Cutaneous side-effects in cancer patients treated with the antiepidermal growth factor receptor antibody C225

Background C225 is an antibody to the epidermal growth factor receptor (EGFR), and inhibits growth of various tumour cells. The antibody is currently being used as a therapeutic agent in several clinical trials of patients with carcinomas.Objectives To determine and investigate the cutaneous side‐ef...

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Veröffentlicht in:British journal of dermatology (1951) 2001-06, Vol.144 (6), p.1169-1176
Hauptverfasser: Busam, K.J., Capodieci, P., Motzer, R., Kiehn, T., Phelan, D., Halpern, A.C.
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container_end_page 1176
container_issue 6
container_start_page 1169
container_title British journal of dermatology (1951)
container_volume 144
creator Busam, K.J.
Capodieci, P.
Motzer, R.
Kiehn, T.
Phelan, D.
Halpern, A.C.
description Background C225 is an antibody to the epidermal growth factor receptor (EGFR), and inhibits growth of various tumour cells. The antibody is currently being used as a therapeutic agent in several clinical trials of patients with carcinomas.Objectives To determine and investigate the cutaneous side‐effects in cancer patients treated with C225.Methods We clinically examined 10 patients treated with C225, and performed immunohistochemical and in situ hybridization studies on skin biopsies.Results The most common cutaneous reaction to C225 therapy was the development of an acneiform follicular eruption, which was most pronounced on the face, chest and upper back and typically manifested a week after the onset of treatment. The consistency of the morphology and timing of the clinical findings in 10 different patients following monotherapy with C225 strongly suggested a direct biological effect of the antibody. Additional dermatological side‐effects included focal areas of tender paronychial inflammation of toes and fingers and small aphthous ulcers of the oral mucosa. Serial punch biopsies of chest skin before and after treatment (at 8 days) revealed two main reaction patterns: a superficial dermal inflammatory cell infiltrate surrounding hyperkeratotic and ectatic follicular infundibula, and a suppurative superficial folliculitis. In two biopsies focal intraepidermal acantholysis was found. Microbiological cultures failed to reveal an infectious aetiology. Immunohistochemical and in situ hybridization studies on a subset of the biopsies showed an increase in the expression of p27Kip1 in epidermal keratinocytes after treatment with C225.Conclusions Our findings support the concept that p27Kip1 plays a part in the in vivo regulation of follicular and epidermal homeostasis by EGFR.
doi_str_mv 10.1046/j.1365-2133.2001.04226.x
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The antibody is currently being used as a therapeutic agent in several clinical trials of patients with carcinomas.Objectives To determine and investigate the cutaneous side‐effects in cancer patients treated with C225.Methods We clinically examined 10 patients treated with C225, and performed immunohistochemical and in situ hybridization studies on skin biopsies.Results The most common cutaneous reaction to C225 therapy was the development of an acneiform follicular eruption, which was most pronounced on the face, chest and upper back and typically manifested a week after the onset of treatment. The consistency of the morphology and timing of the clinical findings in 10 different patients following monotherapy with C225 strongly suggested a direct biological effect of the antibody. Additional dermatological side‐effects included focal areas of tender paronychial inflammation of toes and fingers and small aphthous ulcers of the oral mucosa. Serial punch biopsies of chest skin before and after treatment (at 8 days) revealed two main reaction patterns: a superficial dermal inflammatory cell infiltrate surrounding hyperkeratotic and ectatic follicular infundibula, and a suppurative superficial folliculitis. In two biopsies focal intraepidermal acantholysis was found. Microbiological cultures failed to reveal an infectious aetiology. Immunohistochemical and in situ hybridization studies on a subset of the biopsies showed an increase in the expression of p27Kip1 in epidermal keratinocytes after treatment with C225.Conclusions Our findings support the concept that p27Kip1 plays a part in the in vivo regulation of follicular and epidermal homeostasis by EGFR.</description><identifier>ISSN: 0007-0963</identifier><identifier>EISSN: 1365-2133</identifier><identifier>DOI: 10.1046/j.1365-2133.2001.04226.x</identifier><identifier>PMID: 11422037</identifier><identifier>CODEN: BJDEAZ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Aged ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal, Humanized ; Antineoplastic Agents - adverse effects ; Biological and medical sciences ; C225 ; Carcinoma, Renal Cell - therapy ; Cell Cycle Proteins ; Cetuximab ; Cyclin-Dependent Kinase Inhibitor p27 ; Drug Eruptions - etiology ; Drug Eruptions - metabolism ; Drug Eruptions - pathology ; Drug toxicity and drugs side effects treatment ; epidermal growth factor receptor ; ErbB Receptors - antagonists &amp; inhibitors ; ErbB Receptors - immunology ; Female ; folliculitis ; Folliculitis - chemically induced ; Humans ; Immunoenzyme Techniques ; Kidney Neoplasms - therapy ; Male ; Medical sciences ; Microtubule-Associated Proteins - metabolism ; Middle Aged ; Pharmacology. 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The antibody is currently being used as a therapeutic agent in several clinical trials of patients with carcinomas.Objectives To determine and investigate the cutaneous side‐effects in cancer patients treated with C225.Methods We clinically examined 10 patients treated with C225, and performed immunohistochemical and in situ hybridization studies on skin biopsies.Results The most common cutaneous reaction to C225 therapy was the development of an acneiform follicular eruption, which was most pronounced on the face, chest and upper back and typically manifested a week after the onset of treatment. The consistency of the morphology and timing of the clinical findings in 10 different patients following monotherapy with C225 strongly suggested a direct biological effect of the antibody. Additional dermatological side‐effects included focal areas of tender paronychial inflammation of toes and fingers and small aphthous ulcers of the oral mucosa. Serial punch biopsies of chest skin before and after treatment (at 8 days) revealed two main reaction patterns: a superficial dermal inflammatory cell infiltrate surrounding hyperkeratotic and ectatic follicular infundibula, and a suppurative superficial folliculitis. In two biopsies focal intraepidermal acantholysis was found. Microbiological cultures failed to reveal an infectious aetiology. Immunohistochemical and in situ hybridization studies on a subset of the biopsies showed an increase in the expression of p27Kip1 in epidermal keratinocytes after treatment with C225.Conclusions Our findings support the concept that p27Kip1 plays a part in the in vivo regulation of follicular and epidermal homeostasis by EGFR.</description><subject>Aged</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal, Humanized</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Biological and medical sciences</subject><subject>C225</subject><subject>Carcinoma, Renal Cell - therapy</subject><subject>Cell Cycle Proteins</subject><subject>Cetuximab</subject><subject>Cyclin-Dependent Kinase Inhibitor p27</subject><subject>Drug Eruptions - etiology</subject><subject>Drug Eruptions - metabolism</subject><subject>Drug Eruptions - pathology</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>epidermal growth factor receptor</subject><subject>ErbB Receptors - antagonists &amp; inhibitors</subject><subject>ErbB Receptors - immunology</subject><subject>Female</subject><subject>folliculitis</subject><subject>Folliculitis - chemically induced</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Kidney Neoplasms - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Recombinant Fusion Proteins - adverse effects</subject><subject>Severity of Illness Index</subject><subject>Toxicity: skin, dermoskeleton</subject><subject>Tumor Suppressor Proteins</subject><issn>0007-0963</issn><issn>1365-2133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1v1DAQhi1ERbeFv4AsxDXBH3HsHjhA6AdlBRyKkLhYjj2mWXaTYDva3X-P010Vjpw88jzvjOZBCFNSUlLVb1Yl5bUoGOW8ZITQklSM1eXuCVo8Np6iBSFEFuSi5qfoLMZVBjkR5Bk6pTTzhMsF2jRTMj0MU8Sxc1CA92BTxF2PrektBDya1EGfv1IAk8DhbZfucboHbPrcGXMqbMwa_wzDNje8sWkIOICFcS5mqB3cHjeMiefoxJt1hBfH9xx9u7q8a26K5Zfrj827ZWErcVEXtDUKmDPccUGdUMpLCUo451te53sUIQyUUqZShILwtRdWMW-VaQ2ruOTn6NVh7hiG3xPEpFfDFPq8Us-6si2pMqQOkA1DjAG8HkO3MWGvKdGzZr3Ss00923zI6QfNepejL4_zp3YD7m_w6DUDr4-Aidasfcguu_jPgoozzjP29oBtuzXs_3u_fn_7Ya5yvjjku5hg95g34ZeuJZdCf_98rT_dff3BSLPUkv8BwKOnZg</recordid><startdate>200106</startdate><enddate>200106</enddate><creator>Busam, K.J.</creator><creator>Capodieci, P.</creator><creator>Motzer, R.</creator><creator>Kiehn, T.</creator><creator>Phelan, D.</creator><creator>Halpern, A.C.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>200106</creationdate><title>Cutaneous side-effects in cancer patients treated with the antiepidermal growth factor receptor antibody C225</title><author>Busam, K.J. ; Capodieci, P. ; Motzer, R. ; Kiehn, T. ; Phelan, D. ; Halpern, A.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4596-1ba8e2da3d351d588f77e85ddfb360968002e888a4801e5f6f5c82fc8aba24373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Aged</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal, Humanized</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Biological and medical sciences</topic><topic>C225</topic><topic>Carcinoma, Renal Cell - therapy</topic><topic>Cell Cycle Proteins</topic><topic>Cetuximab</topic><topic>Cyclin-Dependent Kinase Inhibitor p27</topic><topic>Drug Eruptions - etiology</topic><topic>Drug Eruptions - metabolism</topic><topic>Drug Eruptions - pathology</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>epidermal growth factor receptor</topic><topic>ErbB Receptors - antagonists &amp; inhibitors</topic><topic>ErbB Receptors - immunology</topic><topic>Female</topic><topic>folliculitis</topic><topic>Folliculitis - chemically induced</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Kidney Neoplasms - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microtubule-Associated Proteins - metabolism</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Recombinant Fusion Proteins - adverse effects</topic><topic>Severity of Illness Index</topic><topic>Toxicity: skin, dermoskeleton</topic><topic>Tumor Suppressor Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Busam, K.J.</creatorcontrib><creatorcontrib>Capodieci, P.</creatorcontrib><creatorcontrib>Motzer, R.</creatorcontrib><creatorcontrib>Kiehn, T.</creatorcontrib><creatorcontrib>Phelan, D.</creatorcontrib><creatorcontrib>Halpern, A.C.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><jtitle>British journal of dermatology (1951)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Busam, K.J.</au><au>Capodieci, P.</au><au>Motzer, R.</au><au>Kiehn, T.</au><au>Phelan, D.</au><au>Halpern, A.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cutaneous side-effects in cancer patients treated with the antiepidermal growth factor receptor antibody C225</atitle><jtitle>British journal of dermatology (1951)</jtitle><addtitle>Br J Dermatol</addtitle><date>2001-06</date><risdate>2001</risdate><volume>144</volume><issue>6</issue><spage>1169</spage><epage>1176</epage><pages>1169-1176</pages><issn>0007-0963</issn><eissn>1365-2133</eissn><coden>BJDEAZ</coden><abstract>Background C225 is an antibody to the epidermal growth factor receptor (EGFR), and inhibits growth of various tumour cells. The antibody is currently being used as a therapeutic agent in several clinical trials of patients with carcinomas.Objectives To determine and investigate the cutaneous side‐effects in cancer patients treated with C225.Methods We clinically examined 10 patients treated with C225, and performed immunohistochemical and in situ hybridization studies on skin biopsies.Results The most common cutaneous reaction to C225 therapy was the development of an acneiform follicular eruption, which was most pronounced on the face, chest and upper back and typically manifested a week after the onset of treatment. The consistency of the morphology and timing of the clinical findings in 10 different patients following monotherapy with C225 strongly suggested a direct biological effect of the antibody. Additional dermatological side‐effects included focal areas of tender paronychial inflammation of toes and fingers and small aphthous ulcers of the oral mucosa. Serial punch biopsies of chest skin before and after treatment (at 8 days) revealed two main reaction patterns: a superficial dermal inflammatory cell infiltrate surrounding hyperkeratotic and ectatic follicular infundibula, and a suppurative superficial folliculitis. In two biopsies focal intraepidermal acantholysis was found. Microbiological cultures failed to reveal an infectious aetiology. Immunohistochemical and in situ hybridization studies on a subset of the biopsies showed an increase in the expression of p27Kip1 in epidermal keratinocytes after treatment with C225.Conclusions Our findings support the concept that p27Kip1 plays a part in the in vivo regulation of follicular and epidermal homeostasis by EGFR.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>11422037</pmid><doi>10.1046/j.1365-2133.2001.04226.x</doi><tpages>8</tpages></addata></record>
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subjects Aged
Antibodies, Monoclonal - adverse effects
Antibodies, Monoclonal, Humanized
Antineoplastic Agents - adverse effects
Biological and medical sciences
C225
Carcinoma, Renal Cell - therapy
Cell Cycle Proteins
Cetuximab
Cyclin-Dependent Kinase Inhibitor p27
Drug Eruptions - etiology
Drug Eruptions - metabolism
Drug Eruptions - pathology
Drug toxicity and drugs side effects treatment
epidermal growth factor receptor
ErbB Receptors - antagonists & inhibitors
ErbB Receptors - immunology
Female
folliculitis
Folliculitis - chemically induced
Humans
Immunoenzyme Techniques
Kidney Neoplasms - therapy
Male
Medical sciences
Microtubule-Associated Proteins - metabolism
Middle Aged
Pharmacology. Drug treatments
Recombinant Fusion Proteins - adverse effects
Severity of Illness Index
Toxicity: skin, dermoskeleton
Tumor Suppressor Proteins
title Cutaneous side-effects in cancer patients treated with the antiepidermal growth factor receptor antibody C225
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