Predictive value of PD-L1 based on mRNA level in the treatment of stage IV melanoma with ipilimumab
Introduction PD-L1 is established as a predictive marker for therapy of non-small cell lung cancer with pembrolizumab. Furthermore, PD-L1 positive melanoma has shown more favorable outcomes when treated with anti-PD1 antibodies and dacarbazine compared to PD-L1 negative melanoma. However, the role o...
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container_title | Journal of cancer research and clinical oncology |
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creator | Brüggemann, C. Kirchberger, M. C. Goldinger, S. M. Weide, B. Konrad, A. Erdmann, M. Schadendorf, D. Croner, R. S. Krähenbühl, L. Kähler, K. C. Hafner, C. Leisgang, W. Kiesewetter, F. Dummer, R. Schuler, G. Stürzl, M. Heinzerling, L. |
description | Introduction
PD-L1 is established as a predictive marker for therapy of non-small cell lung cancer with pembrolizumab. Furthermore, PD-L1 positive melanoma has shown more favorable outcomes when treated with anti-PD1 antibodies and dacarbazine compared to PD-L1 negative melanoma. However, the role of PD-L1 expression with regard to response to checkpoint inhibition with anti-CTLA-4 is not clear, yet. In addition, the lack of standardization in the immunohistochemical assessment of PD-L1 makes the comparison of results difficult. In this study, we investigated the PD-L1 gene expression with a new fully automated technique via RT-PCR and correlated the findings with the response to the anti-CTLA-4 antibody ipilimumab.
Materials and methods
Within a retrospective multi-center trial, PD-L1 gene expression was evaluated in 78 melanoma patients in a total of 111 pre-treatment tumor samples from 6 skin cancer centers and analyzed with regard to response to ipilimumab. For meaningful statistical analysis, the cohort was enriched for responders with 30 responders and 48 non-responders. Gene expression was assessed by quantitative RT-PCR after extracting mRNA from formalin-fixed paraffin embedded tumor tissue and correlated with results from immunohistochemical (IHC) stainings.
Results and discussion
The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab. The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab. |
doi_str_mv | 10.1007/s00432-017-2450-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1910339750</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1938809200</sourcerecordid><originalsourceid>FETCH-LOGICAL-c372t-b9d3a143a0f63d1d8887a35e60615a52c36032f82bbcc848a96f864684588ca73</originalsourceid><addsrcrecordid>eNp1kUFv1DAQhS0EotvCD-CCLHHhEhjbseMcqxZKpVVbVcDVcpxJ6ypOFttZxL_H0RaEkHoaeeab56d5hLxh8IEBNB8TQC14BaypeC2h4s_Ihq0dJoR8TjZlwCrJmToixyk9QHnLhr8kR1wrphpgG-JuIvbeZb9HurfjgnQe6M15tWW0swl7Ok803F6d0hH3OFI_0XyPNEe0OeCUVzple4f08jsNONppDpb-9Pme-p0ffViC7V6RF4MdE75-rCfk2-dPX8--VNvri8uz023lRMNz1bW9sMW-hUGJnvVa68YKiQoUk1ZyJxQIPmjedc7pWttWDVrVStdSa2cbcULeH3R3cf6xYMom-ORwLK5wXpJhLQMh2kZCQd_9hz7MS5yKu0IJraHlsFLsQLk4pxRxMLvog42_DAOzJmAOCZhyWLMmYHjZefuovHQB-78bf05eAH4AUhlNdxj_-fpJ1d9OdI3a</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1938809200</pqid></control><display><type>article</type><title>Predictive value of PD-L1 based on mRNA level in the treatment of stage IV melanoma with ipilimumab</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Brüggemann, C. ; Kirchberger, M. C. ; Goldinger, S. M. ; Weide, B. ; Konrad, A. ; Erdmann, M. ; Schadendorf, D. ; Croner, R. S. ; Krähenbühl, L. ; Kähler, K. C. ; Hafner, C. ; Leisgang, W. ; Kiesewetter, F. ; Dummer, R. ; Schuler, G. ; Stürzl, M. ; Heinzerling, L.</creator><creatorcontrib>Brüggemann, C. ; Kirchberger, M. C. ; Goldinger, S. M. ; Weide, B. ; Konrad, A. ; Erdmann, M. ; Schadendorf, D. ; Croner, R. S. ; Krähenbühl, L. ; Kähler, K. C. ; Hafner, C. ; Leisgang, W. ; Kiesewetter, F. ; Dummer, R. ; Schuler, G. ; Stürzl, M. ; Heinzerling, L.</creatorcontrib><description>Introduction
PD-L1 is established as a predictive marker for therapy of non-small cell lung cancer with pembrolizumab. Furthermore, PD-L1 positive melanoma has shown more favorable outcomes when treated with anti-PD1 antibodies and dacarbazine compared to PD-L1 negative melanoma. However, the role of PD-L1 expression with regard to response to checkpoint inhibition with anti-CTLA-4 is not clear, yet. In addition, the lack of standardization in the immunohistochemical assessment of PD-L1 makes the comparison of results difficult. In this study, we investigated the PD-L1 gene expression with a new fully automated technique via RT-PCR and correlated the findings with the response to the anti-CTLA-4 antibody ipilimumab.
Materials and methods
Within a retrospective multi-center trial, PD-L1 gene expression was evaluated in 78 melanoma patients in a total of 111 pre-treatment tumor samples from 6 skin cancer centers and analyzed with regard to response to ipilimumab. For meaningful statistical analysis, the cohort was enriched for responders with 30 responders and 48 non-responders. Gene expression was assessed by quantitative RT-PCR after extracting mRNA from formalin-fixed paraffin embedded tumor tissue and correlated with results from immunohistochemical (IHC) stainings.
Results and discussion
The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab. The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-017-2450-2</identifier><identifier>PMID: 28616701</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antibodies ; B7-H1 Antigen - biosynthesis ; B7-H1 Antigen - genetics ; B7-H1 Antigen - immunology ; Cancer Research ; Case-Control Studies ; Chemotherapy ; CTLA-4 protein ; Dacarbazine ; Female ; Gene Expression ; Hematology ; Humans ; Immunohistochemistry ; Immunotherapy ; Internal Medicine ; Ipilimumab - administration & dosage ; L1 gene ; Male ; Medical prognosis ; Medicine ; Medicine & Public Health ; Melanoma ; Melanoma - drug therapy ; Melanoma - genetics ; Melanoma - immunology ; Melanoma - pathology ; MicroRNAs ; Middle Aged ; Monoclonal antibodies ; Neoplasm Staging ; Non-small cell lung carcinoma ; Oncology ; Original Article – Cancer Research ; Paraffin ; PD-1 protein ; PD-L1 protein ; Polymerase chain reaction ; Predictive Value of Tests ; Real-Time Polymerase Chain Reaction ; Retrospective Studies ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Skin cancer ; Skin Neoplasms - drug therapy ; Skin Neoplasms - genetics ; Skin Neoplasms - immunology ; Skin Neoplasms - pathology ; Standardization ; Statistical analysis ; Targeted cancer therapy</subject><ispartof>Journal of cancer research and clinical oncology, 2017-10, Vol.143 (10), p.1977-1984</ispartof><rights>Springer-Verlag GmbH Germany 2017</rights><rights>Journal of Cancer Research and Clinical Oncology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-b9d3a143a0f63d1d8887a35e60615a52c36032f82bbcc848a96f864684588ca73</citedby><cites>FETCH-LOGICAL-c372t-b9d3a143a0f63d1d8887a35e60615a52c36032f82bbcc848a96f864684588ca73</cites><orcidid>0000-0002-1862-2065</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00432-017-2450-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00432-017-2450-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28616701$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brüggemann, C.</creatorcontrib><creatorcontrib>Kirchberger, M. C.</creatorcontrib><creatorcontrib>Goldinger, S. M.</creatorcontrib><creatorcontrib>Weide, B.</creatorcontrib><creatorcontrib>Konrad, A.</creatorcontrib><creatorcontrib>Erdmann, M.</creatorcontrib><creatorcontrib>Schadendorf, D.</creatorcontrib><creatorcontrib>Croner, R. S.</creatorcontrib><creatorcontrib>Krähenbühl, L.</creatorcontrib><creatorcontrib>Kähler, K. C.</creatorcontrib><creatorcontrib>Hafner, C.</creatorcontrib><creatorcontrib>Leisgang, W.</creatorcontrib><creatorcontrib>Kiesewetter, F.</creatorcontrib><creatorcontrib>Dummer, R.</creatorcontrib><creatorcontrib>Schuler, G.</creatorcontrib><creatorcontrib>Stürzl, M.</creatorcontrib><creatorcontrib>Heinzerling, L.</creatorcontrib><title>Predictive value of PD-L1 based on mRNA level in the treatment of stage IV melanoma with ipilimumab</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>Introduction
PD-L1 is established as a predictive marker for therapy of non-small cell lung cancer with pembrolizumab. Furthermore, PD-L1 positive melanoma has shown more favorable outcomes when treated with anti-PD1 antibodies and dacarbazine compared to PD-L1 negative melanoma. However, the role of PD-L1 expression with regard to response to checkpoint inhibition with anti-CTLA-4 is not clear, yet. In addition, the lack of standardization in the immunohistochemical assessment of PD-L1 makes the comparison of results difficult. In this study, we investigated the PD-L1 gene expression with a new fully automated technique via RT-PCR and correlated the findings with the response to the anti-CTLA-4 antibody ipilimumab.
Materials and methods
Within a retrospective multi-center trial, PD-L1 gene expression was evaluated in 78 melanoma patients in a total of 111 pre-treatment tumor samples from 6 skin cancer centers and analyzed with regard to response to ipilimumab. For meaningful statistical analysis, the cohort was enriched for responders with 30 responders and 48 non-responders. Gene expression was assessed by quantitative RT-PCR after extracting mRNA from formalin-fixed paraffin embedded tumor tissue and correlated with results from immunohistochemical (IHC) stainings.
Results and discussion
The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab. The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies</subject><subject>B7-H1 Antigen - biosynthesis</subject><subject>B7-H1 Antigen - genetics</subject><subject>B7-H1 Antigen - immunology</subject><subject>Cancer Research</subject><subject>Case-Control Studies</subject><subject>Chemotherapy</subject><subject>CTLA-4 protein</subject><subject>Dacarbazine</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Hematology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Immunotherapy</subject><subject>Internal Medicine</subject><subject>Ipilimumab - administration & dosage</subject><subject>L1 gene</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Melanoma</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma - genetics</subject><subject>Melanoma - immunology</subject><subject>Melanoma - pathology</subject><subject>MicroRNAs</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Neoplasm Staging</subject><subject>Non-small cell lung carcinoma</subject><subject>Oncology</subject><subject>Original Article – Cancer Research</subject><subject>Paraffin</subject><subject>PD-1 protein</subject><subject>PD-L1 protein</subject><subject>Polymerase chain reaction</subject><subject>Predictive Value of Tests</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Retrospective Studies</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Skin cancer</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - immunology</subject><subject>Skin Neoplasms - pathology</subject><subject>Standardization</subject><subject>Statistical analysis</subject><subject>Targeted cancer therapy</subject><issn>0171-5216</issn><issn>1432-1335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kUFv1DAQhS0EotvCD-CCLHHhEhjbseMcqxZKpVVbVcDVcpxJ6ypOFttZxL_H0RaEkHoaeeab56d5hLxh8IEBNB8TQC14BaypeC2h4s_Ihq0dJoR8TjZlwCrJmToixyk9QHnLhr8kR1wrphpgG-JuIvbeZb9HurfjgnQe6M15tWW0swl7Ok803F6d0hH3OFI_0XyPNEe0OeCUVzple4f08jsNONppDpb-9Pme-p0ffViC7V6RF4MdE75-rCfk2-dPX8--VNvri8uz023lRMNz1bW9sMW-hUGJnvVa68YKiQoUk1ZyJxQIPmjedc7pWttWDVrVStdSa2cbcULeH3R3cf6xYMom-ORwLK5wXpJhLQMh2kZCQd_9hz7MS5yKu0IJraHlsFLsQLk4pxRxMLvog42_DAOzJmAOCZhyWLMmYHjZefuovHQB-78bf05eAH4AUhlNdxj_-fpJ1d9OdI3a</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Brüggemann, C.</creator><creator>Kirchberger, M. 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C.</creator><creator>Hafner, C.</creator><creator>Leisgang, W.</creator><creator>Kiesewetter, F.</creator><creator>Dummer, R.</creator><creator>Schuler, G.</creator><creator>Stürzl, M.</creator><creator>Heinzerling, L.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1862-2065</orcidid></search><sort><creationdate>20171001</creationdate><title>Predictive value of PD-L1 based on mRNA level in the treatment of stage IV melanoma with ipilimumab</title><author>Brüggemann, C. ; Kirchberger, M. C. ; Goldinger, S. M. ; Weide, B. ; Konrad, A. ; Erdmann, M. ; Schadendorf, D. ; Croner, R. S. ; Krähenbühl, L. ; Kähler, K. C. ; Hafner, C. ; Leisgang, W. ; Kiesewetter, F. ; Dummer, R. ; Schuler, G. ; Stürzl, M. ; Heinzerling, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-b9d3a143a0f63d1d8887a35e60615a52c36032f82bbcc848a96f864684588ca73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibodies</topic><topic>B7-H1 Antigen - biosynthesis</topic><topic>B7-H1 Antigen - genetics</topic><topic>B7-H1 Antigen - immunology</topic><topic>Cancer Research</topic><topic>Case-Control Studies</topic><topic>Chemotherapy</topic><topic>CTLA-4 protein</topic><topic>Dacarbazine</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Hematology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunotherapy</topic><topic>Internal Medicine</topic><topic>Ipilimumab - administration & dosage</topic><topic>L1 gene</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Melanoma</topic><topic>Melanoma - drug therapy</topic><topic>Melanoma - genetics</topic><topic>Melanoma - immunology</topic><topic>Melanoma - pathology</topic><topic>MicroRNAs</topic><topic>Middle Aged</topic><topic>Monoclonal antibodies</topic><topic>Neoplasm Staging</topic><topic>Non-small cell lung carcinoma</topic><topic>Oncology</topic><topic>Original Article – Cancer Research</topic><topic>Paraffin</topic><topic>PD-1 protein</topic><topic>PD-L1 protein</topic><topic>Polymerase chain reaction</topic><topic>Predictive Value of Tests</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Retrospective Studies</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Skin cancer</topic><topic>Skin Neoplasms - drug therapy</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - immunology</topic><topic>Skin Neoplasms - pathology</topic><topic>Standardization</topic><topic>Statistical analysis</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brüggemann, C.</creatorcontrib><creatorcontrib>Kirchberger, M. 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C.</creatorcontrib><creatorcontrib>Hafner, C.</creatorcontrib><creatorcontrib>Leisgang, W.</creatorcontrib><creatorcontrib>Kiesewetter, F.</creatorcontrib><creatorcontrib>Dummer, R.</creatorcontrib><creatorcontrib>Schuler, G.</creatorcontrib><creatorcontrib>Stürzl, M.</creatorcontrib><creatorcontrib>Heinzerling, L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cancer research and clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brüggemann, C.</au><au>Kirchberger, M. C.</au><au>Goldinger, S. M.</au><au>Weide, B.</au><au>Konrad, A.</au><au>Erdmann, M.</au><au>Schadendorf, D.</au><au>Croner, R. S.</au><au>Krähenbühl, L.</au><au>Kähler, K. C.</au><au>Hafner, C.</au><au>Leisgang, W.</au><au>Kiesewetter, F.</au><au>Dummer, R.</au><au>Schuler, G.</au><au>Stürzl, M.</au><au>Heinzerling, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictive value of PD-L1 based on mRNA level in the treatment of stage IV melanoma with ipilimumab</atitle><jtitle>Journal of cancer research and clinical oncology</jtitle><stitle>J Cancer Res Clin Oncol</stitle><addtitle>J Cancer Res Clin Oncol</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>143</volume><issue>10</issue><spage>1977</spage><epage>1984</epage><pages>1977-1984</pages><issn>0171-5216</issn><eissn>1432-1335</eissn><abstract>Introduction
PD-L1 is established as a predictive marker for therapy of non-small cell lung cancer with pembrolizumab. Furthermore, PD-L1 positive melanoma has shown more favorable outcomes when treated with anti-PD1 antibodies and dacarbazine compared to PD-L1 negative melanoma. However, the role of PD-L1 expression with regard to response to checkpoint inhibition with anti-CTLA-4 is not clear, yet. In addition, the lack of standardization in the immunohistochemical assessment of PD-L1 makes the comparison of results difficult. In this study, we investigated the PD-L1 gene expression with a new fully automated technique via RT-PCR and correlated the findings with the response to the anti-CTLA-4 antibody ipilimumab.
Materials and methods
Within a retrospective multi-center trial, PD-L1 gene expression was evaluated in 78 melanoma patients in a total of 111 pre-treatment tumor samples from 6 skin cancer centers and analyzed with regard to response to ipilimumab. For meaningful statistical analysis, the cohort was enriched for responders with 30 responders and 48 non-responders. Gene expression was assessed by quantitative RT-PCR after extracting mRNA from formalin-fixed paraffin embedded tumor tissue and correlated with results from immunohistochemical (IHC) stainings.
Results and discussion
The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab. The evaluation of PD-L1 expression based on mRNA level is feasible. Correlation between PD-L1 expression as assessed by IHC and RT-PCR showed varying levels of concordance depending on the antibody employed. RT-PCR should be further investigated to measure PD-L1 expression, since it is a semi-quantitative method with observer-independent evaluation. With this approach, there was no statistical significant difference in the PD-L1 expression between responders and non-responders to the therapy with ipilimumab.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28616701</pmid><doi>10.1007/s00432-017-2450-2</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-1862-2065</orcidid></addata></record> |
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recordid | cdi_proquest_miscellaneous_1910339750 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Adult Aged Aged, 80 and over Antibodies B7-H1 Antigen - biosynthesis B7-H1 Antigen - genetics B7-H1 Antigen - immunology Cancer Research Case-Control Studies Chemotherapy CTLA-4 protein Dacarbazine Female Gene Expression Hematology Humans Immunohistochemistry Immunotherapy Internal Medicine Ipilimumab - administration & dosage L1 gene Male Medical prognosis Medicine Medicine & Public Health Melanoma Melanoma - drug therapy Melanoma - genetics Melanoma - immunology Melanoma - pathology MicroRNAs Middle Aged Monoclonal antibodies Neoplasm Staging Non-small cell lung carcinoma Oncology Original Article – Cancer Research Paraffin PD-1 protein PD-L1 protein Polymerase chain reaction Predictive Value of Tests Real-Time Polymerase Chain Reaction Retrospective Studies RNA, Messenger - genetics RNA, Messenger - metabolism Skin cancer Skin Neoplasms - drug therapy Skin Neoplasms - genetics Skin Neoplasms - immunology Skin Neoplasms - pathology Standardization Statistical analysis Targeted cancer therapy |
title | Predictive value of PD-L1 based on mRNA level in the treatment of stage IV melanoma with ipilimumab |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T09%3A23%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Predictive%20value%20of%20PD-L1%20based%20on%20mRNA%20level%20in%20the%20treatment%20of%20stage%20IV%20melanoma%20with%20ipilimumab&rft.jtitle=Journal%20of%20cancer%20research%20and%20clinical%20oncology&rft.au=Br%C3%BCggemann,%20C.&rft.date=2017-10-01&rft.volume=143&rft.issue=10&rft.spage=1977&rft.epage=1984&rft.pages=1977-1984&rft.issn=0171-5216&rft.eissn=1432-1335&rft_id=info:doi/10.1007/s00432-017-2450-2&rft_dat=%3Cproquest_cross%3E1938809200%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1938809200&rft_id=info:pmid/28616701&rfr_iscdi=true |