Clinical significance of half‐lives of tumor markers α‐fetoprotein and des‐γ‐carboxy prothrombin after hepatectomy for hepatocellular carcinoma

Aim The prognostic significance of the half‐lives (HLs) of α‐fetoprotein (AFP) and des‐γ‐carboxy prothrombin (DCP) in patients undergoing hepatectomy for hepatocellular carcinoma (HCC) is unclear. We evaluated the HLs of AFP and DCP in a cohort of such patients. Methods This study included data on 2...

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Veröffentlicht in:Hepatology research 2018-02, Vol.48 (3), p.E183-E193
Hauptverfasser: Tsukamoto, Masayo, Nitta, Hidetoshi, Imai, Katsunori, Higashi, Takaaki, Nakagawa, Shigeki, Okabe, Hirohisa, Arima, Kota, Kaida, Takayoshi, Taki, Katsunobu, Hashimoto, Daisuke, Chikamoto, Akira, Ishiko, Takatoshi, Beppu, Toru, Baba, Hideo
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container_end_page E193
container_issue 3
container_start_page E183
container_title Hepatology research
container_volume 48
creator Tsukamoto, Masayo
Nitta, Hidetoshi
Imai, Katsunori
Higashi, Takaaki
Nakagawa, Shigeki
Okabe, Hirohisa
Arima, Kota
Kaida, Takayoshi
Taki, Katsunobu
Hashimoto, Daisuke
Chikamoto, Akira
Ishiko, Takatoshi
Beppu, Toru
Baba, Hideo
description Aim The prognostic significance of the half‐lives (HLs) of α‐fetoprotein (AFP) and des‐γ‐carboxy prothrombin (DCP) in patients undergoing hepatectomy for hepatocellular carcinoma (HCC) is unclear. We evaluated the HLs of AFP and DCP in a cohort of such patients. Methods This study included data on 202 patients with HCC who underwent curative hepatectomy and had preoperative AFP concentrations ≥100 ng/mL or DCP ≥200 mAU/mL. We calculated the HLs of AFP and DCP from their values just before and 1 month after hepatectomy. We identified three groups: a normalization group, tumor marker concentrations within normal range 1 month post‐hepatectomy; a long group, HL of AFP ≥7 days or DCP ≥4 days; and a short group, remaining patients. We evaluated associations between HL and prognosis. Results Three‐year recurrence‐free survival (RFS) in the normalization (n = 70), short (n = 71), and long groups (n = 61) was 41.3%, 46.0%, and 16.8%, respectively (P = 0.002). Five‐year overall survival (OS) of normalization, short, and long groups was 72.6, 70.6 and 43.8%, respectively (P = 0.002). Multivariate analysis revealed that long HL is an independent risk factor for poor RFS (hazard ratio [HR] 2.21, P = 0.0006) and poor OS (HR 2.70, P = 0.004). The extrahepatic recurrence rate was 21.3% (13/61) in the long group, which is higher than in the normalization group (8.6%, 6/70) (P = 0.04) and short group (9.9%, 7/71) (P = 0.07). Conclusion Post‐hepatectomy HLs of AFP and DCP are predictors of long‐term outcome in patients with HCC.
doi_str_mv 10.1111/hepr.12942
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We evaluated the HLs of AFP and DCP in a cohort of such patients. Methods This study included data on 202 patients with HCC who underwent curative hepatectomy and had preoperative AFP concentrations ≥100 ng/mL or DCP ≥200 mAU/mL. We calculated the HLs of AFP and DCP from their values just before and 1 month after hepatectomy. We identified three groups: a normalization group, tumor marker concentrations within normal range 1 month post‐hepatectomy; a long group, HL of AFP ≥7 days or DCP ≥4 days; and a short group, remaining patients. We evaluated associations between HL and prognosis. Results Three‐year recurrence‐free survival (RFS) in the normalization (n = 70), short (n = 71), and long groups (n = 61) was 41.3%, 46.0%, and 16.8%, respectively (P = 0.002). Five‐year overall survival (OS) of normalization, short, and long groups was 72.6, 70.6 and 43.8%, respectively (P = 0.002). Multivariate analysis revealed that long HL is an independent risk factor for poor RFS (hazard ratio [HR] 2.21, P = 0.0006) and poor OS (HR 2.70, P = 0.004). The extrahepatic recurrence rate was 21.3% (13/61) in the long group, which is higher than in the normalization group (8.6%, 6/70) (P = 0.04) and short group (9.9%, 7/71) (P = 0.07). Conclusion Post‐hepatectomy HLs of AFP and DCP are predictors of long‐term outcome in patients with HCC.</description><identifier>ISSN: 1386-6346</identifier><identifier>EISSN: 1872-034X</identifier><identifier>DOI: 10.1111/hepr.12942</identifier><identifier>PMID: 28796412</identifier><language>eng</language><publisher>Netherlands: Wiley Subscription Services, Inc</publisher><subject>alpha‐fetoprotein ; Clinical significance ; des‐γ ‐carboxy prothrombin ; half‐life time ; Hepatectomy ; Hepatocellular carcinoma ; Liver cancer ; Medical prognosis ; Multivariate analysis ; Prothrombin ; tumor marker ; Tumor markers</subject><ispartof>Hepatology research, 2018-02, Vol.48 (3), p.E183-E193</ispartof><rights>2017 The Japan Society of Hepatology</rights><rights>2017 The Japan Society of Hepatology.</rights><rights>2018 The Japan Society of Hepatology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3932-a8b81f385322799582772139bf184d16ad61ef5b0b318ad7894bf3f642823fb33</citedby><cites>FETCH-LOGICAL-c3932-a8b81f385322799582772139bf184d16ad61ef5b0b318ad7894bf3f642823fb33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhepr.12942$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhepr.12942$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28796412$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsukamoto, Masayo</creatorcontrib><creatorcontrib>Nitta, Hidetoshi</creatorcontrib><creatorcontrib>Imai, Katsunori</creatorcontrib><creatorcontrib>Higashi, Takaaki</creatorcontrib><creatorcontrib>Nakagawa, Shigeki</creatorcontrib><creatorcontrib>Okabe, Hirohisa</creatorcontrib><creatorcontrib>Arima, Kota</creatorcontrib><creatorcontrib>Kaida, Takayoshi</creatorcontrib><creatorcontrib>Taki, Katsunobu</creatorcontrib><creatorcontrib>Hashimoto, Daisuke</creatorcontrib><creatorcontrib>Chikamoto, Akira</creatorcontrib><creatorcontrib>Ishiko, Takatoshi</creatorcontrib><creatorcontrib>Beppu, Toru</creatorcontrib><creatorcontrib>Baba, Hideo</creatorcontrib><title>Clinical significance of half‐lives of tumor markers α‐fetoprotein and des‐γ‐carboxy prothrombin after hepatectomy for hepatocellular carcinoma</title><title>Hepatology research</title><addtitle>Hepatol Res</addtitle><description>Aim The prognostic significance of the half‐lives (HLs) of α‐fetoprotein (AFP) and des‐γ‐carboxy prothrombin (DCP) in patients undergoing hepatectomy for hepatocellular carcinoma (HCC) is unclear. We evaluated the HLs of AFP and DCP in a cohort of such patients. Methods This study included data on 202 patients with HCC who underwent curative hepatectomy and had preoperative AFP concentrations ≥100 ng/mL or DCP ≥200 mAU/mL. We calculated the HLs of AFP and DCP from their values just before and 1 month after hepatectomy. We identified three groups: a normalization group, tumor marker concentrations within normal range 1 month post‐hepatectomy; a long group, HL of AFP ≥7 days or DCP ≥4 days; and a short group, remaining patients. We evaluated associations between HL and prognosis. Results Three‐year recurrence‐free survival (RFS) in the normalization (n = 70), short (n = 71), and long groups (n = 61) was 41.3%, 46.0%, and 16.8%, respectively (P = 0.002). Five‐year overall survival (OS) of normalization, short, and long groups was 72.6, 70.6 and 43.8%, respectively (P = 0.002). Multivariate analysis revealed that long HL is an independent risk factor for poor RFS (hazard ratio [HR] 2.21, P = 0.0006) and poor OS (HR 2.70, P = 0.004). The extrahepatic recurrence rate was 21.3% (13/61) in the long group, which is higher than in the normalization group (8.6%, 6/70) (P = 0.04) and short group (9.9%, 7/71) (P = 0.07). Conclusion Post‐hepatectomy HLs of AFP and DCP are predictors of long‐term outcome in patients with HCC.</description><subject>alpha‐fetoprotein</subject><subject>Clinical significance</subject><subject>des‐γ ‐carboxy prothrombin</subject><subject>half‐life time</subject><subject>Hepatectomy</subject><subject>Hepatocellular carcinoma</subject><subject>Liver cancer</subject><subject>Medical prognosis</subject><subject>Multivariate analysis</subject><subject>Prothrombin</subject><subject>tumor marker</subject><subject>Tumor markers</subject><issn>1386-6346</issn><issn>1872-034X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kU9u1DAUxi1ERUthwwGQJTYIKUP8J4m9RKMpU2kkKgQSu8hOnhkXJx7spDQ7jtBtj4G4Rw_Rk-AwAwsWeGG_5_fzp0_-EHpG8gVJ6_UWdmFBqOT0ATohoqJZzvinh6lmosxKxstj9DjGyzwnVU75I3RMRSVLTugJul0629tGORzt596aVPYNYG_wVjlz__3G2SuIcz-MnQ-4U-ELhIjvfqSZgcHvgh_A9lj1LW4hptu7n2lrVND-esLzeBt8p2fEDBBwcqsGaAbfTdj4Q-8bcG50KuD0sLG979QTdGSUi_D0cJ6ij2erD8t1tnn39nz5ZpM1TDKaKaEFMUwUjNJKykLQqqKESW2I4C0pVVsSMIXONSNCtZWQXBtmSk4FZUYzdope7nWT1a8jxKHubJztqB78GGsiaSVYQQVP6It_0Es_hj65S5SUQpCCz4Kv9lQTfIwBTL0LNv3bVJO8ngOr58Dq34El-PlBctQdtH_RPwklgOyBb9bB9B-per26eL8X_QVQ8qhq</recordid><startdate>201802</startdate><enddate>201802</enddate><creator>Tsukamoto, Masayo</creator><creator>Nitta, Hidetoshi</creator><creator>Imai, Katsunori</creator><creator>Higashi, Takaaki</creator><creator>Nakagawa, Shigeki</creator><creator>Okabe, Hirohisa</creator><creator>Arima, Kota</creator><creator>Kaida, Takayoshi</creator><creator>Taki, Katsunobu</creator><creator>Hashimoto, Daisuke</creator><creator>Chikamoto, Akira</creator><creator>Ishiko, Takatoshi</creator><creator>Beppu, Toru</creator><creator>Baba, Hideo</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>201802</creationdate><title>Clinical significance of half‐lives of tumor markers α‐fetoprotein and des‐γ‐carboxy prothrombin after hepatectomy for hepatocellular carcinoma</title><author>Tsukamoto, Masayo ; Nitta, Hidetoshi ; Imai, Katsunori ; Higashi, Takaaki ; Nakagawa, Shigeki ; Okabe, Hirohisa ; Arima, Kota ; Kaida, Takayoshi ; Taki, Katsunobu ; Hashimoto, Daisuke ; Chikamoto, Akira ; Ishiko, Takatoshi ; Beppu, Toru ; Baba, Hideo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3932-a8b81f385322799582772139bf184d16ad61ef5b0b318ad7894bf3f642823fb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>alpha‐fetoprotein</topic><topic>Clinical significance</topic><topic>des‐γ ‐carboxy prothrombin</topic><topic>half‐life time</topic><topic>Hepatectomy</topic><topic>Hepatocellular carcinoma</topic><topic>Liver cancer</topic><topic>Medical prognosis</topic><topic>Multivariate analysis</topic><topic>Prothrombin</topic><topic>tumor marker</topic><topic>Tumor markers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsukamoto, Masayo</creatorcontrib><creatorcontrib>Nitta, Hidetoshi</creatorcontrib><creatorcontrib>Imai, Katsunori</creatorcontrib><creatorcontrib>Higashi, Takaaki</creatorcontrib><creatorcontrib>Nakagawa, Shigeki</creatorcontrib><creatorcontrib>Okabe, Hirohisa</creatorcontrib><creatorcontrib>Arima, Kota</creatorcontrib><creatorcontrib>Kaida, Takayoshi</creatorcontrib><creatorcontrib>Taki, Katsunobu</creatorcontrib><creatorcontrib>Hashimoto, Daisuke</creatorcontrib><creatorcontrib>Chikamoto, Akira</creatorcontrib><creatorcontrib>Ishiko, Takatoshi</creatorcontrib><creatorcontrib>Beppu, Toru</creatorcontrib><creatorcontrib>Baba, Hideo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Hepatology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsukamoto, Masayo</au><au>Nitta, Hidetoshi</au><au>Imai, Katsunori</au><au>Higashi, Takaaki</au><au>Nakagawa, Shigeki</au><au>Okabe, Hirohisa</au><au>Arima, Kota</au><au>Kaida, Takayoshi</au><au>Taki, Katsunobu</au><au>Hashimoto, Daisuke</au><au>Chikamoto, Akira</au><au>Ishiko, Takatoshi</au><au>Beppu, Toru</au><au>Baba, Hideo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical significance of half‐lives of tumor markers α‐fetoprotein and des‐γ‐carboxy prothrombin after hepatectomy for hepatocellular carcinoma</atitle><jtitle>Hepatology research</jtitle><addtitle>Hepatol Res</addtitle><date>2018-02</date><risdate>2018</risdate><volume>48</volume><issue>3</issue><spage>E183</spage><epage>E193</epage><pages>E183-E193</pages><issn>1386-6346</issn><eissn>1872-034X</eissn><abstract>Aim The prognostic significance of the half‐lives (HLs) of α‐fetoprotein (AFP) and des‐γ‐carboxy prothrombin (DCP) in patients undergoing hepatectomy for hepatocellular carcinoma (HCC) is unclear. We evaluated the HLs of AFP and DCP in a cohort of such patients. Methods This study included data on 202 patients with HCC who underwent curative hepatectomy and had preoperative AFP concentrations ≥100 ng/mL or DCP ≥200 mAU/mL. We calculated the HLs of AFP and DCP from their values just before and 1 month after hepatectomy. We identified three groups: a normalization group, tumor marker concentrations within normal range 1 month post‐hepatectomy; a long group, HL of AFP ≥7 days or DCP ≥4 days; and a short group, remaining patients. We evaluated associations between HL and prognosis. Results Three‐year recurrence‐free survival (RFS) in the normalization (n = 70), short (n = 71), and long groups (n = 61) was 41.3%, 46.0%, and 16.8%, respectively (P = 0.002). Five‐year overall survival (OS) of normalization, short, and long groups was 72.6, 70.6 and 43.8%, respectively (P = 0.002). Multivariate analysis revealed that long HL is an independent risk factor for poor RFS (hazard ratio [HR] 2.21, P = 0.0006) and poor OS (HR 2.70, P = 0.004). The extrahepatic recurrence rate was 21.3% (13/61) in the long group, which is higher than in the normalization group (8.6%, 6/70) (P = 0.04) and short group (9.9%, 7/71) (P = 0.07). Conclusion Post‐hepatectomy HLs of AFP and DCP are predictors of long‐term outcome in patients with HCC.</abstract><cop>Netherlands</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28796412</pmid><doi>10.1111/hepr.12942</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects alpha‐fetoprotein
Clinical significance
des‐γ ‐carboxy prothrombin
half‐life time
Hepatectomy
Hepatocellular carcinoma
Liver cancer
Medical prognosis
Multivariate analysis
Prothrombin
tumor marker
Tumor markers
title Clinical significance of half‐lives of tumor markers α‐fetoprotein and des‐γ‐carboxy prothrombin after hepatectomy for hepatocellular carcinoma
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