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Sofosbuvir/velpatasvir shows high cure rate in HIV/HCV co-infection study
Liz Highleyman, 2016-07-21 14:10:00
The once-daily co-formulation of sofosbuvir and velpatasvir was highly effective against all hepatitis C virus (HCV) genotypes in HIV/HCV co-infected patients and was safe and well tolerated in the ASTRAL-5 trial, according to results presented yesterday at the 21st International AIDS Conference (AIDS 2016) in Durban, South Africa. A related analysis showed that sofosbuvir/velpatasvir can be safely combined with most widely used antiretrovirals, with the exception of efavirenz.
HIV-positive people co-infected with HCV experience more rapid liver disease progression than those with hepatitis C alone, and liver disease remains a major cause of morbidity and mortality among people living with HIV.
The advent of direct-acting antiviral agents for hepatitis C has enabled shorter, better tolerated and much more effective treatment. The latest interferon-free regimens demonstrate cure rates approaching 100%, and unlike the older interferon-based therapy, they work as well for people with and without HIV co-infection.
But most of the new drugs work best against HCV genotype 1, which is the most prevalent type in Europe and the US. Genotype 3 is now considered the most difficult to treat, while genotypes 4, 5 and 6 do not have as much data. A pangenotypic regimen - one that is active against all genotypes - would simplify treatment because it could be prescribed without the need for genotype testing.
Norbert Bräu of the Icahn School of Medicine at Mt Sinai in New York City presented findings from ASTRAL-5, a phase 3 trial of HIV/HCV co-infected patients evaluating Gilead Sciences' pangenotypic co-formulation combining the HCV NS5B polymerase inhibitor sofosbuvir (marketed alone as Sovaldi) and the second-generation NS5A inhibitor velpatasvir (formerly GS-5816). European and US regulators recently approved the co-formulation, marketed as Epclusa.
As reported at last year's AASLD Liver Meeting, the sofosbuvir/velpatasvir combination demonstrated high sustained response rates for HIV-negative hepatitis C mono-infected patients in the ASTRAL-1 (genotypes 1, 2, 4, 5 and 6), ASTRAL-2 (genotype 2 only), ASTRAL-3 (genotype 3) andASTRAL-4 (decompensated liver disease) trials.
ASTRAL-5 enrolled 106 HIV-positive chronic hepatitis C patients in the US with any HCV genotype. A majority (62%) had HCV genotype 1a, followed by 1b (11%), 2 (10%), 3 (11%) and 4 (5%); none had genotypes 5 or 6.
Most participants (86%) were men, 45% were black and the mean age was 54 years. Just under a third were previously treated for hepatitis C and 18% had compensated liver cirrhosis. At baseline the mean HCV RNA level was 6.3 log10.
Looking at HIV status, participants were on stable antiretroviral therapy (ART) for at least 8 weeks with undetectable HIV viral load and a mean CD4 T-cell count of approximately 600 cells/mm3. They were taking a variety of ART regimens, most often including the HIV protease inhibitors atazanavir (Reyataz), darunavir (Prezista) or lopinavir/ritonavir (Kaletra) (47% on a PI); the integrase inhibitors raltegravir (Isentress) or elvitegravir (Vitekta) (34% taking this class); or the NNRTI rilpivirine (Edurant; 12%). Most used NRTI backbones containing tenofovir in a boosted (53%) or unboosted (33%) regimen.
All participants in this open-label study received 400mg sofosbuvir plus 100mg velpatasvir taken as a once-daily co-formulation for 12 weeks. They were followed for 12 weeks after completing treatment to assess sustained virological response (SVR12), or continued undetectable HCV viral load.
At the end of post-treatment follow-up the overall SVR12 rate was 95% (101 out of 106 treated patients) - similar to cure rates seen in studies of HIV-negative hepatitis C patients. Response rates ranged from 92% for genotypes 1b and 3 (reflecting a single drop-out in each arm), to 95% for genotype 1a (two relapses and one drop-out), to 100% for genotypes 2 and 4.
Cure rates were similar regardless of the presence or absence of cirrhosis (100% and 94%, respectively) and for hepatitis C treatment-naive and treatment-experienced patients (93% and 97%, respectively). HCV drug resistance also did not have a notable effect, as the 12 participants with NS5A resistance-associated variants at baseline all achieved SVR12.
The sofosbuvir/velpatasvir combination was generally safe and well tolerated. There were two serious adverse events not attributed to the study drugs and two treatment discontinuations due to adverse events; 18% experienced grade 3 or 4 laboratory abnormalities (mostly elevated bilirubin in people taking boosted atazanavir). The most common side effects were fatigue (25%) and headache (13%). No one experienced HIV viral rebound while on hepatitis C treatment.
The researchers took a closer look at kidney function, to see whether boosted tenofovir was associated with kidney toxicity when combined with the hepatitis C drugs. Creatinine clearance remained stable over time in all ART regimen arms. It was lower (indicating more impairment) among people taking boosted versus unboosted tenofovir, but lowest among people not taking tenofovir.
"Sofosbuvir/velpatasvir for 12 weeks provides a simple, safe and highly effective treatment for patients coinfected with HIV-1 and HCV," the researchers concluded.
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