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Independent Risk Factors for Hepatocellular Carcinoma Recurrence after Direct-Acting Antiviral Therapy in Patients with Chronic Hepatitis C
Background/Aims: This study was performed to evaluate the efficacy of direct-acting antivirals (DAAs) in Korean patients with hepatitis C virus (HCV)-related hepatocellular carcinoma (HCC) and to investigate the risk factors associated with HCC recurrence. Methods: A total of 100 patients with HCV-r...
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Published in: | Gut and liver 2021-05, Vol.15 (3), p.410 |
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container_title | Gut and liver |
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creator | Young-hwan Ahn Heirim Lee Do Young Kim Hye Won Lee Su Jong Yu Young Youn Cho Jeong Won Jang Byoung Kuk Jang Chang Wook Kim Hee Yeon Kim Hana Park Hyo Jung Cho Bumhee Park Soon Sun Kim Jae Youn Cheong |
description | Background/Aims: This study was performed to evaluate the efficacy of direct-acting antivirals (DAAs) in Korean patients with hepatitis C virus (HCV)-related hepatocellular carcinoma (HCC) and to investigate the risk factors associated with HCC recurrence.
Methods: A total of 100 patients with HCV-related HCC, who were treated with DAAs between May 2015 and December 2016, were recruited from seven university hospitals in Korea. Claim data of 526 patients with HCC obtained from the Health Insurance Review and Assessment Service in South Korea were used for external validation of the results.
Results: Among the 100 patients, 88% achieved a sustained virological response (SVR) 12 weeks after the end of DAA therapy (SVR12), and 37% experienced HCC recurrence after DAA therapy. Short last HCC treatment durability ( |
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fullrecord | <record><control><sourceid>kiss</sourceid><recordid>TN_cdi_kiss_primary_3887664</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><kiss_id>3887664</kiss_id><sourcerecordid>3887664</sourcerecordid><originalsourceid>FETCH-kiss_primary_38876643</originalsourceid><addsrcrecordid>eNp9jbtuwkAQAK8gUsjjC2j2ByyBDbYpkRNEOoTo0eqyxgvHnbW7JOIb8tMgkZpmpphiBm44mVdllud18exeVA_jcTnJq9nQ_X3Fb-rphmiwYT3CEr0lUWiTwIp6tOQphHNAgQbFc0wnhA35swhFT4CtkcAHC3nLFt447mERjX9YMMC2I8H-Ahxhjca3i8IvWwdNJymyvy_YWKF5c08tBqX3f7-60fJz26yyI6vueuETymVX1HVVltPicb0CShdOtw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Independent Risk Factors for Hepatocellular Carcinoma Recurrence after Direct-Acting Antiviral Therapy in Patients with Chronic Hepatitis C</title><source>PubMed Central</source><creator>Young-hwan Ahn ; Heirim Lee ; Do Young Kim ; Hye Won Lee ; Su Jong Yu ; Young Youn Cho ; Jeong Won Jang ; Byoung Kuk Jang ; Chang Wook Kim ; Hee Yeon Kim ; Hana Park ; Hyo Jung Cho ; Bumhee Park ; Soon Sun Kim ; Jae Youn Cheong</creator><creatorcontrib>Young-hwan Ahn ; Heirim Lee ; Do Young Kim ; Hye Won Lee ; Su Jong Yu ; Young Youn Cho ; Jeong Won Jang ; Byoung Kuk Jang ; Chang Wook Kim ; Hee Yeon Kim ; Hana Park ; Hyo Jung Cho ; Bumhee Park ; Soon Sun Kim ; Jae Youn Cheong</creatorcontrib><description>Background/Aims: This study was performed to evaluate the efficacy of direct-acting antivirals (DAAs) in Korean patients with hepatitis C virus (HCV)-related hepatocellular carcinoma (HCC) and to investigate the risk factors associated with HCC recurrence.
Methods: A total of 100 patients with HCV-related HCC, who were treated with DAAs between May 2015 and December 2016, were recruited from seven university hospitals in Korea. Claim data of 526 patients with HCC obtained from the Health Insurance Review and Assessment Service in South Korea were used for external validation of the results.
Results: Among the 100 patients, 88% achieved a sustained virological response (SVR) 12 weeks after the end of DAA therapy (SVR12), and 37% experienced HCC recurrence after DAA therapy. Short last HCC treatment durability (<12 months) before DAA commencement was independently associated with HCC recurrence (hazard ratio [HR], 2.89; p=0.011). In the nationwide validation cohort, 20.3% of the patients experienced HCC recurrence. The last HCC treatment with a noncurative method, a short last HCC treatment durability (<12 months), and a longer total duration of HCC treatment (≥18 months) were independently related with HCC recurrence (HR 3.73, p<0.001; HR 3.34, p<0.001; and HR 1.74, p=0.006; respectively).
Conclusions: DAA therapy showed an acceptable SVR12 rate in patients with HCV-related HCC. Short last HCC treatment durability (<12 months) was associated with HCC recurrence after DAA therapy. This finding suggests that the last HCC treatment durability is an important predictor of HCC recurrence after DAA therapy. (Gut Liver 2021;15:410-419)</description><identifier>ISSN: 1976-2283</identifier><language>kor</language><publisher>대한간학회</publisher><subject>Antiviral agents ; Carcinoma ; chronic ; Hepatitis C ; hepatocellular ; Re-currence ; Risk factors</subject><ispartof>Gut and liver, 2021-05, Vol.15 (3), p.410</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Young-hwan Ahn</creatorcontrib><creatorcontrib>Heirim Lee</creatorcontrib><creatorcontrib>Do Young Kim</creatorcontrib><creatorcontrib>Hye Won Lee</creatorcontrib><creatorcontrib>Su Jong Yu</creatorcontrib><creatorcontrib>Young Youn Cho</creatorcontrib><creatorcontrib>Jeong Won Jang</creatorcontrib><creatorcontrib>Byoung Kuk Jang</creatorcontrib><creatorcontrib>Chang Wook Kim</creatorcontrib><creatorcontrib>Hee Yeon Kim</creatorcontrib><creatorcontrib>Hana Park</creatorcontrib><creatorcontrib>Hyo Jung Cho</creatorcontrib><creatorcontrib>Bumhee Park</creatorcontrib><creatorcontrib>Soon Sun Kim</creatorcontrib><creatorcontrib>Jae Youn Cheong</creatorcontrib><title>Independent Risk Factors for Hepatocellular Carcinoma Recurrence after Direct-Acting Antiviral Therapy in Patients with Chronic Hepatitis C</title><title>Gut and liver</title><addtitle>Gut and Liver</addtitle><description>Background/Aims: This study was performed to evaluate the efficacy of direct-acting antivirals (DAAs) in Korean patients with hepatitis C virus (HCV)-related hepatocellular carcinoma (HCC) and to investigate the risk factors associated with HCC recurrence.
Methods: A total of 100 patients with HCV-related HCC, who were treated with DAAs between May 2015 and December 2016, were recruited from seven university hospitals in Korea. Claim data of 526 patients with HCC obtained from the Health Insurance Review and Assessment Service in South Korea were used for external validation of the results.
Results: Among the 100 patients, 88% achieved a sustained virological response (SVR) 12 weeks after the end of DAA therapy (SVR12), and 37% experienced HCC recurrence after DAA therapy. Short last HCC treatment durability (<12 months) before DAA commencement was independently associated with HCC recurrence (hazard ratio [HR], 2.89; p=0.011). In the nationwide validation cohort, 20.3% of the patients experienced HCC recurrence. The last HCC treatment with a noncurative method, a short last HCC treatment durability (<12 months), and a longer total duration of HCC treatment (≥18 months) were independently related with HCC recurrence (HR 3.73, p<0.001; HR 3.34, p<0.001; and HR 1.74, p=0.006; respectively).
Conclusions: DAA therapy showed an acceptable SVR12 rate in patients with HCV-related HCC. Short last HCC treatment durability (<12 months) was associated with HCC recurrence after DAA therapy. This finding suggests that the last HCC treatment durability is an important predictor of HCC recurrence after DAA therapy. (Gut Liver 2021;15:410-419)</description><subject>Antiviral agents</subject><subject>Carcinoma</subject><subject>chronic</subject><subject>Hepatitis C</subject><subject>hepatocellular</subject><subject>Re-currence</subject><subject>Risk factors</subject><issn>1976-2283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9jbtuwkAQAK8gUsjjC2j2ByyBDbYpkRNEOoTo0eqyxgvHnbW7JOIb8tMgkZpmpphiBm44mVdllud18exeVA_jcTnJq9nQ_X3Fb-rphmiwYT3CEr0lUWiTwIp6tOQphHNAgQbFc0wnhA35swhFT4CtkcAHC3nLFt447mERjX9YMMC2I8H-Ahxhjca3i8IvWwdNJymyvy_YWKF5c08tBqX3f7-60fJz26yyI6vueuETymVX1HVVltPicb0CShdOtw</recordid><startdate>20210530</startdate><enddate>20210530</enddate><creator>Young-hwan Ahn</creator><creator>Heirim Lee</creator><creator>Do Young Kim</creator><creator>Hye Won Lee</creator><creator>Su Jong Yu</creator><creator>Young Youn Cho</creator><creator>Jeong Won Jang</creator><creator>Byoung Kuk Jang</creator><creator>Chang Wook Kim</creator><creator>Hee Yeon Kim</creator><creator>Hana Park</creator><creator>Hyo Jung Cho</creator><creator>Bumhee Park</creator><creator>Soon Sun Kim</creator><creator>Jae Youn Cheong</creator><general>대한간학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>20210530</creationdate><title>Independent Risk Factors for Hepatocellular Carcinoma Recurrence after Direct-Acting Antiviral Therapy in Patients with Chronic Hepatitis C</title><author>Young-hwan Ahn ; Heirim Lee ; Do Young Kim ; Hye Won Lee ; Su Jong Yu ; Young Youn Cho ; Jeong Won Jang ; Byoung Kuk Jang ; Chang Wook Kim ; Hee Yeon Kim ; Hana Park ; Hyo Jung Cho ; Bumhee Park ; Soon Sun Kim ; Jae Youn Cheong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_38876643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2021</creationdate><topic>Antiviral agents</topic><topic>Carcinoma</topic><topic>chronic</topic><topic>Hepatitis C</topic><topic>hepatocellular</topic><topic>Re-currence</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Young-hwan Ahn</creatorcontrib><creatorcontrib>Heirim Lee</creatorcontrib><creatorcontrib>Do Young Kim</creatorcontrib><creatorcontrib>Hye Won Lee</creatorcontrib><creatorcontrib>Su Jong Yu</creatorcontrib><creatorcontrib>Young Youn Cho</creatorcontrib><creatorcontrib>Jeong Won Jang</creatorcontrib><creatorcontrib>Byoung Kuk Jang</creatorcontrib><creatorcontrib>Chang Wook Kim</creatorcontrib><creatorcontrib>Hee Yeon Kim</creatorcontrib><creatorcontrib>Hana Park</creatorcontrib><creatorcontrib>Hyo Jung Cho</creatorcontrib><creatorcontrib>Bumhee Park</creatorcontrib><creatorcontrib>Soon Sun Kim</creatorcontrib><creatorcontrib>Jae Youn Cheong</creatorcontrib><collection>KISS</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>Gut and liver</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Young-hwan Ahn</au><au>Heirim Lee</au><au>Do Young Kim</au><au>Hye Won Lee</au><au>Su Jong Yu</au><au>Young Youn Cho</au><au>Jeong Won Jang</au><au>Byoung Kuk Jang</au><au>Chang Wook Kim</au><au>Hee Yeon Kim</au><au>Hana Park</au><au>Hyo Jung Cho</au><au>Bumhee Park</au><au>Soon Sun Kim</au><au>Jae Youn Cheong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Independent Risk Factors for Hepatocellular Carcinoma Recurrence after Direct-Acting Antiviral Therapy in Patients with Chronic Hepatitis C</atitle><jtitle>Gut and liver</jtitle><addtitle>Gut and Liver</addtitle><date>2021-05-30</date><risdate>2021</risdate><volume>15</volume><issue>3</issue><spage>410</spage><pages>410-</pages><issn>1976-2283</issn><abstract>Background/Aims: This study was performed to evaluate the efficacy of direct-acting antivirals (DAAs) in Korean patients with hepatitis C virus (HCV)-related hepatocellular carcinoma (HCC) and to investigate the risk factors associated with HCC recurrence.
Methods: A total of 100 patients with HCV-related HCC, who were treated with DAAs between May 2015 and December 2016, were recruited from seven university hospitals in Korea. Claim data of 526 patients with HCC obtained from the Health Insurance Review and Assessment Service in South Korea were used for external validation of the results.
Results: Among the 100 patients, 88% achieved a sustained virological response (SVR) 12 weeks after the end of DAA therapy (SVR12), and 37% experienced HCC recurrence after DAA therapy. Short last HCC treatment durability (<12 months) before DAA commencement was independently associated with HCC recurrence (hazard ratio [HR], 2.89; p=0.011). In the nationwide validation cohort, 20.3% of the patients experienced HCC recurrence. The last HCC treatment with a noncurative method, a short last HCC treatment durability (<12 months), and a longer total duration of HCC treatment (≥18 months) were independently related with HCC recurrence (HR 3.73, p<0.001; HR 3.34, p<0.001; and HR 1.74, p=0.006; respectively).
Conclusions: DAA therapy showed an acceptable SVR12 rate in patients with HCV-related HCC. Short last HCC treatment durability (<12 months) was associated with HCC recurrence after DAA therapy. This finding suggests that the last HCC treatment durability is an important predictor of HCC recurrence after DAA therapy. (Gut Liver 2021;15:410-419)</abstract><pub>대한간학회</pub><tpages>10</tpages></addata></record> |
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subjects | Antiviral agents Carcinoma chronic Hepatitis C hepatocellular Re-currence Risk factors |
title | Independent Risk Factors for Hepatocellular Carcinoma Recurrence after Direct-Acting Antiviral Therapy in Patients with Chronic Hepatitis C |
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