Blood clots (pulmonary embolism) and stage 4 MBC

erikaknew
erikaknew Member Posts: 11

Anyone else develop blood clots along the way with our diagnosis? I went to the hospital last month for chest pain on my right side and they found 2 small blood clots in my left lung. Now I'm on lovenox injections for life. When I asked my oncologist how this happened he said it's a side effect of cancer.

What? No one told me about this. Should cancer patients get screened for blood clots then? I'm thankful for the pain on the right side then because I would have never known.


Comments

  • blainejennifer
    blainejennifer Member Posts: 1,848
    edited December 2017

    There's not a whole lot of reliable data on cancer and clotting; it's mainly anecdotal. I was familiar with it from the veterinary world, so when I was diagnosed with stage 4, I started on one baby aspirin a day. My MO is OK with that dosing.

    The bright side is that all those blood thinners seem to impair a tumor's ability to establish a good blood supply.

    I'm so glad you got through the episode without any major harm. You are a smart patient.

  • erikaknew
    erikaknew Member Posts: 11
    edited December 2017

    Thsnks Jen and I think we should all be doing the aspirin regimen or something as preventative. The blood clots scare me more than the cancer does be honest.


    That's good to know about the blood supply and tumors. I'm going to research that some more. It's just more to add to the list of stressful things. Now I feel like a hypochondriac. Every little thing I'm wondering if I should go to the hospital. SMH.


    Thanks for reading and responding!!

  • Kkrenz
    Kkrenz Member Posts: 100
    edited December 2017

    I just had a pulmonary embolism two days ago..MO is blaming tamoxifen...I also have clots in both arms. MO thinks I need to be on a blood thinner for only three months. Interesting about tumor blood supply. I am going to research that as well. I wish everyone a pain free weekend

  • erikaknew
    erikaknew Member Posts: 11
    edited December 2017

    Interesting. I was on tamoxifen as my first line of treatment after stage 4 diagnosis. It stopped working in June. Switched to ibrance and letrozole. Failed after 3 cycles now I'm on Ibrance at a lower dose of 100mg and falsodex.

    I didn't ask what caused it was just told that it comes with cancer. But 3 months sounds better than for life. Learning to give myself injections has been tough and I have to remember to take it the same time every day which I'm not always good at.

    I'm having chest pains in the center of my chest but I've been in bed all day so maybe that was it. I'm up now eating something. But I'm hopeful for an uneventful weekend.

  • Lula73
    Lula73 Member Posts: 1,824
    edited December 2017

    so I’m not stage 4 but did end up with DVT and bilateral PEs from the tamoxifen just 2 months after starting it. Discovered as My left calf was cramped terribly for days (unfortunately it was cold & rainy and I chalked it up to that) and then taking a deep breath became increasingly uncomfortable followed by just regular breathing causing chest/shoulder pain. Lovenox given in the hospital and then discharged on Xarelto. Used lovenox as a bridge before a liver biopsy and before hysterectomy & stage 2 recon. Every doc I’ve seen (ER doc, Hospitalist doc, MO, IM, OB/GYN, BS & PS) all agree the standard is 6 months of therapy on blood thinners even though the clots are typically not visible on imaging at 3 months.

    Kkrenz--I’d ask just to be sure if 3 months of therapy is the gold standard and if not why aren’t they recommending the tried and true for you.

    Erika-did your doc say why you couldn’t take Xarelto or Eliquis instead of Lovenox? The needles in the lovenox shots are crappy and cause pain and bruising. (I deal with insulin needles that length and shorter and the lovenox manufacturer has a lot to learn about making subcutaneous injections comfortable). The only thing I’ve heard anyone mention as a differentiator safetywise is they can reverse the effects of lovenox with potassium...but it still takes 1-2 days. And it takes 1-2 days for the Xarelto or Eliquis to leave the system simply by just not taking it so it’s 6 of 1, 1/2 a dozen of the other. If your MO prescribed it that may be the issue-I learned far more from the IM & ER dr about blood thinners than from my MO. Just trying to look at options so you don’t have to inject...

  • MelissaDallas
    MelissaDallas Member Posts: 7,268
    edited December 2017

    I got PE with ovarian cancer before my surgery or any treatment and was told cancer predisposed me to it. I was tested for all kinds of clotting disorders & had none. Can't take prophylacric tamoxifen or Evista now

  • erikaknew
    erikaknew Member Posts: 11
    edited December 2017

    A place for those managing the ups & downs of a Stage IV/metastatic breast cancer diagnosis. **************Please respect that this forum is for Stage IV members only.*********There is a separate forum For Family and Caregivers of People with a STAGE IV Diagnosis.

  • erikaknew
    erikaknew Member Posts: 11
    edited December 2017

    A place for those managing the ups & downs of a Stage IV/metastatic breast cancer diagnosis. Please respect that this forum is for Stage IV members only. There is a separate forum For Family and Caregivers of People with a STAGE IV Diagnosis.

  • Kkrenz
    Kkrenz Member Posts: 100
    edited December 2017

    Lula-thanks for the info...I will enquire at my next appt. I suspect three months only because the clots were very small and essentially asymptomatic. The only reason they were found is that I was experiencing dizziness, so I went through a whole series of scans to ensure adequate blood supply as well as no brain mets. Thankfully....no brain mets. I can deal with small clots. I will have another series of scans in 3 months. Stage 4 folks are monitored very closely. My MO is also a hematologist. Have a good weekend.

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