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Feasibility of sorafenib combined with local radiotherapy in advanced hepatocellular carcinoma
Sorafenib is an effective systemic agent for advanced hepatocellular carcinoma. To increase its efficacy, we evaluated the feasibility and benefit of sorafenib combined with radiotherapy. From July 2007 to July 2011, 31 patients were treated with a daily dose of 800 mg of sorafenib and radiotherapy....
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Published in: | Yonsei medical journal 2013, 54(5), , pp.1178-1185 |
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description | Sorafenib is an effective systemic agent for advanced hepatocellular carcinoma. To increase its efficacy, we evaluated the feasibility and benefit of sorafenib combined with radiotherapy.
From July 2007 to July 2011, 31 patients were treated with a daily dose of 800 mg of sorafenib and radiotherapy. Among them, 13 patients who received radiotherapy on the bone metastasis were excluded. Thirteen patients received 30-54 Gy of radiotherapy on the primary tumor (primary group) and 5 patients received 30-58.4 Gy on the measurable metastatic lesions (measurable metastasis group). Tumor responses at 1 month after the completion of radiotherapy and overall survival were evaluated.
The in-field response rate was 100% in the primary group and 60% in the measurable metastasis group. A decrease of more than 80% in the tumor marker α-fetoprotein was observed in 7 patients in the primary group (54%). Toxicities of grades 3-4 were hand-foot syndrome in 3 (17%) patients, duodenal bleeding in 1 (6%) patient, thrombocytopenia in 3 (17%) patients and elevation of aspartate transaminase in 1 (6%) patient. The median overall survival was 7.8 months (95% confidence interval, 3.0-12.6).
The combined treatment of sorafenib and radiotherapy was feasible and induced substantial tumor responses in the target lesions. The results of this study emphasize the importance of individualized approach in the management of advanced hepatocellular carcinoma and encourage the initiation of a controlled clinical trial. |
doi_str_mv | 10.3349/ymj.2013.54.5.1178 |
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From July 2007 to July 2011, 31 patients were treated with a daily dose of 800 mg of sorafenib and radiotherapy. Among them, 13 patients who received radiotherapy on the bone metastasis were excluded. Thirteen patients received 30-54 Gy of radiotherapy on the primary tumor (primary group) and 5 patients received 30-58.4 Gy on the measurable metastatic lesions (measurable metastasis group). Tumor responses at 1 month after the completion of radiotherapy and overall survival were evaluated.
The in-field response rate was 100% in the primary group and 60% in the measurable metastasis group. A decrease of more than 80% in the tumor marker α-fetoprotein was observed in 7 patients in the primary group (54%). Toxicities of grades 3-4 were hand-foot syndrome in 3 (17%) patients, duodenal bleeding in 1 (6%) patient, thrombocytopenia in 3 (17%) patients and elevation of aspartate transaminase in 1 (6%) patient. The median overall survival was 7.8 months (95% confidence interval, 3.0-12.6).
The combined treatment of sorafenib and radiotherapy was feasible and induced substantial tumor responses in the target lesions. The results of this study emphasize the importance of individualized approach in the management of advanced hepatocellular carcinoma and encourage the initiation of a controlled clinical trial.</description><identifier>ISSN: 0513-5796</identifier><identifier>EISSN: 1976-2437</identifier><identifier>DOI: 10.3349/ymj.2013.54.5.1178</identifier><identifier>PMID: 23918567</identifier><language>eng</language><publisher>Korea (South): Yonsei University College of Medicine</publisher><subject>Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - adverse effects ; Antineoplastic Agents - therapeutic use ; Carcinoma, Hepatocellular - drug therapy ; Carcinoma, Hepatocellular - pathology ; Carcinoma, Hepatocellular - radiotherapy ; Chemotherapy, Adjuvant ; Feasibility Studies ; Female ; Humans ; Liver Neoplasms - drug therapy ; Liver Neoplasms - pathology ; Liver Neoplasms - radiotherapy ; Male ; Niacinamide - administration & dosage ; Niacinamide - adverse effects ; Niacinamide - analogs & derivatives ; Niacinamide - therapeutic use ; Original ; Phenylurea Compounds - administration & dosage ; Phenylurea Compounds - adverse effects ; Phenylurea Compounds - therapeutic use ; Radiation Dosage ; Radiotherapy - adverse effects ; 의학일반</subject><ispartof>Yonsei Medical Journal, 2013, 54(5), , pp.1178-1185</ispartof><rights>Copyright: Yonsei University College of Medicine 2013 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-b8f72b8f7a362b0ba2d221d137cc28aa235681d083cc2e64db9b197c2a2614b43</citedby><cites>FETCH-LOGICAL-c435t-b8f72b8f7a362b0ba2d221d137cc28aa235681d083cc2e64db9b197c2a2614b43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743177/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743177/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23918567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001794707$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Cha, Jihye</creatorcontrib><creatorcontrib>Seong, Jinsil</creatorcontrib><creatorcontrib>Lee, Ik Jae</creatorcontrib><creatorcontrib>Kim, Jun Won</creatorcontrib><creatorcontrib>Han, Kwang-Hyub</creatorcontrib><title>Feasibility of sorafenib combined with local radiotherapy in advanced hepatocellular carcinoma</title><title>Yonsei medical journal</title><addtitle>Yonsei Med J</addtitle><description>Sorafenib is an effective systemic agent for advanced hepatocellular carcinoma. To increase its efficacy, we evaluated the feasibility and benefit of sorafenib combined with radiotherapy.
From July 2007 to July 2011, 31 patients were treated with a daily dose of 800 mg of sorafenib and radiotherapy. Among them, 13 patients who received radiotherapy on the bone metastasis were excluded. Thirteen patients received 30-54 Gy of radiotherapy on the primary tumor (primary group) and 5 patients received 30-58.4 Gy on the measurable metastatic lesions (measurable metastasis group). Tumor responses at 1 month after the completion of radiotherapy and overall survival were evaluated.
The in-field response rate was 100% in the primary group and 60% in the measurable metastasis group. A decrease of more than 80% in the tumor marker α-fetoprotein was observed in 7 patients in the primary group (54%). Toxicities of grades 3-4 were hand-foot syndrome in 3 (17%) patients, duodenal bleeding in 1 (6%) patient, thrombocytopenia in 3 (17%) patients and elevation of aspartate transaminase in 1 (6%) patient. The median overall survival was 7.8 months (95% confidence interval, 3.0-12.6).
The combined treatment of sorafenib and radiotherapy was feasible and induced substantial tumor responses in the target lesions. The results of this study emphasize the importance of individualized approach in the management of advanced hepatocellular carcinoma and encourage the initiation of a controlled clinical trial.</description><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Carcinoma, Hepatocellular - drug therapy</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Carcinoma, Hepatocellular - radiotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Liver Neoplasms - pathology</subject><subject>Liver Neoplasms - radiotherapy</subject><subject>Male</subject><subject>Niacinamide - administration & dosage</subject><subject>Niacinamide - adverse effects</subject><subject>Niacinamide - analogs & derivatives</subject><subject>Niacinamide - therapeutic use</subject><subject>Original</subject><subject>Phenylurea Compounds - administration & dosage</subject><subject>Phenylurea Compounds - adverse effects</subject><subject>Phenylurea Compounds - therapeutic use</subject><subject>Radiation Dosage</subject><subject>Radiotherapy - adverse effects</subject><subject>의학일반</subject><issn>0513-5796</issn><issn>1976-2437</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpVkU1LxDAQhoMoun78AQ-So5fWJJM07UUQ8QsEQfRqmKSpG22bJa3K_nu7ropeZhjmfd9heAg55CwHkNXJsnvJBeOQK5mrnHNdbpAZr3SRCQl6k8yY4pApXRU7ZHcYXhgTmjOxTXYEVLxUhZ6Rp0uPQ7ChDeOSxoYOMWHj-2Cpi50Nva_pRxjntI0OW5qwDnGc-4SLJQ09xfodezdp5n6BY3S-bd9aTNRhcqGPHe6TrQbbwR989z3yeHnxcH6d3d5d3Zyf3WZOghozWzZarApCISyzKGoheM1BOydKRAGqKHnNSphmX8jaVnZ61AkUBZdWwh45Xuf2qTGvLpiI4as_R_OazNn9w40B4FKJSXq6li7ebOdr5_sxYWsWKXSYll_G_5s-zKeYdwNaAtd6ChDrAJfiMCTf_Ho5MyswZgJjVmCMkkaZFZjJdPT36q_lhwR8AvNcjOI</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Cha, Jihye</creator><creator>Seong, Jinsil</creator><creator>Lee, Ik Jae</creator><creator>Kim, Jun Won</creator><creator>Han, Kwang-Hyub</creator><general>Yonsei University College of Medicine</general><general>연세대학교의과대학</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>5PM</scope><scope>ACYCR</scope></search><sort><creationdate>20130901</creationdate><title>Feasibility of sorafenib combined with local radiotherapy in advanced hepatocellular carcinoma</title><author>Cha, Jihye ; Seong, Jinsil ; Lee, Ik Jae ; Kim, Jun Won ; Han, Kwang-Hyub</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-b8f72b8f7a362b0ba2d221d137cc28aa235681d083cc2e64db9b197c2a2614b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Carcinoma, Hepatocellular - drug therapy</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Carcinoma, Hepatocellular - radiotherapy</topic><topic>Chemotherapy, Adjuvant</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Liver Neoplasms - pathology</topic><topic>Liver Neoplasms - radiotherapy</topic><topic>Male</topic><topic>Niacinamide - administration & dosage</topic><topic>Niacinamide - adverse effects</topic><topic>Niacinamide - analogs & derivatives</topic><topic>Niacinamide - therapeutic use</topic><topic>Original</topic><topic>Phenylurea Compounds - administration & dosage</topic><topic>Phenylurea Compounds - adverse effects</topic><topic>Phenylurea Compounds - therapeutic use</topic><topic>Radiation Dosage</topic><topic>Radiotherapy - adverse effects</topic><topic>의학일반</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cha, Jihye</creatorcontrib><creatorcontrib>Seong, Jinsil</creatorcontrib><creatorcontrib>Lee, Ik Jae</creatorcontrib><creatorcontrib>Kim, Jun Won</creatorcontrib><creatorcontrib>Han, Kwang-Hyub</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Yonsei medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cha, Jihye</au><au>Seong, Jinsil</au><au>Lee, Ik Jae</au><au>Kim, Jun Won</au><au>Han, Kwang-Hyub</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Feasibility of sorafenib combined with local radiotherapy in advanced hepatocellular carcinoma</atitle><jtitle>Yonsei medical journal</jtitle><addtitle>Yonsei Med J</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>54</volume><issue>5</issue><spage>1178</spage><epage>1185</epage><pages>1178-1185</pages><issn>0513-5796</issn><eissn>1976-2437</eissn><abstract>Sorafenib is an effective systemic agent for advanced hepatocellular carcinoma. To increase its efficacy, we evaluated the feasibility and benefit of sorafenib combined with radiotherapy.
From July 2007 to July 2011, 31 patients were treated with a daily dose of 800 mg of sorafenib and radiotherapy. Among them, 13 patients who received radiotherapy on the bone metastasis were excluded. Thirteen patients received 30-54 Gy of radiotherapy on the primary tumor (primary group) and 5 patients received 30-58.4 Gy on the measurable metastatic lesions (measurable metastasis group). Tumor responses at 1 month after the completion of radiotherapy and overall survival were evaluated.
The in-field response rate was 100% in the primary group and 60% in the measurable metastasis group. A decrease of more than 80% in the tumor marker α-fetoprotein was observed in 7 patients in the primary group (54%). Toxicities of grades 3-4 were hand-foot syndrome in 3 (17%) patients, duodenal bleeding in 1 (6%) patient, thrombocytopenia in 3 (17%) patients and elevation of aspartate transaminase in 1 (6%) patient. The median overall survival was 7.8 months (95% confidence interval, 3.0-12.6).
The combined treatment of sorafenib and radiotherapy was feasible and induced substantial tumor responses in the target lesions. The results of this study emphasize the importance of individualized approach in the management of advanced hepatocellular carcinoma and encourage the initiation of a controlled clinical trial.</abstract><cop>Korea (South)</cop><pub>Yonsei University College of Medicine</pub><pmid>23918567</pmid><doi>10.3349/ymj.2013.54.5.1178</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic Agents - administration & dosage Antineoplastic Agents - adverse effects Antineoplastic Agents - therapeutic use Carcinoma, Hepatocellular - drug therapy Carcinoma, Hepatocellular - pathology Carcinoma, Hepatocellular - radiotherapy Chemotherapy, Adjuvant Feasibility Studies Female Humans Liver Neoplasms - drug therapy Liver Neoplasms - pathology Liver Neoplasms - radiotherapy Male Niacinamide - administration & dosage Niacinamide - adverse effects Niacinamide - analogs & derivatives Niacinamide - therapeutic use Original Phenylurea Compounds - administration & dosage Phenylurea Compounds - adverse effects Phenylurea Compounds - therapeutic use Radiation Dosage Radiotherapy - adverse effects 의학일반 |
title | Feasibility of sorafenib combined with local radiotherapy in advanced hepatocellular carcinoma |
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