeating that mantra, but when I hear it, I just want to slap them. We need docs who will think out of the box instead!

  • Anotherone
    Anotherone Member Posts: 633
    edited July 2019

    yeah I myself am not sure as it is counterintuitive. But then again by the time they can be detected with tests they would have been there for a while anyway..

    Mine got gigantic before they caused symptoms


  • Anonymous
    Anonymous Member Posts: 1,376
    edited July 2019

    BevJen - so much agreement with you on this quote! -- "I've heard that same comment about how it doesn't matter if it's found early. I don't know how much stock I put in that. That assumes that we all have the same end point once metastasis is found. "

    My view is, even if finding mets or progression early doesn't change overall survival (maybe the only thing they are measuring) are they saying it cannot improve QOL? Like right now...my MO had wanted me to go to yearly scans after not quite 15 months of NED. And I disagreed and said I wanted to scan again in six months. And lo and behold ....one of my spine lesions was active again (lytic) should I have waited until I had a fracture to treat it? Not to mention, what are the consequences of walking around with an increased tumor load...and don't mets themselves metastasize and spread elsewhere?

    It is a balancing act as far as I am concerned. I am in agreement with my doctor about not scanning TOO much, but every six months seems about right to me for now.


    As for how my mets were found, I am happy to tell my story again. I am another asymptomatic gal.

    I had not been going for regular mammograms even though I was at the age that I should have been. A 2 cm palpable lump appeared on my breast out of nowhere in a spot where a smaller lump would have easily been detectable (so to me, it must have grown very quickly).

    I went from diagnostic mammo/ultrasound to needle biopsy with u.s. to consult with surgeon, breast MRI, more US and needle biopsy of two other breast areas. No other cancer found thru the biopsies but the breast MRI showed a suspicious spot on my lung. From there, a PET/CT was ordered and ruled out any lung involvement BUT the scan found a number of bone mets. I went from healthy to Stage 2 to Stage 4 de novo in two months without any symptoms. My first tumor marker tests (CA 15-3 and CEA) taken before beginning chemo were in a normal range.

    Without the breast MRI showing a false positive, followed by the PET scan, I would not have known about the bone mets, at all.

  • vampeyes
    vampeyes Member Posts: 1,227
    edited July 2019

    Question - 5 months ago I had a CT, a cyst was found on my liver and follow up CT was to be completed. Got the results back and of course everything starts with likely.... so likely a cyst on my liver grew very little 0.5 to 0.6, tiny renal cysts, there are some findings that could suggest chronic bowel malabsorption, bilateral ovarian cysts are likely present - this one makes me laugh as I know I have the cysts and they state they are likely follicle, but nope one is and the other is complex. So my question is how the heck do we know if they are actually cysts and not cancer? Why are they not following up to see if they grow more?

    Thanks for any help.

    HUGS

  • BevJen
    BevJen Member Posts: 2,523
    edited July 2019

    Vampeyes,

    Another puzzler from my perspective. When I had my MRI of my abdomen that showed my liver mets this May, that scan also showed some type of cyst at either end of my pancreas. NO ONE has mentioned these since May. I actually forgot about them, intending to ask my MO if I should be seeing a gastroenterologist or someone else. So I don't know the answer to your question or to mine. I'm not sure what warrants a followup and what doesn't -- and how the heck would WE know?

  • Spoonie77
    Spoonie77 Member Posts: 925
    edited July 2019

    Has anyone been dxd with METs to the Thyroid?

    They found a nodule on last week's US due to swollen lymph nodes. Family hx of Thyroid cancer so maybe "just" Thyroid cancer. But am worried.

    TIA for responses.

    It is no longer the time to disregard thyroid metastases from breast cancer: a case report and review of the literature

    "This case report and first review of the literature on metastases to thyroid from breast cancer highlight the importance of a correct early diagnostic work-up in such cases. Indeed, a primary lesion should be distinguished from metastases given the different treatment protocol related to primary cancer and the clinical impact on prognosis."

  • GlobalGal
    GlobalGal Member Posts: 63
    edited July 2019

    Breast cancer mets to my neck's 3 central lymph nodes here--with no evidence of primary breast cancer or other metastases (so far).

    As for the unexplained weight loss mentioned earlier in this thread, a dear friend of mine with breast cancer in remission for 6 years recently started losing a pound a day, despite eating like a stevedore, which set off alarm bells with all her physicians and led to an intense round diagnostic testing/scans.

    Turns out that she went from hypothyroid to hyperthyroid.

    They lowered her thyroid medication and she's all back to normal.

  • Spoonie77
    Spoonie77 Member Posts: 925
    edited July 2019

    Thanks Globalgal! I had no idea a switch from Hypo to Hyper could happen. Good to know for the future. Wish that was my case but my PCP checked my Thyroid labs earlier this week & all is in range. Monday is almost here. Fingers crossed my MO can tell me not to worry

  • Houston2016
    Houston2016 Member Posts: 317
    edited July 2019

    Hi Simone80,

    I also felt like my right side lymph node under my jaw has a little lump while the left side is flat. I've been losing weight 5-10 lbs in the course of 2 months. Which Dr. Do you see about this?

    Thank you

  • Simone80
    Simone80 Member Posts: 988
    edited July 2019

    Hi Houston,

    I went to a head and neck surgeon who has experience with cancer. He did a biopsy the same day. My insurance doesn't require referals. You might need to see your primary first. Good luck to you.

  • mccathyg
    mccathyg Member Posts: 38
    edited July 2019

    I have a question about when you are considered stage IV. I have just been dx with my 4th recurrence. It is obvious that conventional treatment is not working and I have progression. Just not sure if I am now classed as stage IV because my recurrences are in same area. I don’t know why it is important but I think because of the treatments I am now investigating. With every recurrence my knowledge of treatments increases...

    Thanks and love to everyone....

  • chrissyb
    chrissyb Member Posts: 16,818
    edited July 2019

    Hi mccathyg. The term Stage IV is applied when cancer recurs outside the breast. The bones, liver, lungs and brain being the most common but can also occur in the peritoneal cavity and in the plural. If your recurrences are all in the same breast then that is still the lower stage.

    Hope this helps.

    Love n hugs. Chrissy

Categories