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anti pd1 treatment

Forums General Melanoma Community anti pd1 treatment

  • Post
    starletwoman2007
    Participant
    Hi

    Can anyone using anti pd1 tell me how they are getting on? Is the drug as good the reports say

    Thanks

Viewing 5 reply threads
  • Replies
      Bubbles
      Participant

      I started Nivo in December 2010, in a phase 1, 2 1/2 year trial at Moffit, NED arm, after SRS to a brain met and lobectomy to remove a lung met. So…I was NED at the start and remain so today, 9 months after my last infusion in June 2013. The details of my trial, results and experiences of my arm as well as the sister NON resected arm as I learned them at my visits, along with a lot of melanoma data, are on my blog if you're interested. Yours, celeste

      Bubbles
      Participant

      I started Nivo in December 2010, in a phase 1, 2 1/2 year trial at Moffit, NED arm, after SRS to a brain met and lobectomy to remove a lung met. So…I was NED at the start and remain so today, 9 months after my last infusion in June 2013. The details of my trial, results and experiences of my arm as well as the sister NON resected arm as I learned them at my visits, along with a lot of melanoma data, are on my blog if you're interested. Yours, celeste

      Bubbles
      Participant

      I started Nivo in December 2010, in a phase 1, 2 1/2 year trial at Moffit, NED arm, after SRS to a brain met and lobectomy to remove a lung met. So…I was NED at the start and remain so today, 9 months after my last infusion in June 2013. The details of my trial, results and experiences of my arm as well as the sister NON resected arm as I learned them at my visits, along with a lot of melanoma data, are on my blog if you're interested. Yours, celeste

      sweetaugust
      Participant

      Hi there,

      My primary melanoma was in 2000, 2.0mm deep on my upper right arm.  My melanoma metastesized to Stage IV to a lymph node in my right arm pit in Sept 2012 at 39 yrs old.  The scan revealed that met, as well as several other nodes in my other arm pit, behind my chest wall, wrapped around my heart, and a mass on my liver.

      I was able to get into a clinical trial for the anti pd1, MK-3475. It has been working great for me.  I started MK-3475 (highest dose – every 3 weeks) Oct 31, 2012…and it is now March 21, 2014 and i am doing great.  I am at Dana Farber in Boston.

      At the 3 month mark, all other large nodes shrank to normal and the mass on liver disappeared.  But the met node was aggressive and doubled in size.  At the 6 month mark, my met node blew up and died and now it has been shrinking by about 15% every 5 weeks that I scan.  My most recent scan was two days ago and my met node is now smaller than it was at the beginning of the trial, and nothing else showed up on my scan, so all is fantastic.

      Side effects for me:  Living a basically normal life.  Still working fulltime and feeling good.  Have nausea usually the first week after treatment and then some in the second and third week, but I have still never thrown up.  Have the itchy rash on my chest, neck, and back of head, but it goes away in the summer months.  I get a little fatigue, but really that is probably just from working and my social life.  I just started getting joint pain this week in my hip and shoulder. 

      Otherwise all is great.  I don't take any prescription medications and I try to eat mostly raw organic fruits and veggies to help my body stay healthy. No meat or dairy or refined sugars.   I originally signed up for treatment for 2 years, but back in November they changed it to no end date.

      Laurie

      sweetaugust
      Participant

      Hi there,

      My primary melanoma was in 2000, 2.0mm deep on my upper right arm.  My melanoma metastesized to Stage IV to a lymph node in my right arm pit in Sept 2012 at 39 yrs old.  The scan revealed that met, as well as several other nodes in my other arm pit, behind my chest wall, wrapped around my heart, and a mass on my liver.

      I was able to get into a clinical trial for the anti pd1, MK-3475. It has been working great for me.  I started MK-3475 (highest dose – every 3 weeks) Oct 31, 2012…and it is now March 21, 2014 and i am doing great.  I am at Dana Farber in Boston.

      At the 3 month mark, all other large nodes shrank to normal and the mass on liver disappeared.  But the met node was aggressive and doubled in size.  At the 6 month mark, my met node blew up and died and now it has been shrinking by about 15% every 5 weeks that I scan.  My most recent scan was two days ago and my met node is now smaller than it was at the beginning of the trial, and nothing else showed up on my scan, so all is fantastic.

      Side effects for me:  Living a basically normal life.  Still working fulltime and feeling good.  Have nausea usually the first week after treatment and then some in the second and third week, but I have still never thrown up.  Have the itchy rash on my chest, neck, and back of head, but it goes away in the summer months.  I get a little fatigue, but really that is probably just from working and my social life.  I just started getting joint pain this week in my hip and shoulder. 

      Otherwise all is great.  I don't take any prescription medications and I try to eat mostly raw organic fruits and veggies to help my body stay healthy. No meat or dairy or refined sugars.   I originally signed up for treatment for 2 years, but back in November they changed it to no end date.

      Laurie

      sweetaugust
      Participant

      Hi there,

      My primary melanoma was in 2000, 2.0mm deep on my upper right arm.  My melanoma metastesized to Stage IV to a lymph node in my right arm pit in Sept 2012 at 39 yrs old.  The scan revealed that met, as well as several other nodes in my other arm pit, behind my chest wall, wrapped around my heart, and a mass on my liver.

      I was able to get into a clinical trial for the anti pd1, MK-3475. It has been working great for me.  I started MK-3475 (highest dose – every 3 weeks) Oct 31, 2012…and it is now March 21, 2014 and i am doing great.  I am at Dana Farber in Boston.

      At the 3 month mark, all other large nodes shrank to normal and the mass on liver disappeared.  But the met node was aggressive and doubled in size.  At the 6 month mark, my met node blew up and died and now it has been shrinking by about 15% every 5 weeks that I scan.  My most recent scan was two days ago and my met node is now smaller than it was at the beginning of the trial, and nothing else showed up on my scan, so all is fantastic.

      Side effects for me:  Living a basically normal life.  Still working fulltime and feeling good.  Have nausea usually the first week after treatment and then some in the second and third week, but I have still never thrown up.  Have the itchy rash on my chest, neck, and back of head, but it goes away in the summer months.  I get a little fatigue, but really that is probably just from working and my social life.  I just started getting joint pain this week in my hip and shoulder. 

      Otherwise all is great.  I don't take any prescription medications and I try to eat mostly raw organic fruits and veggies to help my body stay healthy. No meat or dairy or refined sugars.   I originally signed up for treatment for 2 years, but back in November they changed it to no end date.

      Laurie

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