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Brain mets but unknown original source?

Forums General Melanoma Community Brain mets but unknown original source?

  • Post
    azurliene
    Participant

      My dad had (removed 1) two brain mets (recent melanoma diagnosis) but after a full body CT, PET and skin and eye exams, they are still unable to find signs of melanoma anywhere else in his body..

      My dad had (removed 1) two brain mets (recent melanoma diagnosis) but after a full body CT, PET and skin and eye exams, they are still unable to find signs of melanoma anywhere else in his body.. is this the case with anyone els out there? I am thankful he does not have tumors in other organs, but the unknown of it coming from somewhere else but not being able to identify the location scares me… we are dealing with removing the brain mets right now, but for others in a similar situation, did you use a particular drug or treatment to try to prevent tumors from popping up in other parts of the body or did you just monitor the whole body through frequent CT/PET Scans? If so, how often do you have these all body scans?

      I realize the original source can recess and disapear, but this has me extra scared that it is going to pop up somewhere and we are going to realize it quick enough…

      Also, they haven't classified him in a "stage" is this common?

      Than you  for any info/perspectives…this forum is quickly beoming my lifeline

    Viewing 11 reply threads
    • Replies
        azurliene
        Participant

          anybody? ๐Ÿ™

          azurliene
          Participant

            anybody? ๐Ÿ™

            azurliene
            Participant

              anybody? ๐Ÿ™

              FormerCaregiver
              Participant

                Cases with an unknown primary tumour are fairly rare. I remember a friend's husband
                having this many years ago. Here is some info about melanoma with an unknown primary:
                http://www.asco.org/ascov2/Meetings/Abstracts?vmview=abst_detail_view&abstractID=31120&confID=55

                CT/PET scans are normally done according to the schedule that the oncologist feels is
                appropriate.

                If there is no evidence of disease (also known as NED), many oncologists will suggest
                monitoring the situation with regular scans without any specific systemic treatments.

                However, it is always wise to have a plan in place if the melanoma returns. These are
                some treatments that show promise and are worth looking at, depending on
                eligibility criteria and availability: GM-CSF (Leukine) and surgery when needed, Yervoy,
                BRAF and similar inhibitors, IL-2, and anti PD-1 (MDX-1106). I feel that TIL
                treatment (adoptive cell therapy) is the option that may give suitable patients the best
                chance of achieving a durable remission.

                Sometimes the concept of "stage" is not really helpful, and I can see why oncologists
                don't say alot about this. I think that once melanoma cells are present in the
                bloodstream, then it is more helpful to view melanoma as a chronic systemic disease.

                Hope this helps.

                Frank from Australia

                FormerCaregiver
                Participant

                  Cases with an unknown primary tumour are fairly rare. I remember a friend's husband
                  having this many years ago. Here is some info about melanoma with an unknown primary:
                  http://www.asco.org/ascov2/Meetings/Abstracts?vmview=abst_detail_view&abstractID=31120&confID=55

                  CT/PET scans are normally done according to the schedule that the oncologist feels is
                  appropriate.

                  If there is no evidence of disease (also known as NED), many oncologists will suggest
                  monitoring the situation with regular scans without any specific systemic treatments.

                  However, it is always wise to have a plan in place if the melanoma returns. These are
                  some treatments that show promise and are worth looking at, depending on
                  eligibility criteria and availability: GM-CSF (Leukine) and surgery when needed, Yervoy,
                  BRAF and similar inhibitors, IL-2, and anti PD-1 (MDX-1106). I feel that TIL
                  treatment (adoptive cell therapy) is the option that may give suitable patients the best
                  chance of achieving a durable remission.

                  Sometimes the concept of "stage" is not really helpful, and I can see why oncologists
                  don't say alot about this. I think that once melanoma cells are present in the
                  bloodstream, then it is more helpful to view melanoma as a chronic systemic disease.

                  Hope this helps.

                  Frank from Australia

                  FormerCaregiver
                  Participant

                    Cases with an unknown primary tumour are fairly rare. I remember a friend's husband
                    having this many years ago. Here is some info about melanoma with an unknown primary:
                    http://www.asco.org/ascov2/Meetings/Abstracts?vmview=abst_detail_view&abstractID=31120&confID=55

                    CT/PET scans are normally done according to the schedule that the oncologist feels is
                    appropriate.

                    If there is no evidence of disease (also known as NED), many oncologists will suggest
                    monitoring the situation with regular scans without any specific systemic treatments.

                    However, it is always wise to have a plan in place if the melanoma returns. These are
                    some treatments that show promise and are worth looking at, depending on
                    eligibility criteria and availability: GM-CSF (Leukine) and surgery when needed, Yervoy,
                    BRAF and similar inhibitors, IL-2, and anti PD-1 (MDX-1106). I feel that TIL
                    treatment (adoptive cell therapy) is the option that may give suitable patients the best
                    chance of achieving a durable remission.

                    Sometimes the concept of "stage" is not really helpful, and I can see why oncologists
                    don't say alot about this. I think that once melanoma cells are present in the
                    bloodstream, then it is more helpful to view melanoma as a chronic systemic disease.

                    Hope this helps.

                    Frank from Australia

                    lhaley
                    Participant

                      At this point the original primary doesn't matter, it just needs to be dealt with now.   We have several on the board that also have unknown primaries.  

                      Right now I have the fairly large brain tumor but my other PET showed all is clear.  As of this last discussion I am dealing right now just with the brain, nothing systemic.   Now, if the brain doesn't get cleared from either the SRS or a crainectomy (decision being made in 3 weeks) then systemic would be discussed.

                      Their are different thoughts with different Drs but many will not treat without a tumor (stage IV) watch to see if there is a response.  If you read through trials almost all want at least a tumor of 1cm size.  There are a few trials out there like an antipd1 trial in Moffitt, but the person also has to have an hla0201 positve for the vaccine that goes along.   I would have to think that the brain has to have been clear for a certain amount of time.

                      I don't know how often your dad will be given an mri but am assuming his PET scans are every 3 months.  I'm surprised they haven't discussed your stage.  Even though the mel is in only one organ – the brain – I have to imagine he is stage IV. 

                      Right now there happens to be many of us with recent brain tumors.   Scary……   I had been stage IV for 5 years and  was NED (no evidence of the disease) at the time.   

                      Linda

                      lhaley
                      Participant

                        At this point the original primary doesn't matter, it just needs to be dealt with now.   We have several on the board that also have unknown primaries.  

                        Right now I have the fairly large brain tumor but my other PET showed all is clear.  As of this last discussion I am dealing right now just with the brain, nothing systemic.   Now, if the brain doesn't get cleared from either the SRS or a crainectomy (decision being made in 3 weeks) then systemic would be discussed.

                        Their are different thoughts with different Drs but many will not treat without a tumor (stage IV) watch to see if there is a response.  If you read through trials almost all want at least a tumor of 1cm size.  There are a few trials out there like an antipd1 trial in Moffitt, but the person also has to have an hla0201 positve for the vaccine that goes along.   I would have to think that the brain has to have been clear for a certain amount of time.

                        I don't know how often your dad will be given an mri but am assuming his PET scans are every 3 months.  I'm surprised they haven't discussed your stage.  Even though the mel is in only one organ – the brain – I have to imagine he is stage IV. 

                        Right now there happens to be many of us with recent brain tumors.   Scary……   I had been stage IV for 5 years and  was NED (no evidence of the disease) at the time.   

                        Linda

                        lhaley
                        Participant

                          At this point the original primary doesn't matter, it just needs to be dealt with now.   We have several on the board that also have unknown primaries.  

                          Right now I have the fairly large brain tumor but my other PET showed all is clear.  As of this last discussion I am dealing right now just with the brain, nothing systemic.   Now, if the brain doesn't get cleared from either the SRS or a crainectomy (decision being made in 3 weeks) then systemic would be discussed.

                          Their are different thoughts with different Drs but many will not treat without a tumor (stage IV) watch to see if there is a response.  If you read through trials almost all want at least a tumor of 1cm size.  There are a few trials out there like an antipd1 trial in Moffitt, but the person also has to have an hla0201 positve for the vaccine that goes along.   I would have to think that the brain has to have been clear for a certain amount of time.

                          I don't know how often your dad will be given an mri but am assuming his PET scans are every 3 months.  I'm surprised they haven't discussed your stage.  Even though the mel is in only one organ – the brain – I have to imagine he is stage IV. 

                          Right now there happens to be many of us with recent brain tumors.   Scary……   I had been stage IV for 5 years and  was NED (no evidence of the disease) at the time.   

                          Linda

                          azurliene
                          Participant

                            Thank you both – I really appreciate advice, the link and the list of treatment suggestions. The "tumor board" came and said their recommendation for the remaining tumor is "inconclusive" they don't know whether to recommend a 2nd craniotomy or gamma/WBR – we go tomorrow to discuss again. They were also able to get in for a 2nd opinion with MD Anderson in TX on the 14th so trying to decide whether to wait or not and to do surgery or radiation… I'll feel much better once we are able to (hopefully) get rid of this tumor…

                            thanks again

                            Aften

                            azurliene
                            Participant

                              Thank you both – I really appreciate advice, the link and the list of treatment suggestions. The "tumor board" came and said their recommendation for the remaining tumor is "inconclusive" they don't know whether to recommend a 2nd craniotomy or gamma/WBR – we go tomorrow to discuss again. They were also able to get in for a 2nd opinion with MD Anderson in TX on the 14th so trying to decide whether to wait or not and to do surgery or radiation… I'll feel much better once we are able to (hopefully) get rid of this tumor…

                              thanks again

                              Aften

                              azurliene
                              Participant

                                Thank you both – I really appreciate advice, the link and the list of treatment suggestions. The "tumor board" came and said their recommendation for the remaining tumor is "inconclusive" they don't know whether to recommend a 2nd craniotomy or gamma/WBR – we go tomorrow to discuss again. They were also able to get in for a 2nd opinion with MD Anderson in TX on the 14th so trying to decide whether to wait or not and to do surgery or radiation… I'll feel much better once we are able to (hopefully) get rid of this tumor…

                                thanks again

                                Aften

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