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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of cancer research and clinical oncology 2017-10, Vol.143 (10), p.1977-1984
Hauptverfasser: 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.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1984
container_issue 10
container_start_page 1977
container_title Journal of cancer research and clinical oncology
container_volume 143
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 &amp; dosage ; L1 gene ; Male ; Medical prognosis ; Medicine ; Medicine &amp; 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 &amp; dosage</subject><subject>L1 gene</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine &amp; 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. C.</creator><creator>Goldinger, S. M.</creator><creator>Weide, B.</creator><creator>Konrad, A.</creator><creator>Erdmann, M.</creator><creator>Schadendorf, D.</creator><creator>Croner, R. S.</creator><creator>Krähenbühl, L.</creator><creator>Kähler, K. 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 &amp; dosage</topic><topic>L1 gene</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine &amp; 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. 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><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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Health &amp; 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>
fulltext fulltext
identifier ISSN: 0171-5216
ispartof Journal of cancer research and clinical oncology, 2017-10, Vol.143 (10), p.1977-1984
issn 0171-5216
1432-1335
language eng
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