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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
Main Authors: 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
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container_issue 10
container_start_page 1601
container_title Supportive care in cancer
container_volume 19
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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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. 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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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subjects Antibiotics
Drug therapy
Epidermal growth factor
Rash (Dermatology)
title Prophylactic tetracycline does not diminish the severity of epidermal growth factor receptor
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