Skeletal Muscle Mass Influences Tolerability and Prognosis in Hepatocellular Carcinoma Patients Treated with Lenvatinib
Background: Low skeletal muscle mass is significantly associated with severe adverse events (AEs) from chemotherapy, and low tolerability leads to decreased survival. We aimed to investigate whether body skeletal muscle mass is correlated with tolerability and prognosis in patients with hepatocellul...
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Veröffentlicht in: | Liver cancer (Basel ) 2020-04, Vol.9 (2), p.193-206 |
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creator | Uojima, Haruki Chuma, Makoto Tanaka, Yoshiaki Hidaka, Hisashi Nakazawa, Takahide Iwabuchi, Shogo Kobayashi, Satoshi Hattori, Nobuhiro Ogushi, Katsuaki Morimoto, Manabu Kagawa, Tatehiro Tanaka, Katsuaki Kako, Makoto Koizumi, Wasaburo |
description | Background: Low skeletal muscle mass is significantly associated with severe adverse events (AEs) from chemotherapy, and low tolerability leads to decreased survival. We aimed to investigate whether body skeletal muscle mass is correlated with tolerability and prognosis in patients with hepatocellular carcinoma (HCC) treated with lenvatinib. Methods: This multicenter, retrospective study was conducted at five locations in Japan. We included 100 patients with HCC treated with lenvatinib. Skeletal muscle mass was measured by computed tomography and normalized for height in m 2 as skeletal muscle index (SMI). The assessment criteria for low SMI were taken from the sarcopenia criteria of the Japan Society of Hepatology. We investigated the influence of low SMI on drug withdrawal due to severe AEs in the first 2 months and on time to treatment failure (TTF) and overall survival (OS). Results: The numbers of high- and low-SMI patients were 41 and 59, respectively. Those with severe AEs leading to withdraw in the high- and low-SMI groups were 7 and 23, respectively. The low-SMI group had a higher withdrawal rate than the high-SMI group (p = 0.042). The median TTF in the low- and high-SMI groups was 139 and 230 days, respectively. The median OS in the low- and high-SMI groups was 264 and 353 days, respectively. Patients in the low-SMI group experienced significantly worse OS and TTF than those in the high-SMI group (log-rank test for trend: TTF, p = 0.010; OS, p = 0.021). Conclusion: Decreased skeletal muscle mass is associated with the occurrence of severe AEs and worse TTF and OS. Skeletal muscle mass can be used as a predictive marker for tolerability and prognosis to lenvatinib in patients with HCC. |
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We aimed to investigate whether body skeletal muscle mass is correlated with tolerability and prognosis in patients with hepatocellular carcinoma (HCC) treated with lenvatinib. Methods: This multicenter, retrospective study was conducted at five locations in Japan. We included 100 patients with HCC treated with lenvatinib. Skeletal muscle mass was measured by computed tomography and normalized for height in m 2 as skeletal muscle index (SMI). The assessment criteria for low SMI were taken from the sarcopenia criteria of the Japan Society of Hepatology. We investigated the influence of low SMI on drug withdrawal due to severe AEs in the first 2 months and on time to treatment failure (TTF) and overall survival (OS). Results: The numbers of high- and low-SMI patients were 41 and 59, respectively. Those with severe AEs leading to withdraw in the high- and low-SMI groups were 7 and 23, respectively. The low-SMI group had a higher withdrawal rate than the high-SMI group (p = 0.042). The median TTF in the low- and high-SMI groups was 139 and 230 days, respectively. The median OS in the low- and high-SMI groups was 264 and 353 days, respectively. Patients in the low-SMI group experienced significantly worse OS and TTF than those in the high-SMI group (log-rank test for trend: TTF, p = 0.010; OS, p = 0.021). Conclusion: Decreased skeletal muscle mass is associated with the occurrence of severe AEs and worse TTF and OS. Skeletal muscle mass can be used as a predictive marker for tolerability and prognosis to lenvatinib in patients with HCC.</description><identifier>ISSN: 2235-1795</identifier><identifier>EISSN: 1664-5553</identifier><identifier>DOI: 10.1159/000504604</identifier><identifier>PMID: 32399433</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Ascites ; Cancer ; Cancer therapies ; Chemotherapy ; Development and progression ; Drug dosages ; Hepatoma ; Laboratories ; Liver cancer ; Liver diseases ; Medical imaging ; Medical prognosis ; Metastasis ; Muscles ; Musculoskeletal system ; Original Paper ; Prognosis ; Tumors ; Vascular endothelial growth factor</subject><ispartof>Liver cancer (Basel ), 2020-04, Vol.9 (2), p.193-206</ispartof><rights>2019 The Author(s) Published by S. Karger AG, Basel</rights><rights>Copyright © 2020 by S. Karger AG, Basel.</rights><rights>COPYRIGHT 2020 S. Karger AG</rights><rights>2019 The Author(s) Published by S. Karger AG, Basel . This work is licensed under the Creative Commons Attribution – Non-Commercial – No Derivatives License http://creativecommons.org/licenses/by-nc-nd/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2020 by S. Karger AG, Basel 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c519t-5580bea8133abf9961ea3c164a8e7518983082a4f98654cac7a8c538ca473c983</citedby><cites>FETCH-LOGICAL-c519t-5580bea8133abf9961ea3c164a8e7518983082a4f98654cac7a8c538ca473c983</cites><orcidid>0000-0002-3940-9634</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206580/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206580/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27635,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32399433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uojima, Haruki</creatorcontrib><creatorcontrib>Chuma, Makoto</creatorcontrib><creatorcontrib>Tanaka, Yoshiaki</creatorcontrib><creatorcontrib>Hidaka, Hisashi</creatorcontrib><creatorcontrib>Nakazawa, Takahide</creatorcontrib><creatorcontrib>Iwabuchi, Shogo</creatorcontrib><creatorcontrib>Kobayashi, Satoshi</creatorcontrib><creatorcontrib>Hattori, Nobuhiro</creatorcontrib><creatorcontrib>Ogushi, Katsuaki</creatorcontrib><creatorcontrib>Morimoto, Manabu</creatorcontrib><creatorcontrib>Kagawa, Tatehiro</creatorcontrib><creatorcontrib>Tanaka, Katsuaki</creatorcontrib><creatorcontrib>Kako, Makoto</creatorcontrib><creatorcontrib>Koizumi, Wasaburo</creatorcontrib><title>Skeletal Muscle Mass Influences Tolerability and Prognosis in Hepatocellular Carcinoma Patients Treated with Lenvatinib</title><title>Liver cancer (Basel )</title><addtitle>Liver Cancer</addtitle><description>Background: Low skeletal muscle mass is significantly associated with severe adverse events (AEs) from chemotherapy, and low tolerability leads to decreased survival. We aimed to investigate whether body skeletal muscle mass is correlated with tolerability and prognosis in patients with hepatocellular carcinoma (HCC) treated with lenvatinib. Methods: This multicenter, retrospective study was conducted at five locations in Japan. We included 100 patients with HCC treated with lenvatinib. Skeletal muscle mass was measured by computed tomography and normalized for height in m 2 as skeletal muscle index (SMI). The assessment criteria for low SMI were taken from the sarcopenia criteria of the Japan Society of Hepatology. We investigated the influence of low SMI on drug withdrawal due to severe AEs in the first 2 months and on time to treatment failure (TTF) and overall survival (OS). Results: The numbers of high- and low-SMI patients were 41 and 59, respectively. Those with severe AEs leading to withdraw in the high- and low-SMI groups were 7 and 23, respectively. The low-SMI group had a higher withdrawal rate than the high-SMI group (p = 0.042). The median TTF in the low- and high-SMI groups was 139 and 230 days, respectively. The median OS in the low- and high-SMI groups was 264 and 353 days, respectively. Patients in the low-SMI group experienced significantly worse OS and TTF than those in the high-SMI group (log-rank test for trend: TTF, p = 0.010; OS, p = 0.021). Conclusion: Decreased skeletal muscle mass is associated with the occurrence of severe AEs and worse TTF and OS. Skeletal muscle mass can be used as a predictive marker for tolerability and prognosis to lenvatinib in patients with HCC.</description><subject>Ascites</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Development and progression</subject><subject>Drug dosages</subject><subject>Hepatoma</subject><subject>Laboratories</subject><subject>Liver cancer</subject><subject>Liver diseases</subject><subject>Medical imaging</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Muscles</subject><subject>Musculoskeletal system</subject><subject>Original Paper</subject><subject>Prognosis</subject><subject>Tumors</subject><subject>Vascular endothelial growth factor</subject><issn>2235-1795</issn><issn>1664-5553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>M--</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkkFrGzEQhZfS0pg0h95LEfTSHpxKq9VKuhSCaRuDQwNNz2JWnnWUyJIr7Sbk31fGrtOUoINA881788RU1VtGTxkT-jOlVNCmpc2LasLatpkKIfjLalLXXEyZ1OKoOsn5pmBUUSq1fF0d8Zpr3XA-qe5_3qLHATy5GLP1SC4gZzIPvR8xWMzkKnpM0DnvhgcCYUkuU1yFmF0mLpBz3MAQLXo_ekhkBsm6ENdALmFwGIbSnxAGXJJ7N1yTBYa7Ugiue1O96sFnPNnfx9Wvb1-vZufTxY_v89nZYmoF00PJomiHoBjn0PVatwyBW9Y2oFAKprTiVNXQ9Fq1orFgJSgruLLQSG5L9bj6stPdjN0al7bMlMCbTXJrSA8mgjNPK8Fdm1W8M7KmbTEvAh_3Ain-HjEPZu3yNjAEjGM2dUPrhuu6ZgX98B96E8cUSjxTi5YrIaVsHqkVeDQu9LH42q2oOZN1q5VUXBbq9BmqnCWunY0Be1fenzR82jXYFHNO2B8yMmq2i2IOi1LY9_9-yoH8uxaPM95CWmE6AIv5bCdhNsu-UO-epfYufwDe58yq</recordid><startdate>20200401</startdate><enddate>20200401</enddate><creator>Uojima, Haruki</creator><creator>Chuma, Makoto</creator><creator>Tanaka, Yoshiaki</creator><creator>Hidaka, Hisashi</creator><creator>Nakazawa, Takahide</creator><creator>Iwabuchi, Shogo</creator><creator>Kobayashi, Satoshi</creator><creator>Hattori, Nobuhiro</creator><creator>Ogushi, Katsuaki</creator><creator>Morimoto, Manabu</creator><creator>Kagawa, Tatehiro</creator><creator>Tanaka, Katsuaki</creator><creator>Kako, Makoto</creator><creator>Koizumi, Wasaburo</creator><general>S. Karger AG</general><scope>M--</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3940-9634</orcidid></search><sort><creationdate>20200401</creationdate><title>Skeletal Muscle Mass Influences Tolerability and Prognosis in Hepatocellular Carcinoma Patients Treated with Lenvatinib</title><author>Uojima, Haruki ; Chuma, Makoto ; Tanaka, Yoshiaki ; Hidaka, Hisashi ; Nakazawa, Takahide ; Iwabuchi, Shogo ; Kobayashi, Satoshi ; Hattori, Nobuhiro ; Ogushi, Katsuaki ; Morimoto, Manabu ; Kagawa, Tatehiro ; Tanaka, Katsuaki ; Kako, Makoto ; Koizumi, Wasaburo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c519t-5580bea8133abf9961ea3c164a8e7518983082a4f98654cac7a8c538ca473c983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Ascites</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Development and progression</topic><topic>Drug dosages</topic><topic>Hepatoma</topic><topic>Laboratories</topic><topic>Liver cancer</topic><topic>Liver diseases</topic><topic>Medical imaging</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Muscles</topic><topic>Musculoskeletal system</topic><topic>Original Paper</topic><topic>Prognosis</topic><topic>Tumors</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uojima, Haruki</creatorcontrib><creatorcontrib>Chuma, Makoto</creatorcontrib><creatorcontrib>Tanaka, Yoshiaki</creatorcontrib><creatorcontrib>Hidaka, Hisashi</creatorcontrib><creatorcontrib>Nakazawa, Takahide</creatorcontrib><creatorcontrib>Iwabuchi, Shogo</creatorcontrib><creatorcontrib>Kobayashi, Satoshi</creatorcontrib><creatorcontrib>Hattori, Nobuhiro</creatorcontrib><creatorcontrib>Ogushi, Katsuaki</creatorcontrib><creatorcontrib>Morimoto, Manabu</creatorcontrib><creatorcontrib>Kagawa, Tatehiro</creatorcontrib><creatorcontrib>Tanaka, Katsuaki</creatorcontrib><creatorcontrib>Kako, Makoto</creatorcontrib><creatorcontrib>Koizumi, Wasaburo</creatorcontrib><collection>Karger Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Liver cancer (Basel )</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uojima, Haruki</au><au>Chuma, Makoto</au><au>Tanaka, Yoshiaki</au><au>Hidaka, Hisashi</au><au>Nakazawa, Takahide</au><au>Iwabuchi, Shogo</au><au>Kobayashi, Satoshi</au><au>Hattori, Nobuhiro</au><au>Ogushi, Katsuaki</au><au>Morimoto, Manabu</au><au>Kagawa, Tatehiro</au><au>Tanaka, Katsuaki</au><au>Kako, Makoto</au><au>Koizumi, Wasaburo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Skeletal Muscle Mass Influences Tolerability and Prognosis in Hepatocellular Carcinoma Patients Treated with Lenvatinib</atitle><jtitle>Liver cancer (Basel )</jtitle><addtitle>Liver Cancer</addtitle><date>2020-04-01</date><risdate>2020</risdate><volume>9</volume><issue>2</issue><spage>193</spage><epage>206</epage><pages>193-206</pages><issn>2235-1795</issn><eissn>1664-5553</eissn><abstract>Background: Low skeletal muscle mass is significantly associated with severe adverse events (AEs) from chemotherapy, and low tolerability leads to decreased survival. We aimed to investigate whether body skeletal muscle mass is correlated with tolerability and prognosis in patients with hepatocellular carcinoma (HCC) treated with lenvatinib. Methods: This multicenter, retrospective study was conducted at five locations in Japan. We included 100 patients with HCC treated with lenvatinib. Skeletal muscle mass was measured by computed tomography and normalized for height in m 2 as skeletal muscle index (SMI). The assessment criteria for low SMI were taken from the sarcopenia criteria of the Japan Society of Hepatology. We investigated the influence of low SMI on drug withdrawal due to severe AEs in the first 2 months and on time to treatment failure (TTF) and overall survival (OS). Results: The numbers of high- and low-SMI patients were 41 and 59, respectively. Those with severe AEs leading to withdraw in the high- and low-SMI groups were 7 and 23, respectively. The low-SMI group had a higher withdrawal rate than the high-SMI group (p = 0.042). The median TTF in the low- and high-SMI groups was 139 and 230 days, respectively. The median OS in the low- and high-SMI groups was 264 and 353 days, respectively. Patients in the low-SMI group experienced significantly worse OS and TTF than those in the high-SMI group (log-rank test for trend: TTF, p = 0.010; OS, p = 0.021). Conclusion: Decreased skeletal muscle mass is associated with the occurrence of severe AEs and worse TTF and OS. Skeletal muscle mass can be used as a predictive marker for tolerability and prognosis to lenvatinib in patients with HCC.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>32399433</pmid><doi>10.1159/000504604</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-3940-9634</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Ascites Cancer Cancer therapies Chemotherapy Development and progression Drug dosages Hepatoma Laboratories Liver cancer Liver diseases Medical imaging Medical prognosis Metastasis Muscles Musculoskeletal system Original Paper Prognosis Tumors Vascular endothelial growth factor |
title | Skeletal Muscle Mass Influences Tolerability and Prognosis in Hepatocellular Carcinoma Patients Treated with Lenvatinib |
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