Corticosteroid Therapy for Crizotinib-induced, Allergy-mediated Liver Injury: a Case Report
Background. Crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor used to treat ALK-positive lung adenocarcinoma, has been shown to cause hepatic dysfunction; however, the appropriate treatment for crizotinib-induced hepatic injury has not yet been established. Case. We describe a case involving...
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Veröffentlicht in: | Haigan 2015/02/20, Vol.55(1), pp.48-52 |
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description | Background. Crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor used to treat ALK-positive lung adenocarcinoma, has been shown to cause hepatic dysfunction; however, the appropriate treatment for crizotinib-induced hepatic injury has not yet been established. Case. We describe a case involving a 68-year-old woman with lung adenocarcinoma (cT4N3M1b, brain metastasis). After treatment for the brain metastasis, she was prescribed 500 mg/day of crizotinib. A drug eruption and elevation of the serum hepatic enzyme levels (aspartate transaminase [AST] 44 IU/l, alanine transaminase [ALT] 43 IU/l) and peripheral blood eosinophil ratio (7.0%) were noted on day 13 after beginning crizotinib treatment. On day 21, crizotinib was discontinued due to deterioration of the patient's hepatic function (AST 134 IU/l, ALT 207 IU/l). Four days later, she presented with a fever, worsening of the drug eruption and aggravation of the hepatic injury (AST 1823 IU/l, ALT 2756 IU/l), suggesting drug-induced, allergy-mediated liver injury. Subsequently, 250 mg/day of methylprednisolone was administered intravenously for three days, and her symptoms and the hepatic injury rapidly improved. Conclusions. Corticosteroids represent a promising treatment for crizotinib-related, allergy-mediated liver injury. Because crizotinib is a key drug for treating ALK-positive lung adenocarcinoma, further studies are needed to establish the most appropriate management strategy for crizotinib-induced liver injury. |
doi_str_mv | 10.2482/haigan.55.48 |
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Crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor used to treat ALK-positive lung adenocarcinoma, has been shown to cause hepatic dysfunction; however, the appropriate treatment for crizotinib-induced hepatic injury has not yet been established. Case. We describe a case involving a 68-year-old woman with lung adenocarcinoma (cT4N3M1b, brain metastasis). After treatment for the brain metastasis, she was prescribed 500 mg/day of crizotinib. A drug eruption and elevation of the serum hepatic enzyme levels (aspartate transaminase [AST] 44 IU/l, alanine transaminase [ALT] 43 IU/l) and peripheral blood eosinophil ratio (7.0%) were noted on day 13 after beginning crizotinib treatment. On day 21, crizotinib was discontinued due to deterioration of the patient's hepatic function (AST 134 IU/l, ALT 207 IU/l). Four days later, she presented with a fever, worsening of the drug eruption and aggravation of the hepatic injury (AST 1823 IU/l, ALT 2756 IU/l), suggesting drug-induced, allergy-mediated liver injury. Subsequently, 250 mg/day of methylprednisolone was administered intravenously for three days, and her symptoms and the hepatic injury rapidly improved. Conclusions. Corticosteroids represent a promising treatment for crizotinib-related, allergy-mediated liver injury. Because crizotinib is a key drug for treating ALK-positive lung adenocarcinoma, further studies are needed to establish the most appropriate management strategy for crizotinib-induced liver injury.</description><identifier>ISSN: 0386-9628</identifier><identifier>EISSN: 1348-9992</identifier><identifier>DOI: 10.2482/haigan.55.48</identifier><language>eng ; jpn</language><publisher>The Japan Lung Cancer Society</publisher><subject>Allergy-mediated liver injury ; Corticosteroid ; Crizotinib</subject><ispartof>Haigan, 2015/02/20, Vol.55(1), pp.48-52</ispartof><rights>2015 by The Japan Lung Cancer Society</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2448-ec32c1b0cc1f40cc5d3e0ca295a0ada906cb5ef03c63c4eba0955c85e9c6eba13</citedby><cites>FETCH-LOGICAL-c2448-ec32c1b0cc1f40cc5d3e0ca295a0ada906cb5ef03c63c4eba0955c85e9c6eba13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Oonuma, Hitoshi</creatorcontrib><creatorcontrib>Kato, Jin-ichi</creatorcontrib><creatorcontrib>Oyama, Kazuyuki</creatorcontrib><creatorcontrib>Kawahara, Ritsuko</creatorcontrib><creatorcontrib>Seki, Kunihiko</creatorcontrib><creatorcontrib>Inoue, Yuzuru</creatorcontrib><title>Corticosteroid Therapy for Crizotinib-induced, Allergy-mediated Liver Injury: a Case Report</title><title>Haigan</title><addtitle>JJLC</addtitle><description>Background. Crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor used to treat ALK-positive lung adenocarcinoma, has been shown to cause hepatic dysfunction; however, the appropriate treatment for crizotinib-induced hepatic injury has not yet been established. Case. We describe a case involving a 68-year-old woman with lung adenocarcinoma (cT4N3M1b, brain metastasis). After treatment for the brain metastasis, she was prescribed 500 mg/day of crizotinib. A drug eruption and elevation of the serum hepatic enzyme levels (aspartate transaminase [AST] 44 IU/l, alanine transaminase [ALT] 43 IU/l) and peripheral blood eosinophil ratio (7.0%) were noted on day 13 after beginning crizotinib treatment. On day 21, crizotinib was discontinued due to deterioration of the patient's hepatic function (AST 134 IU/l, ALT 207 IU/l). Four days later, she presented with a fever, worsening of the drug eruption and aggravation of the hepatic injury (AST 1823 IU/l, ALT 2756 IU/l), suggesting drug-induced, allergy-mediated liver injury. Subsequently, 250 mg/day of methylprednisolone was administered intravenously for three days, and her symptoms and the hepatic injury rapidly improved. Conclusions. Corticosteroids represent a promising treatment for crizotinib-related, allergy-mediated liver injury. Because crizotinib is a key drug for treating ALK-positive lung adenocarcinoma, further studies are needed to establish the most appropriate management strategy for crizotinib-induced liver injury.</description><subject>Allergy-mediated liver injury</subject><subject>Corticosteroid</subject><subject>Crizotinib</subject><issn>0386-9628</issn><issn>1348-9992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNpNkM9Kw0AQhxdRsFZvPsA-QFM3u9mw60VK8E-hIEg9eQiTyaTdkiZlNxXi05sSKV5mGOabH8PH2H0s5jIx8mELbgPNXOt5Yi7YJFaJiay18pJNhDJpZFNprtlNCDshUqlTNWFfWes7h23oyLeu5OsteTj0vGo9z7z7aTvXuCJyTXlEKmd8UdfkN320p9JBRyVfuW_yfNnsjr5_5MAzCMQ_6DDE3rKrCupAd399yj5fntfZW7R6f11mi1WEMhk-JFQS40IgxlUyVF0qEgjSahBQghUpFpoqoTBVmFABwmqNRpPFdJhiNWWzMRd9G4KnKj94twff57HIT2LyUUyudZ6YAX8a8V3oYENnGE4iavoHx-PFeYNb8Dk16hegGXEg</recordid><startdate>20150220</startdate><enddate>20150220</enddate><creator>Oonuma, Hitoshi</creator><creator>Kato, Jin-ichi</creator><creator>Oyama, Kazuyuki</creator><creator>Kawahara, Ritsuko</creator><creator>Seki, Kunihiko</creator><creator>Inoue, Yuzuru</creator><general>The Japan Lung Cancer Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20150220</creationdate><title>Corticosteroid Therapy for Crizotinib-induced, Allergy-mediated Liver Injury: a Case Report</title><author>Oonuma, Hitoshi ; Kato, Jin-ichi ; Oyama, Kazuyuki ; Kawahara, Ritsuko ; Seki, Kunihiko ; Inoue, Yuzuru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2448-ec32c1b0cc1f40cc5d3e0ca295a0ada906cb5ef03c63c4eba0955c85e9c6eba13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>2015</creationdate><topic>Allergy-mediated liver injury</topic><topic>Corticosteroid</topic><topic>Crizotinib</topic><toplevel>online_resources</toplevel><creatorcontrib>Oonuma, Hitoshi</creatorcontrib><creatorcontrib>Kato, Jin-ichi</creatorcontrib><creatorcontrib>Oyama, Kazuyuki</creatorcontrib><creatorcontrib>Kawahara, Ritsuko</creatorcontrib><creatorcontrib>Seki, Kunihiko</creatorcontrib><creatorcontrib>Inoue, Yuzuru</creatorcontrib><collection>CrossRef</collection><jtitle>Haigan</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oonuma, Hitoshi</au><au>Kato, Jin-ichi</au><au>Oyama, Kazuyuki</au><au>Kawahara, Ritsuko</au><au>Seki, Kunihiko</au><au>Inoue, Yuzuru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corticosteroid Therapy for Crizotinib-induced, Allergy-mediated Liver Injury: a Case Report</atitle><jtitle>Haigan</jtitle><addtitle>JJLC</addtitle><date>2015-02-20</date><risdate>2015</risdate><volume>55</volume><issue>1</issue><spage>48</spage><epage>52</epage><pages>48-52</pages><issn>0386-9628</issn><eissn>1348-9992</eissn><abstract>Background. Crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor used to treat ALK-positive lung adenocarcinoma, has been shown to cause hepatic dysfunction; however, the appropriate treatment for crizotinib-induced hepatic injury has not yet been established. Case. We describe a case involving a 68-year-old woman with lung adenocarcinoma (cT4N3M1b, brain metastasis). After treatment for the brain metastasis, she was prescribed 500 mg/day of crizotinib. A drug eruption and elevation of the serum hepatic enzyme levels (aspartate transaminase [AST] 44 IU/l, alanine transaminase [ALT] 43 IU/l) and peripheral blood eosinophil ratio (7.0%) were noted on day 13 after beginning crizotinib treatment. On day 21, crizotinib was discontinued due to deterioration of the patient's hepatic function (AST 134 IU/l, ALT 207 IU/l). Four days later, she presented with a fever, worsening of the drug eruption and aggravation of the hepatic injury (AST 1823 IU/l, ALT 2756 IU/l), suggesting drug-induced, allergy-mediated liver injury. Subsequently, 250 mg/day of methylprednisolone was administered intravenously for three days, and her symptoms and the hepatic injury rapidly improved. Conclusions. Corticosteroids represent a promising treatment for crizotinib-related, allergy-mediated liver injury. Because crizotinib is a key drug for treating ALK-positive lung adenocarcinoma, further studies are needed to establish the most appropriate management strategy for crizotinib-induced liver injury.</abstract><pub>The Japan Lung Cancer Society</pub><doi>10.2482/haigan.55.48</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Allergy-mediated liver injury Corticosteroid Crizotinib |
title | Corticosteroid Therapy for Crizotinib-induced, Allergy-mediated Liver Injury: a Case Report |
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