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C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse, Villejuif, France

C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

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Page 1: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

HCV PRE AND POST-LIVER TRANSPLANTATION

Professor Didier SAMUEL

Centre Hépatobiliaire,

Inserm Unit 785, Paris XI University

Hopital Paul Brousse, Villejuif, France

Page 2: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Evolution of Liver Transplantation for Viral Cirrhosis

in Europe.

With HCCWithout HCC

0

100

200

300

400

500

600

700

800

1986 1987 1988 1989 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009

Virus Delta Virus B Virus C

0

100

200

300

400

500

600

700

800

1986 1987 1988 1989 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009

Virus Delta Virus B Virus C

www.eltr.org

Page 3: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Trends in Waiting List for HCV Cirrhosis in USA

Kim Gastroenterology 2009

Page 4: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

PATTERN OF HCV RECURRENCE POST OLTx

OLT

DEATH50%

NO HEPATITIS20%

CHRONIC HEPATITIS

ACUTE HEPATITIS70%

CHOLESTATIC HEPATITIS

< 10 %

VIRAL RECURRENCE

1 MTH

6 MTH

CHRONIC HEPATITIS CIRRHOSIS

?

6 MTH1 MTH

1 MTH

Adapted From McCaughanAdapted From McCaughan

Page 5: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

McCaughanJ Hepatol 2011

CHOLESTATIC HEPATITIS C

Page 6: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

FIBROSING CHOLESTATIC HEPATITIS C

Antonini AJT 2011

Page 7: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

FCH in HCV-HIV Coinfected PatienstImpact on Survival

Antonini AJT 2011

Page 8: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Immunosuppression

ProliferationProliferation

ApoptosisApoptosis

FibrosisFibrosis

HCV load Inflammation +

IFN- related genes IFN- response

-

Acute Rejection

Inflammation

Stress Response

The immune response

-

+

Pathobiology of Chronic HCV Post LT

McCaughan and Zekry J.Hepatol 2004, Samuel Easl Hepatol 2006

Stimulation of the IMMUNE RESPONSE by more HCV WINS

Page 9: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

• Liver Biopsy

Gold Standard,

Bring additional information than fibrosis stage

. HPVG

Invasive, can be done with liver biopsy

Not routine for many Centres

. Non invasive tests

Biochemical

Elastometry (fibroscan)

. Time post-LT as an adding variable

EVALUATION OF THE SEVERITY OF HCV RECURRENCE

Page 10: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Blasco Hepatology 2006; 43: 492-499

HPVG, Fibrosis at 1 Year Post-Transplant and Outcome

Page 11: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Gallegos-Orozco Liver Transplant 2009

Fibrosis Stage at 12 months at Liver Biopsy and Survival

Page 12: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Carrion Gastro 2010

Non Invasive 3-MALG Test and

Decompensation and Survival Post-Transplant

Page 13: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Carrion Hepatology 2010

Liver Stiffness and Severity of HCV Recurrence

Page 14: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Donor and Host Factorsof

HCV Recurrence

Page 15: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Belli Liver Transplant 2007; 13: 733-740

Fibrosis on the Graft In HCV+ve Liver Transplant Patients According to Donor Age and Gender

Risk of Fibrosis: Stable over years, Higher in women receiving old donors

Page 16: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

STEROIDS AND HCV

• Controversial role

– Increase viral load (Fong Gastro 1994, Gane Gastro 1996)

– Increase viral hepatocyte entry (Gastro 2010)

– Boluses of steroids deleterious (Berenguer J Hepatol 2000)

– Rapid withdrawal deleterious (Berenguer Hepatology 2003, McCaughan J Hepatol 2004, Vivarelli J Hepatol 2007)

» Immune rebound?

– Immunosuppression without steroids: not yet proven beneficial (Klintmaln Liver Transplant 2007)

Page 17: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

No Impact of Steroid-Free IS on Graft HCV Fibrosis

Klintmalm Liver Transplant 2011

Page 18: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

HCV Recurrence , Cyclosporine vs Tacrolimus

• There is currently no proof of superiority of one vs another

– Antiviral effect of Cyclosporine only in vitro

– Better efficacy of IFN in Ciclosporine patients not confirmed

– Randomized studies showed earlier reinfection with Tac but no

difference in fibrosis stage, better survival with Tac?

Samonakis, J Hepatol 2012 in Press, Berenguer Nat Rev Gastroenterol 2011

Page 19: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

ANTIVIRAL TREATMENT BEFORE LIVER TRANSPLANTATION

– Difficult to manage in decompensated cirrhotic patients

– Risk of deterioration of liver function

– Risk of sepsis, severe neutropenia, and anemia

– Poor antiviral effect at this stage

– However, some patients candidates to LT:

» Have preserved liver function (those with HCC)

» Have a long expected waiting time for LT

» Have never been treated or are ”false” non responders

Page 20: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

ANTIVIRAL TREATMENT BEFORE LIVER TRANSPLANTATION

» 124 patients

• 56 Child A, 45 Child B, 23 Child C

• 86 Genotype 1, 16 Genotype 2, 17 Genotype 3

» SVR:

• 50% in genotype non-1,

• 13% in genotype 1

» 22 complications in 15 patients ( 21 in Child B and C), 4 died

» No HCV recurrence in sustained responders.

Everson Hepatology 2005

Page 21: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B

Authors Patients Child Treatment Virologic Response EOT

SVR

Post-LT

Tolerance

Forns

(2003)

30

(Time pre-LT 4

mths)

G1:83%

A 50%

B 43%

C 7%

INF 3M/d

+RBV 800mg

Mean Duration :

12 wks

(2-33 wks)

9 (30%)

Factors for response : viral

laod pre-LT,

Decrease viral load≥ 2 log Wk 4

6/30

(20%)

Decrease INF 60%, RBV

23%

Stop 20%

Sepsis: 2

Liver Failure: 4

Carrion

(2008)

51

G1:80%

51 controls

Meld 11

Peg2a 180g/wk

+RBV

0,8-1g/d

Mean duration: 15 Wks

15 (29%)

Factors response: G non 1,

RVR Wk4

10/51

(20%)

infectious risk

increased by Trt (NS)

ANTIVIRAL TREATMENT PRE-LT

Forns J Hepatol 2003, Carrion J Hepatol 2008

Page 22: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Antiviral Treatment in Patients Waiting

for Liver Transplantation, Risk of Sepsis Related to CPT

Carrión JA et al. J Hepatol. 2009;50:719-28.

Page 23: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Antiviral Treatment in Patients Waiting

for Liver Transplantation, Norfloxacin Prophylaxis

Carrión JA et al. J Hepatol. 2009;50:719-28.

Page 24: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Roche, Samuel Liver Int 2012

Antiviral Treatment Before Transplantation

Page 25: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Direct Antiviral Agents Before LTA New Challenge

• Data In cirrhotic patients are lacking

• Therapies with IFN will remain poorly tolerated

• Increase possibility to achieve SVR or on treatment

virologic response

• Increase risk of virologic breakthrough

• Duration, safety issues to be analysed

• Therapies without IFN awaited

Page 26: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Zeisel J Hepatol 2011

Mechanism of HCV Entry

Page 27: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Feray J Hepatol 2011

Strategies Before and After Transplantation

Page 28: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Roche, Samuel Liver Transplant 2010

Antiviral Treatment Immediately after Transplantation

Page 29: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Antiviral Therapy PegINF+ RBV Post-TransplantationAntiviral Therapy PegINF+ RBV Post-TransplantationAuthors Studie

sPatients Years ETVR SVR Tolerance AR Factors

linked with SVR

Wang 21 (1RCT)

587 1980-05 42%(30-37)

27% (23-31)

Reduction 66% (61-70%)Stop: 26% ( 20-32)

5%(3-7)

No prior antiviral tt post-LTNon-1 G

Berenguer 19 (2RCT)

611 2004-07 42%(17-68)

30%G1: 28%G2: 71-100%G3:41% (30-77%)

Reduction:68%Stop 28%

6.4% EVRG2AdherenceBaseline viremia

Xirouchakis 6 RCT 264 2005-07 - 30%G1: 29%G2: 71-100%G3: 41% ( 30-77)

- 5%

Roche, Samuel Liver Int 2012, Wang AJT 2006, Berenguer J Hepatol 2008, Xirouchakis J Viral Hep 2008

Page 30: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Auto(Allo)immune Hepatitis and IFN

Sharma Liver Transplant 2007

Page 31: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Treatment with PEG IFN + RBV After LT

SVR Dependent of Fibrosis stage

• 27 Pts mild Hepatitis C (F1-F2): SVR 48%

• 27 Pts severe hepatitis C (F3-F4), Cholestatic Hepatitis: SVR 18%

• F3-4: 4/15

• Cholestatic hepatitis, 1/12 (Carrion Gastro 2007)

• 20% F3-F4 vs 1% F1 Patients died or were retransplanted ( Roche

Liver transplant 2008)

Page 32: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

SVR and IL28 in all Genotype Transplant Patients

Lange J Hepatol 11

Page 33: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

SVR According to IL 28

Charlton Hepatology 2011

Page 34: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Survival (Death and Graft Loss) According to IL 28

Charlton Hepatology 2011

IL 28 Recipient IL 28 Donor

Page 35: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

IL 28 In the Donor should be determined on Graft Reperfusion Biopsy or PBMC, not on follow-up Biopsies

Coto-Llorena J Hepatol 2012

Page 36: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

SVR According to IL 28 in Recipient, Donor, and FU Biopsy

Coto-Llorena J Hepatol 2012

Page 37: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Histological Outcome in Relation with Virological Response to PEGIFN+ Ribavirine

Carrion Gastroenterology 2007

Variables associated with Histological improvement: EVR, BR, SVR

Page 38: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Piciotto J Hepatol 2007

Impact of SVR on Suvival in Transplant HCV + Patients

Berenguer M AJT 2008

Page 39: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Direct Antiviral Agents After LTA New Challenge

• Increase possibility to achieve SVR or on treatment virologic

response

• Interaction between anti NS3 protease and calcineurin

inhibitors

• Duration, safety issues to be analysed

• Therapies without IFN awaited

Page 40: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

Garg Hepatology 2011

Telaprevir and Cyclosprine and Tacrolimus Interactions

Cmax increased by 1.4X

AUC Increased by 4.1-4.6X

T1/2 increased by 4 X

Cmax increased by 9.3X

AUC Increased by 70X

T1/2 increased by 5 X

Page 41: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Evolution of Liver Transplantation for Viral Cirrhosis

in Europe.

With HCCWithout HCC

www.eltr.org

Page 42: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

Evolution of Patient Survival after LT for Virus C

Cirrhosis without HCC in Europe (ELTR: 1988-2010)www.eltr.org

Page 43: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

CONCLUSION

• Survival still affected by HCV recurrence

• Monitoring combining liver biopsy and non invasive methods

• Treatment before Transplantation poorly effective

– SVR before LT , no recurrence post-LT

– HCVRNA negativity at LT, Risk of post transplant recurrence

reduced by 70%

• Treatment after transplantation :

– Effective at time of Chronic hepatitis before the F3 stage

» 30-40% SVR in G1 Patients

» 70% SVR in G2-G3 Patients

Page 44: C.H.B. HCV PRE AND POST-LIVER TRANSPLANTATION Professor Didier SAMUEL Centre Hépatobiliaire, Inserm Unit 785, Paris XI University Hopital Paul Brousse,

C.H.B.

CONCLUSION

• Advent of Direct antiviral agents will open a new era

• Before LT: Presence of IFN in the treatment arm will remain a

limitating factor

• After LT: new strategies will arise

• Viral breakthrough, tolerance, interaction with calcineurin

inhibitors, treatment duration:

– Open questions for the close future