The Effect of Antiviral Therapy on Liver Fibrosis in...
Transcript of The Effect of Antiviral Therapy on Liver Fibrosis in...
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Jidong JiaBeijing Friendship Hospital,
Capital Medical University2016-5-29 1
The Effect of Antiviral Therapy on Liver Fibrosis in CHC
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Disclosure
Consultation for Abbvie, BMS, Gilead, MSD, Novartis and Roche pharmaceutical companies.
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Outline • Natural history of hepatitis C infection• The effect of antiviral therapy on liver fibrosis• Summary
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Liver fibrosis is a common pathway to advanced liver disease
Pellicoro A,et al. Nat Rev Immunol 2014;14:181-94
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HCV-induced fibrosis and cirrhosis
Inflammation
Fibrosis Cirrhosis
Mild inflammation
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Puche JE, et al. Compr Physiol 2013;3:1473-92
HSCs play a key role in pathogenesis of liver fibrosis
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Resolved
Acute hepatitis
Chronic hepatitis
Cirrhosis
HCC
( 20%)
(80%)
(3-5% / yr)
(20%)
Natural History of Hepatitis C
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Progression of Fibrosis inChronic Hepatitis C
Years10 20 30
RapidMedium
Slow
4
3
2
1
Poynard et al. Lancet. 1997;349:825
Fibr
osis
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1382 HALT-C patients screened
Screen Ishak score cohorts:2=36, 3=177, 4=67, 5=80, 6=83
545 Patients pre-study with725 Liver biopsy
Rate of Progression of fibrosis in CHC
344 Liver biopsy >10mm, >4 yr interval
Compensated CHC failed to past IFN therapy
Analysis GROUP rate of progression slopes
Analysis INDIVIDUAL rate of progression slopes
Go backwards to include previous biopsies
—
+
0
Time flowGastroenterology 2011;141:900–8
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Ishak score at screening
Group slope Years ± screening
2 .005 -6.4 yr to +4.3 yr
3 .062 -5.8 yr to + 4.3 yr
4 .090 -5.1 yr to +4.0 yr
5 .076 -6.8 yr to +4.2 yr
6 .124 -5.9 yr to +4.3 yr
Rapid fibrosis score progression(RFSP)>0.2 occurred in 26.7% of HALT-C Trial patients
Gastroenterology 2011;141:900–8
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The RFSP in individuals is 0.35 to 0.97 Ishak units/year
Patients with progression in fibrosis over time
Patients without significant change in fibrosis over time
Gastroenterology 2011;141:900–8
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Fibrosis Progression Rate
0.12–0.14 units / year 1 unit: 7 to 8 years Evolution to cirrhosis:
28 – 32 years
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Viral factors Host factors
HCV genotypes
Quasispecies
Virus load
Co-infection
Gender
Age at infection
Aging process
Race
ALT elevation
Genetic factors (IL-28)
Viral and host factors related to HCV spontaneous clearance and disease progress
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IL-28 and fibrosis progression in CHC:
Associated?
YES
cohort
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IL-28 and fibrosis progression in CHC:
Associated?
Gastroenterology 2012;143:1244–52
YES !
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NO
Results from Beijing Friendship Hospital in 2012: rs12979860 and rs8099917 polymorphisms were NOTsignificantly associated with the FibroScan measurements
Cong R, You H
NO
NOT Associated?IL-28 and fibrosis progression in CHC:
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HCV RNA Negative (n=27, 31.8%)
Patients with HCV-Ab positive (n=85)
Recipients from One Blood Donor (n=105)
Twenty person missed, died or HCV-Ab (-)
One HCV genotype1b donor
HCV RNA Positive(n=58, 68.2%)
1998
20024 years
9-12 years
2009
2010
Without Clearance
Spontaneous Clearance
Outcome of patients infected with the one resourse of HCV
Chronic Hepatitis(n=13, 22.4%)
Decomp Cirrhosis or HCC (n=0 )
Cirrhosis(n=3, 5.2%)
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Age, not IL-28B, plays important role in both HCV spontaneous clearance and disease progress
Gender (male vs. female)
Odds Ratio (95% CI)
Age <20 years vs. >20 years*<40 years vs. >40 years
.01 1.5 5 10 15
IL-28 rs10853728 CC vs. CG
rs12979860, 8099917, 12980275
1.11 (0.59-2.08)
2.04 (1.13-3.69)
0.81 (0.43-1.54)
1.89 (0.91-3.91) 2.28 (0.63-8.32)
30
Gender (male vs. female)
Odds Ratio (95% CI)
Age <20 years vs. >20 years
<40 years vs. >40 years*
.01 1.5 5 10 15
IL-28 rs 12979860 CC vs. CT
rs 8099917 TT vs. TG
1.56 (0.41-5.90)
0.78 (0.11-5.58)
0.13 (0.03-0.65)
0.87 (0.65-1.18)
30
HCV Spontaneous Clearance
HCV Disease Progress
0.87 (0.65-1.18)
A
B
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2012 APASL, Poster PP13-037
12 Week
HCV RNA Positive(n=58)
HCV RNA Negative (n=27)
Patients with HCV-Ab positive (n=85)2009
2010
Treat with conventional IFN alpha-2b plus ribavirin(n=47, 45 patients complete the treatment)
RNA (-)OR(n=41)
2009-2010
Follow-up
0 Week
24 Week
RNA (+)(n=4)
RNA (+)(n=2)
RNA (-)(n=39)
RNA (-)(n=2)
48 Week RNA (+)(n=3)
RNA (-)(n=36)
RNA (+)(n=2)
RNA (-)(n=2)
72 Week
IFN+R
IB
RNA (-)(n=2)
RNA (+)(n=1)
RNA (-)(n=35)
RNA (+)(n=2)
RNA (-)(n=1)
RNA (+)(n=2)
Two withdraw at week 5 or 12 for side effects
RNA (+)(n=2)
RNA (+)(n=2)
RNA (+)(n=2)
Single source HCV 1b-infected group results support treatment response, not IL-28, as accurate predictor of sustained viral response
SVR=78.7%
IL-28 SNPs (p=0.355~0.504)
Response 24W (p = 0.013*)
Fibroscan (p =0.033*)
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A Seven-Gene Signature (Cirrhosis Risk Score) Predicts Liver Fibrosis Progression
Advantages Disadvantages
All 7 SNPs were associated with therisk of cirrhosis with odds ratios 1.86 to 3.23
Cutoff values may only distinguish patients with a very high risk ofcirrhosis
Unique variable associated with fibrosis progression in multivariate analysis, including gender and alcohol intake
Identified in Caucasian patients so it may not be applicable to all ethnic groups
Mean CRS was significantly higher in untreated in whom fibrosis progressed
J Hepatol 2012; 57 :1110–25Hepatology 2009;50: 1038-44
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Outline Natural history of hepatitis C infection The effect of antiviral therapy on liver
fibrosis Summary
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22
Lee YA, et al. Gut 2015;64:830–41.
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Changes in hepatic inflammation components in the 38 pre- and posttreatment liver biopsies
23
D’Ambrosio R, et al. Hepatology 2012;56:532-43
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METAVIR score for fibrosis before and after an SVR
24
D’Ambrosio R, et al. Hepatology 2012;56:532-43
F4
F3
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Changes in the areas of fibrosis assessed by morphometryof pre- and posttreatment liver biopsies
25
D’Ambrosio R, et al. Hepatology 2012;56:532-43
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Mean change from baseline in METAVIR necroinflammatory(NIF) activity and fibrosis scores (pooled analysis of 1571
patients in 8 trials of phase 2 to 4)
26
Pockros PJ, et al. Hepatology 2010;52:1193-1200
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Regression of fibrosis according to treatment response to IFN/PEG-IFN±RBV
27
Poynard T, et al.J Hepatol 2013; 59:675–83
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Forty-nine paired pre-treatment and long-term follow-up biopsies in patients with SVR
28
Pre-treatmentIshak fibrosis scores ≥ 4Pretreatment Ishak scores ≤3
George SL, et al. Hepatology . 2009; 49: 729–38.
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Cumulative risk of liver cirrhosis in elderly CHC following treatment
29
Tseng CW, et al. Clinical Interventions in Aging 2016
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Improvement of platelets after SVR among CHC patients with advanced hepatic fibrosis
30
van der Meer, AJ, et al. JGH 2016, in press
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Improvement in hepatic inflammation is associated with less fibrosis progression (HALT-C)
31
Morishima C, et al. Am J Gastroenterol 2012
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Impact of the 10 different regimens on fibrosis stage
32
Poynard T, Et Al. Gastroenterology 2002;122:1303–13
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Evidence for the regression of liver fibrosis in patients treated for CHC
Ellis EL, et al. J Hepatol 2012; 56:1171–80
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Liver-related event and death in patients ±SVR (Left) and in patients ± regression of cirrhosis (Right)
after IFN-based therapy
34Mallet V, et al. Ann Intern Med. 2008;149:399-403.
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Survivals in CHC Patients With Advanced Fibrosis ± SVR
35
van der Meer AJ, et al. JAMA 2012
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Could DAA therapies improve liver fibrosis in CHC?
So far no DAA clinical trials use liver histology as endpointThe efficacy is too highThe duration of treatment is too shortLong-term follow-up studies on the
histological or clinical outcomes (including development of cirrhosis, decompensation, HCC or survival) are warranted
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Outline Natural history of hepatitis C infection The effect of antiviral therapy on liver
fibrosis Summary
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Summary HCV infection carries a high risk of
progression of liver fibrosis SVR induced by IFN-based therapy could
attenuate the progression or accelerate the regression of liver fibrosis
Regression of liver fibrosis reduces the liver events and improves survival
DAA therapy should also achieve the same but needs to be verified by long-term follow-up studies
38