Hepatitis C in HIV Coinfection. Annie Luetkemeyer, MD Division of HIV, ID and Global Medicine ZSFG, UCSF
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1 Hepatitis C in HIV Coinfection Annie Luetkemeyer, MD Division of HIV, ID and Global Medicine ZSFG, UCSF
2 Disclosures I have received research grant support to UCSF related to HCV from the following: Abbvie Bristol Myers Squibb (BMS) Gilead Merck Pfizer ACTG (NIH)
3 HCV Deaths vs. Other Notifiable Infectious Diseases (including HIV, TB & HBV) in US Globally HCV ~ million ~ 3.5 million Ab+ (2.7 HCV RNA, likely underestimate ) HIV 36 million 1.2 million HIV-HCV > 2 million ~ 25% US Ly CID 2016
4 Natural history of HCV in HIV Higher HCV viral load in HIV If HCV untreated, faster progression to cirrhosis Higher incidenceof hepatocellular carcinoma which can present with more aggressive and widespread forms in HIV
5 Good news about HIV/HCV Excellent and generally equivalent cure rates (>95% cure rate) Generally same HCV treatment recommendations & duration HCV treatment options available for nearly every ART regimen
6 Less Good News Managing ART /DAA drug interactions can be complex Good data available and many excellent resources AASLD/IDSA Guidelines: University of Liverpool HCV Drug interactions:
7 ART + DAA Scorecard SOF Ledipasvir VEL Daclatasvir P/r/O + D EBR/GZP ATV/r No data LDV ; ATV a VEL ; ATV a DCV * ATV ; PAR GZP & EBV, ATV DRV/r SOF ; DRV LDV ; DRV a VEL ; DRV a DCV, DRV DRV ; PAR / GZP & ELB ; DRV LPV/r No data No data VEL ; LPV a DCV, LPV LPV ; PAR GZP & EBR ; DRV EFV SOF ; EFV LDV EFV VEL ; EFV DCV ** No PK data** GZP & EBR, EFV RPV SOF ; RPV LDV ; RPV VEL ; RPV No PK data (clinical trial data ok) PAR ; RPV GZP & EBR ; RPV ETV No data No data No Data DCV ** No data No data RAL SOF ; RAL LDV ; RAL VEL ; RAL No PK data (clinical trial data ok) PrOD ; RAL GZP & EBR ; RAL ELV/cob Cobi ; SOF a LDV ; SOF a VEL ; COBI No data No data GZP & EBV, ATV DTG No data LDV ; DOL VEL ; RAL DCV ; TFV PAR ; DOL GZP & EBR ; DOL MVC No data No data No Data No data No data No data TDF SOF ;TFV LDV ; TFV VEL ; TFV DCV ; TFV PrOD ; TFV GZP & EBR ; TFV TAF SOF ;TFV LDV ;TFV VEL ;TFV No Data No Data No Data Decrease DCV dose to 30mg QD, **Increase DCV dose to 90mg QD, *** 3D + EFV led to premature study discontinuation due to toxicities, a only of concern when coadministered with TDF Adapted from Jennifer Kiser
8 ART with least interactions with DAAs SOF Ledipasvir VEL Daclatasvir P/r/O + D EBR/GZP ATV/r No data LDV ; ATV a VEL ; ATV a DCV * ATV ; PAR GZP & EBV, ATV DRV/r SOF ; DRV LDV ; DRV a VEL ; DRV a DCV, DRV DRV ; PAR / GZP & ELB ; DRV LPV/r No data No data VEL ; LPV a DCV, LPV LPV ; PAR GZP & EBR ; DRV EFV SOF ; EFV LDV EFV VEL ; EFV DCV ** No PK data** GZP & EBR, EFV RPV SOF ; RPV LDV ; RPV VEL ; RPV No PK data (clinical trial data ok) PAR ; RPV GZP & EBR ; RPV ETV No data No data No Data DCV ** No data No data RAL SOF ; RAL LDV ; RAL VEL ; RAL No PK data (clinical trial data ok) PrOD ; RAL GZP & EBR ; RAL ELV/cob Cobi ; SOF a LDV ; SOF a VEL ; COBI No data No data GZP & EBV, ATV DTG No data LDV ; DOL VEL ; RAL DCV ; TFV PAR ; DOL GZP & EBR ; DOL MVC No data No data No Data No data No data No data TDF SOF ;TFV LDV ; TFV VEL ; TFV DCV ; TFV PrOD ; TFV GZP & EBR ; TFV TAF SOF ;TFV LDV ;TFV VEL ;TFV No Data No Data No Data Decrease DCV dose to 30mg QD, **Increase DCV dose to 90mg QD, *** 3D + EFV led to premature study discontinuation due to toxicities, a only of concern when coadministered with TDF Adapted from Jennifer Kiser
9 The bad news: Reinfection in HIV+ MSM Meta-analysis of 5 year HCV reinfection risk High and equivalent SVR rates Risk for reinfection NEAT European Cohort HIV+ MSM 25% reinfection rate over 12 yrs 7.3/100py Not Just HIV+ MSM at risk: MSM on PREP with sexually acquired HCV Simmons CID March 2016, Inglitz J Hep 2016, Volk CID 2015:60
10 2016 HCV Report card Whom to treat: everyone Evidence clearly supports treatment in all HCVinfected persons except those with limited life expectancy (less than 12 months) due to non liver related comorbid conditions (AASLD/IDSA guidelines) First pangenotype, single pill therapy approved Duration for most patients: 8-12 weeks >95% cure in vast majority of patients Most do not require ribavirin Effective options for historically hardest to treat populations HIV/HCV coinfected Active injection drug users & those on opiate substitution therapy Cirrhotics, including decompensated Prior treatment failures Renal failure Genotype 3
11 Than Thank you!
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