Forum Replies Created

Viewing 15 posts - 16 through 30 (of 66 total)
  • Author
    Posts
  • in reply to: DAAs and Liver Cancer Risk #21904
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    Hi Gaj, thanks for your efforts about clarification of such things. Possibly, some waiting for more confident data may be an appropriate decision for many people with compensated cirrhosis.

    I agree with most of your doubts about confidence in study’s statistics. Really, group is quite small, and HCC incidence may vary according to disease severity, age… Probably, HCC rate in group of young compensated cirrhotics will be lower than in group of old sub/decompensated cirrhotics. There are many people with child B cirrhosis in group – it is unlikely that such people are interferon eligible. Hence, interferon-treated group, in average, is more helathy than DAA treated group – such difference may affects HCC rate. Five of the nineteen relapsed, probably, is not an issue, because they are “subgroup with HCC” of full cohort. Real SVR rate in full cohort may be much higher.

    Another small study – http://dx.doi.org.sci-hub.cc/10.1016/j.jhep.2016.07.027 – “High incidence of hepatocellular carcinoma following successful interferon-free antiviral therapy for hepatitis C associated cirrhosis” 4 HCC ocurrence per 54 patients – 7.4% rate. 7.4% rate is quite high – 1:13 chance. Nearly 30% of HCC recurrence rate from other studies seems extremely high… From the other side, some studies do not show increased HCC rate – http://www.natap.org/2016/EASL/EASL_76.htm Results of studies seem contradictory – probably, time will tell…


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: DAAs and Liver Cancer Risk #21903
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    Hi beaches, I wish you to achieve SVR with your therapy!

    Yes, cirrhosis is something like time bomb, and question is – whether cure is worse than disease or not. I have some problems with joints too (not very serious), some sleep disorder – but i am not sure that HCV is a cause of such problems instead of other factors… Some of my friends have much more serious joint problems without HCV infection. Really, if i correctly understand, “medical evidence” for many “extrahepatic manifestations” of HCV is not very strong.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: DAAs and Liver Cancer Risk #21869
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    Hi Gaj,

    My concern is – if DAA treatment increases HCC risk (compared to “no treatment”;), then, whether benefits of treatment outweigh its harm “in long-term perspective” or not? It seems, that data from studies look like little bit controversial…

    I was diagnosed with HCV-cirrhosis in 2005 and up to now cirrhosis is compensated, and i had not events of decompensation (such as ascites, variceal bleeding, HCC etc.) My lab report (regarding to liver function) is not worse than in 2005. I feel relatively good and not sure that SVR “itself” will sufficiently improve my health… Of course, i want to achieve SVR (and already bought generics for the therapy), but possibility of increased HCC risk after DAA treatment is my main worry. Good managing of HCC requires good medical facilities, it may be difficult for many people in my country. Hope that, really, DAA treatment is not increases HCC risk.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: DAAs and Liver Cancer Risk #21864
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    A possible question is – whether DAA treatment increases probability of getting HCC for cirrhotics (comparing to “no treatment”;) or not? If yes, then things may become complicated… 6.6% per year for treated and 5.2% for people with SVR (data from http://www.journal-of-hepatology.eu/article/S0168-8278(16)30271-9/fulltext) may seems quite high. Survival with beginning (MELD < 11) compensated HCV-cirrhosis may seems as 80% for 10 years (http://www.nature.com.sci-hub.cc/ajg/journal/v104/n5/abs/ajg200931a.html). If i correctly understand, with annual 5.2% (if these data are correct), probability of getting HCC with SVR after DAA treatment during 10 years may be close to 50% for cirrhotics.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: DAAs and Liver Cancer Risk #21804
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    “Unexpected high incidence of hepatocellular carcinoma in cirrhotic patients with sustained virologic response following interferon-free direct-acting antiviral treatment” – http://www.journal-of-hepatology.eu/article/S0168-8278(16)30271-9/fulltext

    Unfortunately, there are two cases of occurence of HCC after sof-dac treatment on russian-spoken forum, without previous history of HCC.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: Sofosvel (velpatasvir) #21627
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    Hi beaconbdd!

    Thank you for information. Could you please clarify your current price for Sofosvel medication?

    Best wishes,
    Serg


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: SVR 24. détected again #21599
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg
    jeanmarc wrote:

    I finished my 3 monts treatment with twinvir 6 months ago and got a non detected result!
    yesterday I got the result of my new viral 6 months after EOT and it’s detected again :(
    So what I should do now ?
    Thank you

    Sorry to hear this. Firstly, I think it is better for you to retest PCR in different good laboratory. In my country (Russia), quality of lab analyses often is not best, and many “false positive” PCR results are registered on internet forums.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: G1a relapse #21467
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg
    tweakmax wrote:

    just read the updated aasld guidelines 7 july 2016. Sof+vel+riba for 24 weeks is good for retreatment, regardless of ravs, according to studies by prof gane.

    Please be careful there – this study supports 24 weeks of sof/vel/rib after failed 4-12 weeks of NS5A (vel) containing regimen – http://www.natap.org/2016/EASL/EASL_11.htm .

    We need data from studies about retreatment with sof/vel after failure of 24 weeks course of sof/dac or sof/led. If such data will be good, then sof/vel generics may become “second line” therapy for relapsers after 24 weeks course.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    in reply to: Reduction of liver fibrosis without antiviral treatment #21317
    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg
    Price wrote:

    HCV RNA Persists in Liver Explants of Most Patients Awaiting Liver Transplantation Treated With an Interferon-Free Regimen.

    http://www.ncbi.nlm.nih.gov/m/pubmed/27373513/#

    Is this correct that liver explants, mostly, were analyzed by PCR before the treatment cessation, at the time of transplantation? If yes, then these findings do not prove that virus persists in liver after SVR12.

    We assessed the presence of hepatitis C virus (HCV) RNA in liver explants from 39 patients awaiting liver transplantation who were treated with an interferon-free regimen and had undetectable serum HCV RNA at the time of liver transplantation.

    only 6 patients (15%) had finalized the treatment course at the moment of LT (mean time off-treatment 25 days [range 6-61]).


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    Full article is available via sci-hub: http://dx.doi.org.sci-hub.cc/10.1053/j.gastro.2016.06.025


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg
    Price wrote:

    Serg, I also think that you need to take into consideration whether you treated and failed treatment previously because studies have shown that may impact their health in the future.

    Yes, of course.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    fitz, I did not wrote that “Big Pharma dispenses treatment to everyone”, please do not ascribe to me such thoughts. I will skip some your “ad hominem” arguments, but i agree that these discussed things about “semantics” may seems like some “offtopic” there… And, anyway, we cannot change current “semantic” in this area.

    Best wishes,
    Serg


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg
    Gaj wrote:

    LFTs within nominal range that drop on treatment is evidence of that.

    If i correctly understand, LFTs and PCR are signs, not symptoms. A quote about such things (really, i dont agree with all statements of this relatively old article):

    let us consider the difference between signs and symptoms. Signs are typically abnormal blood tests; these are the tests that doctors order to monitor patients. Some signs measure the degree of inflammation (such as enzymes called aminotransferases, known by patients as “ALT” or “AST”). While the ALT or AST test is often called a “liver function test”, it really does not measure any function that the liver performs, but simply assesses the presence of liver cell damage. It is more appropriately denoted as a “liver enzyme test”. The other test (sign) that we need to consider is the one that measures the number of hepatitis C particles that are present in the blood (known as “viral load” or “viral titer”). Traditionally, the success of treatment has been measured by the absence of detectable viral particles in the blood at least six months after the therapy has been stopped. This prolonged clearance of virus from the blood stream is known as a “sustained viral response” or SVR.
    Symptoms are the things that affect the quality and quantity of life; it is the development of symptoms that concerns patients. Symptoms of liver failure include internal bleeding from dilated veins (called varices), excessive fluid accumulation in the legs (called edema) and abdomen (called ascites), and slowing down of thinking with confusion and even coma (called hepatic encephalopathy). Another symptomatic complication of cirrhosis is the development of hepatocellular carcinoma.
    The point is that if only the enzyme tests remain abnormal, and symptoms of liver failure never occur, there is no clinical “dis-ease”. Treatment is irrelevant because it is impossible to make an asymptomatic patient feel better and, at the time of treatment, patients do not have symptoms of end-stage liver disease.

    (http://www.news-medical.net/health/Hepatitis-C-treatment-no-benefits-and-possible-harm.aspx)


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg
    Gaj wrote:

    Errr….Google says that TTW is a computer game that can get infected with the SHuer3 virus??? (Take one subscription to Norton annually. ;) )

    Oh, i am sorry for error – of course, TTV virus, not TTW. :)


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

    Serg
    • Topics: 4
    • Replies: 66
    • Total: 70
    • Recovery Champion
    • ★★★★
    @serg

    Serg, If you don’t believe you have a disease, may I ask what benefit or purpose there is to your participation here?

    fitz, I have F4 (cirrhosis) – hence, i definitely have a disease.

    Your argument seems to be that the only rationale for treatment, or credible indicator of ‘disease’ would be if one is actually dying of cirrhosis – which is exactly the operative assumption of Big Phama and Big Insurance for denying treatment to Hep C patients until one is by their definition “sick enough”.

    No, i dont think this way. If treatment is “prophylaxis” of cirrhosis/extrahepatic manifestations – people should have full rights to prevent cirrhosis/extrahepatic manifestations – whether they are sick or not.

    Rather, semantics of “hcv is a disease in every infected”, “everyone must undergo treatment”, and “achieve a cure” may be promoted by Big Pharma for maximizing their profit. If we can convince infected people that they are all “sick” – it is much simple to sell him medication with huge prices, than sell prophylactic drugs to healthy people.


    Probably infected in 1977
    2005 – diagnosed with HCV 1b, compensated F4, 15 mln viral load, ALT 320
    2005-2006 – PegIFN/rib 48 weeks treatment, relapse
    2016 – compensated F4, MELD 8-9, ALT 100-160
    2018 – compensated F4, MELD 8, ALT 91

Viewing 15 posts - 16 through 30 (of 66 total)