Home › Forums › Main Forum › Experts Corner › Viral Load and SVR › Viral Load On Treatment – What To Expect
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31 December 2015 at 9:59 am #7625
Hi Jill,
Yep definitely the disease progression can be unpredictable – main reason in my decision to jump on tx just in case, despite being F0
if you haven’t had a fibroscan, i understand.
GT1a since 1988, diagnosed 1990
F0, tx naive
VL 262,000 ALT 40 AST 26 GGT 13 Fibroscan 04/12/15 – 2.9
Started Mesochem sof/dac 12 weeks 01/01/2016
11/02/2016 – 6 weeks UNDETECTED
AST 26
ALT 2631 December 2015 at 10:53 am #7632Yeah I agree zhuk, even if fibrosis is low, it’s still in there doing damage.
In fact, it’s doing harm all over your body ,
so get into battle mode & get the b@stards!!
x
J the young dragon slayer is:
HepC 1a since birth
Male aged 15
VL 2000000
Started Twinvir/ 10-11-15-then Sof/led.
NO sides so far !
after one week VL : 37
after 4 wks VL : UND !
EOT 2/2/16 UND.!
4 wks. post tx results….pending….
7/3/16 VL result : 4 week post tx: SVR !
12 weeks SVR !
24 wks SVR yeeaa!!31 December 2015 at 11:11 am #7633You said it Cindi – it affects numerous body systems. Be interesting to sift out which symptoms are the hep & which are other stuff…gotta say I’m curious to find out
I’m thinking of tx like machine gunning the virus…for personal preference an M60 lol. Let the battle be joined!
GT1a since 1988, diagnosed 1990
F0, tx naive
VL 262,000 ALT 40 AST 26 GGT 13 Fibroscan 04/12/15 – 2.9
Started Mesochem sof/dac 12 weeks 01/01/2016
11/02/2016 – 6 weeks UNDETECTED
AST 26
ALT 2631 December 2015 at 12:17 pm #7636”James-Freeman-facebook” wrote:2) The advice re prolongation of treatment based on HCV viral load monitoring is incorrect. There is no relationship between on-treatment monitoring and treatment outcome (assuming high level adherence, as in clinical trials). In fact, many patients in clinical trials have had “detectable” HCV RNA at end-of-treatment and still achieve sustained viral clearance. There is clearly no relationship between week 4 (or other timepoints) and sustained viral clearance, so extending treatment duration (as we did with interferon-based treatment) does not make sense in the interferon-free era..
Thank you Dr. James.
This is one of my major concerns. If 12 weeks is enough to cure hep C in my case. You pointed out very clear that there’s no need to the prolongation of the treatment based only on viral load during treatment.
By the way mine VL was big at the beginning. That’s why I decided to get rid of the viruses.
But being on generics is important at psychological level to check if treatment is going in the right direction. illy:' />
HCV since I don’t know. Diagnosed in 2010.
GT1b, F0/F1, VL 9M, ALT 44, AST 42, Tx naive,
started 12 wks Twinvir on 06.12.2015. Feeling great and grateful 🙂
virus not detected 06.02.2016 & SVR24
isaing4@gmail.com3 January 2016 at 3:12 am #7854By the way mine VL was big at the beginning.
In the ION-3 trial (Harvoni GT1, naive, non cirrhotics)
http://www.hepatitisc.uw.edu/page/treatment/clinical-trials/61
It was observed that SVR rates were nearly identical for 8 weeks vs 12 weeks treatment where the initial viral load was < 6 million.
YMMV
3 January 2016 at 12:55 pm #7880My gastro said that the few viruses I had left would be killed off by my immune system. Extended treatment wasn’t necessary. So far my immune system ain’t done right by me so I decided to extend treatment for a few more months. Maybe that’s why I am having some health problems but I will deal with them as they arise. No more virus for me after 42 years.
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