Cabozantinib-induced serum creatine kinase elevation and musculoskeletal complaints
Summary Cabozantinib is a multikinase inhibitor approved for the treatment of metastatic medullary thyroid cancer and advanced renal cell carcinoma (RCC) in patients who have received prior anti-angiogenic therapy. While associations between serum creatine kinase (CK) elevations and other tyrosine k...
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Veröffentlicht in: | Investigational new drugs 2018-12, Vol.36 (6), p.1143-1146 |
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creator | Stump, Sarah E. Whang, Young E. Crona, Daniel J. |
description | Summary
Cabozantinib is a multikinase inhibitor approved for the treatment of metastatic medullary thyroid cancer and advanced renal cell carcinoma (RCC) in patients who have received prior anti-angiogenic therapy. While associations between serum creatine kinase (CK) elevations and other tyrosine kinase inhibitors used for the treatment of solid malignancies have been previously reported, we report a case of cabozantinib-associated CK elevation that was associated with musculoskeletal complaints by an RCC patient. Nine days following initiation of cabozantinib, the patient reported muscle cramps and serum CK had increased from levels 12 months earlier that were within normal limits to a grade 1 elevation of 244 units/L. Despite a dose reduction, her CK continued to rise over the next 2 months, leading to a peak CK of 914 units/L. Due to this grade 3 elevation, cabozantinib was permanently discontinued, and her CK subsequently returned to a grade 1 elevation within one week and then to baseline within 3 weeks. The temporal relationship between drug exposure and CK increase strongly suggests causality. To the authors’ knowledge, this is the first reported case of CK elevation attributed to cabozantinib, but cabozantinib-induced CK elevations could be under-reported, and providers should monitor for musculoskeletal complaints during cabozantinib therapy. |
doi_str_mv | 10.1007/s10637-018-0629-2 |
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Cabozantinib is a multikinase inhibitor approved for the treatment of metastatic medullary thyroid cancer and advanced renal cell carcinoma (RCC) in patients who have received prior anti-angiogenic therapy. While associations between serum creatine kinase (CK) elevations and other tyrosine kinase inhibitors used for the treatment of solid malignancies have been previously reported, we report a case of cabozantinib-associated CK elevation that was associated with musculoskeletal complaints by an RCC patient. Nine days following initiation of cabozantinib, the patient reported muscle cramps and serum CK had increased from levels 12 months earlier that were within normal limits to a grade 1 elevation of 244 units/L. Despite a dose reduction, her CK continued to rise over the next 2 months, leading to a peak CK of 914 units/L. Due to this grade 3 elevation, cabozantinib was permanently discontinued, and her CK subsequently returned to a grade 1 elevation within one week and then to baseline within 3 weeks. The temporal relationship between drug exposure and CK increase strongly suggests causality. To the authors’ knowledge, this is the first reported case of CK elevation attributed to cabozantinib, but cabozantinib-induced CK elevations could be under-reported, and providers should monitor for musculoskeletal complaints during cabozantinib therapy.</description><identifier>ISSN: 0167-6997</identifier><identifier>EISSN: 1573-0646</identifier><identifier>DOI: 10.1007/s10637-018-0629-2</identifier><identifier>PMID: 29956055</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Angiogenesis ; Anilides - adverse effects ; Case reports ; Cramps ; Creatine ; Creatine kinase ; Creatine Kinase - blood ; Female ; Humans ; Inhibitor drugs ; Kidney cancer ; Medicine ; Medicine & Public Health ; Metastases ; Middle Aged ; Muscle Cramp - chemically induced ; Muscles ; Musculoskeletal Diseases - blood ; Musculoskeletal Diseases - chemically induced ; Musculoskeletal Diseases - enzymology ; Oncology ; Patients ; Pharmacology/Toxicology ; Protein-tyrosine kinase ; Pyridines - adverse effects ; Renal cell carcinoma ; Short Report ; Targeted cancer therapy ; Therapy ; Thyroid ; Thyroid cancer ; Tyrosine</subject><ispartof>Investigational new drugs, 2018-12, Vol.36 (6), p.1143-1146</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Investigational New Drugs is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-86638e924ed139546c553065119f2cba9612e96068bfc8e0d7ef5543a0bdc9333</citedby><cites>FETCH-LOGICAL-c372t-86638e924ed139546c553065119f2cba9612e96068bfc8e0d7ef5543a0bdc9333</cites><orcidid>0000-0003-3742-8863</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/s10637-018-0629-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10637-018-0629-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29956055$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stump, Sarah E.</creatorcontrib><creatorcontrib>Whang, Young E.</creatorcontrib><creatorcontrib>Crona, Daniel J.</creatorcontrib><title>Cabozantinib-induced serum creatine kinase elevation and musculoskeletal complaints</title><title>Investigational new drugs</title><addtitle>Invest New Drugs</addtitle><addtitle>Invest New Drugs</addtitle><description>Summary
Cabozantinib is a multikinase inhibitor approved for the treatment of metastatic medullary thyroid cancer and advanced renal cell carcinoma (RCC) in patients who have received prior anti-angiogenic therapy. While associations between serum creatine kinase (CK) elevations and other tyrosine kinase inhibitors used for the treatment of solid malignancies have been previously reported, we report a case of cabozantinib-associated CK elevation that was associated with musculoskeletal complaints by an RCC patient. Nine days following initiation of cabozantinib, the patient reported muscle cramps and serum CK had increased from levels 12 months earlier that were within normal limits to a grade 1 elevation of 244 units/L. Despite a dose reduction, her CK continued to rise over the next 2 months, leading to a peak CK of 914 units/L. Due to this grade 3 elevation, cabozantinib was permanently discontinued, and her CK subsequently returned to a grade 1 elevation within one week and then to baseline within 3 weeks. The temporal relationship between drug exposure and CK increase strongly suggests causality. To the authors’ knowledge, this is the first reported case of CK elevation attributed to cabozantinib, but cabozantinib-induced CK elevations could be under-reported, and providers should monitor for musculoskeletal complaints during cabozantinib therapy.</description><subject>Angiogenesis</subject><subject>Anilides - adverse effects</subject><subject>Case reports</subject><subject>Cramps</subject><subject>Creatine</subject><subject>Creatine kinase</subject><subject>Creatine Kinase - blood</subject><subject>Female</subject><subject>Humans</subject><subject>Inhibitor drugs</subject><subject>Kidney cancer</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Middle Aged</subject><subject>Muscle Cramp - chemically induced</subject><subject>Muscles</subject><subject>Musculoskeletal Diseases - blood</subject><subject>Musculoskeletal Diseases - chemically induced</subject><subject>Musculoskeletal Diseases - enzymology</subject><subject>Oncology</subject><subject>Patients</subject><subject>Pharmacology/Toxicology</subject><subject>Protein-tyrosine kinase</subject><subject>Pyridines - adverse effects</subject><subject>Renal cell carcinoma</subject><subject>Short Report</subject><subject>Targeted cancer therapy</subject><subject>Therapy</subject><subject>Thyroid</subject><subject>Thyroid cancer</subject><subject>Tyrosine</subject><issn>0167-6997</issn><issn>1573-0646</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1kE1LxDAURYMozjj6A9xIwY2baj6apFnK4BcMuFDXIU1fpTNtOiatoL_elI4KgquQm_PuCwehU4IvCcbyKhAsmEwxyVMsqErpHpoTLlm8ZWIfzTERMhVKyRk6CmGNMWZKZodoRpXiAnM-R09LU3SfxvW1q4u0duVgoUwC-KFNrAcTc0g2tTMBEmjgPQadS4wrk3YIdmi6sIlxb5rEdu22MbXrwzE6qEwT4GR3LtDL7c3z8j5dPd49LK9XqWWS9mkuBMtB0QxKwhTPhOWcYcEJURW1hVGCUFACi7yobA64lFBxnjGDi9IqxtgCXUy9W9-9DRB63dbBQtMYB90QNI1SciYYURE9_4Ouu8G7-LuRIpRyLkaKTJT1XQgeKr31dWv8hyZYj8b1ZFxH43o0rmmcOds1D0UL5c_Et-II0AkI8cm9gv9d_X_rF4zbi0w</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Stump, Sarah E.</creator><creator>Whang, Young E.</creator><creator>Crona, Daniel J.</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>K60</scope><scope>K6~</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>L.-</scope><scope>M0C</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3742-8863</orcidid></search><sort><creationdate>20181201</creationdate><title>Cabozantinib-induced serum creatine kinase elevation and musculoskeletal complaints</title><author>Stump, Sarah E. ; Whang, Young E. ; Crona, Daniel J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-86638e924ed139546c553065119f2cba9612e96068bfc8e0d7ef5543a0bdc9333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Angiogenesis</topic><topic>Anilides - adverse effects</topic><topic>Case reports</topic><topic>Cramps</topic><topic>Creatine</topic><topic>Creatine kinase</topic><topic>Creatine Kinase - blood</topic><topic>Female</topic><topic>Humans</topic><topic>Inhibitor drugs</topic><topic>Kidney cancer</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Middle Aged</topic><topic>Muscle Cramp - chemically induced</topic><topic>Muscles</topic><topic>Musculoskeletal Diseases - blood</topic><topic>Musculoskeletal Diseases - chemically induced</topic><topic>Musculoskeletal Diseases - enzymology</topic><topic>Oncology</topic><topic>Patients</topic><topic>Pharmacology/Toxicology</topic><topic>Protein-tyrosine kinase</topic><topic>Pyridines - adverse effects</topic><topic>Renal cell carcinoma</topic><topic>Short Report</topic><topic>Targeted cancer therapy</topic><topic>Therapy</topic><topic>Thyroid</topic><topic>Thyroid cancer</topic><topic>Tyrosine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stump, Sarah E.</creatorcontrib><creatorcontrib>Whang, Young E.</creatorcontrib><creatorcontrib>Crona, Daniel J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>ABI/INFORM Collection</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ABI/INFORM Global (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Business Premium Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Business Premium Collection (Alumni)</collection><collection>Health Research Premium Collection</collection><collection>ABI/INFORM Global (Corporate)</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Business Collection (Alumni Edition)</collection><collection>ProQuest Business Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ABI/INFORM Professional Advanced</collection><collection>ABI/INFORM Global</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Business</collection><collection>ProQuest One Business (Alumni)</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 Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Investigational new drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stump, Sarah E.</au><au>Whang, Young E.</au><au>Crona, Daniel J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cabozantinib-induced serum creatine kinase elevation and musculoskeletal complaints</atitle><jtitle>Investigational new drugs</jtitle><stitle>Invest New Drugs</stitle><addtitle>Invest New Drugs</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>36</volume><issue>6</issue><spage>1143</spage><epage>1146</epage><pages>1143-1146</pages><issn>0167-6997</issn><eissn>1573-0646</eissn><abstract>Summary
Cabozantinib is a multikinase inhibitor approved for the treatment of metastatic medullary thyroid cancer and advanced renal cell carcinoma (RCC) in patients who have received prior anti-angiogenic therapy. While associations between serum creatine kinase (CK) elevations and other tyrosine kinase inhibitors used for the treatment of solid malignancies have been previously reported, we report a case of cabozantinib-associated CK elevation that was associated with musculoskeletal complaints by an RCC patient. Nine days following initiation of cabozantinib, the patient reported muscle cramps and serum CK had increased from levels 12 months earlier that were within normal limits to a grade 1 elevation of 244 units/L. Despite a dose reduction, her CK continued to rise over the next 2 months, leading to a peak CK of 914 units/L. Due to this grade 3 elevation, cabozantinib was permanently discontinued, and her CK subsequently returned to a grade 1 elevation within one week and then to baseline within 3 weeks. The temporal relationship between drug exposure and CK increase strongly suggests causality. To the authors’ knowledge, this is the first reported case of CK elevation attributed to cabozantinib, but cabozantinib-induced CK elevations could be under-reported, and providers should monitor for musculoskeletal complaints during cabozantinib therapy.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29956055</pmid><doi>10.1007/s10637-018-0629-2</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0003-3742-8863</orcidid></addata></record> |
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subjects | Angiogenesis Anilides - adverse effects Case reports Cramps Creatine Creatine kinase Creatine Kinase - blood Female Humans Inhibitor drugs Kidney cancer Medicine Medicine & Public Health Metastases Middle Aged Muscle Cramp - chemically induced Muscles Musculoskeletal Diseases - blood Musculoskeletal Diseases - chemically induced Musculoskeletal Diseases - enzymology Oncology Patients Pharmacology/Toxicology Protein-tyrosine kinase Pyridines - adverse effects Renal cell carcinoma Short Report Targeted cancer therapy Therapy Thyroid Thyroid cancer Tyrosine |
title | Cabozantinib-induced serum creatine kinase elevation and musculoskeletal complaints |
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