The Long-awaited Results …
I know many of you have been waiting anxiously to hear back on the results. We have been so busy the last few days trying to juggle normal life (work, school etc. with the appointments with the doctors) that it has been difficult to share this information any earlier with anyone.
Here’s a quick summary:
First the good news:
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The bone marrow biopsy indicated that there are 6% plasma cells in the marrow (down from 11%), however more importantly, there are no monoclonal cells in the sample taken indicating no trace of myeloma cells. We need to remember that this was a sampling from one area of the bone marrow and hope that it’s true for all of the marrow.
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There appears to be no further damage/lesions to Alpesh’s bones etc. However, the damage that has been done is unfortunately significant but with time and the right medication, he might be able to repair the bones.
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Cycle 4 blood work shows no trace of the M protein in his blood at all!
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All the heart/lung tests were normal – so nothing new to worry about. Thank Goodness!
The not so great news
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Unfortunately the plasmacytomas did not shrink. The one in the sacrum is the same size but is not pressing against any bones/nerves so is not causing the pain and limp that it initially caused. The one near the lung is now three different smaller tumors (it was probably always 3 tumors but they could not see the definitions before). This is actually good news because these appear to have shrunk a little.
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Dr Lonial and Dr Z both concur that this is nothing to be too alarmed about since they may have limited “hot spots” now (active myeloma cells) within the tumors so they may just be dead tissue that will be in Alpesh’s body forever. They won’t do any harm but will probably calcify at some point.
The Gameplan II (at the moment anyway)
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We will harvest Alpesh’s stem cells in February as planned. The cells will be stored if Alpesh needs to do an autologous transplant in the future.
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Alpesh will have a Pet Scan to determine if there are any hot spots in the tumors. If there are any, both Dr Lonial and Dr Z recommend using radiation therapy to “zap” them once and for all to kill active myeloma cells. They are pretty confident that this will be achieved.
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Alpesh will then do another 4 cycles of chemo using the same drugs as before, Revlimid, Velcade and Dexamethasone to kill off any microscopic myeloma cells that might be still be in his body after the radiation.
This is a very top line summary of what the doctors have indicated. In general the news is very good. Even though the tumors are still there, the doctors are confident the radiation will kill off the cells so we feel very hopeful. If Alpesh can sustain the next four cycles, Dr Lonial and Dr Z both have suggested that he may go into remission. For how long? We are not sure but it will at least buy us some time and that is what we need.
Alpesh’s spirits are up – the bone marrow results were a real bonus for us. No monoclonal cells and no trace of the M protein in his blood – Wow!
Thank you all for your thoughts and prayers…..I think you’re being heard.
[by Sima]
January 22nd, 2009 at 9:46 am
Sima,
Thank you for all these updates. I had a long talk with Alpesh about a month and a half ago on the phone (don’t know if he told you) and told him how much inspiration he has given me and so many other people over the years. He continues to inspire everyone around him now with this battle. I read through these posts and I find it hard to keep from breaking down when I think about what your family and he are going through. This disease always seems to strike those of us who least deserve it…
Rachel and I offer our prayers and thoughts to your family in this most difficult time, and we continue to be inspired by Alpesh. He is a special guy, and I’m sure you are very proud of him. This last post is encouraging, and more proof that he is going to pull though this as we all know he can.
Warmest Regards,
Bob
January 22nd, 2009 at 1:25 pm
Sima,
This is good news indeed. My wife and I, and members of our church that I have shared this with pray for you each week and I can assure you the prayers are heard. I told Alpesh last week how impressed I was with your information and management of the communications to us. You are doing a wonderful thing keeping us posted and helping us all learn and begin to understand the circumstances you, Alpesh and the boys are experiencing. As you know, you can always reach out if you need anything.
Best wishes,
Darrell