Hep C Discussion Forum

Members Login
Username 
 
Password 
    Remember Me  
Chatbox
Please log in to join the chat!
Post Info TOPIC: Question about treatment


Guru

Status: Offline
Posts: 3398
Date:
RE: Question about treatment
Permalink  
 


Hi again Ranelle,

To decide whether you can wait for treatment, you need to know how much liver damage you have. I'm afraid a blood test ( probably FibroSure or FibroTest) isn't very reliable. You need a liver biopsy or Fibroscan to get an accurate picture. These are the only tests accepted by the Drug Companies in assessing patients for Trials. This is more important than viral load or liver function tests. Good luck.



__________________

Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm



Guru

Status: Offline
Posts: 895
Date:
Permalink  
 

Hi Nurschic,

I am also 1 million in viral count, and had all the blood tests and scan. Despite this my doctor insisted I have a biospsy as the deciding factor to treat or wait for new DDAs. There are cases of people that have normal test results and still have fibroses. Good luck with your decision, personally I am warehousing until next year. x

 



__________________

Genotype: 3b

VL.�over 15, 000 000

Failed TX 2014: Interferon/Riba.

Cured using Sof/Dak combination.

I can eat cake again! <3 



Senior Member

Status: Offline
Posts: 143
Date:
Permalink  
 

I have never had a liver biopsy. a long time ago did have some blood work completed that  my doctor said showed liver damage just like a biopsy. I forget the name of the test. hoping that the blood work that I got done on Monday has that same test in it. My genotype is 1a.

i have just over a week to my dr appt to review labs and do treatment teaching. I'm nervous yet getting excited about the end results. 



__________________

Dx:2007; Genotype 1; VL 1.4mil, start triple therapy (peg/rib/inc) 6/2/13 (Failed), Harvoni 12 weeks EOT undetected, 6 month EOT UNDETECTED!



Guru

Status: Offline
Posts: 3398
Date:
Permalink  
 

Hi Ranelle,

The Viral Load can vary greatly. Yours is moderate. As JoAnne said, a liver biopsy is the best way to check how much liver damage you have. That is more important than the VL level.

Do you know your Genotype? That may make a difference in any treatment decision. Get as much information as you can. Good luck.



__________________

Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm



Guru

Status: Offline
Posts: 1077
Date:
Permalink  
 

Have you had a liver biospy?
It gives an accurate evaluation
Of the condition of your liver.
That's the gauge I used in determining
To do treatment. VL doesn't tell enough.
Are your enzymes above normal?
Biospy gives facts!
Best wishes to you and glad you found
The forum. It's great bunch of people going
Thru same thing....


__________________

JoAnne

Genotype 1a, Triple therapy w/Invicek started May 19, 2012

DET 4 wk. UND 2,6,12,24 48 treatment. Achieved SVR 2013!



Senior Member

Status: Offline
Posts: 168
Date:
Permalink  
 

With the current RX's, a lower VL does appear to clear quicker but that dosen't indicate weather SVR will be acheived. Many members have gone UND in 4 weeks only to have the virus return once treatment ended. As for weather to treat now or to wait, that's a question only you can answer. There are some really good Rxs now on the market, for the most part they are "ugly" drugs, but pretty effective. If you can wait a few years, there look to be some very promising drugs in testing now that may have minimal sides. Best of luck to ya.



__________________

KCCO

 

 



Senior Member

Status: Offline
Posts: 143
Date:
Permalink  
 

I was wondering, does someone that has a fairly low VL (in the 1mil) do better on treatment? My dr keeps saying that I could wait on treatment if I want, but why wait if if my chances are better?



__________________

Dx:2007; Genotype 1; VL 1.4mil, start triple therapy (peg/rib/inc) 6/2/13 (Failed), Harvoni 12 weeks EOT undetected, 6 month EOT UNDETECTED!

Page 1 of 1  sorted by
 
Quick Reply

Please log in to post quick replies.

Legal Disclaimer:

THIS FORUM, IT'S OWNERS, ADMINISTRATORS, MODERATORS AND MEMBERS DO NOT AT ANY TIME GIVE MEDICAL ADVICE AND IN ALL CASES REFER ANYONE HERE TO SEEK APPROPRIATE MEDICAL ADVICE FROM THEIR DOCTOR.