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The week my Neutrophils dropped my WBC was 1.7. When I re-tested a week later (last week), my WBC was 2.1 but the lab screwed up the test and they could't do the Neutrophils. I'm hoping a rise in WBC correlates with a rise in Neutrophils. We'll see this week but your experience is reassuring.
My doc doesn't prescribe Procrit until the Neutrophils, Absolute drops below 500. I understand some may prescribe earlier, maybe around 750. Above that, it really isn't necessary, so why put it into your system. Good luck!
Talk to the doc about having them monitor your serum response to the Neupogen to keep you on the minimum number of shots needed for an acceptable ANC/WBC level. In my case there reached a point where I was told to do two shots a week, and knew that it was overkill. So I asked to be cut back to one, and that worked out fine until the end of my tx.
As far as being cautious with the low ANC levels (neutropenia), the generally accepted belief is that there is no great need to be worried about your immune system being overwhelmed by some outside invader (see - <a href="http://www.hcvadvocate.org/hepatitis/About_Hepatitis_pdf/1.1_Hepatits_C/Neutropenia.pdf">Neutropenia during combination therapy of interferon alfa and ribavirin for chronic
hepatitis C</a>.(from the paper: "<i>In conclusion, neutropenia is frequent during treatment of hepatitis C with interferon and ribavirin, but it is not commonly associated with infections.</i>") and <a href="http://www.hivandhepatitis.com/2003icr/DDW2003/docs/052803g.html">Neutropenia Associated with HCV Therapy May Not Be Associated with Serious Adverse Events</a> (from the paper: "<i>(2) Infectious [serious adverse events] generally did not occur at the time of nadir ANC.</i>") and <a href="http://www.natap.org/2003/hepUpdate/day5.htm">
Threshold for neutropenia in the adjustment of interferon treatment in HCV infection</a> (from the paper: "<i>Based on these preliminary data, it can be concluded that the onset of neutropenia during combination therapy with interferon and ribavirin is not associated with subsequent infection, even in patients with post-hepatitis C cirrhosis.</i>")). Rather, the more common concerns are of longer and slower healing times and of lessening resistance leaving one open to lingering low-level maladies that may not fully resolve until the interferon is ended and the ANC rebounds.
Here's some further reading on managing sx's during tx: <a href="http://www.ccjm.org/PDFFILES/hepadOng.pdf">Managing the hematologic side effects of antiviral therapy for chronic hepatitis C: Anemia, neutropenia, and thrombocytopenia</a>.
TnHepGuy
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Thanks for the advice and links.
Re "monitoring" are you talking about WBC and Neutrophils Absolute, or some other blood tests? Also, how often did you have your blood tested when you started the Neupogen?
Right now I have major bloodwork done monthly, but I'd imagine I should have at least my CBC done weekly once I started Neupogen, at least until I stabilized.
My first shot occured early on - at week 5 - and they monitored my CBC weekly thereafter for the next few weeks (eventually switching to every two weeks). This first shot was a temporary 'boost' (of sorts), as my overall ANC trend numbers were going down, but hadn't yet consistantly hit rock-bottom. Between weeks #5 and weeks #22 I did only a couple more shots, but it became inevitable that at some point I would be on it for good. (It was also inevitable given that the reason I was taken off of mono interferon tx way back in 1993 was due to low ANC and WBC). Starting at week #30 (having been on Neupogen full-time by then) they switched me to doing bloodwork every 4 weeks (with a six week gap actually taking place on my last one (from week 42 till week 48).
As far as my experience with the sx's go, I didn't have any for the first couple of shots. But by the third one or so, I came to realize that with every shot I would feel the bone pain and fatigue the following day. Others who have been on it have no sx's or less severe ones - very individual.
But more than anything else, I was very grateful to know that it (Neupogen) was available for me to be on to maintain full-dosage interferon - and to make it the full 48 weeks. I believe the biggest crisis I experienced was at the week #5 point, when my GIPA wanted to lower my dosage rather than allow me to wait a few more days (over the weekend) to get Neupogen delivered. It was a crazy, wild, stressful and hectic few hours - but I was able to find a vial (actually 10) and avoided any dose reduction or skips.
TnHepGuy
I see the difference between wbc and nuetrophils. Thanks for responding.
TnHepGuy_,
Well again thanks for the sites. I also found your information helpful to my experience. I'll be on shot 15 this weekend and most likely will start on neupogin after I see a Hematologist.
I have heard that mono therapy (interferon) was a real bear. Is this the same tx that was/is given to cancer patients?
As far as the shot. I had some bone pain and can't tell if I had more fatigue than usual. I pretty much feel incapacitated anyway.
Good luck to you,
-cbee
Hope you are doing well otherwise.
Scott