Follicular Transformed to Diffuse B Large Cell..Scared

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  • catwink22
    catwink22 Member Posts: 281
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    Me too

    Hi Christine,

    I was just wondering if you received your 2nd opinion? I too was just recently diagnosed with DLCL after having been treated for Follicular w Rituxan only, but I have mutations so I am considered "double hit". I was originally scheduled to start R-Chop but they changed my chemo to Hyper-CVAD the night before. It sounds as though you have had many more complications. I too suffered for almost a year with hip pain & they told me it was muscle spasms. Looking back I was so relieved I didn't want to believe anything else. I have a large tumor that has done bone damage. The not knowing what to do or are we doing the right things, or are the right choices being made are the hardest parts for me. There are so many success stories here & they are so inspiring. Thank you everyone for sharing your stories it does make us stronger.

  • Brazzi2008
    Brazzi2008 Member Posts: 1
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    Very anxious as well

     Had non-Hodgkin's lymphoma and transformed into diffuse large B cell. On my fourth chemo treatment and everything seems clear so far. Very thankful there was none in my bone marrow or any of my organs. Still, very scared and unsure about the future, but keeping all my trust in God .   I really believe I am going to beat this and encourage you to believe the same. Cancer is no longer a death sentence, however it is a challenge. Keep yourself positive and trust in the Lord. You can't beat this. They are recommending that I get a stEm cell transplant to increase the chances of it not coming back.

  • Max Former Hodgkins Stage 3
    Max Former Hodgkins Stage 3 Member Posts: 3,812 Member
    edited January 2017 #24
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    Scanexity

    Brazzi, cat, misujih,

    A regular here about three years ago coined a term for the fear of relapse that we all have: "Scanexity"; anxiety during annual or periodic follow-up scans.  I am not certain of the writer, but believe that it was Roc.

    mis, Follicular is indolent, as you  know better than me, and the indolent strains are more prone to repapse; I know, having had NLPHL, which is an indolent HL that has an approximately 15% relapse rate after full remission.  And this can happen 10, 15, any number of years later.  I focus on the fact that these numbers mean also that the disease has an 85% liklihood to not relapse. In the cancer world, that is astronomical.  The late and great Pennsylvania Senator Arlen Spector's first lymphoma was NLPHL....he had two subsequent relapses in differing strains, all spaced far apart, before his end.

    Brazzi, your attitude is the best, and the perfect way to face an uncertain medical future.  We lymphomaniacs do not die from lymphoma so much as we live with it.  But this is not to say the life is easy.  It is also not to deny the reality of dying:  20,000 a year in the US are taken by lymphoma. But among the millions living with it,  this seems like better chances than most cancer patients have.  My indolent strain has a high relapse rate, and like many indolent strains, also commonly comes back as a more aggressive form: usually either a large-B or, a leukemia.   If it ever does recur (I am lymphoma-clean going on seven years now) I do not think I will fear death, but rather dread the amount of work and disability that salvage treatment involves.  I would recommend that you do substantial research before deciding on a SCT.  Newer modalities for many forms of relapsed lymphomas work as well and are less draconian than SCT.

    Wishing the best for all,

    max

  • lindary
    lindary Member Posts: 711 Member
    edited January 2017 #25
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    SCT

    Max is right about researching the SCT. I was all set to start SCT after the collection. However we ran into problems during collection. After 2 days they had collect barely 1/3 of what they wanted. We went in for a third day of collection but the Dr stopped it before it started. My platelets had kept dropping and the counts that mroning were too low to continue. So the Dr. decided to put it on hold (this was the second time that was done). Two months later they did what was the 3rd set of scans after my RICE treatments had ended. The scans came back clean. A month later the SCT Dr told me they were taking me off the SCT list. Recommendation was to do the 2 years of Rituxan maintenance. When I asked about the stem cells that had been collected she told me that they had been frozen but chances are if the cancer comes back there will be newer drugs and treatments.  I am not really sure why the Dr decided to not do the SCT but I am glad to be going down the road I am on. I just hope for the best.

     

  • ggraphix
    ggraphix Member Posts: 4
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    Transformation

    Our family doctor saw "cancer" in my husband's abdomen in Oct 2014.  A CAT scan of his abdomen, done to fine the cause of an unexplained fever, showed multiple enlarged lymph nodes.  She came to us in tears with the diagnosis and sent us up to Huntsman Cancer Institute in Salt Lake City.  Earlier that year, he had a stage 1B melanoma removed from his right thigh, followed by an epic infection that took 2 months to heal.  We had to make the appointment for the abdominal cancer in the dermatology department, because our doctor assumed that it was relapsed Melanoma.  The Oncologist had a couple of radiologists look over the scan, and they said it was "nothing", that the lymph nodes were the same size they were on his April 2014 scan, and not to worry about it.

    In October 2016 he was having trouble eating.  He was complaining that food was getting stuck going down.  I took him to the ER, and they admitted him.  Assuming it was a bleeding ulcer (there was blood in his urine by then), they did a biopsy, which came back as DLBCL with a "triple hit". He had MYC, BCL2, and BCL6 mutations.  He went back to Huntsman, this time to Hematology, and has just finished 2 long cycles of CODOX-M/R-IVAC.  He came through the treatment alive, but with side effects.

    From everything I've read, I'm convinced that he did have some sort of indolent lymphoma in 2014 that transformed.  His doctors (HEM) refuse to look at the earlier scans done in 2014 (DERM) at the same hospital, saying it would not make a difference.  I think they are just trying to protect their collegue.

     

  • Max Former Hodgkins Stage 3
    Max Former Hodgkins Stage 3 Member Posts: 3,812 Member
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    ggraphix said:

    Transformation

    Our family doctor saw "cancer" in my husband's abdomen in Oct 2014.  A CAT scan of his abdomen, done to fine the cause of an unexplained fever, showed multiple enlarged lymph nodes.  She came to us in tears with the diagnosis and sent us up to Huntsman Cancer Institute in Salt Lake City.  Earlier that year, he had a stage 1B melanoma removed from his right thigh, followed by an epic infection that took 2 months to heal.  We had to make the appointment for the abdominal cancer in the dermatology department, because our doctor assumed that it was relapsed Melanoma.  The Oncologist had a couple of radiologists look over the scan, and they said it was "nothing", that the lymph nodes were the same size they were on his April 2014 scan, and not to worry about it.

    In October 2016 he was having trouble eating.  He was complaining that food was getting stuck going down.  I took him to the ER, and they admitted him.  Assuming it was a bleeding ulcer (there was blood in his urine by then), they did a biopsy, which came back as DLBCL with a "triple hit". He had MYC, BCL2, and BCL6 mutations.  He went back to Huntsman, this time to Hematology, and has just finished 2 long cycles of CODOX-M/R-IVAC.  He came through the treatment alive, but with side effects.

    From everything I've read, I'm convinced that he did have some sort of indolent lymphoma in 2014 that transformed.  His doctors (HEM) refuse to look at the earlier scans done in 2014 (DERM) at the same hospital, saying it would not make a difference.  I think they are just trying to protect their collegue.

     

    Similiar

    Your husband's case, in a very general way, is somewhat similiar to mine: I have so many issues, that doctors cannot grapple with all at once, and focus on just this or that.  But your husband's case is so convoluted that, most likely, it will never be known when he contracted what, or why.

    The only positive approach is to address what is known now, and move forward as aggressively as possible. Your last sentence is conjectural, and would have the doctors operating in a highly unethical manner, fortunately something that I have never encountered myself.

    max