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Prophylactic tetracycline does not diminish the severity of epidermal growth factor receptor
Purpose Previous studies suggest tetracycline and other antibiotics lessen the severity of epidermal growth factor receptor (EGFR) inhibitor-induced rash. This study sought to confirm such findings. Methods Patients starting an EGFR inhibitor were eligible for this randomized, double-blinded, placeb...
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Published in: | Supportive care in cancer 2011-10, Vol.19 (10), p.1601 |
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creator | Jatoi, Aminah Dakhil, Shaker R Sloan, Jeff A Kugler, John W Rowland, Kendrith M., Jr Schaefer, Paul L Novotny, Paul J Wender, Donald B Gross, Howard M Loprinzi, Charles L |
description | Purpose Previous studies suggest tetracycline and other antibiotics lessen the severity of epidermal growth factor receptor (EGFR) inhibitor-induced rash. This study sought to confirm such findings. Methods Patients starting an EGFR inhibitor were eligible for this randomized, double-blinded, placebo-controlled study and had to be rash-free. They were then randomly assigned to tetracycline 500 mg orally twice a day for 28 days versus a placebo. Rash development and severity (monthly physician assessment and weekly patient-reported questionnaires), quality of life (SKINDEX-16), and adverse events were monitored during the 4-week intervention and then for an additional 4 weeks. The primary objective was to compare the incidence of grade 2 or worse rash between study arms; 32 patients per group provided a 90% probability of detecting a 40% difference in incidence with a type I error rate of 0.05 (two-sided). Results Sixty-five patients were enrolled, and groups were balanced on baseline characteristics. During the first 4 weeks, healthcare provider-reported data found that 27 tetracycline-treated patients (82%) and 24 placebo-exposed patients (75%) developed a rash. This rash was a grade 2+ in 17 (52%) and 14 (44%), respectively (p=0.62). Comparable grade 2+ rash rates were observed during weeks 5 through 8 as well as with patient-reported rash data throughout the study period. Quality of life was comparable across study arms, and tetracycline was well tolerated. Conclusion Although previous studies suggest otherwise, this randomized, double-blinded, placebo-controlled study did not find that tetracycline lessened rash incidence or severity in patients who were taking EGFR inhibitors. Keywords Tetracycline * Rash * EGFR inhibitor * EGFR inhibitor-induced rash |
doi_str_mv | 10.1007/s00520-010-0988-5 |
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fullrecord | <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_infotracmisc_A357967683</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A357967683</galeid><sourcerecordid>A357967683</sourcerecordid><originalsourceid>FETCH-LOGICAL-g673-a61c7926e418f74be7a9366f4f8339b55dcb6ce238ccd60edc4be887ab61efb43</originalsourceid><addsrcrecordid>eNptj0tLxDAUhbNQcKz-AHcB1x2Tpnl0OQy-YEAXsxSGNLmZRtpmSILSf29EFy7kcLmHy7kfHIRuKFlTQuRdIoQ3pCa0TKdUzc_QinQtrVvG-QW6TOmdEColb1bo7TWG07CM2mRvcIYctVnM6GfANkDCc8jY-snPPg04D4ATfED0ecHBYTh5C3HSIz7G8JkH7AomRBzBwKmYK3Tu9Jjg-ndXaP9wv98-1buXx-ftZlcfhWS1FtTIrhHQUuVk24PUHRPCtU4x1vWcW9MLAw1TxlhBwJqSUUrqXlBwfcsqdPuDPeoRDn524bvF5JM5bBiXnZCikCq0_idVZGHyJszgfLn_efgCuqRlFQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Prophylactic tetracycline does not diminish the severity of epidermal growth factor receptor</title><source>Social Science Premium Collection</source><source>Springer Nature</source><source>Sociology Collection</source><creator>Jatoi, Aminah ; Dakhil, Shaker R ; Sloan, Jeff A ; Kugler, John W ; Rowland, Kendrith M., Jr ; Schaefer, Paul L ; Novotny, Paul J ; Wender, Donald B ; Gross, Howard M ; Loprinzi, Charles L</creator><creatorcontrib>Jatoi, Aminah ; Dakhil, Shaker R ; Sloan, Jeff A ; Kugler, John W ; Rowland, Kendrith M., Jr ; Schaefer, Paul L ; Novotny, Paul J ; Wender, Donald B ; Gross, Howard M ; Loprinzi, Charles L</creatorcontrib><description>Purpose Previous studies suggest tetracycline and other antibiotics lessen the severity of epidermal growth factor receptor (EGFR) inhibitor-induced rash. This study sought to confirm such findings. Methods Patients starting an EGFR inhibitor were eligible for this randomized, double-blinded, placebo-controlled study and had to be rash-free. They were then randomly assigned to tetracycline 500 mg orally twice a day for 28 days versus a placebo. Rash development and severity (monthly physician assessment and weekly patient-reported questionnaires), quality of life (SKINDEX-16), and adverse events were monitored during the 4-week intervention and then for an additional 4 weeks. The primary objective was to compare the incidence of grade 2 or worse rash between study arms; 32 patients per group provided a 90% probability of detecting a 40% difference in incidence with a type I error rate of 0.05 (two-sided). Results Sixty-five patients were enrolled, and groups were balanced on baseline characteristics. During the first 4 weeks, healthcare provider-reported data found that 27 tetracycline-treated patients (82%) and 24 placebo-exposed patients (75%) developed a rash. This rash was a grade 2+ in 17 (52%) and 14 (44%), respectively (p=0.62). Comparable grade 2+ rash rates were observed during weeks 5 through 8 as well as with patient-reported rash data throughout the study period. Quality of life was comparable across study arms, and tetracycline was well tolerated. Conclusion Although previous studies suggest otherwise, this randomized, double-blinded, placebo-controlled study did not find that tetracycline lessened rash incidence or severity in patients who were taking EGFR inhibitors. Keywords Tetracycline * Rash * EGFR inhibitor * EGFR inhibitor-induced rash</description><identifier>ISSN: 0941-4355</identifier><identifier>DOI: 10.1007/s00520-010-0988-5</identifier><language>eng</language><publisher>Springer</publisher><subject>Antibiotics ; Drug therapy ; Epidermal growth factor ; Rash (Dermatology)</subject><ispartof>Supportive care in cancer, 2011-10, Vol.19 (10), p.1601</ispartof><rights>COPYRIGHT 2011 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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>Jatoi, Aminah</creatorcontrib><creatorcontrib>Dakhil, Shaker R</creatorcontrib><creatorcontrib>Sloan, Jeff A</creatorcontrib><creatorcontrib>Kugler, John W</creatorcontrib><creatorcontrib>Rowland, Kendrith M., Jr</creatorcontrib><creatorcontrib>Schaefer, Paul L</creatorcontrib><creatorcontrib>Novotny, Paul J</creatorcontrib><creatorcontrib>Wender, Donald B</creatorcontrib><creatorcontrib>Gross, Howard M</creatorcontrib><creatorcontrib>Loprinzi, Charles L</creatorcontrib><title>Prophylactic tetracycline does not diminish the severity of epidermal growth factor receptor</title><title>Supportive care in cancer</title><description>Purpose Previous studies suggest tetracycline and other antibiotics lessen the severity of epidermal growth factor receptor (EGFR) inhibitor-induced rash. This study sought to confirm such findings. Methods Patients starting an EGFR inhibitor were eligible for this randomized, double-blinded, placebo-controlled study and had to be rash-free. They were then randomly assigned to tetracycline 500 mg orally twice a day for 28 days versus a placebo. Rash development and severity (monthly physician assessment and weekly patient-reported questionnaires), quality of life (SKINDEX-16), and adverse events were monitored during the 4-week intervention and then for an additional 4 weeks. The primary objective was to compare the incidence of grade 2 or worse rash between study arms; 32 patients per group provided a 90% probability of detecting a 40% difference in incidence with a type I error rate of 0.05 (two-sided). Results Sixty-five patients were enrolled, and groups were balanced on baseline characteristics. During the first 4 weeks, healthcare provider-reported data found that 27 tetracycline-treated patients (82%) and 24 placebo-exposed patients (75%) developed a rash. This rash was a grade 2+ in 17 (52%) and 14 (44%), respectively (p=0.62). Comparable grade 2+ rash rates were observed during weeks 5 through 8 as well as with patient-reported rash data throughout the study period. Quality of life was comparable across study arms, and tetracycline was well tolerated. Conclusion Although previous studies suggest otherwise, this randomized, double-blinded, placebo-controlled study did not find that tetracycline lessened rash incidence or severity in patients who were taking EGFR inhibitors. Keywords Tetracycline * Rash * EGFR inhibitor * EGFR inhibitor-induced rash</description><subject>Antibiotics</subject><subject>Drug therapy</subject><subject>Epidermal growth factor</subject><subject>Rash (Dermatology)</subject><issn>0941-4355</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptj0tLxDAUhbNQcKz-AHcB1x2Tpnl0OQy-YEAXsxSGNLmZRtpmSILSf29EFy7kcLmHy7kfHIRuKFlTQuRdIoQ3pCa0TKdUzc_QinQtrVvG-QW6TOmdEColb1bo7TWG07CM2mRvcIYctVnM6GfANkDCc8jY-snPPg04D4ATfED0ecHBYTh5C3HSIz7G8JkH7AomRBzBwKmYK3Tu9Jjg-ndXaP9wv98-1buXx-ftZlcfhWS1FtTIrhHQUuVk24PUHRPCtU4x1vWcW9MLAw1TxlhBwJqSUUrqXlBwfcsqdPuDPeoRDn524bvF5JM5bBiXnZCikCq0_idVZGHyJszgfLn_efgCuqRlFQ</recordid><startdate>20111001</startdate><enddate>20111001</enddate><creator>Jatoi, Aminah</creator><creator>Dakhil, Shaker R</creator><creator>Sloan, Jeff A</creator><creator>Kugler, John W</creator><creator>Rowland, Kendrith M., Jr</creator><creator>Schaefer, Paul L</creator><creator>Novotny, Paul J</creator><creator>Wender, Donald B</creator><creator>Gross, Howard M</creator><creator>Loprinzi, Charles L</creator><general>Springer</general><scope/></search><sort><creationdate>20111001</creationdate><title>Prophylactic tetracycline does not diminish the severity of epidermal growth factor receptor</title><author>Jatoi, Aminah ; Dakhil, Shaker R ; Sloan, Jeff A ; Kugler, John W ; Rowland, Kendrith M., Jr ; Schaefer, Paul L ; Novotny, Paul J ; Wender, Donald B ; Gross, Howard M ; Loprinzi, Charles L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g673-a61c7926e418f74be7a9366f4f8339b55dcb6ce238ccd60edc4be887ab61efb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Antibiotics</topic><topic>Drug therapy</topic><topic>Epidermal growth factor</topic><topic>Rash (Dermatology)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jatoi, Aminah</creatorcontrib><creatorcontrib>Dakhil, Shaker R</creatorcontrib><creatorcontrib>Sloan, Jeff A</creatorcontrib><creatorcontrib>Kugler, John W</creatorcontrib><creatorcontrib>Rowland, Kendrith M., Jr</creatorcontrib><creatorcontrib>Schaefer, Paul L</creatorcontrib><creatorcontrib>Novotny, Paul J</creatorcontrib><creatorcontrib>Wender, Donald B</creatorcontrib><creatorcontrib>Gross, Howard M</creatorcontrib><creatorcontrib>Loprinzi, Charles L</creatorcontrib><jtitle>Supportive care in cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jatoi, Aminah</au><au>Dakhil, Shaker R</au><au>Sloan, Jeff A</au><au>Kugler, John W</au><au>Rowland, Kendrith M., Jr</au><au>Schaefer, Paul L</au><au>Novotny, Paul J</au><au>Wender, Donald B</au><au>Gross, Howard M</au><au>Loprinzi, Charles L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prophylactic tetracycline does not diminish the severity of epidermal growth factor receptor</atitle><jtitle>Supportive care in cancer</jtitle><date>2011-10-01</date><risdate>2011</risdate><volume>19</volume><issue>10</issue><spage>1601</spage><pages>1601-</pages><issn>0941-4355</issn><abstract>Purpose Previous studies suggest tetracycline and other antibiotics lessen the severity of epidermal growth factor receptor (EGFR) inhibitor-induced rash. This study sought to confirm such findings. Methods Patients starting an EGFR inhibitor were eligible for this randomized, double-blinded, placebo-controlled study and had to be rash-free. They were then randomly assigned to tetracycline 500 mg orally twice a day for 28 days versus a placebo. Rash development and severity (monthly physician assessment and weekly patient-reported questionnaires), quality of life (SKINDEX-16), and adverse events were monitored during the 4-week intervention and then for an additional 4 weeks. The primary objective was to compare the incidence of grade 2 or worse rash between study arms; 32 patients per group provided a 90% probability of detecting a 40% difference in incidence with a type I error rate of 0.05 (two-sided). Results Sixty-five patients were enrolled, and groups were balanced on baseline characteristics. During the first 4 weeks, healthcare provider-reported data found that 27 tetracycline-treated patients (82%) and 24 placebo-exposed patients (75%) developed a rash. This rash was a grade 2+ in 17 (52%) and 14 (44%), respectively (p=0.62). Comparable grade 2+ rash rates were observed during weeks 5 through 8 as well as with patient-reported rash data throughout the study period. Quality of life was comparable across study arms, and tetracycline was well tolerated. Conclusion Although previous studies suggest otherwise, this randomized, double-blinded, placebo-controlled study did not find that tetracycline lessened rash incidence or severity in patients who were taking EGFR inhibitors. Keywords Tetracycline * Rash * EGFR inhibitor * EGFR inhibitor-induced rash</abstract><pub>Springer</pub><doi>10.1007/s00520-010-0988-5</doi></addata></record> |
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title | Prophylactic tetracycline does not diminish the severity of epidermal growth factor receptor |
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