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DOI 10.1007/s00535-017-1396-0

Медицинская библиотека · Journal of gastroenterology · 2017

Efficacy and safety of glecaprevir/pibrentasvir in HCV-infected Japanese patients with prior DAA experience, severe renal impairment, or genotype 3 infection.

Kumada Hiromitsu, Watanabe Tsunamasa, Suzuki Fumitaka, Ikeda Kenji, Sato Ken, Toyoda Hidenori, Atsukawa Masanori, Ido Akio, Takaki Akinobu, Enomoto Nobuyuki, Kato Koji, Alves Katia, Burroughs Margaret, Redman Rebecca, Pugatch David, Pilot-Matias Tami J, Krishnan Preethi, Oberoi Rajneet K, Xie Wangang, Chayama Kazuaki

Клиническое исследование III фазыСтатьяМногоцентровое исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Once-daily, orally administered, co-formulated glecaprevir (NS3/4A protease inhibitor) and pibrentasvir (NS5A inhibitor) (G/P) demonstrated pangenotypic activity and high sustained virologic response (SVR) rates in studies outside Japan. Here we report safety and efficacy in a subset of Japanese patients with chronic HCV infection who received G/P 300/120 mg in a phase 3, open-label, multicenter study (CERTAIN-1).

METHODS

This analysis focuses on three difficult-to-treat subgroups: HCV GT1/2-infected patients who failed to achieve SVR after treatment with a direct acting antiviral (DAA)-containing regimen; GT1/2-infected patients with severe renal impairment (estimated glomerular filtration rate < 30 mL/min/1.73 m2); and GT3-infected patients. Patients in the renal impairment and GT3 cohorts were treatment-naive or interferon treatment-experienced. Noncirrhotic GT1/2-infected, DAA-naïve patients in the renal impairment cohort received G/P for 8 weeks; all other patients were treated for 12 weeks. Primary outcome was SVR (HCV RNA < 15 IU/mL) 12 weeks post-treatment (SVR12).

RESULTS

The study enrolled 33 GT1/2-infected patients who failed previous DAA treatment (four with cirrhosis); 12 GT1/2-infected patients with severe renal impairment (two with cirrhosis); and 12 GT3-infected patients (two with cirrhosis). SVR12 was achieved by 31/33 (93.9%), 12/12 (100%), and 10/12 (83.3%) patients, respectively. One serious adverse event (fluid overload, not related to G/P) occurred in a patient on chronic intermittent hemodialysis.

CONCLUSIONS

G/P achieved high SVR12 rates and was well tolerated in three difficult-to-treat patient subgroups with limited treatment options in Japan (DAA-experienced patients, patients with severe renal impairment, and GT3-infected patients). These results support the potential suitability of this regimen for these special populations in Japan.

Для цитирования: Kumada Hiromitsu, Watanabe Tsunamasa, Suzuki Fumitaka, Ikeda Kenji, Sato Ken, Toyoda Hidenori, Atsukawa Masanori, Ido Akio, Takaki Akinobu, Enomoto Nobuyuki, Kato Koji, Alves Katia, Burroughs Margaret, Redman Rebecca, Pugatch David, Pilot-Matias Tami J, Krishnan Preethi, Oberoi Rajneet K, Xie Wangang, Chayama Kazuaki. Efficacy and safety of glecaprevir/pibrentasvir in HCV-infected Japanese patients with prior DAA experience, severe renal impairment, or genotype 3 infection.. Journal of gastroenterology. 2017. DOI: 10.1007/s00535-017-1396-0.

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