Norma I Rallón, Jose M. Benito, Pablo Barreiro, Eugenia Vispo, Pablo Labarga, Sonia Rodriguez-Novoa & Vincent Soriano Infectious Diseases Department, Hospital.

Slides:



Advertisements
Similar presentations
HIV/HCV Coinfection News – HCV Protease Inhibitors
Advertisements

Hepatitis B & Hepatitis C in HIV
José M. Miró, 1 Miguel Montejo, 2 Lluis Castells, 3 Antonio Rimola, 1 Antonio Rafecas, 4 Pilar Miralles, 5 Jesús Fortún, 6 Marino Blanes, 7 Manuel de la.
Using genetic markers in clinical practice David Thomas Advisor: Merck Clinical trial: Gilead and Merck.
Overview: Treatment of HCV Infection Jürgen Rockstroh Department of Medicine I, University of Bonn, Germany ICVH Baltimore 20114/22/2011.
Durability of Response and Rate of Re-emergence of Wild Type at Boceprevir (BOC) Resistance-Associated Variant (RAV) Loci in Genotype 1a and 1b Patients:
Douglas T. Dieterich, Juergen K. Rockstroh, Kenneth E. Sherman, Nathalie Adda, Lisa Mahnke, Varun Garg, Shahin Gharakhanian, Scott McCallister, Vincente.
Frequencies of Resistance-Associated Amino Acid Variants Following Combination Treatment with Boceprevir (BOC) Plus PEGINTRON (PegInterferon Alfa-2b) and.
Slide 1 Healthcare Utilization and Mortality associated with HIV and HCV: How to address the burden of liver disease Susanna Naggie 1,2, Lawrence Park.
Adherence to HCV Therapy: Relation with Virologic Outcomes and Changes in Adherence Over Time Vincent Lo Re, MD, MSCE V. Teal, R. Localio, V. Amorosa,
Acute HCV in HIV-infected Men The ‘new’ STD
Optimal therapy in genotype 1 patients 3 rd Paris Hepatitis Conference January 2009 Stefan Zeuzem, MD J.W. Goethe University Hospital Frankfurt,
The basics for simulations
1..
Benjamin Banneker Charter Academy of Technology Making AYP Benjamin Banneker Charter Academy of Technology Making AYP.
HCV Infection in Marginalized Populations
Analyzing Genes and Genomes
Management of non naïve patients with hepatitis C "Non-Responders" 3rd Paris Hepatitis Conference, Paris, Christoph Sarrazin J. W. Goethe-University.
New Lesions versus Growth of Existing Disease: Does it impact prognosis? Axel Grothey¹, James Heun¹, Megan Branda¹, Richard M. Goldberg², Dan Sargent¹.
Sanaa Kamal, M.D., Ph.D. Professor Ain Shams University, Cairo, Egypt Clinical Challenges in the Management of Hepatitis C Genotype 4.
How to Optimize Treatment of Genotype 4 Patients Rami MOUCARI MD, PhD Bellevue Medical Center – Saint Joseph University, Beirut, Lebanon.
Institute for Public Health, Medical Decision Making and Health Technology Assessment 1 Results of the PanEuropean Hepatitis C Project 3 rd Paris Hepatitis.
Hepatitis C & HIV in 2011 Vincent Soriano Infectious Diseases Department Hospital Carlos III, Madrid, Spain.
What’s new in HCV genotype 2? Alessandra Mangia S.Giovanni Rotondo,ITALY PARIS HEPATITIS CONFERENCE January 2012.
Optimal therapy in genotype 2 and 3 patients Antonio Craxì Liver & GI Unit, Di.Bi.M.I.S., University of Palermo, Italy
CBG metaprotein composition shown in Figure 2. Associations also found between the IL28B rs genotype and SVR (p = 5.06×10 -5 ) and between CBG.
Testing of Patients with Chronic Hepatitis C: What do I really need? Hepatitis C Choices in Care Greg Everson, MD.
Clinical managment of hepatitis C in an environment with limited acces to treatment Andrzej Horban Hospital of Infectious Diseases Warsaw, Poland.
Hepatitis web study Hepatitis web study Simeprevir in HIV Coinfection, GT-1 C212 Trial Phase 3 Treatment Naïve and Treatment Experienced Dieterich D, et.
Hepatitis web study H EPATITIS W EB S TUDY H. Nina Kim, MD Assistant Professor of Medicine Division of Infectious Diseases University of Washington School.
Host Genetics of HCV: Relevance for the study of HCV in Africa Thomas J. Urban, PharmD, PhD Center for Human Genome Variation Duke University Medical Center.
Norma I. Rallón 1, José Medrano 1, Salvador Resino 2, Clara Restrepo 1, Vincent Soriano 1 and José M. Benito 1 1 Department of Infectious Diseases, Hospital.
How to optimize the treatment of HCV-4 patients? Nabil Antaki MD, FRCPC Aleppo, Syria Paris, January 30, 2012.
Liver fibrosis regression after anti HCV therapy and the rate of death, liver-related death, liver- related complications, and hospital.
Peginterferon Alfa-2a plus Ribavirin vs Peginterferon Alfa-2b plus Ribavirin for Chronic Hepatitis C Virus Infection in HIV- Infected Patients J Berenguer.
LDV/SOF 90/400 mg qd Non-randomised Open-label N = 21 W12 SVR 12 NIAID SYNERGY GT4 Kohli A. Lancet Infect Dis 2015; Juky 15, ePub ahead of print ≥ 18 years.
OBV/PTV/r + DSV + RBV OBV/PTV/r + DSV Randomisation* 1 : 1 Open label years Chronic HCV infection Genotype 1b Prior failure to PEG-IFN + RBV HCV.
Twice Weekly Peg-IFN-alpha-2a with Ribavirin Improves Early Viral Kinetics over Standard Therapy Among HIV/HCV Co-Infected African American Patients Alison.
SMV + PEG-IFN + RBV Open-label W12 W24* or W48* N = years Chronic HCV infection Genotype 4 Treatment-naïve or experienced with relapse or partial.
Randomisation* 2 : 1 Double blind *Randomisation was stratified on genotype (1a or 1b or other) and IL28B genotype (CC, CT or TT) N = 133 N = 260 W24W48.
Simplification from Protease Inhibitors to Once or Twice Daily Raltegravir: the ODIS trial Eugenia Vispo, Pablo Barreiro, Francisco Blanco, Sonia Rodríguez-Novoa*,
SMV SOF 400 Open-label OPTIMIST-2 Study: SMV + SOF for genotype 1 and cirrhosis W12  Objective –Superiority of SVR 12 (HCV RNA historical control.
Reddy KR. Lancet Infect Dis. 2015;15:27-35 ATTAIN SMV + TVR placebo + PEG-IFN + RBV TVR + SMV placebo + PEG-IFN + RBV Randomisation* 1 : 1 Double-blind.
Progressive histological liver improvement after sustained virological response to therapy in HCV / HIV coinfected patients. Jose L. Casado,
Distinct hepatitis C virus kinetics in HIV- infected patients treated with ribavirin plus either pegylated interferon α-2a or α-2b Eugenia Vispo, Pablo.
Sources of Hepatitis C Infection (U.S.) Previously Acquired (
W24 ≥ 18 years Chronic HCV infection Genotype 1 Treatment naïve Early fibrosis to compensated cirrhosis No HBV or HIV co-infection N = 10 SOF + weight-based.
SOLAR-1 LDV/SOF + RBV Randomisation* of the 7 groups 1 : 1 Open-label SOLAR-1 Study: LDV/SOF + RBV in advanced liver disease  Design W12W24 ≥ 18 years.
Evolution of the Functional Profile of HIV-Specific CD8+ T cells in a Cohort of Long Term Nonprogressors M López, N Rallón, A Peris, M Salgado, B Rodés,
SOF/VEL 400/100 mg qd N = 500 N = 100 W12 Placebo > 18 years Chronic HCV infection Genotype 1, 2, 4, 5 or 6 Naïve or pre-treatment with IFN-based regimen.
 Objective –SVR 12 (HCV RNA < 25 IU/ml), with 95% CI, next observation carried backward DCV + SOF + RBV Randomised* 1:1 Open-label ALLY-3+ study: DCV.
Open-label W24 ≥ 18 years Chronic HCV infection All genotypes HCV RNA ≥ 10,000 IU/ml Liver transplantation months earlier Child Pugh ≤ 7 and MELD.
Update on Genetic Links to HCV Clearance Todd Wills, MD ETAC Infectious Disease Specialist HEPATITIS C TREATMENT EXPANSION INITIATIVE MULTISITE CONFERENCE.
36 year old HCV+ woman, Risk factor: occasional IVDU 15 years ago First treatment with PEG-IFN/RBV in 2002 –only qualitative PCR available : positive at.
Previous SVR With Interferon-Based Therapy for HCV Lowers Risk of Hepatotoxicity in HIV/HCV-Coinfected Individuals on Antiretroviral Therapy Slideset on:
Acute HCV genotype 1 infection * No HBV or HIV co-infection
Higher rate of antiretroviral therapy reinitiation among HIV-HBV coinfected patients in the episodic arm of the SMART study Dore G.1, Soriano V.2, Neuhaus.
Long-term impact of response to interferon-based therapy in patients with chronic HCV in relation to liver function, survival and cause of death Philip.
A. Stepanov, A. Kruk, N. Polovinkina, A. Vinogradova
Viral Kinetics of Hepatitis C Virus genotype 5 in South African patients treated with Pegylated-Interferon-alfa and Ribavirin Martin Nieuwoudt , Schalk.
LEAGUE-1 study: daclatasvir + SMV + RBV for genotype 1
The Aging Liver in the Aging HIV and HCV Patients
Influence of hepatitis C and hepatitis G virus co-infection on viral and cellular dynamics in patients infected with human immunodeficiency virus following.
Simeprevir in HIV Coinfection, GT-1 C212 Trial
Ombitasvir + Paritaprevir + Ritonavir +/- Ribavirin in HCV GT4 PEARL-I
Volume 139, Issue 5, Pages e1 (November 2010)
ARV-trial.com IMPACT Study: SMV + DCV + SOF in HCV genotype 1 with decompensated liver disease Design Open label ≥ 18 years Chronic HCV infection Genotype.
Ledipasvir-Sofosbuvir +/- Ribavirin in HCV Genotype 1 ION-2
Incidence of HCC after HCV treatment with DAAs: ERCHIVES
Sequencing cohorts Open-label Design W8 W12 ≥ 18 years
Presentation transcript:

Norma I Rallón, Jose M. Benito, Pablo Barreiro, Eugenia Vispo, Pablo Labarga, Sonia Rodriguez-Novoa & Vincent Soriano Infectious Diseases Department, Hospital Carlos III, Madrid, Spain. Broader Influence of IL28B Gene Polymorphisms and Interferon λ3 Plasma Levels on HCV Outcomes in HIV Patients Financial Disclosure No financial relationships to disclose within the past 12 months relevant to my presentation. No discussion of off-label or investigational drugs

IL28B Gene Genetic Variation HCV-Monoinfected Patients % SVR to pegIFN+RBV by rs genotypes Ge et al. Nature 2009; 461:

IL28B Gene Genetic Variation HCV-Monoinfected Patients % SVR to pegIFN+RBV by rs genotypes Ge et al. Nature 2009; 461: % spontaneous HCV clearance by rs genotypes Thomas et al. Nature 2009; 461:

DESCRIPTION Hospital Carlos III Cohort 650 HIV/HCV Co-infected individuals VariablenIL28BEffectReference Spontaneous HCV clearance24CCEnhanced in genotypes 1 and 4 Rallón et al. AIDS 2010 Response to pegIFNα-RBV therapy 164CCIncreased SVR mainly in genotypes 1 and 4 Response to pegIFNα-RBV therapy 159/86CCPredictive of SVR (Prometheus index)Medrano et al., Clin Inf Dis 2010 Early viral kinetics on therapy196CCIncreased RVR and EVR mainly in genotypes 1 and 4 Rallón et al. AIDS 2011 (in press) Response to pegIFNα-RBV therapy in prior non-response or relapse patients 62CCIncreased SVR only in genotypes 1 and 4 prior true non-responders Labarga et al. AIDS 2011 (in press) Serum HCV-RNA levels289CC/CTGreater viral loadLabarga et al. AIDS 2011 (in press) Liver fibrosis progression304CCGreater rate of cirrhosisBarreiro et al. J Infect Dis 2011 (in press) Liver enzymes elevation304CCIncreased ALT levels Serum IFN λ3 levels112CCNo impact at baseline but greater increase during IFNα therapy Rallon et al. CROI 2011

LESSONS LEARNED

Higher prevalence of CC genotype in patients who spontaneously clear HCV compared with chronically infected HCV patients Rallón et al. AIDS 2010; 24:F23-9 HCV/HIV-Coinfected Patients rs genotypes 75% 46% 25% 54% Spontaneous HCV clearance Chronic HCV infected p=0.007 n=164n=24 % of patients CT/TT patients CC patients

The rs CC genotype exerts a beneficial effect on the probability of SVR to pegIFN+RBV, mainly in HIV/HCV- coinfected patients with HCV G1/4 Rallón et al. AIDS 2010; 24:F23-9 Rate of SVR in distinct HCV genotypes according to rs SNP CT/TT patients CC patients

The rs CC genotype exerts a beneficial effect on the probability of SVR to pegIFN+RBV, mainly in HIV/HCV- coinfected patients with HCV G1/4 Rallón et al. AIDS 2010; 24:F23-9 Rate of SVR in distinct HCV genotypes according to rs SNP Predictors of SVR to pegIFNα/RBV therapy in HIV/HCV coinfected patients CT/TT patients CC patients

Baseline prediction of the likelihood of SVR to pegIFN-RBV Medrano et al. Clin Infect Dis 2010; 51: PROMETHEUS INDEX HCV genotype (1/4) Serum log 10 HCV-RNA Stiffness (KPa) IL28B rs (CT/TT)

Baseline prediction of the likelihood of SVR to pegIFN-RBV Medrano et al. Clin Infect Dis 2010; 51: Diagnostic performance in the derivation and validation groups PROMETHEUS INDEX HCV genotype (1/4) Serum log 10 HCV-RNA Stiffness (KPa) IL28B rs (CT/TT)

The CC genotype increases the rate of RVR and EVR in G1/4 patients, potentially driven by faster viral kinetics during the first weeks of therapy CT/TT patients CC patients Rallón et al. AIDS 2011; in press % % % % % % % % % % (n=135)

The CC genotype increases the rate of RVR and EVR in G1/4 patients, potentially driven by faster viral kinetics during the first weeks of therapy CT/TT patients CC patients Rallón et al. AIDS 2011; in press % % % % % % % % % % (n=135)

Marginal effect of IL28B variants on G2/3, potentially due to similar viral kinetics during the first weeks of therapy CT/TT patients CC patients Rallón et al. AIDS 2011; in press % % % % % % % % % % (n=61)

Marginal effect of IL28B variants on G2/3, potentially due to similar viral kinetics during the first weeks of therapy CT/TT patients CC patients Rallón et al. AIDS 2011; in press % % % % % % % % % % (n=61)

The rs CC genotype increases the probability of SVR in prior true non-responders infected with G1/4 Labarga et al. AIDS 2011; in press p= p=0.0 2 p=0.3 6 % of patients with SVR No

Patients with the C allele harbor higher serum HCV-RNA Labarga et al. AIDS 2011; in press Median serum HCV-RNA in HIV-HCV coinfected patients with distinct IL28B genotypes

Patients with the C allele harbor higher serum HCV-RNA Labarga et al. AIDS 2011; in press Median serum HCV-RNA in HIV-HCV coinfected patients with distinct IL28B genotypes Proportion of HIV-HCV coinfected patients with HCV-RNA >600,000 IU/ml according to IL28B genotypes

The CC genotype is associated to a higher rate of liver cirrhosis in HIV/HCV coinfected patients CT/TT patients CC patients 24% 28% 22% 18% 13% 15% 6% 15% AllHCV genotype patients p=0.01 p=0.04 p=0.23 n=170n=96n=38n=304 Barreiro et al. J Infect Dis 2011; in press Proportion of patients with liver cirrhosis by IL28B variants and HCV genotype % of patients with liver cirrhosis

The CC genotype is associated to a higher rate of liver cirrhosis in HIV/HCV coinfected patients CT/TT patients CC patients 24% 28% 22% 18% 13% 15% 6% 15% AllHCV genotype patients p=0.01 p=0.04 p=0.23 n=170n=96n=38n= length of infection (years) HR= 3.02 (95% CI, ), p= Cumulative proportion of cirrhotic patients (%) CT/TT patients CC patients Barreiro et al. J Infect Dis 2011; in press Proportion of patients with liver cirrhosis by IL28B variants and HCV genotype Risk for liver cirrhosis over time of HCV infection according to IL28B rs genotype % of patients with liver cirrhosis

IFN-λ3 is significantly up-regulated after 4 weeks of pegIFNα+RBV therapy only in CC carriers Median IFN-λ3 plasma levels during pegIFN-α/RBV therapy according to rs IL28B genotypes Rallón et al. CROI 2011 All patientsSVR patientsNon-responder patients

IFN-λ3 is significantly up-regulated after 4 weeks of pegIFNα+RBV therapy only in CC carriers Median IFN-λ3 plasma levels during pegIFN-α/RBV therapy according to rs IL28B genotypes Rallón et al. CROI 2011 All patientsSVR patientsNon-responder patients

IFN-λ3 is significantly up-regulated after 4 weeks of pegIFNα+RBV therapy only in CC carriers Median IFN-λ3 plasma levels during pegIFN-α/RBV therapy according to rs IL28B genotypes Rallón et al. CROI 2011 All patientsSVR patientsNon-responder patients

TAKE HOME MESSAGES Important role of IL28B genotypes on the rate of spontaneous clearance and on likelihood of response to pegIFNα-RBV therapy in HIV/HCV-coinfected individuals, including prior IFNα-experienced patients. Broader influence of IL28B genotypes on HCV disease, including viral replication and liver injury. IMPLICATIONS Universal IL28B testing in all individuals with chronic hepatitis C. Cheap and once in life. The Prometheus index might be a helpful baseline tool to guide therapeutic decisions. Given the faster progression to cirrhosis and increased response to therapy, IL28B CC carriers should be prioritized

ACKNOWLEDGMENTS Duke Clinical Research Institute, Durham, NC Susanna Naggie Alex Thompson Kevin Shianna John McHutchison Institute for Genome Sciences and Policy, Durham, NC David Goldstein NEAT European Project (LSHP- CT ) Infectious Diseases Department, Hospital Carlos III, Madrid, Spain José M. Benito Tamara Bar-Magen Eugenia Vispo Clara Restrepo Pablo Labarga Sonia Rodriguez-Novoa José Medrano Pablo Barreiro Luz Martin-Carbonero Eva Poveda Norma I. Rallón Vincent Soriano Infectious Diseases Unit, Hospital de Valme, Sevilla, Spain Juan A. Pineda Karin Neukam Juan Macias José A. Mirá Federico Di Lello Hospital Universitario Reina Sofía, Cordoba, Spain Antonio Rivero Angela Camacho Molecular Biology Dept, Jaen University, Jaen, Spain Antonio Caruz On behalf of CoRIS (Spain) Enrique Bernal, Hosp Reina Sofía, Murcia Javier Pinilla, Hosp San Pedro, Logroño José Hernández-Quero, Hosp San Cecilio, Granada Santiago Moreno, Hosp Ramón y Cajal, Madrid José M Miró, Hosp Clínic, Barcelona Manuel Leal, Hosp Virgen del Rocío, Sevilla Felix Gutierrez, Hosp de Elche, Elche Joaquin Portilla, Hosp de Alicante, Alicante Molecular Epidemiology, Infectious Diseases Lab National Centre of Microbiology, ISCIII, Madrid, Spain Salvador Resino Aida Calvino