Hepatitis C Virus Cure Rates Are Reduced in Patients With Active but Not Inactive Hepatocellular Carcinoma: A Practice Implication

Author:

Ogawa Eiichi1,Toyoda Hidenori2,Iio Etsuko3,Jun Dae Won4,Huang Chung-Feng5,Enomoto Masaru6,Hsu Yao-Chun7,Haga Hiroaki8,Iwane Shinji9,Wong Grace1011,Lee Dong Hyun12,Tada Toshifumi2,Liu Chen-Hua1314,Chuang Wan-Long5,Hayashi Jun15,Cheung Ramsey1617,Yasuda Satoshi2,Tseng Cheng-Hao7,Takahashi Hirokazu918,Tran Sally16,Yeo Yee Hui16,Henry Linda16,Barnett Scott D16,Nomura Hideyuki19,Nakamuta Makoto20,Dai Chia-Yen5,Huang Jee-Fu5,Yang Hwai-I21,Lee Mei-Hsuan22,Jun Mi Jung12,Kao Jia-Horng1314,Eguchi Yuichiro9,Ueno Yoshiyuki8,Tamori Akihiro6,Furusyo Norihiro1,Yu Ming-Lung5,Tanaka Yasuhito3,Nguyen Mindie H16,

Affiliation:

1. Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan

2. Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan

3. Department of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan

4. Department of Gastroenterology, Hanyang University, Seoul, South Korea

5. Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan

6. Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan

7. Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Hospital, Kaohsiung, Taiwan

8. Department of Gastroenterology, Yamagata University Faculty of Medicine, Yamagata, Japan

9. Liver Center, Saga University Hospital, Saga, Japan

10. Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong

11. State Key Laboratory of Digestive Disease, The Chinese University of Hong Kong, Hong Kong

12. Department of Gastroenterology, Good Gang-An Hospital, Busan, Korea

13. Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan

14. Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan

15. Kyushu General Internal Medicine Center, Haradoi Hospital, Fukuoka, Japan

16. Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA

17. Division of Gastroenterology and Hepatology, Veterans Affairs Palo Alto Health Care System, Palo Alto, California, USA

18. Division of Metabolism and Endocrinology, Saga University Faculty of Medicine, Saga, Japan

19. The Center for Liver Disease, Shin-Kokura Hospital, Kitakyushu, Japan

20. Department of Gastroenterology, Kyushu Medical Center, National Hospital Organization, Fukuoka, Japan

21. Genomics Research Center, Academia Sinica, Taipei, Taiwan

22. Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan

Abstract

Abstract Background Cure rates of hepatitis C virus (HCV) treatment with direct-acting antivirals (DAAs) for patients with active and inactive hepatocellular carcinoma (HCC) may differ, but well-controlled studies are limited. We aimed to evaluate DAA outcomes in a large East Asian HCV/HCC population compared with HCV/non-HCC patients. Methods Using data from the Real-World Evidence from the Asia Liver Consortium (REAL-C) registry (Hong Kong, Japan, South Korea, and Taiwan), we used propensity score matching (PSM) to match HCC and non-HCC (1:1) groups for age, sex, cirrhosis, prior treatment, HCV genotype, treatment regimen, baseline platelet count, HCV RNA, total bilirubin, alanine aminotransferase, and albumin levels to evaluate DAA treatment outcomes in a large population of HCV/HCC compared with HCV/non-HCC patients. Results We included 6081 patients (HCC, n = 465; non-HCC, n = 5 616) treated with interferon-free DAAs. PSM of the entire study population yielded 436 matched pairs with similar baseline characteristics. There was no statistically significant difference in the overall SVR rate of HCC (92.7%) and non-HCC (95.0%) groups. Rates of treatment discontinuation, adverse effects, and death were also similar between HCC and non-HCC groups. Among patients with HCC, those with active HCC had a lower SVR than inactive HCC cases (85.5% vs 93.7%; P = .03). On multivariable analysis, active HCC, but not inactive HCC, was significantly associated with lower SVR (OR, 0.28; P = .01) when compared with non-HCC. Conclusions Active HCC but not inactive HCC was independently associated with lower SVR compared with non-HCC patients undergoing DAA therapy, although cure rate was still relatively high (85%) in active HCC patients.

Funder

Gilead Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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