Tumor Markers, Ibrance or Xeloda

Curlysue50
Curlysue50 Member Posts: 22

I been on Ibrance and Faslodex since December 2016 (dx Stage IV in October 2016). My tumor markers have steadily gone up to the high 400s. My question has anyone experienced tumor markers increasing with Ibrance and Faslodex? I feel fine and normal other than the fatigue from lowered hemoglobin from Ibrance. My new onc had wanted me to originally start on Xeloda. Anyone had Xeloda and success with reducing tumor markers? I'm scheduled for a rescan in May.

Cheers from Chicago

Comments

  • susan_02143
    susan_02143 Member Posts: 7,209
    edited April 2017

    Sue,

    Ibrance did absolutely nothing for me but make me too ill to enjoy life. At the 6 month scans, it was clear that my cancer was not fooled by Ibrance even a little bit so we moved on to Xeloda. I found it to be far easier on my system, and it worked for 14 months. Before the Ibrance I maintained NED status for 5 years on Faslodex so obviously our cancers respond differently to these treatments.

    Susan [who once had curly hair too]

  • cive
    cive Member Posts: 709
    edited April 2017

    Curlysue, I'm only on my second round of Ibrance/faslodex and after the first round my TMs went from 1700 to 3000.  My MO and I agreed to finish the second round just in case it is tumor flare.  I feel fine except for being a little tired and my liver tests are now back to normal.  My MO was talking zeloda or havalan if we continue to see rapidly rising tumor markers.

  • Curlysue50
    Curlysue50 Member Posts: 22
    edited April 2017

    Cive

    Are your tumor markers the 27-29?

  • zarovka
    zarovka Member Posts: 3,607
    edited April 2017

    Curly - My tumor markers doubled in the first 4 months on Ibrance and then leveled off. During that 4 month period, my tumor load decreased by 85%. I am at cycle 16 and doing well, but once my tumor markers stabilized, I stopped seeing any more reduction in tumor load. This is a protocol that takes 6-9 months to kick in. Be patient if you can. Wait for scans. Unfortunately, your tumor marker increase could be advancing disease or dying cancer and there is really no way to know without a scan.

    >Z<

  • SandiBeach57
    SandiBeach57 Member Posts: 1,617
    edited April 2017

    My TM Ca15.3 declined on AC and continued to decline on 3 cycles of Ibrance/Letrozole. It is now 67. Will see next week what TM is doing on 4th cycle. How is tumor load measured?

  • zarovka
    zarovka Member Posts: 3,607
    edited April 2017

    By tumor load, I mean, the number and size of tumor. I had 5-7 lesions less than 2cm's in my liver. They are barely visible now. I had some impacted lymph nodes, also gone. The primary tumor remains, but a fraction of its original size.

    >Z<

  • Deborajoy
    Deborajoy Member Posts: 3
    edited April 2017

    please tell me something positive ... I am about to start war on cancer with ibrance and amidrex . stage IV breast metastised no chemo ,no rrad, no surgery...just ibrance and arimidex.. pray for me i'm a newbie with hope. 2nd occurance now IV.. I'm scared but trust OCO should I ?

  • cive
    cive Member Posts: 709
    edited April 2017

    Yes Curley tm is ca.27-29.

  • SandiBeach57
    SandiBeach57 Member Posts: 1,617
    edited April 2017

    Thank you Zarovka for explaining the terminology "tumor load".

    Deborajoy, there is a good topic titled "Ibrance" in the Stage IV section that might help your anxiety. It was started by a lovely woman named Hope, who sadly left us last year. I would go back about 6 months as there are quite a few posts. It has helped me as I was diagnosed Stage IV in Oct 2016 and started Ibrance/letrozole in Jan 2017. I have completed 4 cyles (following IV chemo AC) and it has really helped with tumor death.

    Sorry you are here, but the folks on BCO community are very supportive.

  • bigbhome
    bigbhome Member Posts: 840
    edited April 2017

    Deborajoy, been on Ibrance and Letrozole for 18 mos. Have done well! Chin up, smile on and power thru. I hope out works for you.

    Know this group is the best for support! I have only been on a few days but have already gotten great tips on managing se of radiation. Great supporters!

  • BetzPrit
    BetzPrit Member Posts: 3
    edited December 2017

    [A little back story: I suddenly became severely anemic in January. Whist trying to find the cause of the anemia, they did a bone marrow biopsy which showed the metastasized breast cancer. This was in April. It was a shock as no one on either side of my family had ever had any type of cancer. In fact, I'd had a mammogram in June of 2016 which was completely normal. February of this year I'd had an ultrasound of the breasts . . . no cancer found. But in April, my HGB was 8.5 and I had to have two packed red cell transfusions. My mammogram and ultra sound still showed nothing, and the PET scan showed no active tumors, but when they did a 3D mammogram, they found a diffuse tumor on the distal side of the right breast, and two malignant lymph glands in the right axilla. They have not done surgery.]

    I have Stage IV Metstatic Invasive Lobular Pleomorphic Carcinoma of the Breast. I was diagnosed in May 2017. I began Letrozol and IBRANCE in June. My tumor marker was 400. I was on 125 mg of IBRANCE. I was on it for three weeks and off for one week. Had my labs done in July and the WBC was down from 4.8 to 1.3 and but my HGB was up to 9.7 and my tumor marker had fallen to 176. So my doc told me to hold off of the IBRANCE for one more week, then I restarted it with a lower dose (100 mg.), which I took for 3 weeks, then I was off for one week. The only side effects I've noticed are some slight thinning of my hair, a small growth of black stiff chin hairs, and my voice deepening from Soprano to Tenor (due to the estrogen blocker).

    In August at my follow-up appointment, my tumor marker was 109.2. The HGB was up to 11.2 and the WBC was up to 3.0!!!

    In September my tumor marker was 78.6, my HGB was 11.8, and my WBC was still 3.0.

    In October my tumor marker was 55.5, my HGB was 12.5, and my WBC was still 3.0.

    Nov. 2nd my tumor marker was 45.2, my HGB was 12.1 and my WBC was 3.6.

    Nov. 30th, my tumor marker was 41.2, my HGB was 12.2, and my WBC was 2.9 (a bit worrisome).

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