Targeted therapy in patients with non-small cell lung cancer previously treated with chemotherapy
A case of successful and prolonged treatment of metastatic non-small cell lung cancer with the epidermal growth factor receptor antagonist erlotinib is presented. A never-smoker female was diagnosed with stage IV lung cancer in December 2005. A chest CT scan showed soft tissue mass 35×34 mm in size...
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Veröffentlicht in: | Medicina (Kaunas, Lithuania) Lithuania), 2011-01, Vol.47 (9), p.520-525 |
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creator | Drobnienė, Monika Cicėnienė, Audronė Zelvienė, Teresė Pipirienė Grigienė, Rūta Lachej, Nadežda Steponavičienė, Laura Aleknavičius, Eduardas |
description | A case of successful and prolonged treatment of metastatic non-small cell lung cancer with the epidermal growth factor receptor antagonist erlotinib is presented. A never-smoker female was diagnosed with stage IV lung cancer in December 2005. A chest CT scan showed soft tissue mass 35×34 mm in size in the right lung with metastases in the lymph nodes and in the left lung. A biopsy revealed a poorly differentiated adenocarcinoma. The disease showed poor response to the first-line and second-line chemotherapy. Targeted therapy with erlotinib was started in February 2007. The most severe adverse event observed was grade 3 skin rash. The disease was stable until February 2009 when brain metastases were detected. Erlotinib was continued until May 2009 when disease progression in the lungs was confirmed. The patient died due to ongoing disease progression in December 2009. Retrospective genetic analysis of a tumor specimen was performed, and no mutations in EGFR exons 18-21 were detected. The patient had a significant clinical benefit for the period of 24 months. These results are consistent with previous reports in literature that clinical characteristics such as female gender, nonsmoker, adenocarcinoma histology, and severe cutaneous toxicity seem to predict good response to erlotinib. In the present case, erlotinib proved to be effective even in heavily pretreated, chemotherapy-resistant lung adenocarcinoma. So far, no exact predictive biomarkers of erlotinib effectiveness have been determined; and their further analyses are essential. |
doi_str_mv | 10.3390/medicina47090069 |
format | Article |
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A never-smoker female was diagnosed with stage IV lung cancer in December 2005. A chest CT scan showed soft tissue mass 35×34 mm in size in the right lung with metastases in the lymph nodes and in the left lung. A biopsy revealed a poorly differentiated adenocarcinoma. The disease showed poor response to the first-line and second-line chemotherapy. Targeted therapy with erlotinib was started in February 2007. The most severe adverse event observed was grade 3 skin rash. The disease was stable until February 2009 when brain metastases were detected. Erlotinib was continued until May 2009 when disease progression in the lungs was confirmed. The patient died due to ongoing disease progression in December 2009. Retrospective genetic analysis of a tumor specimen was performed, and no mutations in EGFR exons 18-21 were detected. The patient had a significant clinical benefit for the period of 24 months. These results are consistent with previous reports in literature that clinical characteristics such as female gender, nonsmoker, adenocarcinoma histology, and severe cutaneous toxicity seem to predict good response to erlotinib. In the present case, erlotinib proved to be effective even in heavily pretreated, chemotherapy-resistant lung adenocarcinoma. So far, no exact predictive biomarkers of erlotinib effectiveness have been determined; and their further analyses are essential.</description><identifier>ISSN: 1648-9144</identifier><identifier>EISSN: 1648-9144</identifier><identifier>DOI: 10.3390/medicina47090069</identifier><identifier>PMID: 22156604</identifier><language>eng</language><publisher>Switzerland</publisher><subject>Adenocarcinoma - diagnostic imaging ; Adenocarcinoma - drug therapy ; Adenocarcinoma - pathology ; Carcinoma, Non-Small-Cell Lung - diagnostic imaging ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - pathology ; Erlotinib Hydrochloride ; Fatal Outcome ; Female ; Humans ; Lung Neoplasms - diagnostic imaging ; Lung Neoplasms - drug therapy ; Lung Neoplasms - pathology ; Middle Aged ; Molecular Targeted Therapy ; Neoplasm Staging ; Prognosis ; Protein Kinase Inhibitors - therapeutic use ; Quinazolines - therapeutic use ; Receptor, Epidermal Growth Factor - antagonists & inhibitors ; Tomography, X-Ray Computed</subject><ispartof>Medicina (Kaunas, Lithuania), 2011-01, Vol.47 (9), p.520-525</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-fc40627e714033b15fc2df97692a1426e5851ad0ac3054fdc6e02ceb0025e15c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22156604$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Drobnienė, Monika</creatorcontrib><creatorcontrib>Cicėnienė, Audronė</creatorcontrib><creatorcontrib>Zelvienė, Teresė Pipirienė</creatorcontrib><creatorcontrib>Grigienė, Rūta</creatorcontrib><creatorcontrib>Lachej, Nadežda</creatorcontrib><creatorcontrib>Steponavičienė, Laura</creatorcontrib><creatorcontrib>Aleknavičius, Eduardas</creatorcontrib><title>Targeted therapy in patients with non-small cell lung cancer previously treated with chemotherapy</title><title>Medicina (Kaunas, Lithuania)</title><addtitle>Medicina (Kaunas)</addtitle><description>A case of successful and prolonged treatment of metastatic non-small cell lung cancer with the epidermal growth factor receptor antagonist erlotinib is presented. A never-smoker female was diagnosed with stage IV lung cancer in December 2005. A chest CT scan showed soft tissue mass 35×34 mm in size in the right lung with metastases in the lymph nodes and in the left lung. A biopsy revealed a poorly differentiated adenocarcinoma. The disease showed poor response to the first-line and second-line chemotherapy. Targeted therapy with erlotinib was started in February 2007. The most severe adverse event observed was grade 3 skin rash. The disease was stable until February 2009 when brain metastases were detected. Erlotinib was continued until May 2009 when disease progression in the lungs was confirmed. The patient died due to ongoing disease progression in December 2009. Retrospective genetic analysis of a tumor specimen was performed, and no mutations in EGFR exons 18-21 were detected. The patient had a significant clinical benefit for the period of 24 months. These results are consistent with previous reports in literature that clinical characteristics such as female gender, nonsmoker, adenocarcinoma histology, and severe cutaneous toxicity seem to predict good response to erlotinib. In the present case, erlotinib proved to be effective even in heavily pretreated, chemotherapy-resistant lung adenocarcinoma. So far, no exact predictive biomarkers of erlotinib effectiveness have been determined; and their further analyses are essential.</description><subject>Adenocarcinoma - diagnostic imaging</subject><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - pathology</subject><subject>Carcinoma, Non-Small-Cell Lung - diagnostic imaging</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Erlotinib Hydrochloride</subject><subject>Fatal Outcome</subject><subject>Female</subject><subject>Humans</subject><subject>Lung Neoplasms - diagnostic imaging</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - pathology</subject><subject>Middle Aged</subject><subject>Molecular Targeted Therapy</subject><subject>Neoplasm Staging</subject><subject>Prognosis</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Quinazolines - therapeutic use</subject><subject>Receptor, Epidermal Growth Factor - antagonists & inhibitors</subject><subject>Tomography, X-Ray Computed</subject><issn>1648-9144</issn><issn>1648-9144</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkM1Lw0AQxRdRbK3ePcnePEVnP9M9SvELCl7qOWw3k3Yl2cTdVOl_b2qriJeZgXnvx-MRcsngRggDtw2W3vlgZQ4GQJsjMmZaTjPDpDz-c4_IWUpvAIKrnJ-SEedMaQ1yTOzCxhX2WNJ-jdF2W-oD7WzvMfSJfvp-TUMbstTYuqYOh1Fvwoo6GxxG2kX88O0m1VvaR7Q7zLfFrbFpD8BzclLZOuHFYU_I68P9YvaUzV8en2d388wJCX1WOQma55gzCUIsmaocLyuTa8Mtk1yjmipmS7BOgJJV6TQCd7gE4AqZcmJCrvfcLrbvG0x90fi0S2wDDhELw4yRRjE1KGGvdLFNKWJVdNE3Nm4LBsWu1-J_r4Pl6gDfLIfnr-GnSPEF7rd21w</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Drobnienė, Monika</creator><creator>Cicėnienė, Audronė</creator><creator>Zelvienė, Teresė Pipirienė</creator><creator>Grigienė, Rūta</creator><creator>Lachej, Nadežda</creator><creator>Steponavičienė, Laura</creator><creator>Aleknavičius, Eduardas</creator><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>7X8</scope></search><sort><creationdate>20110101</creationdate><title>Targeted therapy in patients with non-small cell lung cancer previously treated with chemotherapy</title><author>Drobnienė, Monika ; 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A never-smoker female was diagnosed with stage IV lung cancer in December 2005. A chest CT scan showed soft tissue mass 35×34 mm in size in the right lung with metastases in the lymph nodes and in the left lung. A biopsy revealed a poorly differentiated adenocarcinoma. The disease showed poor response to the first-line and second-line chemotherapy. Targeted therapy with erlotinib was started in February 2007. The most severe adverse event observed was grade 3 skin rash. The disease was stable until February 2009 when brain metastases were detected. Erlotinib was continued until May 2009 when disease progression in the lungs was confirmed. The patient died due to ongoing disease progression in December 2009. Retrospective genetic analysis of a tumor specimen was performed, and no mutations in EGFR exons 18-21 were detected. The patient had a significant clinical benefit for the period of 24 months. These results are consistent with previous reports in literature that clinical characteristics such as female gender, nonsmoker, adenocarcinoma histology, and severe cutaneous toxicity seem to predict good response to erlotinib. In the present case, erlotinib proved to be effective even in heavily pretreated, chemotherapy-resistant lung adenocarcinoma. So far, no exact predictive biomarkers of erlotinib effectiveness have been determined; and their further analyses are essential.</abstract><cop>Switzerland</cop><pmid>22156604</pmid><doi>10.3390/medicina47090069</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - diagnostic imaging Adenocarcinoma - drug therapy Adenocarcinoma - pathology Carcinoma, Non-Small-Cell Lung - diagnostic imaging Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - pathology Erlotinib Hydrochloride Fatal Outcome Female Humans Lung Neoplasms - diagnostic imaging Lung Neoplasms - drug therapy Lung Neoplasms - pathology Middle Aged Molecular Targeted Therapy Neoplasm Staging Prognosis Protein Kinase Inhibitors - therapeutic use Quinazolines - therapeutic use Receptor, Epidermal Growth Factor - antagonists & inhibitors Tomography, X-Ray Computed |
title | Targeted therapy in patients with non-small cell lung cancer previously treated with chemotherapy |
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