Non‐liver‐related mortality in the DAA era: Insights from post‐SVR patients with and without previous HCC history

Author:

Miuma Satoshi1ORCID,Miyaaki Hisamitsu1,Ichikawa Tatsuki2,Matsuzaki Toshihisa3,Goto Takashi4,Kamo Yasuhiro5,Shigeno Masaya6,Hino Naoyuki7,Ario Keisuke7,Yanagi Kenji8,Tsutsumi Takuya8,Fukushima Nobuyoshi9,Nakashiki Suguru10,Yamasaki Kazufumi11,Hamasaki Keisuke12,Shibata Hidetaka13,Arima Kazuhiko14ORCID,Yamamichi Shinobu2,Yamashima Mio2,Takahashi Kosuke1,Nakao Yasuhiko1,Fukushima Masanori115,Haraguchi Masafumi1,Sasaki Ryu1,Ozawa Eisuke1,Taura Naota1,Nakao Kazuhiko1

Affiliation:

1. Department of Gastroenterology and Hepatology Nagasaki University Graduate School of Biomedical Sciences Nagasaki Japan

2. Department of Gastroenterology Nagasaki Harbor Medical Center City Hospital Nagasaki Japan

3. Department of Gastroenterology Sasebo City General Medical Center Sasebo Japan

4. Department of Gastroenterology Nagasaki Rosai Hospital Sasebo Japan

5. Department of Gastroenterology Hakujujikai Sasebo Chuo Hospital Sasebo Japan

6. Department of Gastroenterology Japanese Red Cross Nagasaki Genbaku Hospital Nagasaki Japan

7. Department of Gastroenterology National Hospital Organization Ureshino Medical Center Ureshino Japan

8. Department of Gastroenterology Nijigaoka Hospital Nagasaki Japan

9. Department of Gastroenterology Nagasaki Goto Chuo Hospital Goto Japan

10. Department of Gastroenterology Inoue Hospital Nagasaki Japan

11. Department of Gastroenterology Saint Francis Hospital Nagasaki Japan

12. Department of Gastroenterology Caritas Clinic Nagasaki Japan

13. Gastroenterology and Hepatology Shibata Chokodo Hospital Shimabara Japan

14. Department of Public Health Nagasaki University Graduate School of Biomedical Sciences Nagasaki Japan

15. Department of Gastroenterology Koebaru Chuo Hospital Nagasaki Japan

Abstract

AbstractBackground and AimsMortality after sustained virological response (SVR) with interferon‐free direct‐acting antiviral (IFN‐free DAA) therapy is crucial for optimizing post‐SVR patient care, but it remains unclear, especially regarding non‐liver‐related mortality.MethodsConsecutive post‐SVR patients from 14 institutions were stratified into three cohorts: A (without advanced fibrosis and without prior HCC), B (with advanced fibrosis and without prior HCC), and C (curative HCC treatment). We assessed mortality (per 1000 person‐years [/1000PY]) post‐SVR. Mortality rates were compared between cohorts A and B and the general population using age‐ and sex‐adjusted standardized mortality ratio (SMR). Comparison of survival between each cohort was performed using propensity‐score (PS) matching with sex, age, and comorbidity.ResultsIn cohort A (n = 762; median age, 65 years), 22 patients died (median follow‐up, 36 months); all‐cause mortality was 10.0/1000PY, with 86.4% non‐liver‐related deaths. In cohort B (n = 519; median age, 73 years), 27 patients died (median follow‐up, 39 months); all‐cause mortality was 16.7/1000PY, with 88.9% non‐liver‐related deaths. In both cohorts, malignant neoplasm was the most common cause of death; all‐cause mortality was comparable to that of the general population (SMR: 0.96 and 0.92). In cohort C (n = 108; median age, 75 years), 15 patients died (median follow‐up, 51 months); all‐cause mortality was 36.0/1000PY, with 53.3% liver‐related deaths. PS matching showed no significant survival differences between cohorts A and B, both of which had better survival than cohort C.ConclusionsMortality varies based on HCC history in the DAA era; nevertheless, attention should be paid to non‐liver‐related deaths in all post‐SVR patients.

Publisher

Wiley

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