new hopeful her2neu trials

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hopefultreatment
hopefultreatment Member Posts: 5
new hopeful her2neu trials

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  • hopefultreatment
    hopefultreatment Member Posts: 5
    edited May 2012

    Check out this hopeful new trial starting soon thru mayo/tapimmune, and possible game changer



    http://www.youtube.com/watch?v=TobrcGEyzbo&feature=youtube_gdata_player

  • hopefultreatment
    hopefultreatment Member Posts: 5
    edited May 2012

    More information about the agreement, which will soon lead to trials: 

    http://www.tapimmune.com

     Looks very promising! Going to watch this intently as it progresses!

  • Joanne58
    Joanne58 Member Posts: 1,117
    edited April 2012

    This looks very promising, especiallly as I think of my 3 daughters' future.  How I hope they can escape my dx with the help of a vaccine like this--wow!  Thanks for posting good news :)

  • hopefultreatment
    hopefultreatment Member Posts: 5
    edited April 2012

    I agree and hope the same for your daughters :)

     Let us hope this works out:

    "The existing products in the market don't go the same pathway and so they're not as effective; and so we think that with our other approaches to HER2/neu, we'll have a real advantage and give us a leading position in development of a vaccine for HER2/neu -- both for therapeutic and hopefully in the future, prophylactic."

  • joyful57
    joyful57 Member Posts: 3
    edited April 2012

    This is my very first post and not even sure if i am posting in the correct place but here goes.  Just began my treatment of chemo with herceptin this past Thursday.  My cancer is her2 positive so I am very hopeful knowing what I have learned just recently about the sucess of herceptin.  I will receive TCH for 6 treatments every 21 days followed by radiation for 5 weeks.  The herceptin will continue for a year.....I was diagnosed in March 5th after a mastectomy.  Four of my nodes were positive also.  If any of you have advice as this is so very new for me, I would appreciate.  Coping very well thus far but understand I am about to hit a brick wall within  a day or two.  We will see!!!!  I am most competitive, even with myself so I am fighting this......thanks girls!!!!!

  • Joanne58
    Joanne58 Member Posts: 1,117
    edited April 2012

    joyful--sounds like you have a good attitude for chemo, which will carry you through the down days you may have.  I think you'll have more good days than bad (just my hunch), so enjoy those good days before the next tx (treatment) and know that the time goes by and you'll be done in a few months. 

    Herceptin alone is a breeze for most of us.  Runny nose seems to be the most common SE--no big deal.

    I will always be grateful for the sisters who led the way here on this forum, and now people like me can assure those starting out like you that it will be OK--you can do hard things!  ;) 

    Best to you, jp!

    --Joanne

  • joyful57
    joyful57 Member Posts: 3
    edited April 2012

    Thank you Joanne for your reply.  I couldn't wait to arise to see if anyone would have written me.  And there you were!!!!  The power of technology is wonderful!!!!!  Feeling good again today so I am up early ready to take on the day.  Mom and sister visiting tomorrow for a night with me from out of town so about to plan the menu.  Every day is a good day when feeling well enough to carry on.  The sun is shining here so all is good.  Enjoy your day too.!!!!!!!

     jp 

  • Joanne58
    Joanne58 Member Posts: 1,117
    edited April 2012

    Wow, joyful!  I'm impressed that you're planning a menu for your visiting family!  So glad you're feeling well enough to do this, but I'll bet they insist on helping ;)  Enjoy your mom and sister!

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited May 2012
    Hey joyful !!  Come join some of us gals on the April/May Chemo Lounge Hangout on the Chemotherapy section.  I had my first chemo round a week ago (6 rounds of Taxotere/ Cytoxan every three weeks plus Herceptin for a year).  I'm in the Herceptin B-47 clinical trial to determine whether low HER2 patients benefit from the receipt of Herceptin.  Normally, I would not have received Herceptin as a part of my chemo but I was randomized under the study to receive the Herceptin.  At any rate, please come visit the chemo thread where you will find lots of wonderful gals, support and a place to vent since that part is good for the soul.  HUGS to you!!!!
  • hopefultreatment
    hopefultreatment Member Posts: 5
    edited May 2012

    oops, sorry, here is the link again:

     www.tapimmune.com

  • LoriKnous
    LoriKnous Member Posts: 80
    edited May 2012

    @joyfull57 This is also my first post. In April of 2007 I was diagnosed with a her2neu pos. breast tumor. My treatment was as follows. Adrimiocin/Cytoxin 6 rounds x3wks. Then Taxol/Herceptin for 12 wks. Then I had a mastectomy with clear margins and 12 lymph nodes removed. All said to be clear. Radiation and finished my Herceptin in Sept. of '08. Everything was fine until Jan 2012. I had blood in my urine so the Dr. visits began again. In March I was told by the Dr.s that my cancer had returned. It is settled in my bladder/ovary area and acities (fluid in the abdomin) had set in.......all the way to my lungs. My suggestion is to talk to your Dr. about staying on Herceptin. It seems to be the best fighter of this type of cancer.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2012

    Joyful, sounds like you might be triple positive. Join the triple positive thread. Lots of good info.



    I just started a phase 2 vaccine trial for her2+ early stage people. I go to Wake forest medical center every three to four weeks for the vaccine/placebo. Hope it turns out to be something positive.

  • LoriKnous
    LoriKnous Member Posts: 80
    edited June 2012

    @Fluffqueen0...Is this the new medication that was just released for Her2Neu+ ?

  • SpecialK
    SpecialK Member Posts: 16,486
    edited June 2012

    Lori - here is the vaccine link - I am in the same one as fluff but I go to Sibley Memorial (Johns Hopkins) in Washington, DC.

    http://clinicaltrials.gov/show/NCT00524277

  • LoriKnous
    LoriKnous Member Posts: 80
    edited June 2012

    Thank you SpecialK, gonna check out the info.

  • LoriKnous
    LoriKnous Member Posts: 80
    edited June 2012

    Just heard of a new drug for Her2neu+ cancer. Not sure of the spelling but, it was refered to as Projetta. I haven't been able to find anything online, has anyone else heard anything about it, or the propper spelling? I have an appointment with my Dr. on Monday and chemo to follow so I am going to ask everyone.

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