Icotinib combined with rapamycin in a renal transplant recipient with epidermal growth factor receptor-mutated non-small cell lung cancer: A case report
As kidney transplant recipients are at increased risk of developing cancer, regular monitoring should be undertaken to monitor the balance between immunosuppression and graft function and to identify malignancy. The present study reports the outcome of the treatment of adenocarcinoma of the lung (T1...
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Veröffentlicht in: | Oncology letters 2014-01, Vol.7 (1), p.171-176 |
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description | As kidney transplant recipients are at increased risk of developing cancer, regular monitoring should be undertaken to monitor the balance between immunosuppression and graft function and to identify malignancy. The present study reports the outcome of the treatment of adenocarcinoma of the lung (T1aN0M1a, stage IV) using the molecular-targeted therapy, icotinib, in a 66-year-old male renal transplant patient receiving rapamycin and prednisolone as ongoing renal immunosuppressive therapy. An initial partial response to icotinib was achieved, and graft function remained good. However, the patient subsequently developed interstitial pneumonitis. The plasma concentrations of rapamycin and icotinib were within the normal ranges, which excluded the possibility of a pharmacokinetic drug interaction and indicated that the interstitial pneumonitis was likely to be associated with the side-effects of icotinib. Drug therapy was discontinued and the patient underwent a segmentectomy. Tacrolimus was administered for ongoing renal graft immunosuppression. To the best of our knowledge, this is the first report of the concomitant administration of icotinib and rapamycin in post-transplant de novo lung cancer. It is also the first report of interstitial pneumonitis associated with icotinib in a post-transplant patient. |
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The present study reports the outcome of the treatment of adenocarcinoma of the lung (T1aN0M1a, stage IV) using the molecular-targeted therapy, icotinib, in a 66-year-old male renal transplant patient receiving rapamycin and prednisolone as ongoing renal immunosuppressive therapy. An initial partial response to icotinib was achieved, and graft function remained good. However, the patient subsequently developed interstitial pneumonitis. The plasma concentrations of rapamycin and icotinib were within the normal ranges, which excluded the possibility of a pharmacokinetic drug interaction and indicated that the interstitial pneumonitis was likely to be associated with the side-effects of icotinib. Drug therapy was discontinued and the patient underwent a segmentectomy. Tacrolimus was administered for ongoing renal graft immunosuppression. To the best of our knowledge, this is the first report of the concomitant administration of icotinib and rapamycin in post-transplant de novo lung cancer. It is also the first report of interstitial pneumonitis associated with icotinib in a post-transplant patient.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2013.1657</identifier><identifier>PMID: 24348843</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Antigens ; Antineoplastic agents ; Biomarkers ; Biopsy ; Cancer therapies ; Case reports ; Complications and side effects ; Development and progression ; Diagnosis ; Dosage and administration ; icotinib ; Immunotherapy ; interstitial pneumonitis ; Kidney transplantation ; Kidney transplants ; Lung cancer ; Medical imaging ; Mutation ; Non-small cell lung cancer ; Oncology ; Patient outcomes ; Patients ; rapamycin ; Risk factors ; Smoking ; Transplants & implants ; Tumors</subject><ispartof>Oncology letters, 2014-01, Vol.7 (1), p.171-176</ispartof><rights>Copyright © 2014, Spandidos Publications</rights><rights>COPYRIGHT 2014 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2014</rights><rights>Copyright © 2014, Spandidos Publications 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-6c6ca2f8e5d2b8978f542a9677436dee1233dc16734ad64651e410aa2d30d5643</citedby><cites>FETCH-LOGICAL-c541t-6c6ca2f8e5d2b8978f542a9677436dee1233dc16734ad64651e410aa2d30d5643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861587/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861587/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,5571,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24348843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ZHAO, QIONG</creatorcontrib><creatorcontrib>WANG, YINA</creatorcontrib><creatorcontrib>TANG, YEMIN</creatorcontrib><creatorcontrib>PENG, LING</creatorcontrib><title>Icotinib combined with rapamycin in a renal transplant recipient with epidermal growth factor receptor-mutated non-small cell lung cancer: A case report</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>As kidney transplant recipients are at increased risk of developing cancer, regular monitoring should be undertaken to monitor the balance between immunosuppression and graft function and to identify malignancy. The present study reports the outcome of the treatment of adenocarcinoma of the lung (T1aN0M1a, stage IV) using the molecular-targeted therapy, icotinib, in a 66-year-old male renal transplant patient receiving rapamycin and prednisolone as ongoing renal immunosuppressive therapy. An initial partial response to icotinib was achieved, and graft function remained good. However, the patient subsequently developed interstitial pneumonitis. The plasma concentrations of rapamycin and icotinib were within the normal ranges, which excluded the possibility of a pharmacokinetic drug interaction and indicated that the interstitial pneumonitis was likely to be associated with the side-effects of icotinib. Drug therapy was discontinued and the patient underwent a segmentectomy. Tacrolimus was administered for ongoing renal graft immunosuppression. To the best of our knowledge, this is the first report of the concomitant administration of icotinib and rapamycin in post-transplant de novo lung cancer. It is also the first report of interstitial pneumonitis associated with icotinib in a post-transplant patient.</description><subject>Antigens</subject><subject>Antineoplastic agents</subject><subject>Biomarkers</subject><subject>Biopsy</subject><subject>Cancer therapies</subject><subject>Case reports</subject><subject>Complications and side effects</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Dosage and administration</subject><subject>icotinib</subject><subject>Immunotherapy</subject><subject>interstitial pneumonitis</subject><subject>Kidney transplantation</subject><subject>Kidney transplants</subject><subject>Lung cancer</subject><subject>Medical imaging</subject><subject>Mutation</subject><subject>Non-small cell lung cancer</subject><subject>Oncology</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>rapamycin</subject><subject>Risk factors</subject><subject>Smoking</subject><subject>Transplants & implants</subject><subject>Tumors</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptkt9rFDEQxxdRbKl981kWBPHBPfNrs1kfhKP4o1DwRZ9DLsnepWSTNcm29D_xz3XW1ruemIRkmHzmO2QyVfUSoxUVPXkf_YogTFeYt92T6hR3PWkwEuTp3u7YSXWe8zWC0XIsBH9enRBGmRCMnla_LnUsLrhNreO4ccGa-taVXZ3UpMY77UINS9XJBuXrklTIk1ehgEO7yVmw_uB2csamEZhtirfgGJQuMS2YncBoxrmoAuIhhiYD52ttYfNz2NZaBW3Th3oNVrYQM8VUXlTPBuWzPX84z6ofnz99v_jaXH37cnmxvmp0y3BpuOZakUHY1pCN6DsxtIyonncdo9xYiwmlRmPeUaYMZ7zFlmGkFDEUmZYzelZ9vNed5s1ojYYnJeXllNyo0p2Mysnjm-B2chtvJBUct6IDgbcPAin-nG0ucnR5eZwKNs5ZYkHgc1osMKCv_0Gv45ygskD1lHCCUY8O1FZ5K10YIuTVi6hcM9zynvf9orX6DwXT2NHpGOzgwH8U8OZRwM4qX3Y5-rm4GPIx-O4e1CnmnOywLwZGcuk6Gb1cuk4uXQf4q8cF3MN_e-yQOE8qGGdiPlTXN6hrEIbVYfobhYTfYQ</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>ZHAO, QIONG</creator><creator>WANG, YINA</creator><creator>TANG, YEMIN</creator><creator>PENG, LING</creator><general>D.A. Spandidos</general><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140101</creationdate><title>Icotinib combined with rapamycin in a renal transplant recipient with epidermal growth factor receptor-mutated non-small cell lung cancer: A case report</title><author>ZHAO, QIONG ; WANG, YINA ; TANG, YEMIN ; PENG, LING</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c541t-6c6ca2f8e5d2b8978f542a9677436dee1233dc16734ad64651e410aa2d30d5643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antigens</topic><topic>Antineoplastic agents</topic><topic>Biomarkers</topic><topic>Biopsy</topic><topic>Cancer therapies</topic><topic>Case reports</topic><topic>Complications and side effects</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Dosage and administration</topic><topic>icotinib</topic><topic>Immunotherapy</topic><topic>interstitial pneumonitis</topic><topic>Kidney transplantation</topic><topic>Kidney transplants</topic><topic>Lung cancer</topic><topic>Medical imaging</topic><topic>Mutation</topic><topic>Non-small cell lung cancer</topic><topic>Oncology</topic><topic>Patient outcomes</topic><topic>Patients</topic><topic>rapamycin</topic><topic>Risk factors</topic><topic>Smoking</topic><topic>Transplants & implants</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ZHAO, QIONG</creatorcontrib><creatorcontrib>WANG, YINA</creatorcontrib><creatorcontrib>TANG, YEMIN</creatorcontrib><creatorcontrib>PENG, LING</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ZHAO, QIONG</au><au>WANG, YINA</au><au>TANG, YEMIN</au><au>PENG, LING</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Icotinib combined with rapamycin in a renal transplant recipient with epidermal growth factor receptor-mutated non-small cell lung cancer: A case report</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>7</volume><issue>1</issue><spage>171</spage><epage>176</epage><pages>171-176</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>As kidney transplant recipients are at increased risk of developing cancer, regular monitoring should be undertaken to monitor the balance between immunosuppression and graft function and to identify malignancy. The present study reports the outcome of the treatment of adenocarcinoma of the lung (T1aN0M1a, stage IV) using the molecular-targeted therapy, icotinib, in a 66-year-old male renal transplant patient receiving rapamycin and prednisolone as ongoing renal immunosuppressive therapy. An initial partial response to icotinib was achieved, and graft function remained good. However, the patient subsequently developed interstitial pneumonitis. The plasma concentrations of rapamycin and icotinib were within the normal ranges, which excluded the possibility of a pharmacokinetic drug interaction and indicated that the interstitial pneumonitis was likely to be associated with the side-effects of icotinib. Drug therapy was discontinued and the patient underwent a segmentectomy. Tacrolimus was administered for ongoing renal graft immunosuppression. 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subjects | Antigens Antineoplastic agents Biomarkers Biopsy Cancer therapies Case reports Complications and side effects Development and progression Diagnosis Dosage and administration icotinib Immunotherapy interstitial pneumonitis Kidney transplantation Kidney transplants Lung cancer Medical imaging Mutation Non-small cell lung cancer Oncology Patient outcomes Patients rapamycin Risk factors Smoking Transplants & implants Tumors |
title | Icotinib combined with rapamycin in a renal transplant recipient with epidermal growth factor receptor-mutated non-small cell lung cancer: A case report |
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