Differences in RRM1 protein expression between diagnostic biopsies and resection specimens, and changes during carboplatin and paclitaxel treatment, in non-small-cell lung cancer
Aims It is of interest whether expression of potentially predictive biomarkers changes during chemotherapy, for accurate evaluation after first‐line chemotherapy. This study aimed to evaluate changes in RRM1 expression during chemotherapy. Materials and methods RRM1 immunohistochemistry was performe...
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Veröffentlicht in: | Histopathology 2014-02, Vol.64 (3), p.412-420 |
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description | Aims
It is of interest whether expression of potentially predictive biomarkers changes during chemotherapy, for accurate evaluation after first‐line chemotherapy. This study aimed to evaluate changes in RRM1 expression during chemotherapy.
Materials and methods
RRM1 immunohistochemistry was performed on tumour samples from a total of 118 NSCLC patients with stage T1‐4N0‐2M0 disease. Samples were included from 65 patients treated with paclitaxel and carboplatin before surgery [neoadjuvant chemotherapy (NAC) group], and 53 patients who had undergone surgery but not chemotherapy [operation (OP) group].
Results
Discordant RRM1 expression (low versus high) was observed in 32% and 43% of paired diagnostic and subsequent resection specimens in the OP group and NAC group, respectively (P = 0.913). Ten (33%) and 12 (23%) tumours in the NAC group and the OP group, respectively, had increased RRM1 expression in the resection specimens (P = 0.289), and 12 (40%) and 19 (36%) tumours had decreased expression (P = 0.707). Eleven (50%) lymph node metastases had higher RRM1 expression following chemotherapy, and two (7%) had decreased expression.
Conclusions
The substantial discordance between paired samples emphasizes the need for sufficient tumour tissue in biopsies when RRM1 expression is evaluated. No change in RRM1 expression was observed in primary tumours, but expression seemed to be higher in N2 lymph node metastases following chemotherapy. Tumour heterogeneity and potential post‐chemotherapy changes should be considered when RRM1 expression is evaluated. |
doi_str_mv | 10.1111/his.12264 |
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It is of interest whether expression of potentially predictive biomarkers changes during chemotherapy, for accurate evaluation after first‐line chemotherapy. This study aimed to evaluate changes in RRM1 expression during chemotherapy.
Materials and methods
RRM1 immunohistochemistry was performed on tumour samples from a total of 118 NSCLC patients with stage T1‐4N0‐2M0 disease. Samples were included from 65 patients treated with paclitaxel and carboplatin before surgery [neoadjuvant chemotherapy (NAC) group], and 53 patients who had undergone surgery but not chemotherapy [operation (OP) group].
Results
Discordant RRM1 expression (low versus high) was observed in 32% and 43% of paired diagnostic and subsequent resection specimens in the OP group and NAC group, respectively (P = 0.913). Ten (33%) and 12 (23%) tumours in the NAC group and the OP group, respectively, had increased RRM1 expression in the resection specimens (P = 0.289), and 12 (40%) and 19 (36%) tumours had decreased expression (P = 0.707). Eleven (50%) lymph node metastases had higher RRM1 expression following chemotherapy, and two (7%) had decreased expression.
Conclusions
The substantial discordance between paired samples emphasizes the need for sufficient tumour tissue in biopsies when RRM1 expression is evaluated. No change in RRM1 expression was observed in primary tumours, but expression seemed to be higher in N2 lymph node metastases following chemotherapy. Tumour heterogeneity and potential post‐chemotherapy changes should be considered when RRM1 expression is evaluated.</description><identifier>ISSN: 0309-0167</identifier><identifier>EISSN: 1365-2559</identifier><identifier>DOI: 10.1111/his.12264</identifier><identifier>PMID: 24266856</identifier><identifier>CODEN: HISTDD</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; biomarker ; Biopsy ; Carboplatin - administration & dosage ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - metabolism ; Carcinoma, Non-Small-Cell Lung - pathology ; chemotherapy ; Female ; Humans ; Immunohistochemistry ; Lung Neoplasms - drug therapy ; Lung Neoplasms - metabolism ; Lung Neoplasms - pathology ; Lymphatic Metastasis ; Male ; Middle Aged ; Neoadjuvant Therapy ; non-small-cell lung cancer ; Paclitaxel - administration & dosage ; RRM1 ; Treatment Outcome ; Tumor Suppressor Proteins - metabolism</subject><ispartof>Histopathology, 2014-02, Vol.64 (3), p.412-420</ispartof><rights>2013 John Wiley & Sons Ltd</rights><rights>2013 John Wiley & Sons Ltd.</rights><rights>Copyright © 2014 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhis.12264$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhis.12264$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24266856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jakobsen, Jan N</creatorcontrib><creatorcontrib>Santoni-Rugiu, Eric</creatorcontrib><creatorcontrib>Sørensen, Jens B</creatorcontrib><title>Differences in RRM1 protein expression between diagnostic biopsies and resection specimens, and changes during carboplatin and paclitaxel treatment, in non-small-cell lung cancer</title><title>Histopathology</title><addtitle>Histopathology</addtitle><description>Aims
It is of interest whether expression of potentially predictive biomarkers changes during chemotherapy, for accurate evaluation after first‐line chemotherapy. This study aimed to evaluate changes in RRM1 expression during chemotherapy.
Materials and methods
RRM1 immunohistochemistry was performed on tumour samples from a total of 118 NSCLC patients with stage T1‐4N0‐2M0 disease. Samples were included from 65 patients treated with paclitaxel and carboplatin before surgery [neoadjuvant chemotherapy (NAC) group], and 53 patients who had undergone surgery but not chemotherapy [operation (OP) group].
Results
Discordant RRM1 expression (low versus high) was observed in 32% and 43% of paired diagnostic and subsequent resection specimens in the OP group and NAC group, respectively (P = 0.913). Ten (33%) and 12 (23%) tumours in the NAC group and the OP group, respectively, had increased RRM1 expression in the resection specimens (P = 0.289), and 12 (40%) and 19 (36%) tumours had decreased expression (P = 0.707). Eleven (50%) lymph node metastases had higher RRM1 expression following chemotherapy, and two (7%) had decreased expression.
Conclusions
The substantial discordance between paired samples emphasizes the need for sufficient tumour tissue in biopsies when RRM1 expression is evaluated. No change in RRM1 expression was observed in primary tumours, but expression seemed to be higher in N2 lymph node metastases following chemotherapy. Tumour heterogeneity and potential post‐chemotherapy changes should be considered when RRM1 expression is evaluated.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>biomarker</subject><subject>Biopsy</subject><subject>Carboplatin - administration & dosage</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>chemotherapy</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>non-small-cell lung cancer</subject><subject>Paclitaxel - administration & dosage</subject><subject>RRM1</subject><subject>Treatment Outcome</subject><subject>Tumor Suppressor Proteins - metabolism</subject><issn>0309-0167</issn><issn>1365-2559</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc9u1DAQxi0EokvhwAsgS1w4NK3_JHZyhIV2K1qQFhBHy04mWxevE2xH3b4WT4izW3pgLp7R_L7RJ38IvabklOY6u7HxlDImyidoQbmoClZVzVO0IJw0BaFCHqEXMd4SQiVn7Dk6YiUToq7EAv35aPseAvgWIrYer9fXFI9hSJAH2I0BYrSDxwbSHYDHndUbP8RkW2zsMEabZdp3OHPQppmMI7R2Cz6e7BftjfabDHVTsH6DWx3MMDqd8vl5PerW2aR34HAKoFMWppPZiB98EbfauaIF57Cb9uJsM7xEz3rtIrx6eI_Rj_NP35er4urrxeXy_VVhOZVlYaQWoq0IGFJTbmgtS0273JsS6sow1jDCeJ2rEo3sTW36jjFSCqJF33Dgx-jd4W7-jt8TxKS2Ns5mtIdhioqWDZFCSMEz-vY_9HaYgs_uMiVFKTJZZurNAzWZLXRqDHarw736l0YGzg7AnXVw_7inRM0xqxyz2sesVpff9k1WFAeFjQl2jwodfikhuazUzy8X6vpzvWTr85X6wP8CsWiq_g</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Jakobsen, Jan N</creator><creator>Santoni-Rugiu, Eric</creator><creator>Sørensen, Jens B</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201402</creationdate><title>Differences in RRM1 protein expression between diagnostic biopsies and resection specimens, and changes during carboplatin and paclitaxel treatment, in non-small-cell lung cancer</title><author>Jakobsen, Jan N ; Santoni-Rugiu, Eric ; Sørensen, Jens B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3174-b7a66c50eb0813b1874a1d081b4e85b229202388885697fb8bfd220460a6f93e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>biomarker</topic><topic>Biopsy</topic><topic>Carboplatin - administration & dosage</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - metabolism</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>chemotherapy</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>non-small-cell lung cancer</topic><topic>Paclitaxel - administration & dosage</topic><topic>RRM1</topic><topic>Treatment Outcome</topic><topic>Tumor Suppressor Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jakobsen, Jan N</creatorcontrib><creatorcontrib>Santoni-Rugiu, Eric</creatorcontrib><creatorcontrib>Sørensen, Jens B</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Histopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jakobsen, Jan N</au><au>Santoni-Rugiu, Eric</au><au>Sørensen, Jens B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in RRM1 protein expression between diagnostic biopsies and resection specimens, and changes during carboplatin and paclitaxel treatment, in non-small-cell lung cancer</atitle><jtitle>Histopathology</jtitle><addtitle>Histopathology</addtitle><date>2014-02</date><risdate>2014</risdate><volume>64</volume><issue>3</issue><spage>412</spage><epage>420</epage><pages>412-420</pages><issn>0309-0167</issn><eissn>1365-2559</eissn><coden>HISTDD</coden><abstract>Aims
It is of interest whether expression of potentially predictive biomarkers changes during chemotherapy, for accurate evaluation after first‐line chemotherapy. This study aimed to evaluate changes in RRM1 expression during chemotherapy.
Materials and methods
RRM1 immunohistochemistry was performed on tumour samples from a total of 118 NSCLC patients with stage T1‐4N0‐2M0 disease. Samples were included from 65 patients treated with paclitaxel and carboplatin before surgery [neoadjuvant chemotherapy (NAC) group], and 53 patients who had undergone surgery but not chemotherapy [operation (OP) group].
Results
Discordant RRM1 expression (low versus high) was observed in 32% and 43% of paired diagnostic and subsequent resection specimens in the OP group and NAC group, respectively (P = 0.913). Ten (33%) and 12 (23%) tumours in the NAC group and the OP group, respectively, had increased RRM1 expression in the resection specimens (P = 0.289), and 12 (40%) and 19 (36%) tumours had decreased expression (P = 0.707). Eleven (50%) lymph node metastases had higher RRM1 expression following chemotherapy, and two (7%) had decreased expression.
Conclusions
The substantial discordance between paired samples emphasizes the need for sufficient tumour tissue in biopsies when RRM1 expression is evaluated. No change in RRM1 expression was observed in primary tumours, but expression seemed to be higher in N2 lymph node metastases following chemotherapy. Tumour heterogeneity and potential post‐chemotherapy changes should be considered when RRM1 expression is evaluated.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24266856</pmid><doi>10.1111/his.12264</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - therapeutic use biomarker Biopsy Carboplatin - administration & dosage Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - metabolism Carcinoma, Non-Small-Cell Lung - pathology chemotherapy Female Humans Immunohistochemistry Lung Neoplasms - drug therapy Lung Neoplasms - metabolism Lung Neoplasms - pathology Lymphatic Metastasis Male Middle Aged Neoadjuvant Therapy non-small-cell lung cancer Paclitaxel - administration & dosage RRM1 Treatment Outcome Tumor Suppressor Proteins - metabolism |
title | Differences in RRM1 protein expression between diagnostic biopsies and resection specimens, and changes during carboplatin and paclitaxel treatment, in non-small-cell lung cancer |
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