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Combo Treatment: Baraclude + Viread (results)
Hey guys, I'm new to the forum -- I just found the thread through Google by searching Viread + Baraclude. My apologies if I ask a few stupid questions, I'm still learning a lot about HepB. =]
I want to start off by saying that I have been taking both Baraclude + Viread as part of a study in November. I will try to be specific as possible, but all my paperwork and results are back at home since I'm away for college. I'm a 23 year old Asian male and found out I had chronic HepB.
---------------------------------------------------DATA---------------------------------------------------
• 1st blood results were (taken in 07/18/2008). NOT ON TREATMENT
HEPATITIS B VIRAL DNA, QUANT PCR 1,630,000,000 H <160 copies/mL
• 2nd blood results were (taken in 08/19/2008). NOT ON TREATMENT
HEP B VIRAL DNA QT 1,020,000,000 H <160 copies/mL
*some fluctuation in numbers, but still very high
♦I started the combo drugs sometime in November with the high DNA count above, if not more.
• 3rd blood results were (taken in December 2008): ON TREATMENT
HEP B VIRAL DNA QT 300,000 H <160 copies/mL
• 4th blood results were (taken in January 2009): ON TREATMENT
HEP B VIRAL DNA QT 801 H <160 copies/mL
• 5th blood results were (taken in April 2009): ON TREATMENT
HEP B VIRAL DNA QT 201 H <160 copies/mL
My doctor said the goal is to get my HepBeAG to turn negative as it is the engine behind the whole process, and the viral count to Zero.
At the moment, I'm HepBeAB negative, and HepBeAG positive.
Please feel free to ask any questions, and hopefully I'll be able to do the same as well as provide answers.
Thanks everyone! Will keep everyone up to date!
I want to start off by saying that I have been taking both Baraclude + Viread as part of a study in November. I will try to be specific as possible, but all my paperwork and results are back at home since I'm away for college. I'm a 23 year old Asian male and found out I had chronic HepB.
---------------------------------------------------DATA---------------------------------------------------
• 1st blood results were (taken in 07/18/2008). NOT ON TREATMENT
HEPATITIS B VIRAL DNA, QUANT PCR 1,630,000,000 H <160 copies/mL
• 2nd blood results were (taken in 08/19/2008). NOT ON TREATMENT
HEP B VIRAL DNA QT 1,020,000,000 H <160 copies/mL
*some fluctuation in numbers, but still very high
♦I started the combo drugs sometime in November with the high DNA count above, if not more.
• 3rd blood results were (taken in December 2008): ON TREATMENT
HEP B VIRAL DNA QT 300,000 H <160 copies/mL
• 4th blood results were (taken in January 2009): ON TREATMENT
HEP B VIRAL DNA QT 801 H <160 copies/mL
• 5th blood results were (taken in April 2009): ON TREATMENT
HEP B VIRAL DNA QT 201 H <160 copies/mL
My doctor said the goal is to get my HepBeAG to turn negative as it is the engine behind the whole process, and the viral count to Zero.
At the moment, I'm HepBeAB negative, and HepBeAG positive.
Please feel free to ask any questions, and hopefully I'll be able to do the same as well as provide answers.
Thanks everyone! Will keep everyone up to date!
My ALT and AST according to my FIRST (7/18/08) test results are:
ALT(sgpt) 83 H
AST(sgot) 38
I will try to get my hands on my recent Jan/April 09 results this weekend.
ALT(sgpt) 83 H
AST(sgot) 38
I will try to get my hands on my recent Jan/April 09 results this weekend.
you look good so far.
viral load is considered by some UND . it can still go lower but you're good now
yes the ultimate immediate goal is whatg your doctor told you, the idea is to seroconvert from e antigen positive to negative.. once you reach that goal i believe your doctor will keep you on meds for another period of time 6-12 months and then take you off of meds and have you monitored periodically every 3-6 months
ALT is high obviously, but maybe with your new results it is within range now..
let us know how you feel
good luck
viral load is considered by some UND . it can still go lower but you're good now
yes the ultimate immediate goal is whatg your doctor told you, the idea is to seroconvert from e antigen positive to negative.. once you reach that goal i believe your doctor will keep you on meds for another period of time 6-12 months and then take you off of meds and have you monitored periodically every 3-6 months
ALT is high obviously, but maybe with your new results it is within range now..
let us know how you feel
good luck
Your lab trends look good. You should be UND by now. Since you are only 23, it may take some time for you to "e" seroconvert, could be several years. So be prepare to see your eAntigen stay positive for some time since there is still too much cccDNA taking hold in your liver cells producing too much eAntigen despite UND DNA.
What's the plan after you go UND?
What is the goal of the study?
What's the plan after you go UND?
What is the goal of the study?
Thank you for posting and sharing your lab results.
Recently I discussed Hep B and its various lab readings with a Western medicine trained hepatologist according to whom unlike the assumption of many patients with HBV, particularly new patients, that high HBV DNA is horrible and is what is killing the liver cells, what hurts and damages liver cells in patients with HBV is the human immune system that tries to fight the virus in liver cells. That is why patients with positive HBeAg and very high HBV DNA often do not have correspondingly serious damage in their livers.
Many lab results posted at the Chinese HBV site are proof that antiviral drugs are effective at lowering HBV DNA to UND and ALT/AST to normal range but sadly many patients still complain of pain in liver area, fatigue, no appetite, cirrhosis, firbrosis, fatty livers and HCC.
That is why the view that HBV patients should not be satisfied with UND DNA and normal ALT/AST only but should demand negative HBsAg and positive HBsAB from their treatments.
Recently I discussed Hep B and its various lab readings with a Western medicine trained hepatologist according to whom unlike the assumption of many patients with HBV, particularly new patients, that high HBV DNA is horrible and is what is killing the liver cells, what hurts and damages liver cells in patients with HBV is the human immune system that tries to fight the virus in liver cells. That is why patients with positive HBeAg and very high HBV DNA often do not have correspondingly serious damage in their livers.
Many lab results posted at the Chinese HBV site are proof that antiviral drugs are effective at lowering HBV DNA to UND and ALT/AST to normal range but sadly many patients still complain of pain in liver area, fatigue, no appetite, cirrhosis, firbrosis, fatty livers and HCC.
That is why the view that HBV patients should not be satisfied with UND DNA and normal ALT/AST only but should demand negative HBsAg and positive HBsAB from their treatments.
"That is why the view that HBV patients should not be satisfied with UND DNA and normal ALT/AST only but should demand negative HBsAg and positive HBsAB from their treatments."
how can we "demand" such thing Jim ? you cant demand something that isnt supposedly there. one can offer something one does not have . so if - so far, there isnt a cure that brings you to S antigen negative and antibodies postive , then there isnt much one can ask for.
you and i and a lot of people on here have kids.. and you know not a single day passes without me getting depressed about my hbv even for 5 minutes.. every time i look at the two God created rascals running around in the house i cant help but to worry about their future and mine for that matter. its been a year since i found out i had hbv. i must've gotten it some 15 years ago if i am correct about the symptoms that mightve been the acute stage of hbv that i was experiencing.
this thing has a cure.. eventually that is.. all diseases have a cure.. God has not created a disease without a cure to it.. only two things we can not cure is old age and death. medicine cant cure or prevent that. so it is a matter of time before some cure is found.. hopefully it is found in our time while we are still here.
for how though, i know i can be hopefully and pray to God a cure is here soon but i also know i cant demand it..
one day jim.. one day :-)
how can we "demand" such thing Jim ? you cant demand something that isnt supposedly there. one can offer something one does not have . so if - so far, there isnt a cure that brings you to S antigen negative and antibodies postive , then there isnt much one can ask for.
you and i and a lot of people on here have kids.. and you know not a single day passes without me getting depressed about my hbv even for 5 minutes.. every time i look at the two God created rascals running around in the house i cant help but to worry about their future and mine for that matter. its been a year since i found out i had hbv. i must've gotten it some 15 years ago if i am correct about the symptoms that mightve been the acute stage of hbv that i was experiencing.
this thing has a cure.. eventually that is.. all diseases have a cure.. God has not created a disease without a cure to it.. only two things we can not cure is old age and death. medicine cant cure or prevent that. so it is a matter of time before some cure is found.. hopefully it is found in our time while we are still here.
for how though, i know i can be hopefully and pray to God a cure is here soon but i also know i cant demand it..
one day jim.. one day :-)
"That is why the view that HBV patients should not be satisfied with UND DNA and normal ALT/AST only but should demand negative HBsAg and positive HBsAB from their treatments." -cajim
I take this to mean that HepB patients should push and advocate for continuing research to find a cure.
"and you know not a single day passes without me getting depressed about my hbv even for 5 minutes.. " -bberry
What helps me is to try to adopt a more universal view. Disease is a part of life. When praying, don't just ask God for a cure but remember to thank God that HBV is now a manageable disease.
I take this to mean that HepB patients should push and advocate for continuing research to find a cure.
"and you know not a single day passes without me getting depressed about my hbv even for 5 minutes.. " -bberry
What helps me is to try to adopt a more universal view. Disease is a part of life. When praying, don't just ask God for a cure but remember to thank God that HBV is now a manageable disease.
My view may be wrong but I will share anyway: If we patients are not satisfied with only DNA->UND and ALT/AST->normal range, then the scientists may not stay at the stage of curing by killing indiscriminately. They may spend more efforts at figuring out how to strengthen the internal environment of a patient that will increasingly make it impossible for the virus to stay. We patients also make our share of efforts: we must be willing to do a lot more than just popping a pill into our mouth for our cure.
That's right. Also research needs to realize that chronic HBV like all chronic conditions are not very well treated by methods of kill. Yes, chemo therapy and radiation may have successfully killed all the cancer cells in a patient but at the same time they have so weakened and destroyed their carrier, the human body that the patient also dies with the cancer cells shortly after; Yes, methods of kill have killed HBV viruses to UND but at the same time they have so weakened and poisoned the patient's liver, kidney, and other systems that the patient gets weaker and weaker with UND DNA and normal ALT/AST!
"then the scientists may not stay at the stage of curing by killing indiscriminately"
At the risk of sounding pedantic, I'll say that viruses are not "killed" because they are not really alive.
None of the HBV medicines (as far as I know) actively destroy the virus. They just interfere in the replication process. And the way I understand it, the body's own reproductive mechanisms make the viral load low - by simple dilution - by creating new cells and getting rid of old cells and wastes.
Speaking for myself, I feel a lot better with my undetectable VL. No more feeling bloated all the time, like I used to feel a year ago.
Coming to my own faith: I have faith that this particular disease is fully curable. My reason: most adults get rid of it on their own! Why can't we? Clearly it is curable! I wish they would speed up research on the natural immune response, and find a way to trigger that in us.
At the risk of sounding pedantic, I'll say that viruses are not "killed" because they are not really alive.
None of the HBV medicines (as far as I know) actively destroy the virus. They just interfere in the replication process. And the way I understand it, the body's own reproductive mechanisms make the viral load low - by simple dilution - by creating new cells and getting rid of old cells and wastes.
Speaking for myself, I feel a lot better with my undetectable VL. No more feeling bloated all the time, like I used to feel a year ago.
Coming to my own faith: I have faith that this particular disease is fully curable. My reason: most adults get rid of it on their own! Why can't we? Clearly it is curable! I wish they would speed up research on the natural immune response, and find a way to trigger that in us.
1. Figuratively speaking, "kill" means "hurt", e.g. Adefovir hurts HBV replication just as it hurts patient's kidney, alive or not.
2. I am happy to hear that some patients are happy because they have benefited from UND DNA, but may I venture to assume that they will be happier when they get rid of the virus, not just the bloating.
3. I agree: "most adults get rid of it on their own!" not by antiviral drugs or IFN but by their own body, their immune system, their internal bodily condition.
2. I am happy to hear that some patients are happy because they have benefited from UND DNA, but may I venture to assume that they will be happier when they get rid of the virus, not just the bloating.
3. I agree: "most adults get rid of it on their own!" not by antiviral drugs or IFN but by their own body, their immune system, their internal bodily condition.
"and you know not a single day passes without me getting depressed about my hbv even for 5 minutes.. " -bberry
Personally, I feel fine about it. I ask myself "given this situation, what is the best thing I can do?". Then I try to do it. I have neither hope that medicines will work, nor fear that medicines won't work and the virus will take over. It is always just "Now, what is my best course of action?"
Unlike you, I don't have kids. And I wonder if that makes a difference. I wonder this approach would work if I had kids of my own. If I may hazard a guess, I think it would.
I agree with steven entirely in that disease is a part of life :-).
I'll stop yapping now :-)
Personally, I feel fine about it. I ask myself "given this situation, what is the best thing I can do?". Then I try to do it. I have neither hope that medicines will work, nor fear that medicines won't work and the virus will take over. It is always just "Now, what is my best course of action?"
Unlike you, I don't have kids. And I wonder if that makes a difference. I wonder this approach would work if I had kids of my own. If I may hazard a guess, I think it would.
I agree with steven entirely in that disease is a part of life :-).
I'll stop yapping now :-)
"Personally, I feel fine about it. I ask myself "given this situation, what is the best thing I can do?". Then I try to do it. I have neither hope that medicines will work, nor fear that medicines won't work and the virus will take over. It is always just "Now, what is my best course of action?" "
--I admire this a lot.
"And I wonder if that makes a difference."
--I think it would.
"I agree with steven entirely in that disease is a part of life."
--A quote from Dr. Liu,"A natural life is without disease. That a patient is with a disease is because he/she has made a mistake. Therefore to cure the disease depends to the larger extent on the patient himself/herself and to the smaller extent on the doctor."
--I admire this a lot.
"And I wonder if that makes a difference."
--I think it would.
"I agree with steven entirely in that disease is a part of life."
--A quote from Dr. Liu,"A natural life is without disease. That a patient is with a disease is because he/she has made a mistake. Therefore to cure the disease depends to the larger extent on the patient himself/herself and to the smaller extent on the doctor."
I'm happy to see that people are discussing and giving their perspectives on this disease. It's great to see both hope and sorrow because it's a part of life.
Quick question...what does UND stand for? IFN? Undetectable VL?
As of right now, i feel very healthy, just like anyone else. No signs of any side effects. I exercise as often as I can.
As of January: ALT 31/AST 21
Quick question...what does UND stand for? IFN? Undetectable VL?
As of right now, i feel very healthy, just like anyone else. No signs of any side effects. I exercise as often as I can.
As of January: ALT 31/AST 21
Yes, UND, though not a standard acronym, stands for Undetectable Viral Load around here.
IFN stands for interferon. Though generally IFN could stand for any of the several interferons, in the context of HepB, it stands for peginterferon alfa-2a. Another note, in medical papers, I have come across researchers testing the efficacy of other interferons as well - for HepB - and they abbreviate to IFN as well.
Please do continue to keep us posted.
IFN stands for interferon. Though generally IFN could stand for any of the several interferons, in the context of HepB, it stands for peginterferon alfa-2a. Another note, in medical papers, I have come across researchers testing the efficacy of other interferons as well - for HepB - and they abbreviate to IFN as well.
Please do continue to keep us posted.
""So be prepare to see your eAntigen stay positive for some time since there is still too much cccDNA taking hold in your liver cells producing too much eAntigen despite UND DNA.
What's the plan after you go UND?
What is the goal of the study?""
The goal of the study is to test the efficiency of the combo treatment vs single treatment. Prevent mutations of the HepB virus. My doctor hopes that the virus does not mutate. I'll be on it regardless for the next 1.5 years. The study lasts 2 years.
What's the plan after you go UND?
What is the goal of the study?""
The goal of the study is to test the efficiency of the combo treatment vs single treatment. Prevent mutations of the HepB virus. My doctor hopes that the virus does not mutate. I'll be on it regardless for the next 1.5 years. The study lasts 2 years.
Hat off and a big "thank you" to you for paving the way for safe and effective treatments for people to come.
I just wanted to let you guys know that I didn't forget about this thread.
I will be going back for my scheduled visit this Friday, July 11, 2009, for another usual check-up. (includes a physical and blood test).
I will keep you guys updated!
I will be going back for my scheduled visit this Friday, July 11, 2009, for another usual check-up. (includes a physical and blood test).
I will keep you guys updated!
Thank you all for this discussion that will definitely give some postive spirit to all the patients to fight with the virus.
Hepbinme: i would like to know you are from which place. If you are from India i would like to know the doctur you are consulting.
Hepbinme: i would like to know you are from which place. If you are from India i would like to know the doctur you are consulting.
I have not actually seen my latest results, the last ones were at
• 5th blood results were (taken in April 2009): ON TREATMENT
HEP B VIRAL DNA QT 201 H <160 copies/mL
The 6th blood results should already be out, but I haven't had the chance to review them at the office yet. The doctor said that I should be at a count of at least 0 H (yes, zero). But that doesn't mean that I've cured of it. The treatment only suppresses the virus.
I am still on the combo treatment and will continue to be on it for the next year. The program is for a total of two years.
I apologize that I can not assist you, jammy65, as I am located in California, USA...
• 5th blood results were (taken in April 2009): ON TREATMENT
HEP B VIRAL DNA QT 201 H <160 copies/mL
The 6th blood results should already be out, but I haven't had the chance to review them at the office yet. The doctor said that I should be at a count of at least 0 H (yes, zero). But that doesn't mean that I've cured of it. The treatment only suppresses the virus.
I am still on the combo treatment and will continue to be on it for the next year. The program is for a total of two years.
I apologize that I can not assist you, jammy65, as I am located in California, USA...
Reaching 0H is first step. Please share your success story e-sero conversion (or s-sero conversion)
hi, can you also clear with your doctor if you were in the immune tollernat fase when you started or just cronic hbe +
it is very good to see that such high hbv-dna can be suppressed so fast by the combo of most potent antivirals, any adverse event of ?
did you have a liver bipsy or fibroscan at start of treatment kidneys?
thank you
it is very good to see that such high hbv-dna can be suppressed so fast by the combo of most potent antivirals, any adverse event of ?
did you have a liver bipsy or fibroscan at start of treatment kidneys?
thank you
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