Spectrum of ocular toxicities from epidermal growth factor receptor inhibitors and their intermediate-term follow-up: a five-year review
Purpose Epidermal growth factor receptor (EGFR) inhibitors and kinases are commonly used in the treatment regimen of various solid tumors including non-small cell lung, colorectal, head and neck, breast, and pancreatic cancers. The aim of this study is to describe common ocular adverse effects assoc...
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description | Purpose
Epidermal growth factor receptor (EGFR) inhibitors and kinases are commonly used in the treatment regimen of various solid tumors including non-small cell lung, colorectal, head and neck, breast, and pancreatic cancers. The aim of this study is to describe common ocular adverse effects associated with EGFR inhibitor treatment, outline successful management options, and provide data on intermediate-term follow-up of these patients.
Methods
A retrospective chart review was performed of all patients presenting to the ophthalmology clinic with an adverse ocular effect while on an EGFR inhibitor. Duration of EGFR inhibitor treatment, symptoms, diagnosis, and treatment information were collected. Statistical analyses were done to ascertain differences in adverse effects based on duration and type of EGFR inhibitor treatment using the Fisher exact test.
Results
The two most common EGFR inhibitors in this group of patients were erlotinib and cetuximab. The most common adverse ocular effects for patients on EGFR inhibitors were dysfunctional tear syndrome (DTS), followed by blepharitis and eyelash changes (trichomegaly and trichiasis). Two patients had epithelial defects (corneal abrasions). There was no significant difference in adverse effects based on specific EGFR inhibitor medication or duration of treatment. Almost all patients were successfully managed with treatment regimens that we have outlined in this paper. Intermediate-term follow-up (range 6–17 months) showed a persistence of DTS and eyelash changes.
Conclusion
We present what is, to our knowledge, the largest reported cohort of patients with ocular toxicities from EGFR inhibitors—the spectrum of eye toxicities, their management, and the intermediate-term follow-up of patients with eye toxicities. Awareness of this information is important for oncologists and oncology nurses to facilitate proper counseling and management/referral of patients developing eye toxicity while on EGFR inhibitors. |
doi_str_mv | 10.1007/s00520-012-1645-y |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_1357394085</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A336672515</galeid><sourcerecordid>A336672515</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-bb791dc4353864530b29d6508088ea61a75732e5ac1f3abd94487803a74bbf5a3</originalsourceid><addsrcrecordid>eNp1UcuO1DAQtBCIHRY-gAuyxNnQjuM44bZaLQ9pJQ7A2XKc9oxXSRxsZ4f5Az4bR7M8Lpy61K6q7nYR8pLDGw6g3iYAWQEDXjHe1JKdHpEdr4VgSojuMdlBV3NWCykvyLOU7gC4UrJ6Si4qwWVRqB35-WVBm-M60eBosOtoIs3hh7c-e0zUxTBRXPyAcTIj3cdwzAfqjM0h0ogWlw34-eB7X1CiZh5oPqDfmrmIcPAmI9sgdWEcw5GtyztqqPP3yE5oNpt7j8fn5IkzY8IXD_WSfHt_8_X6I7v9_OHT9dUtszVAZn2vOj7YcpRoy8kC-qobGgkttC2ahhsllahQGsudMP3Q1XWrWhBG1X3vpBGX5PXZd4nh-4op67uwxrmM1FwUbVdDK_-y9mZE7WcXcjR28snqKyGaRlWSbyx-ZtkYUoro9BL9ZOJJc9BbQvqckC4J6S0hfSqaVw_z1778zh_F70gKoToTUnma9xj_WfC_rr8AmxCdIw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1357394085</pqid></control><display><type>article</type><title>Spectrum of ocular toxicities from epidermal growth factor receptor inhibitors and their intermediate-term follow-up: a five-year review</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Borkar, Durga S. ; Lacouture, Mario E. ; Basti, Surendra</creator><creatorcontrib>Borkar, Durga S. ; Lacouture, Mario E. ; Basti, Surendra</creatorcontrib><description>Purpose
Epidermal growth factor receptor (EGFR) inhibitors and kinases are commonly used in the treatment regimen of various solid tumors including non-small cell lung, colorectal, head and neck, breast, and pancreatic cancers. The aim of this study is to describe common ocular adverse effects associated with EGFR inhibitor treatment, outline successful management options, and provide data on intermediate-term follow-up of these patients.
Methods
A retrospective chart review was performed of all patients presenting to the ophthalmology clinic with an adverse ocular effect while on an EGFR inhibitor. Duration of EGFR inhibitor treatment, symptoms, diagnosis, and treatment information were collected. Statistical analyses were done to ascertain differences in adverse effects based on duration and type of EGFR inhibitor treatment using the Fisher exact test.
Results
The two most common EGFR inhibitors in this group of patients were erlotinib and cetuximab. The most common adverse ocular effects for patients on EGFR inhibitors were dysfunctional tear syndrome (DTS), followed by blepharitis and eyelash changes (trichomegaly and trichiasis). Two patients had epithelial defects (corneal abrasions). There was no significant difference in adverse effects based on specific EGFR inhibitor medication or duration of treatment. Almost all patients were successfully managed with treatment regimens that we have outlined in this paper. Intermediate-term follow-up (range 6–17 months) showed a persistence of DTS and eyelash changes.
Conclusion
We present what is, to our knowledge, the largest reported cohort of patients with ocular toxicities from EGFR inhibitors—the spectrum of eye toxicities, their management, and the intermediate-term follow-up of patients with eye toxicities. Awareness of this information is important for oncologists and oncology nurses to facilitate proper counseling and management/referral of patients developing eye toxicity while on EGFR inhibitors.</description><identifier>ISSN: 0941-4355</identifier><identifier>EISSN: 1433-7339</identifier><identifier>DOI: 10.1007/s00520-012-1645-y</identifier><identifier>PMID: 23151647</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Analysis ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal, Humanized - adverse effects ; Cancer ; Care and treatment ; Cetuximab ; Chemotherapy ; Chicago - epidemiology ; Clinical trials ; Colorectal cancer ; Cornea ; Epidermal growth factor ; Erlotinib Hydrochloride ; Eye Diseases - chemically induced ; Eye Diseases - epidemiology ; Female ; Follow-Up Studies ; Humans ; Lung cancer ; Male ; Medical Audit ; Medicine ; Medicine & Public Health ; Metastasis ; Neoplasms - drug therapy ; Nursing ; Nursing Research ; Oncology ; Ophthalmology ; Original Article ; Pain Medicine ; Pancreatic cancer ; Patients ; Quinazolines - adverse effects ; Receptor, Epidermal Growth Factor - antagonists & inhibitors ; Rehabilitation Medicine ; Retrospective Studies ; Toxicity ; Tumors</subject><ispartof>Supportive care in cancer, 2013-04, Vol.21 (4), p.1167-1174</ispartof><rights>Springer-Verlag Berlin Heidelberg 2012</rights><rights>COPYRIGHT 2013 Springer</rights><rights>Springer-Verlag Berlin Heidelberg 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-bb791dc4353864530b29d6508088ea61a75732e5ac1f3abd94487803a74bbf5a3</citedby><cites>FETCH-LOGICAL-c400t-bb791dc4353864530b29d6508088ea61a75732e5ac1f3abd94487803a74bbf5a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00520-012-1645-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00520-012-1645-y$$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/23151647$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borkar, Durga S.</creatorcontrib><creatorcontrib>Lacouture, Mario E.</creatorcontrib><creatorcontrib>Basti, Surendra</creatorcontrib><title>Spectrum of ocular toxicities from epidermal growth factor receptor inhibitors and their intermediate-term follow-up: a five-year review</title><title>Supportive care in cancer</title><addtitle>Support Care Cancer</addtitle><addtitle>Support Care Cancer</addtitle><description>Purpose
Epidermal growth factor receptor (EGFR) inhibitors and kinases are commonly used in the treatment regimen of various solid tumors including non-small cell lung, colorectal, head and neck, breast, and pancreatic cancers. The aim of this study is to describe common ocular adverse effects associated with EGFR inhibitor treatment, outline successful management options, and provide data on intermediate-term follow-up of these patients.
Methods
A retrospective chart review was performed of all patients presenting to the ophthalmology clinic with an adverse ocular effect while on an EGFR inhibitor. Duration of EGFR inhibitor treatment, symptoms, diagnosis, and treatment information were collected. Statistical analyses were done to ascertain differences in adverse effects based on duration and type of EGFR inhibitor treatment using the Fisher exact test.
Results
The two most common EGFR inhibitors in this group of patients were erlotinib and cetuximab. The most common adverse ocular effects for patients on EGFR inhibitors were dysfunctional tear syndrome (DTS), followed by blepharitis and eyelash changes (trichomegaly and trichiasis). Two patients had epithelial defects (corneal abrasions). There was no significant difference in adverse effects based on specific EGFR inhibitor medication or duration of treatment. Almost all patients were successfully managed with treatment regimens that we have outlined in this paper. Intermediate-term follow-up (range 6–17 months) showed a persistence of DTS and eyelash changes.
Conclusion
We present what is, to our knowledge, the largest reported cohort of patients with ocular toxicities from EGFR inhibitors—the spectrum of eye toxicities, their management, and the intermediate-term follow-up of patients with eye toxicities. Awareness of this information is important for oncologists and oncology nurses to facilitate proper counseling and management/referral of patients developing eye toxicity while on EGFR inhibitors.</description><subject>Analysis</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal, Humanized - adverse effects</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Cetuximab</subject><subject>Chemotherapy</subject><subject>Chicago - epidemiology</subject><subject>Clinical trials</subject><subject>Colorectal cancer</subject><subject>Cornea</subject><subject>Epidermal growth factor</subject><subject>Erlotinib Hydrochloride</subject><subject>Eye Diseases - chemically induced</subject><subject>Eye Diseases - epidemiology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Lung cancer</subject><subject>Male</subject><subject>Medical Audit</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastasis</subject><subject>Neoplasms - drug therapy</subject><subject>Nursing</subject><subject>Nursing Research</subject><subject>Oncology</subject><subject>Ophthalmology</subject><subject>Original Article</subject><subject>Pain Medicine</subject><subject>Pancreatic cancer</subject><subject>Patients</subject><subject>Quinazolines - adverse effects</subject><subject>Receptor, Epidermal Growth Factor - antagonists & inhibitors</subject><subject>Rehabilitation Medicine</subject><subject>Retrospective Studies</subject><subject>Toxicity</subject><subject>Tumors</subject><issn>0941-4355</issn><issn>1433-7339</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1UcuO1DAQtBCIHRY-gAuyxNnQjuM44bZaLQ9pJQ7A2XKc9oxXSRxsZ4f5Az4bR7M8Lpy61K6q7nYR8pLDGw6g3iYAWQEDXjHe1JKdHpEdr4VgSojuMdlBV3NWCykvyLOU7gC4UrJ6Si4qwWVRqB35-WVBm-M60eBosOtoIs3hh7c-e0zUxTBRXPyAcTIj3cdwzAfqjM0h0ogWlw34-eB7X1CiZh5oPqDfmrmIcPAmI9sgdWEcw5GtyztqqPP3yE5oNpt7j8fn5IkzY8IXD_WSfHt_8_X6I7v9_OHT9dUtszVAZn2vOj7YcpRoy8kC-qobGgkttC2ahhsllahQGsudMP3Q1XWrWhBG1X3vpBGX5PXZd4nh-4op67uwxrmM1FwUbVdDK_-y9mZE7WcXcjR28snqKyGaRlWSbyx-ZtkYUoro9BL9ZOJJc9BbQvqckC4J6S0hfSqaVw_z1778zh_F70gKoToTUnma9xj_WfC_rr8AmxCdIw</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Borkar, Durga S.</creator><creator>Lacouture, Mario E.</creator><creator>Basti, Surendra</creator><general>Springer-Verlag</general><general>Springer</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>0-V</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88J</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HEHIP</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2R</scope><scope>M2S</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>POGQB</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PRQQA</scope><scope>Q9U</scope></search><sort><creationdate>20130401</creationdate><title>Spectrum of ocular toxicities from epidermal growth factor receptor inhibitors and their intermediate-term follow-up: a five-year review</title><author>Borkar, Durga S. ; Lacouture, Mario E. ; Basti, Surendra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-bb791dc4353864530b29d6508088ea61a75732e5ac1f3abd94487803a74bbf5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analysis</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal, Humanized - adverse effects</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Cetuximab</topic><topic>Chemotherapy</topic><topic>Chicago - epidemiology</topic><topic>Clinical trials</topic><topic>Colorectal cancer</topic><topic>Cornea</topic><topic>Epidermal growth factor</topic><topic>Erlotinib Hydrochloride</topic><topic>Eye Diseases - chemically induced</topic><topic>Eye Diseases - epidemiology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Lung cancer</topic><topic>Male</topic><topic>Medical Audit</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastasis</topic><topic>Neoplasms - drug therapy</topic><topic>Nursing</topic><topic>Nursing Research</topic><topic>Oncology</topic><topic>Ophthalmology</topic><topic>Original Article</topic><topic>Pain Medicine</topic><topic>Pancreatic cancer</topic><topic>Patients</topic><topic>Quinazolines - adverse effects</topic><topic>Receptor, Epidermal Growth Factor - antagonists & inhibitors</topic><topic>Rehabilitation Medicine</topic><topic>Retrospective Studies</topic><topic>Toxicity</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borkar, Durga S.</creatorcontrib><creatorcontrib>Lacouture, Mario E.</creatorcontrib><creatorcontrib>Basti, Surendra</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 Social Sciences Premium Collection</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>Medical Database (Alumni Edition)</collection><collection>Social Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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>Social Science Premium Collection</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 Central Student</collection><collection>Sociology Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Social Science Database</collection><collection>Sociology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest Sociology & Social Sciences Collection</collection><collection>ProQuest One Health & Nursing</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>ProQuest One Social Sciences</collection><collection>ProQuest Central Basic</collection><jtitle>Supportive care in cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borkar, Durga S.</au><au>Lacouture, Mario E.</au><au>Basti, Surendra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spectrum of ocular toxicities from epidermal growth factor receptor inhibitors and their intermediate-term follow-up: a five-year review</atitle><jtitle>Supportive care in cancer</jtitle><stitle>Support Care Cancer</stitle><addtitle>Support Care Cancer</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>21</volume><issue>4</issue><spage>1167</spage><epage>1174</epage><pages>1167-1174</pages><issn>0941-4355</issn><eissn>1433-7339</eissn><abstract>Purpose
Epidermal growth factor receptor (EGFR) inhibitors and kinases are commonly used in the treatment regimen of various solid tumors including non-small cell lung, colorectal, head and neck, breast, and pancreatic cancers. The aim of this study is to describe common ocular adverse effects associated with EGFR inhibitor treatment, outline successful management options, and provide data on intermediate-term follow-up of these patients.
Methods
A retrospective chart review was performed of all patients presenting to the ophthalmology clinic with an adverse ocular effect while on an EGFR inhibitor. Duration of EGFR inhibitor treatment, symptoms, diagnosis, and treatment information were collected. Statistical analyses were done to ascertain differences in adverse effects based on duration and type of EGFR inhibitor treatment using the Fisher exact test.
Results
The two most common EGFR inhibitors in this group of patients were erlotinib and cetuximab. The most common adverse ocular effects for patients on EGFR inhibitors were dysfunctional tear syndrome (DTS), followed by blepharitis and eyelash changes (trichomegaly and trichiasis). Two patients had epithelial defects (corneal abrasions). There was no significant difference in adverse effects based on specific EGFR inhibitor medication or duration of treatment. Almost all patients were successfully managed with treatment regimens that we have outlined in this paper. Intermediate-term follow-up (range 6–17 months) showed a persistence of DTS and eyelash changes.
Conclusion
We present what is, to our knowledge, the largest reported cohort of patients with ocular toxicities from EGFR inhibitors—the spectrum of eye toxicities, their management, and the intermediate-term follow-up of patients with eye toxicities. Awareness of this information is important for oncologists and oncology nurses to facilitate proper counseling and management/referral of patients developing eye toxicity while on EGFR inhibitors.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>23151647</pmid><doi>10.1007/s00520-012-1645-y</doi><tpages>8</tpages></addata></record> |
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subjects | Analysis Antibodies, Monoclonal - adverse effects Antibodies, Monoclonal, Humanized - adverse effects Cancer Care and treatment Cetuximab Chemotherapy Chicago - epidemiology Clinical trials Colorectal cancer Cornea Epidermal growth factor Erlotinib Hydrochloride Eye Diseases - chemically induced Eye Diseases - epidemiology Female Follow-Up Studies Humans Lung cancer Male Medical Audit Medicine Medicine & Public Health Metastasis Neoplasms - drug therapy Nursing Nursing Research Oncology Ophthalmology Original Article Pain Medicine Pancreatic cancer Patients Quinazolines - adverse effects Receptor, Epidermal Growth Factor - antagonists & inhibitors Rehabilitation Medicine Retrospective Studies Toxicity Tumors |
title | Spectrum of ocular toxicities from epidermal growth factor receptor inhibitors and their intermediate-term follow-up: a five-year review |
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