- Category: Experimental HCV Drugs
- Published on Tuesday, 11 March 2014 00:00
- Written by Liz Highleyman
An all-oral regimen of daclatasvir plus simeprevir, without interferon or ribavirin, led to sustained response in 85% to 95% of patients with hepatitis C genotype 1b, but this combination did not work well against genotype 1a, researchers reported last week at the 21st Conference on Retroviruses and Opportunistic Infections (CROI 2014) in Boston.
The advent of direct-acting antivirals that target different steps of the hepatitis C virus (HCV) lifecycle has begun to bring about a revolution in treatment, curing more people in a shorter time without the side-effects of interferon. As new medications emerge from the development pipeline, people with hepatitis C and their doctors are eager for more data about which drugs work best in which combinations and for which patients.
Christophe Hézode from Hôpital Henri Mondor in Paris presented findings from LEAGUE-1, a multicenter European trial evaluating the safety and efficacy of a dual oral regimen of daclatasvir plus simeprevir for treatment-naive people and prior null responders with genotype 1 chronic hepatitis C.
Bristol-Myers Squibb's NS5A inhibitor daclatasvir has shown promising outcomes in all-oral combinations with drugs including the HCV protease inhibitor asunaprevir and Gilead Sciences' recently approved HCV polymerase inhibitor sofosbuvir (Sovaldi). The daclatasvir/asunaprevir combination has been submitted for approval in Japan, and the U.S. FDA has designated it as a "breakthrough therapy" for expedited review. Daclatasvir is pending European Union approval for use with other direct-acting agents.. Janssen's NS3/4A protease inhibitor simeprevir (Olysio) has been approved in the U.S. and Japan, and is awaiting European approval.
The main part of the LEAGUE-1 trial (AI444-062) included 147 participants with HCV genotype 1b, including 104 previously untreated patients and 43 prior null responders. Null responders had little or no response to a prior attempt at interferon-based therapy and are considered the most difficult group to treat. An exploratory part of the study looked at 21 people with harder-to-treat HCV genotype 1a.
Just over half of the genotype 1b patients were women, more than 90% were white and the median age was approximately 55 years. The genotype 1a patients were mostly white men. In both genotype groups, more than one-quarter of treatment-naive patients -- but no more than 5% of null responders -- had the favorable IL28B gene variant associated with good interferon responsiveness. About 15% of untreated patients had liver cirrhosis, as assessed by biopsy or FibroScan, rising to 40% of null responders. (The overall proportion of participants with advanced fibrosis or cirrhosis was capped at 35% in the trial protocol.)
Participants with genotype 1b were randomly assigned to receive 30 mg once-daily daclatasvir plus 150 mg once-daily simeprevir, either with or without weight-based ribavirin. After 12 weeks of treatment, they were re-randomized to either stop all treatment or continue their assigned regimen for an additional 12 weeks. In the exploratory part, all genotype 1a patients received daclatasvir, simeprevir, and ribavirin for 24 weeks.
Simeprevir is processed by the CYP450 enzyme system and can interact with other drugs including daclatasvir. Previous pharmacokinetic studies in healthy volunteers without hepatitis C showed that daclatasvir levels doubled when combined with simeprevir. The 30 mg dose used in in LEAGUE-1 was based on these findings, but the researchers noted that daclatasvir exposure was "less than anticipated" in this study.
The primary study endpoint was sustained virological response at 12 weeks after completing treatment (SVR12).
- Among genotype 1b treatment-naive participants, SVR12 rates were 85% with the dual daclatasvir and simeprevir regimen, and 75% with the triple daclatasvir, simeprevir, and ribavirin regimen in an intent-to-treat analysis.
- In an observed analysis excluding people with missing data at week 12, the SVR12 rates were 90% and 83%, respectively.
- Looking at the effect of treatment duration, 81% of naive patients using the dual regimen for 12 weeks and 89% treated for 24 weeks achieved SVR12.
- Among those receiving the triple regimen, SVR12 rates were 75% for 12 weeks and 74% for 24 weeks, not a significant difference.
- Turning to the genotype 1b prior null responders, SVR12 rates were 65% with the dual regimen and 95% with the triple regimen in an intent-to-treat analysis.
- In an observed analysis, the corresponding rates were 79% and 95%, respectively.
- Looking again at treatment duration, 83% of null responders taking the dual regimen for 12 weeks and 50% treated for 24 weeks achieved SVR12.
- Among those taking the triple regimen, SVR12 rates were 100% for 12 weeks and 89% for 24 weeks.
- Overall, participants with liver cirrhosis did about as well as those without; SVR12 rates were 56%-100% for cirrhotics compared with 71%-94% for non-cirrhotics, but the number of cirrhotic patients in each treatment arm was small.
- Of the 15 cases of observed viral breakthrough during therapy, 11 occurred at or before treatment week 8.
- Of the 6 people who experienced post-treatment relapse, 2 were treated for 12 weeks, 3 were treated for 24 weeks, and 1 stopped treatment prematurely after 2 weeks.
- In the exploratory genotype 1a analysis, 67% of treatment-naive participants achieved SVR12 -- including both patients with cirrhosis -- while 4 of the 12 (33%) experienced viral breakthrough.
- 7 of the 9 genotype 1a null responders experienced viral breakthrough, and they were given the option to add pegylated interferon to their regimen.
- Daclatasvir and simeprevir were generally safe and well-tolerated.
- 9% of people taking the dual regimen and 4% who used ribavirin experienced serious adverse events.
- 3% and 2%, respectively, discontinued treatment due to adverse events.
- 8 people developed elevated bilirubin, all but 1 of them in the ribavirin arms.
- No one in either arm reported serious anemia, a potential side effect of ribavirin.
Based on these findings, the researchers concluded that the all-oral combination of low-dose 30 mg daclatasvir plus 150 mg simeprevir, both once-daily, with or without ribavirin "achieved SVR12 rates of 75-85% in treatment-naive patients and 65-95% in prior null responders with genotype 1b infection," while there was a "high rate of virologic breakthrough in genotype 1a null responders."
Hézode said response rates were similar in ribavirin-containing and ribavirin-sparing arms, "suggesting its possible to treat these patients without ribavirin." Likewise, SVR rates "seem similar" in cirrhotic and non-cirrhotic patients. Finally, the results suggest that 12 weeks of therapy is "optimal," and there was not a significant difference with longer treatment.
Further studies of daclatasvir in direct-acting antiviral studies -- including those with simeprevir -- will use the recommended 60 mg dose of daclatasvir, the researchers noted.
S Zeuzem, C Hezode, JPP Bronowicki, et al (LEAGUE-1 Study Team). Daclatasvir in Combination With Simeprevir ± Ribavirin for Hepatitis C Virus Genotype 1 Infection. 21st Conference on Retroviruses and Opportunistic Infections (CROI 2014). Boston, March 3-6. Abstract 28LB.