Risk of Hepatocellular Cancer Recurrence in Hepatitis C Virus+ Patients Treated with Direct-Acting Antiviral Agents

Background With advent of direct-acting antiviral agents (DAA), hepatitis C virus (HCV) treatment is dramatically increasing. Although few studies reported rates of hepatocellular carcinoma (HCC) recurrence following DAA treatment, there have been no studies that followed sufficient number of DAA-tr...

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Published inDigestive diseases and sciences Vol. 64; no. 11; pp. 3328 - 3336
Main Authors Zou, Winnie Y., Choi, Kati, Kramer, Jennifer R., Yu, Xian, Cao, Yumei, El-Serag, Hashem B., Kanwal, Fasiha
Format Journal Article
LanguageEnglish
Published New York Springer US 01.11.2019
Springer
Springer Nature B.V
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Summary:Background With advent of direct-acting antiviral agents (DAA), hepatitis C virus (HCV) treatment is dramatically increasing. Although few studies reported rates of hepatocellular carcinoma (HCC) recurrence following DAA treatment, there have been no studies that followed sufficient number of DAA-treated patients after successful HCC treatment to examine HCC recurrence. Methods We conducted a cohort study of HCV+ patients who had successfully treated HCC before initiating DAAs. We conducted medical record reviews to confirm HCC diagnosis, treatment, and remission prior to DAA initiation, and subsequent HCC recurrence. We calculated HCC recurrence rate and examined the recurrent tumor characteristics. We used Cox proportional hazard model to identify factors associated with HCC recurrence. Results We identified 264 HCV+ patients who received DAAs after an average of 30.9 (20.6) months following HCC treatment. HCC recurred in 26.1% patients during 23.3 (9.8) months follow-up, at a rate of 0.38 [0.30, 0.48] per 1000 person-month. Most (82.3%) recurrent HCC were early stage. Receiving non-curative treatment for HCC was associated with a higher risk of recurrence than curative treatment (HR adj  = 2.06, [1.24, 3.40]). The risk of HCC recurrence decreased with longer duration between HCC treatment completion and DAA initiation (HR adj  = 0.97, [0.95, 0.99] per additional month). Compared with patients who achieved sustained virological response (SVR), those without SVR had significantly increased risk of HCC recurrence (HR adj  = 4.17, [1.48, 11.75]). Conclusions We conclude that most HCV+ patients with HCC benefit from DAA treatment; however, timing of DAA initiation after HCC treatment should be carefully considered.
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AUTHOR CONTRIBUTIONS
H.B.E. and F.K. conceptualized the study; F.K. supervised all studies performed and is the guarantor of the article; W.Y.Z. and K.C. collected data; W.Y.Z., J.R.K., X.Y., and Y.C. critically analyzed experimental data. W.Y.Z. wrote the manuscript. H.B.E. and F.K. provided critical input in manuscript revision. All authors contributed to the writing or editing of the manuscript and approved the final version of the manuscript.
ISSN:0163-2116
1573-2568
DOI:10.1007/s10620-019-05641-3