Hep C Discussion Forum

Members Login
Username 
 
Password 
    Remember Me  
Chatbox
Please log in to join the chat!
Post Info TOPIC: Pegasys, Riba and Sovaldi nest week...New here...


Member

Status: Offline
Posts: 9
Date:
RE: Pegasys, Riba and Sovaldi nest week...New here...
Permalink  
 


Hope4: I also have always asked my gastro docs if I should wait or not. Five years ago, the opinion was to wait (low vl, no symptoms). This year I was told to do it (still low vl, but starting to climb). My gastro felt the success rate in the 90 percentile was worth 12 weeks. Now that I am done, I am glad to have gone this route. My body is still ridding itself of the meds (low TSH, and platelets), but that should correct itself in a few weeks.

__________________


Guru

Status: Offline
Posts: 1724
Date:
Permalink  
 

Huey wrote:

Actually you can get better, the margin of error can be eliminated thus giving you 100+ the margin , making it 101% or whatever the margin of error is.

Just being a smartelic, evileye


Actually you can get better than 101%.  It can not only cure your virus but when you are done you will look like Brad Pitt or Angelina Jolie (in their prime)!

Just being a wisecracker.  Huey, you remind me of my brother.  Always the smart aleck except he also cracks jokes in the MOST dire situations.  He's lucky nobody has killed him!



__________________

Diagnosed in 2011, Incivek triple in 2011, tx discontinued, Genotype 1a, CT, VL 7mill, cirrhosis dx in 2012, age 67, waiting for new DAAs.



Guru

Status: Offline
Posts: 678
Date:
Permalink  
 

Isiscat2011 wrote:

The best SVR rates are with Sovaldi/Ledipasvir.  For gt1, tx naive, non-cirrhotics, the SVR rate is 100% in clinical trials.  You can't beat that. 

http://www.gilead.com/news/press-releases/2014/6/gilead-announces-phase-3-data-showing-that-the-fixeddose-combination-of-ledipasvirsofosbuvir-achieved-100-percent-sustained-virologic-response-svr12-among-patients-with-chronic-hepatitis-c-in-japan


 Actually you can get better, the margin of error can be eliminated thus giving you 100+ the margin , making it 101% or whatever the margin of error is.

Just being a smartelic, evileye



__________________

  HCV Genotype 3a , now Psot-Tx was on S/riba. First VL was 5.8 mil on 7-5-13 then "und" at 3.8 weeks. 06/13/14 still und. off meds 3 days back on 7/29 Last pill 08/10/14 SVR+4

 



Senior Member

Status: Offline
Posts: 292
Date:
Permalink  
 

absolutely - but that will not be an option for us until October the earliest.



__________________

John   non-responder  

Undetected at week 2 on solvaldi/rib/interferon:  stayed through week 12 but virus came back as soon as I stopped.  on   Harvoni and ribravirin 24 weeks undetected after two. 8/2/15  12 week EOT  UNDETECTED!  SVR

1991-2015 RIP

 



Guru

Status: Offline
Posts: 1724
Date:
Permalink  
 

The best SVR rates are with Sovaldi/Ledipasvir.  For gt1, tx naive, non-cirrhotics, the SVR rate is 100% in clinical trials.  You can't beat that. 

http://www.gilead.com/news/press-releases/2014/6/gilead-announces-phase-3-data-showing-that-the-fixeddose-combination-of-ledipasvirsofosbuvir-achieved-100-percent-sustained-virologic-response-svr12-among-patients-with-chronic-hepatitis-c-in-japan



__________________

Diagnosed in 2011, Incivek triple in 2011, tx discontinued, Genotype 1a, CT, VL 7mill, cirrhosis dx in 2012, age 67, waiting for new DAAs.



Senior Member

Status: Offline
Posts: 292
Date:
Permalink  
 

The best option for 1 a or 1B who has previously failed treatment is sovaldi/interferon/riba

 

O/S are almost as effective, but it is not the first choice in the strongest way to beat this thing.  If you are like me it is interferon triple (I just finished) or wait until October.  This is the research I am getting



__________________

John   non-responder  

Undetected at week 2 on solvaldi/rib/interferon:  stayed through week 12 but virus came back as soon as I stopped.  on   Harvoni and ribravirin 24 weeks undetected after two. 8/2/15  12 week EOT  UNDETECTED!  SVR

1991-2015 RIP

 



Senior Member

Status: Offline
Posts: 479
Date:
Permalink  
 

I had to do the riba & interferon since I had done the incivek 2 yrs ago. they said the incivek was a cousin to the olysio & could  not do it.. it is obviously a part of the pro tease inhibitor.  which i relapsed on. everyone is different.  I am just praying for svr for u...

I had done the interferon & riba two times b4 & then a trial study that really messed with my vision. I am not even sure that one is still around. but then came the golden pill. & it sure was golden for me. u will do this, I know u can.

Tazsmile



__________________

TazKat Genotype 1A null responder x 3 riba & iterferon twice, relapsed from Incivek 2012 with only 12 weeks left to do. stage 4 mild cirrhosis 4/25/2014/ started sovaldi riba & interferon.. finished treatment 7/17/14  results 7/25  cleared..

 

 



Guru

Status: Offline
Posts: 1724
Date:
Permalink  
 

Hope4 wrote:

I had asked doctor what he would do, given my status and the options I had (one being waiting) and he said if he were me, he would take this tx  for  12 weeks now.  So I trusted that.

All that being said, still open for advice.

 


That's an interesting question to pose to your doctor and I'm sure they hear it a lot.  In my experience doctors are willing to push the envelope farther than the average person with treatments for themselves because they feel more in control.  If something happens they can identify the problem faster and counter-act or remedy it. I usually ask them how would they advise their wife, sister, or mother because the answer may be different. That's assuming they are really thinking about the question on a personal as well as professional level and answering with complete honesty.

If you are really still open to advice I would advise you to wait.  But, I certainly understand the desire to get it done now.  Bluegene's position is extreme, and notably, she's never used Int/Riba.  I have.  By all accounts it's a harder tx (and probably less safe) than the all orals which is why I say, given the choice, I'd wait.  



-- Edited by Isiscat2011 on Sunday 27th of July 2014 02:36:20 AM

__________________

Diagnosed in 2011, Incivek triple in 2011, tx discontinued, Genotype 1a, CT, VL 7mill, cirrhosis dx in 2012, age 67, waiting for new DAAs.



Member

Status: Offline
Posts: 25
Date:
Permalink  
 

Thanks, both Bluegene and Misosoup...

OK...Now I'm getting scared...I think I will probably be going forward with it now tho' , because everything is in place and I 've kind of geared myself up to just starting now and being done with it by the end of October .....I, too have a desk job, which I'm hoping to still manage (My boss knows I'm going to take this tx, plus one close co-worker...)  I've got vacation days to plug in here and there as needed.   I am really hoping for the best, but trying to prepare for the worst.  Maybe I'll invest in the Cetaphil cream and ask about the Ambien.

I had asked doctor what he would do, given my status and the options I had (one being waiting) and he said if he were me, he would take this tx  for  12 weeks now.  So I trusted that.

All that being said, still open for advice.

 



__________________

Gen 1a        60 yrs     (was tx naive )   Started tx Pegasys, Ribavirin and Sovaldi on 7/31/14  12 wks.    VL 2,186,415.      Dr. said no cirrhosis, had no biopsy. EOT 10/22/14, undetected.  TX was tolerable, overall.

Still Undetected 4/27/15   SVR 24!!!



Newbie

Status: Offline
Posts: 2
Date:
Permalink  
 

Hi there! I'm more of a lurker than anything, but I started the same treatment two weeks ago tomorrow. It hasn't been so bad, I'm having a bit of trouble sleeping for more than a couple hours straight, but that's about it. Didn't start til Week 2. Headaches for about 12 hours after my injections, but nothing Tylenol doesn't help.

 

I'm following my doctor's advice and drinking absolutely ridiculous amounts of water, cut down the caffeine, and apply Cetaphil cream all over after the shower. They've given me Ambien for sleep, though I haven't tried it properly yet (just got it yesterday). So, I suppose that helps. I'm also aware I'm a young one compared to a lot of people here (just turned 27), so that may play a role.

 

I've got what basically amounts to a desk job with a lot of cognitive effort (graduate student!), and though I've been tired, I've been working fine. Perhaps a little slower than normal since they took away my energy drinks!!



__________________

27 F, genotype 1a, started riba/Pegasys/Sovaldi July 2014



Member

Status: Offline
Posts: 11
Date:
Permalink  
 

hmm To Hope4 and everyone else in her category: non-cirrhotic about to start the peg-ribavirin ride to hell... if you cannot meet the criteria needed for OS treatment, than choose the lesser of two evils and hope the government doesn't put a mandate on this golden health care with OS. The lesser of two evils would be to wait for Gileads miracle pill of the century which is due to be FDA approved by the end of the year. Clinical trials indicate a near 100% cure rate in all catagories including cirrhotics. I myself would have waited, but the virus was about to reach F-5. So I went with the available 96% cure rate-- Golden OS. Am now at day 9 in treatment-no serious side effects.



__________________
?


Member

Status: Offline
Posts: 11
Date:
Permalink  
 

hmmHello Hope. As I explained to maddie and rob the risk greatly outweighs any potential gain when taking riba/peg with or without Sovaldi. The hepatologist (gastrointologist) who prescribed those killer drugs did it more out of insurance company pressure than out of Hippocratic oath. Save yourself unnecessary misery and fight to get the Golden OS all-oral combo. Be assertive with the doctor. Insist. There is criteria that must be met before being eligible for the OS combo so meet it. Find a way. Research. Ask. I don't have the time to coach in this area but Ill tell you now...riba-peg is slow death via torture. Sincerely, Bluegene.



__________________
?


Member

Status: Offline
Posts: 25
Date:
My intro..Pegasys, Riba and Sovaldi next week.....
Permalink  
 



Hi,
anyone else currently undergoing tx now with pegasys, ribavirin and sovaldi...or has finished with it? Just looking for any tips, advice and general moral support. Excited to get
started but pretty nervous about the side effects. Need to keep working and hoping that works out. Grateful that it's only for 12 weeks, so keeping that thought in mind....



-- Edited by Hope4 on Thursday 24th of July 2014 11:44:56 PM

__________________

Gen 1a        60 yrs     (was tx naive )   Started tx Pegasys, Ribavirin and Sovaldi on 7/31/14  12 wks.    VL 2,186,415.      Dr. said no cirrhosis, had no biopsy. EOT 10/22/14, undetected.  TX was tolerable, overall.

Still Undetected 4/27/15   SVR 24!!!



Member

Status: Offline
Posts: 25
Date:
Pegasys, Riba and Sovaldi nest week...New here...
Permalink  
 


Starting tx next week  (Inf, Riba and Sovaldi 12 wks)



__________________

Gen 1a        60 yrs     (was tx naive )   Started tx Pegasys, Ribavirin and Sovaldi on 7/31/14  12 wks.    VL 2,186,415.      Dr. said no cirrhosis, had no biopsy. EOT 10/22/14, undetected.  TX was tolerable, overall.

Still Undetected 4/27/15   SVR 24!!!

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.