Home › Forums › Main Forum › Genotype Specific › Genotype 3 (37%) › Fibrosis/Cirrhosis info corner
- This topic has 8 replies, 6 voices, and was last updated 8 years, 11 months ago by Dr James.
-
AuthorPosts
-
27 December 2015 at 5:42 pm #7381
To the moderator,
I suggest a new topic concerning itself with the latest research, information on the treatment & reversal of fibrosis/cirrhosis. As there is so many of us now cured or on that way. The next & final step is what can I do to repair my liver.
OH WHAT A GREAT THING IT IS TO HAVE QUALITY PROBLEMS !!
So on to the next step remembering the liver is the only human organ that can self repair,
BUT HOW TO HELP IT ALONG.28 December 2015 at 12:03 am #7392Cheers Angus, me too! F4 and cirrhosis 17 years, Treatment is going well with bloods, although I feel worse now after 6 weeks than I did all those years ago on int/rib. But, time will come, in a few months, when I have no virus and can get my poor wrinkly prune of a liver working better. Weight loss for me must help. Am doing well with that.
Genotype 3 30 years, 2x treatment interferon/ribavirin non responder. Cirrhosis 17 years. Fibroscan, decompensating, 40 down to 22 by 29/3/16- now down to 6.5, normal, no cirrhosis. Started Buyers Club Sof/Dac 14 Nov 15. SVR 12 29/0716
28 December 2015 at 1:15 am #7396Hello Hazel,
It will be the Riba making you feel bad. If you read http://fixhepc.com/forum/gt3/369-gt3-high-svr-rates-with-daclatasvir.html you will find an n=468 study (the biggest Sof+Dac study to date) that failed to show any benefit in an subgroup of F3 & F4 GT3 patients by taking Ribavirin. If you are doing 24 weeks this suggests that your results will be equal or better – Riba than + Riba.
Ribavirin has a 1/2 life of 12 days so when you stop it takes 12 days to fall to 1/2 the starting level, 24 days to fall to 1/4, 36 days to fall to 1/8.
I understand why intuitively it might seem “more is better” (and therefore + Riba is better) but the evidence suggests that is not the case.
YMMV
28 December 2015 at 1:24 am #7399will read more
Genotype 3 30 years, 2x treatment interferon/ribavirin non responder. Cirrhosis 17 years. Fibroscan, decompensating, 40 down to 22 by 29/3/16- now down to 6.5, normal, no cirrhosis. Started Buyers Club Sof/Dac 14 Nov 15. SVR 12 29/0716
28 December 2015 at 5:32 am #7408At this point I will be happy if I clear & survive – and the lesions in my liver don’t jettison me into a whole new nightmare.
However the goal posts might hopefully shift – and I agree – it would be good to start developing some evidence based or even compelling alternative data on how the HCV damaged liver, portal hypertension, varices and ascites might be modified and the prospect of HCC inhibited – however, marginally – once they are no longer being fuelled by HCV generated inflammation. good one. archer.
28 December 2015 at 6:13 am #7409Hi Archer,
While only mild C-P/a, I do have the experience of a couple of small HCC (so far successfully resolved) and the basic gist of what my specialist tries to tell me seems to be that clearing the virus and as a result avoiding continuous inflammation and fibrotic activity at the same time as regeneration will significantly reduce the ongoing risk of recurrences although it will require ongoing monitoring. Apparently it should also provide some improvements in the extent of fibrosis and thus cirrhosis over time as long as I look after my liver but he did say the improvement seen varies by case.
So I’m also very interested in the latest developments around optimum liver care post HCV.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
28 December 2015 at 2:33 pm #7435Hi Gaj an Archer,
interesting thoughts. I was F3 in 2012 and I expect while religiously adhering to the “WAIT” my liver would have gradated to F4.
I notice on the med calculator Dr Freeman posted that the chances for SVR for Genotype 3’a’s like me goes from 24:1 with F3, to 9:1 with F3-F4.
Treatment for me being above F3 is twenty four weeks vs 12 weeks for F3.
I hope that getting treated does get the scarring under control a bit as I may increase the odds of a SVR.
Message for people like me aged 60 appears to be get treated asap to get the scarring under control.
yours
J.
28 December 2015 at 5:11 pm #7452Thanks Sabrecat,
That reminded me of a report I read the other week re G3. Basically their comments were that this genotype needs hitting asap with the new DAAs, try to increase metabolic rate, reduce fatty liver disease risks and keep monitoring even non cirrhosis patients post SVR. So not great news but important for us to know.
http://hepatitiscnewdrugs.blogspot.com.au/2015/12/hcv-genotype-3-wolf-in-sheeps-clothing.html
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
1 January 2016 at 8:28 am #7674Happy New Year to you all. May 2016 be extra kind to you.
I have been scrumming through my results over the last 10 months and came across my Fibroscan result. I don’t think the result has ever been explained to me clearly (only that it was “okay” so thought I would run it past those of you that may know what the numbers mean.
Findings: The appearance of the liver is within normal. No focal lesions visible.
AFRI results:ARFI – Median Velocity 1.16 IQR 0.18 The first radiologist
1.15 IQR 0.11 The second radiologistBoth ARFI measurement sets are concordant in the less than F2 range. I was always of the opinion that the Fibroscan was F0 but am starting to wonder now if it was read wrong …….. my GP had not had any past experience in these sorts of scans. I did fax it through to Dr Freeman when I sent all my test results to him but forgot to ask him what it meant.(was too excited about staring my treatment at the time).
Thanks in advance.
YMMV
-
AuthorPosts
- You must be logged in to reply to this topic.