Review
Copyright ©The Author(s) 2015.
World J Hepatol. Jul 28, 2015; 7(15): 1936-1952
Published online Jul 28, 2015. doi: 10.4254/wjh.v7.i15.1936
Table 1 Trials of direct-acting antivirals for chronic hepatitis C infection in human immunodeficiency virus co-infected patients
StudyGTTx regimenTx duration (wk)Hepatitis C characteristicsSVR12
GTFibrosis stageTreatment status
P05411[100]1PegIFNα-2b + RBVBOC: 44Tx naïveBOC
wb (600-1400 mg) +PegIFN/RBV: 48Metavir F0-4GT1: 42/64 (66%)
BOC vs placeboCirrhosis: 3%GT1a: 32/51 (63%)
GT1b: 7/12 (58%)
Placebo GT1: 9/34 (26%)
VX08-950-110[101]1PegIFNα-2a + RBVTPV: 12Tx naïveTPV
800 mg or wbPegIFN/RBV: 48Metavir F0-4GT1: 28/38 (74%)
(1000-1200 mg) +GT1a: 20/27 (74%)
TVR vs placeboGT1b: 7/11 (64%)
Placebo
GT1: 10/22 (45%)
GT1a: 4/14 (29%)
GT1b: 4/6 (67%)
ANRS HC261PegIFNα-2a + RBVTPV: 12Tx expGT1: 55/69 (80%)F1-2Relapse
TelapreVIH[95]wb (1000-1200 mg)PegIFN/RBV (RGT): 44 or 72Metavir F0-4GT1a: 36/48 (75%)34/42 (81%)20/27 (74%)
+ TVRBoth cirrhosis and priorGT1b: 19/21 (90%)F3-4Breakthrough
null-response excluded21/27 (78%)5/6 (83%)
Partial response
15/15 (100%)
Null response
15/21 (71%)
P7977-1910[102]1-4SOF + PegIFNα-2a12Tx naïveAll GTs: 21/23 (91%)
+ RBV wbNo cirrhosisGT1: 17/19 (89%)
(1000-1200 mg)[GT1a: 13/15 (87%)
GT1b: 4/4]
GT2: 1/1
GT3: 2/2
GT4: 1/1
STARTVerso4[103,104]1FDV 240 mg (EFV) or 120 mgFDV: 24 or (12 vs 24),PegIFN/RBV Tx naïveGT1: 221/308 (72%)No CirrhosisTx naïve
(ATV/r or DRV/r) or 120 vs 240 mgPegIFN/RBV (RGT): 48 oror prior relapseGT1a: 171/242 (71%)187/261 (72%)164/239 (69%)
(RAL or MVC or no ART) +24 wk vs 48 wkCompensated cirrhosis: 15%GT1b: 50/66 (76%)CirrhosisRelapse
PegIFNα-2a + RBV wb (1000-1200 mg)33/45 (73%)57/69 (83%)
C212[105]1SMV + PegIFNα-2a + RBV wbSMV: 12PegIFN/RBV Tx naïveGT1: 78/106 (74%)F0-2Tx naïve
(1000-1200 mg)PegIFN/RBV RGT: (24 vs 48)or Tx expGT1a: 62/88 (70%)36/45 (80%)42/53 (79%)
for Tx naïve or prior relapseMetavir F0-4; Cirrhosis:GT1b: 16/18 (89%)F3-4Relapse
or 48 for partial-6%-30% by Tx arm14/22 (64%)13/15 (87%)
or null-response or cirrhosisPartial response
7/10 (70%)
Null response
16/28 (57%)
PHOTON-1[106]1-3SOF + RBV wb (1000-1200 mg)GT 1: 24Tx naïve (GT1-3) or exp (GT2-3)GT1: 87/114 (76%)No CirrhosisTx naïve
GT 2-3 Tx naïve: 12Cirrhosis ≤ 20%[GT1a: 74/90 (82%)GT1: 84/109 (77%)GT1: 87/114 (76%)
GT 2-3 Tx exp: 24GT1b: 13/24 (54%)]GT2: 22/25 (88%)GT2: 23/26 (88%)
GT2: 44/50 (88%)GT3: 24/36 (67%)GT3: 28/42 (67%)
GT3: 44/59 (75%)CirrhosisTx exp
GT1: 3/5 (60%)GT2: 22/24 (92%)
GT2: 1/1GT3: 16/17 (94%)
GT3: 4/6 (67%)
PHOTON-2[107]1-4SOF + RBV wb (1000-1200 mg)GT 1, 3, 4: 24Tx naïve (GT1-4) or exp (GT 2-3)GT1: 95/112 (85%)No CirrhosisTx naïve
GT 2 Tx naïve: 12Compensated cirrhosis: 20% of patients[GT1a: 84/100 (84%)GT1: 84/95 (88%)GT 1: 95/112 (85%)
GT 2 Tx exp: 24GT1b: 10/11 (91%)]GT2: 19/22 (86%)GT2: 17/19 (89%)
GT2: 22/25 (88%)GT3: 73/80 (91%)GT3: 52/57 (91%)
GT3: 94/106 (89%)GT4: 19/23 (83%)GT4: 26/31 (84%)
GT4: 26/31 (84%)CirrhosisTx exp:
GT1: 11/17 (65%)GT2: 5/6 (83%)
GT2: 3/3GT3: 41/49 (84%)
GT3: 21/26 (81%)
GT4: 7/8 (88%)
TURQUOISE-I[108]1Paritaprevir/r/Ombitasvir +12 or 24Tx naïve or PegIFN/RBV expTx for 12 wk
Dasabuvir + RBV wb (1000-1200 mg)Cirrhosis ≤ 30%GT1: 29/31 (94%)
Tx for 24 wk
19/20 (95%)
ERADICATE[109]1SOF/LDV12Tx naïveUntreated HIV Infection
Knodell F0-3GT1: 10/10
C-WORTHY[110]1Grazoprevir + MK-8742 +/- RBV12Tx naïveWith RBV
No cirrhosis28/29 (97%)
Metavir F0-3Without RBV
26/29 (90%)