A case of complete response with rechallenge-lenvatinib plus transcatheter arterial chemoembolization for unresectable hepatocellular carcinoma refractory to multiple molecular-targeted agent treatments
The efficacy of lenvatinib (LEN) plus transcatheter arterial chemoembolization (LEN-TACE) has been reported, but its effect on unresectable hepatocellular carcinoma (HCC) refractory to LEN therapy has not been demonstrated. We report a case of HCC refractory to multiple molecular-targeted agents (MT...
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Veröffentlicht in: | Clinical journal of gastroenterology 2023-06, Vol.16 (3), p.438-443 |
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creator | Tomonari, Tetsu Tanaka, Hironori Tanaka, Takahiro Taniguchi, Tatsuya Sogabe, Masahiro Kawano, Yutaka Okamoto, Koichi Miyamoto, Hiroshi Sato, Yasushi Takayama, Tetsuji |
description | The efficacy of lenvatinib (LEN) plus transcatheter arterial chemoembolization (LEN-TACE) has been reported, but its effect on unresectable hepatocellular carcinoma (HCC) refractory to LEN therapy has not been demonstrated. We report a case of HCC refractory to multiple molecular-targeted agents (MTA) treatments, including LEN, that was successfully treated with LEN-TACE. A 59-year-old man was referred to our department with multiple HCCs and a background of hepatitis B virus infection. TACE was the initial treatment. However, he was determined to be TACE-refractory, and multitargeted therapy was initiated. LEN was started at 12 mg/day but resulted in progressive disease (PD) after 13 months of the administration. The response to second-line sorafenib was PD after 2 months. Third-line therapy with atezolizumab + bevacizumab was stopped after one course because of an immune-related adverse event (i.e., dermatitis). The response to fourth-line regorafenib was PD at 2 months, and the response to fifth-line cabozantinib was PD after 6 months. The efficacy of LEN-TACE was recently reported; therefore, we decided to attempt LEN-TACE therapy as a salvage line. After obtaining the patient’s consent to repeat LEN and TACE, treatment was initiated. The tumor markers levels markedly reduced after LEN-TACE therapy. After three additional TACE treatments with continued LEN administration, the tumor marker levels normalized, and complete response was determined based on RECIST guidelines. LEN-TACE therapy may effectively treat unresectable advanced HCC in the LEN-rechallenge setting and may be a treatment option as a last-line therapeutic option. |
doi_str_mv | 10.1007/s12328-023-01777-y |
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We report a case of HCC refractory to multiple molecular-targeted agents (MTA) treatments, including LEN, that was successfully treated with LEN-TACE. A 59-year-old man was referred to our department with multiple HCCs and a background of hepatitis B virus infection. TACE was the initial treatment. However, he was determined to be TACE-refractory, and multitargeted therapy was initiated. LEN was started at 12 mg/day but resulted in progressive disease (PD) after 13 months of the administration. The response to second-line sorafenib was PD after 2 months. Third-line therapy with atezolizumab + bevacizumab was stopped after one course because of an immune-related adverse event (i.e., dermatitis). The response to fourth-line regorafenib was PD at 2 months, and the response to fifth-line cabozantinib was PD after 6 months. The efficacy of LEN-TACE was recently reported; therefore, we decided to attempt LEN-TACE therapy as a salvage line. After obtaining the patient’s consent to repeat LEN and TACE, treatment was initiated. The tumor markers levels markedly reduced after LEN-TACE therapy. After three additional TACE treatments with continued LEN administration, the tumor marker levels normalized, and complete response was determined based on RECIST guidelines. LEN-TACE therapy may effectively treat unresectable advanced HCC in the LEN-rechallenge setting and may be a treatment option as a last-line therapeutic option.</description><identifier>ISSN: 1865-7257</identifier><identifier>EISSN: 1865-7265</identifier><identifier>DOI: 10.1007/s12328-023-01777-y</identifier><identifier>PMID: 36856957</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Abdominal Surgery ; Carcinoma, Hepatocellular - pathology ; Case Report ; Chemoembolization, Therapeutic - methods ; Colorectal Surgery ; Gastroenterology ; Hepatology ; Humans ; Liver Neoplasms - drug therapy ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Surgical Oncology ; Treatment Outcome</subject><ispartof>Clinical journal of gastroenterology, 2023-06, Vol.16 (3), p.438-443</ispartof><rights>Japanese Society of Gastroenterology 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. Japanese Society of Gastroenterology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-b747671b8f0d58e0fa5c8b7b0adce1b1021c147fe1a691ebb58b6e788248bd783</citedby><cites>FETCH-LOGICAL-c371t-b747671b8f0d58e0fa5c8b7b0adce1b1021c147fe1a691ebb58b6e788248bd783</cites><orcidid>0000-0002-6776-4609</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12328-023-01777-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12328-023-01777-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36856957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tomonari, Tetsu</creatorcontrib><creatorcontrib>Tanaka, Hironori</creatorcontrib><creatorcontrib>Tanaka, Takahiro</creatorcontrib><creatorcontrib>Taniguchi, Tatsuya</creatorcontrib><creatorcontrib>Sogabe, Masahiro</creatorcontrib><creatorcontrib>Kawano, Yutaka</creatorcontrib><creatorcontrib>Okamoto, Koichi</creatorcontrib><creatorcontrib>Miyamoto, Hiroshi</creatorcontrib><creatorcontrib>Sato, Yasushi</creatorcontrib><creatorcontrib>Takayama, Tetsuji</creatorcontrib><title>A case of complete response with rechallenge-lenvatinib plus transcatheter arterial chemoembolization for unresectable hepatocellular carcinoma refractory to multiple molecular-targeted agent treatments</title><title>Clinical journal of gastroenterology</title><addtitle>Clin J Gastroenterol</addtitle><addtitle>Clin J Gastroenterol</addtitle><description>The efficacy of lenvatinib (LEN) plus transcatheter arterial chemoembolization (LEN-TACE) has been reported, but its effect on unresectable hepatocellular carcinoma (HCC) refractory to LEN therapy has not been demonstrated. We report a case of HCC refractory to multiple molecular-targeted agents (MTA) treatments, including LEN, that was successfully treated with LEN-TACE. A 59-year-old man was referred to our department with multiple HCCs and a background of hepatitis B virus infection. TACE was the initial treatment. However, he was determined to be TACE-refractory, and multitargeted therapy was initiated. LEN was started at 12 mg/day but resulted in progressive disease (PD) after 13 months of the administration. The response to second-line sorafenib was PD after 2 months. Third-line therapy with atezolizumab + bevacizumab was stopped after one course because of an immune-related adverse event (i.e., dermatitis). The response to fourth-line regorafenib was PD at 2 months, and the response to fifth-line cabozantinib was PD after 6 months. The efficacy of LEN-TACE was recently reported; therefore, we decided to attempt LEN-TACE therapy as a salvage line. After obtaining the patient’s consent to repeat LEN and TACE, treatment was initiated. The tumor markers levels markedly reduced after LEN-TACE therapy. After three additional TACE treatments with continued LEN administration, the tumor marker levels normalized, and complete response was determined based on RECIST guidelines. LEN-TACE therapy may effectively treat unresectable advanced HCC in the LEN-rechallenge setting and may be a treatment option as a last-line therapeutic option.</description><subject>Abdominal Surgery</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Case Report</subject><subject>Chemoembolization, Therapeutic - methods</subject><subject>Colorectal Surgery</subject><subject>Gastroenterology</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Surgical Oncology</subject><subject>Treatment Outcome</subject><issn>1865-7257</issn><issn>1865-7265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UcuO1DAQjBCIfcAPcEA-csliO5PYe1ytWEBaiQucrbbTmWTlR7Ad0PCJfBU9zLJHLu22XVXdpWqaN4JfCc7V-yJkJ3XLZddyoZRqD8-ac6GHvlVy6J8_9b06ay5KeeB8kFx1L5uzbtD9cN2r8-b3DXNQkKWJuRRWjxVZxrKmSI8_lzrTzc3gPcY9tlR_QF3iYtnqt8Jqhlgc1JlomUGmuoBnbsaQMNjkl18ET5FNKbMtkjC6CtYjm3GFmhx6v3nItEN2S0wBaNyUwdWUD6wmFjZfF9qKheTRHaFthbyncSODPcZKKyDUQF151byYwBd8_XheNt_uPny9_dTef_n4-fbmvnWdErW1aqcGJaye-Nhr5BP0TltlOYwOhRVcCid2akIBw7VAa3ttB1Ray522o9LdZfPupLvm9H3DUk1YytEJRExbMVJpIcVODJKg8gR1OZVC1syalwD5YAQ3xwzNKUNDGZq_GZoDkd4-6m824PhE-RcaAboToNAXxZLNQ9pyJM__k_0DxGuwdA</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Tomonari, Tetsu</creator><creator>Tanaka, Hironori</creator><creator>Tanaka, Takahiro</creator><creator>Taniguchi, Tatsuya</creator><creator>Sogabe, Masahiro</creator><creator>Kawano, Yutaka</creator><creator>Okamoto, Koichi</creator><creator>Miyamoto, Hiroshi</creator><creator>Sato, Yasushi</creator><creator>Takayama, Tetsuji</creator><general>Springer Nature Singapore</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6776-4609</orcidid></search><sort><creationdate>20230601</creationdate><title>A case of complete response with rechallenge-lenvatinib plus transcatheter arterial chemoembolization for unresectable hepatocellular carcinoma refractory to multiple molecular-targeted agent treatments</title><author>Tomonari, Tetsu ; Tanaka, Hironori ; Tanaka, Takahiro ; Taniguchi, Tatsuya ; Sogabe, Masahiro ; Kawano, Yutaka ; Okamoto, Koichi ; Miyamoto, Hiroshi ; Sato, Yasushi ; Takayama, Tetsuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-b747671b8f0d58e0fa5c8b7b0adce1b1021c147fe1a691ebb58b6e788248bd783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abdominal Surgery</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Case Report</topic><topic>Chemoembolization, Therapeutic - methods</topic><topic>Colorectal Surgery</topic><topic>Gastroenterology</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Surgical Oncology</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tomonari, Tetsu</creatorcontrib><creatorcontrib>Tanaka, Hironori</creatorcontrib><creatorcontrib>Tanaka, Takahiro</creatorcontrib><creatorcontrib>Taniguchi, Tatsuya</creatorcontrib><creatorcontrib>Sogabe, Masahiro</creatorcontrib><creatorcontrib>Kawano, Yutaka</creatorcontrib><creatorcontrib>Okamoto, Koichi</creatorcontrib><creatorcontrib>Miyamoto, Hiroshi</creatorcontrib><creatorcontrib>Sato, Yasushi</creatorcontrib><creatorcontrib>Takayama, Tetsuji</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tomonari, Tetsu</au><au>Tanaka, Hironori</au><au>Tanaka, Takahiro</au><au>Taniguchi, Tatsuya</au><au>Sogabe, Masahiro</au><au>Kawano, Yutaka</au><au>Okamoto, Koichi</au><au>Miyamoto, Hiroshi</au><au>Sato, Yasushi</au><au>Takayama, Tetsuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of complete response with rechallenge-lenvatinib plus transcatheter arterial chemoembolization for unresectable hepatocellular carcinoma refractory to multiple molecular-targeted agent treatments</atitle><jtitle>Clinical journal of gastroenterology</jtitle><stitle>Clin J Gastroenterol</stitle><addtitle>Clin J Gastroenterol</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>16</volume><issue>3</issue><spage>438</spage><epage>443</epage><pages>438-443</pages><issn>1865-7257</issn><eissn>1865-7265</eissn><abstract>The efficacy of lenvatinib (LEN) plus transcatheter arterial chemoembolization (LEN-TACE) has been reported, but its effect on unresectable hepatocellular carcinoma (HCC) refractory to LEN therapy has not been demonstrated. We report a case of HCC refractory to multiple molecular-targeted agents (MTA) treatments, including LEN, that was successfully treated with LEN-TACE. A 59-year-old man was referred to our department with multiple HCCs and a background of hepatitis B virus infection. TACE was the initial treatment. However, he was determined to be TACE-refractory, and multitargeted therapy was initiated. LEN was started at 12 mg/day but resulted in progressive disease (PD) after 13 months of the administration. The response to second-line sorafenib was PD after 2 months. Third-line therapy with atezolizumab + bevacizumab was stopped after one course because of an immune-related adverse event (i.e., dermatitis). The response to fourth-line regorafenib was PD at 2 months, and the response to fifth-line cabozantinib was PD after 6 months. The efficacy of LEN-TACE was recently reported; therefore, we decided to attempt LEN-TACE therapy as a salvage line. After obtaining the patient’s consent to repeat LEN and TACE, treatment was initiated. The tumor markers levels markedly reduced after LEN-TACE therapy. After three additional TACE treatments with continued LEN administration, the tumor marker levels normalized, and complete response was determined based on RECIST guidelines. LEN-TACE therapy may effectively treat unresectable advanced HCC in the LEN-rechallenge setting and may be a treatment option as a last-line therapeutic option.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>36856957</pmid><doi>10.1007/s12328-023-01777-y</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-6776-4609</orcidid></addata></record> |
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subjects | Abdominal Surgery Carcinoma, Hepatocellular - pathology Case Report Chemoembolization, Therapeutic - methods Colorectal Surgery Gastroenterology Hepatology Humans Liver Neoplasms - drug therapy Male Medicine Medicine & Public Health Middle Aged Surgical Oncology Treatment Outcome |
title | A case of complete response with rechallenge-lenvatinib plus transcatheter arterial chemoembolization for unresectable hepatocellular carcinoma refractory to multiple molecular-targeted agent treatments |
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