학술논문

Randomised clinical trial: alisporivir combined with peginterferon and ribavirin in treatment-naïve patients with chronic HCV genotype 1 infection (ESSENTIAL II)
Document Type
Academic Journal
Author
Zeuzem, S.Flisiak, R.Vierling, J. M.Mazur, W.Mazzella, G.Thongsawat, S.Abdurakhmanov, D.Van Kính, N.Calistru, P.Heo, J.Stanciu, C.Gould, M.Makara, M.Hsu, S.-J.Buggisch, P.Samuel, D.Mutimer, D.Nault, B.Merz, M.Bao, W.Griffel, L. H.Brass, C.Naoumov, N. V.Tanno, HugoBessone, FernandoTerg, RubenFrider, BernardoBertuzzi, RominaDesmond, PaulZekry, AmanyWeltman, MartinGeorge, JacobCrawford, DarrellMatthews, GailMoreno, ChristopheVan Vlierberghe, HansReynaert, HendrikGould, MichaelLee, SamuelRamji, AlnoorTam, EdwardMarotta, PaulYoshida, EricWong, FlorenceFeld, JordanSamuel, DidierMarcellin, PatrickAlric, LaurentZarski, Jean-PierreZoulim, FabienBuggisch, PeterHinrichsen, HolgerGoeser, TobiasZeuzem, StefanGalle, PeterBerg, ThomasSchott, EckartRasenack, JensGerken, GuidoWedemeyer, HansTsang, OwenYuen, Man-FungChan, HenryHui, Aric JosunMakara, MihalyTornai, IstvanGervain, JuditSzalay, FerencVarga, MartaHorvath, GaborHunyady, BelaVincze, AronMazzella, GiuseppeGaeta, Giovanni BattistaAlberti, AlfredoColombo, MassimoAndreone, PietroRizzetto, MarioAngelico, MarioCraxi, AntonioPicciotto, AntoninoSacchi, PaoloVinci, MariaInvernizzi, PietroBruno, SavinoHeo, JeongLee, YounjaeCho, MongHan, SangyoungLee, JinwooAhn, SanghoonLim, YoungsukHwang, SeonggyuSanchez, JuanMuñoz, LindaMaldonado, HectorMazur, WlodzimierzFlisiak, RobertJablkowski, MaciejKryczka, WieslawHalota, WaldemarCalistru, PetrePrelipcean, CristinaMusa, ManuelaStanciu, CarolManuc, MirceaTanasescu, ComanDumitrascu, DanAbdurakhmanov, DjamalChulanov, VladimirNikitin, IgorZhdanov, KonstantinEsaulenko, ElenaMaevskaya, MarinaZnoyko, OlgaLamoglia, Ricard SolaFerret, Maria ButiGarcia-Samaniego, JavierGomez, Manuel RomeroDiago, MoisesCalleja, Jose LuisHsu, Shih-JerChuang, Wan-LongHu, Tsung-HuiPeng, Cheng-YuanChen, Chi-YiKao, Jia-HorngThongsawat, SatawatSukeepaisarnjaroen, WattanaPiratvisuth, TeerhaTanwandee, TawesakKomolmit, PiyawatAgarwal, KoshMutimer, DavidBrown, AshleyFoster, GrahamMcPherson, StuartRyder, StephenPoulos, JohnRustgi, VinodLyche, KipOmarro, StevenVierling, JohnGhalib, ReemKarnam, UmaprasannaPeine, CraigGalati, JosephPerson, JohnDe La Torre, AndrewRavendhran, NatarajanMushahwar, AndriaOʼLeary, JacquelineLee, WilliamLawitz, EricAnkoma-Sey, VictorKing, JohnPound, DavidScarsella, AnthonyThuluvath, PaulPockros, PaulMailliard, MarkShiffman, MitchellSylvestre, DianaHeiman, DavidJacobson, IraBacon, BruceDimitroff, JamesReindollar, RobertTobias, HillelGodofsky, EliotRodriguez-Torres, MaribelBennett, MichaelBen-Zvi, JeffreyVan, Kinh NguyenDao, LongHuu, Hoang BuiMinh, Yen LamLe Thanh, LyVan Long, Dao
Source
Alimentary Pharmacology & Therapeutics. Oct 01, 2015 42(7):829-844
Subject
Language
English
ISSN
0269-2813
Abstract
BACKGROUND: Alisporivir (ALV) is an oral, host-targeting agent with pangenotypic anti-hepatitis C virus (HCV) activity and a high barrier to resistance. AIM: To evaluate efficacy and safety of ALV plus peginterferon-α2a and ribavirin (PR) in treatment-naïve patients with chronic HCV genotype 1 infection. METHODS: Double-blind, randomised, placebo-controlled, Phase 3 study evaluating ALV 600 mg once daily [response-guided therapy (RGT) for 24 or 48 weeks or 48 weeks fixed duration] or ALV 400 mg twice daily RGT with PR, compared to PR alone. Following a Food and Drug Administration partial clinical hold, ALV/placebo was discontinued and patients completed treatment with PR only. At that time, 87% of patients had received ≥12 weeks and 20% had received ≥24 weeks of ALV/PR triple therapy. RESULTS: A total of 1081 patients were randomised (12% cirrhosis, 55% CT/TT IL28B). Addition of ALV to PR improved virological response in a dose-dependent fashion. Overall, sustained virological response (SVR12; primary endpoint) was 69% in all ALV groups vs. 53% in PR control. Highest SVR12 (90%) was achieved in patients treated with ALV 400 mg twice daily and PR for >24 weeks. Seven cases of pancreatitis were reported, with similar frequency between ALV/PR and PR control groups (0.6% vs. 0.8% respectively). Adverse events seen more frequently with ALV/PR than with PR alone were anaemia, thrombocytopenia, hyperbilirubinaemia and hypertension. CONCLUSIONS: Alisporivir, especially the 400 mg twice daily regimen, increased efficacy of PR therapy in treatment-naïve patients with HCV genotype 1 infection. The mechanism of action and pangenotypic activity suggest that alisporivir could be useful in interferon-free combination regimens.