Either the myeloma has suddenly gone crazy, or something else is going on. This blog is titled Myeloma Hope, so I hope that something else is happening, something good.
My doctor ML warned me in advance that the myeloma markers might not even be measured during the first eight weeks of the current study, because they might go wild (and presumably scare the pants off a simple country boy like me). However, until now the measurements have nevertheless been done, hence today's blog about them.
Myeloma is a cancer of some (most) of the plasma cells that live in the bone marrow, but not ALL of the plasma cells - there are still some good ones. Unfortunately there is no way to evaluate the plasma cells (good or bad) without a bone marrow biopsy, and even then you only get the cells at the exact spot of the biopsy - another spot will give a somewhat different result. However, in my case the good and bad cells both generate Immunoglobulin G, a key constituent of any healthy immune system. The IgG measurement includes the immunoglobulins generated by BOTH the good and the bad cells, and M-spike represents just the useless immunoglobulins made by the malignant cells.
The study drugs are intended to help my immune system recognize the malignant plasma cells as intruders and take action against them, so it is possible that the increase in IgG is actually an increase in the GOOD immunoglobulins which are designed to attack the malignant cells. If so, then perhaps the study therapy is starting to work! This notion is somewhat supported by the fact that M-spike remained constant at 1400 mg/dL (1.4 g/dL) for the week, despite the jump in overall IgG.
I say "somewhat" because I don't quite trust the accuracy of M-spike, in part because a week ago it was actually higher than IgG, an impossible result. That has happened before - Dr WG says they "round up" the numbers. In addition, even before rounding up, I don't believe that the numbers have either the accuracy or the precision of the IgG measurement. Nevertheless a steady M-Spike is better than an increase. I'll take it.
Oh, I hope that this therapy works! It is SO easy to take - I feel full of energy every day, and neuropathy from previous therapies (especially the next-previous study) is gradually disappearing.
At the ninth week of the study I will get another PET scan, and then we will know. If it isn't working I have a plan, but I sure want it to work. Week seven is coming up.
