Option for recurence ?

Hello everybody

Can anyone tell me about treatment options for recurence?

Who has made a recurrence of an endometrial adenocarcinoma? How long have treatments controlled your disease?

Comments

  • Sandrine04
    Sandrine04 Member Posts: 76
    edited June 2017 #2
    Nobody?

    Nobody?

  • NoTimeForCancer
    NoTimeForCancer Member Posts: 3,486 Member

    Nobody?

    Nobody?

    Dear Sandrine, I am not sure

    Dear Sandrine, I am not sure if things are getting lost in translation, but there have been quite a few replies by the ladies here who care about you.

    First, for your anxiety, you may want to ask your doctor for lorazapam.  It may help you find a little peace so you can continue your search.  As for your search, maybe you can ask about Keytruda. (may be considered experimental for gyn cancers)  Some of the ladies have had success with it, but as for topotecan - two reported it did not do anything for their cancer.

    I know you had written about hormone therapy.  Was that tried?  I know you said a doctor had suggested it but I am not sure if you started it.  

    Also, takingcontrol58 had written the following on metformin:

    Sandrine,

    Metformin was approved in 1995 in the US for the treatment of diabetes and insulin resistance (prediabetes).
    Gynecologists also prescribe it for patients with PCOS (polycystic ovary syndrome) which is usually caused by
    insulin resistance.  In 2005, researchers learned of its many anti-cancer benefits.  It is an inexpensive, generic
    medication and is considered one of the 100 most essential medicines by the World Health Organization because of
    its safey, effectiveness and low cost. Metformin has been used in Europe for over 50 years.

    It has been shown to be partularly effective for endometrial cancer because endometrial cancer cells have alot of
    insulin receptors on their surface.  I was insulin resistant (pre-diabetic).I had borderline high glucose levels and
    high IGF-1 (insulin growth factor-1), which is a hormone usually raised before the diagnosis of endometrial cancer.  I don't
    understand why most doctors don't test for this hormone.  If you are diabetic and taking another diabetes medication, you
    should switch to metformin because it is the only diabetes drug proven to have anti-cancer beneficts.  If you are overweight or have
    borderline high glucose levels or high levels of IGF-1 or are insulin resistant, you should ask your doctor to put you on this
    drug.   All these are risk factors for endometrial cancer.  Metformin has many other benefits that target the processes that cause
    cancer cells to grow and metastasize and become immune to chemotherapy. Since there are no effective cancer treatments
    that cure metastatic cancer, I would suggest you try metformin.  All 34cm of my metastases disappeared when I started taking
    metformin, without cutting out any organs or getting additional surgery. You have nothing to lose. 

    If you have had surgery, you should ask to get genomic testing on the tumor they removed.  If you did not have surgery,
    you can request Circulating Tumor Cell testing, which will identify gene mutations through a blood test.  Metformin also 
    targets a mutated pathway found in 80% of all endometrial cancers, the P13K/Akt/Mtor pathway.  This pathway regulates insulin.  
    If you have a mutation on this pathway, metformin might be of even more benefit to you.  I had a mutation on this pathway.

    Let me know if you have any more questions.

    Taking control58

    For all of us based in the U.S., we just don't know the best clinic or cancer centers in France or Europe.  (Traveling in Europe is different than the U.S. - traveling 6 hours in one state in the U.S. can take you through several countries in Europe).  Although two of the ladies have gone to Dr. Herzog's clinic in Germany - daylady and editgrl.  

    The lack of response is not that the ladies don't care - we do.  I hope this wrap up of some of the notes I have found on the chat helps.  Unfortunately, everyone is different, so what works for some of the ladies may not work for you - they just keep throwing things at it...I pray they find a cure.

    Dear Sandrine, I am so sorry you are struggling, I don't have anything else to add though and hope this does not come off mean-spirited in any way - I just have search the boards for some of the responses.  

    Hugs dear one.

  • Sandrine04
    Sandrine04 Member Posts: 76
    Notimeforcancer thanck very

    Notimeforcancer thanck very much. 

    Actually it's not easy for me to find myself in the forum even with a translator.

    Keytruda is not in France as treatment but just in clinical trial. Currently there is no clinical trial. must wait..

    My oncologist said that they will try to operate to eliminate cancer. Scanner and irm are not so bad but I have two nodules on the mesentery. Who knows the mesentery?Before the tumors were too large this is the reason why the surgery was a failure.

    Now, after à second chemo. ... Maybe it's possible.

    If the surgery remains impossible then my oncologist will do the analyzes of my tumor to know which treatment is the best

    But I am distressed because I know that treatments are not numerous and that life expectancy is reduced in this case.

    I have two children, a husband ..

    thanks a lot for your help .

     

  • NoTimeForCancer
    NoTimeForCancer Member Posts: 3,486 Member
    Oh dear, Sandrine.  Of course

    Oh dear, Sandrine.  Of course you are distressed - it is completely understandable.  None of us really know how much time we have with the ones we love.  I think those of us who have/had cancer realize how precious it really is, which is why my chemo nurse told me, "Go out and LIVE!"  I am sure you are spending all the time you can with your husband and children and making so many wonderful memories that even if you lived 100 years they will always treasure them close. 

     

  • ConnieSW
    ConnieSW Member Posts: 1,688 Member
    edited June 2017 #6
    Sandrine

    i don't have any information from experience but my heart aches for you and your family. I am hoping your doctors find a good plan. 

  • TAyers
    TAyers Member Posts: 86 Member
    edited June 2017 #7

    Sandrine, I had a recurrence in my right middle lobe of my lung. I had only one nodule which is odd to only get one, but they surgically removed it and then I had the 6 treatments of carboplatin and pacilitaxol. I will get catscans every 4 months to check and see if any other cancer occurs. I can sense your fear and anxiety and will be praying for you.

  • Sandrine04
    Sandrine04 Member Posts: 76
    Tayers thanck very much 

    Tayers thanck very much 

  • Beebster
    Beebster Member Posts: 20

    Sandrine,

    Eight months after finishing frontline treatment (paclitaxel/carboplatin and brachytherapy), a CT scan showed multiple (never did get a count...2, 3 50??) peritoneal tumors and mets to my liver. Lymph nodes were enlarged. No biopsy, the assumption was that it was from my original cancer. I have been on once-a-month (every 28 days) chemo of liposomal doxirubicin/carboplatin, starting last December. I've had a nearly 4-week delay back in March/April due to a low absolute neutrophil count. In fact, my sixth chemo was supposed to be this morning, but my ANC is too low. Very disappointing. We will give it another go next week. A CT scan in March showed that I was having a significant response (no radiographic evidence of the liver mets or lymphadenopathy, and the main tumor in in peritoneal area had shrunk by over 50%. I will request that my 3-month CT be moved up into June (instead of early July). Better to know now if the chemo is continuing to work, or if my cancer has progressed and it is time to move onto something else! 

    I feel great, always have, so that is an enormous advantage in setting my emotional tone for the day. Things to help limit the anxiety/sadness spiral: step outside and breath the air. Listen to birds chirping, traffic going by...go to the farmer's market, call your best friend and ask how their day is going. And, IMHO, be joyful that Emmanuel Marcon is your president! I sure am. Wink

    Beebster

  • pinky104
    pinky104 Member Posts: 574 Member
    edited June 2017 #10

    Sandrine, I am currently in treatment for a metastasis to my paracolic gutter.  The cancer wrapped itself around my ascending colon and went into the muscle in my right hip, and almost into the bone.  I am taking Carboplatin and Gemzar, having a lot of side effects from the Gemzar.  Last time, 7 years ago, I took Carboplatin and Taxol and had very few side effects.  The chemo is much more difficult for me this time.  Last time, I got through it relatively easily.  I was told that might happen since my bone marrow wouldn't react as well the second time that I had chemo.

  • Sandrine04
    Sandrine04 Member Posts: 76
    Hello pinky104 I already had

    Hello pinky104 I already had two chemo protocols (cisplatin / doxoburine and carboplatin / taxol) so now chemo is no longer an option for me.

    I have cancer on the mesentery. I know nobody who had metastasis at this place

     

  • derMaus
    derMaus Member Posts: 558 Member
    Sandrine, refresh my memory:

    Sandrine, refresh my memory: have you had radiation? I have mets in my retroperitoneal lymph nodes adjacent to my mesentary artery, and will be starting radiation in a week or two. Also, you mentioned earlier that language difference can be cumbersome; I wonder if you'd looked at any cancer centers in the Quebec area? I ask that because I Googled and found several French-language website and facilities there. Your English is far superior to my French, so I couldn't quite follow all the details, but I did  think of you when I saw them. You mentioned possibly coming to the States for treatment, so I thought I'd mention Quebec as it's right next door to us...  

  • Sandrine04
    Sandrine04 Member Posts: 76
    Dermaus,  no...i don't have

    Dermaus,  no...i don't have radiothérapy.Thursday I will finish my chemo just carboplatin and on July 26 the surgeon will try to operate me.

    He does not know if it is possible