Assessing the prognostic value of IMDC risk score for nivolumab-treated patients with renal cancer and malignant melanoma
BACKGROUND: The response of Renal Cell Cancer (RCC) to tyrosine kinase inhibitors (TKI) has been well established. Although these stratifications have been established for TKI response and prognosis, these parameters have recently been used to predict immunotherapy response in RCC. We aimed to use a...
Gespeichert in:
Veröffentlicht in: | Cancer biomarkers : section A of Disease markers 2023-01, Vol.38 (3), p.367-377 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 377 |
---|---|
container_issue | 3 |
container_start_page | 367 |
container_title | Cancer biomarkers : section A of Disease markers |
container_volume | 38 |
creator | Beypınar, Ismail Sözel, Yıldız Önder, Arif Hakan |
description | BACKGROUND:
The response of Renal Cell Cancer (RCC) to tyrosine kinase inhibitors (TKI) has been well established. Although these stratifications have been established for TKI response and prognosis, these parameters have recently been used to predict immunotherapy response in RCC. We aimed to use a combination of clinical parameters of International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk groups and metastatic sites at the time of diagnosis to predict the effectiveness of immune checkpoint inhibitors in malignant melanoma (MM).
METHOD:
In this cross-sectional study, we retrospectively analyzed the demographic information, metastatic sites, and IMDC risk group data. The blood parameters were included in the first cycle of nivolumab treatment.
RESULTS:
The OS was statistically different between the RCC and MM groups in terms of the IMDC. In univariate analysis of stage at diagnosis, CRP levels and bone and bone marrow metastases were confirmed to be prognostic factors in the MM population in terms of OS. Brain metastasis was a prognostic factor for RCC, whereas sex, line of treatment, LDH, bone, and splenic metastasis remained significant in patients with MM in terms of OS. Brain metastasis was prognostic in both cancer types in multivariate analysis in terms of PFS. In addition to brain metastasis, LDH levels and lung, liver, and splenic metastases also affect PFS in patients with MM undergoing nivolumab treatment.
CONCLUSION:
In our study, the IMDC was confirmed to be a prognostic factor for MM. The IMDC groups were similar, except for the favorable RCC and MM groups. Different metastatic sites were prognostic, similar to the IMDC risk group in the MM group. |
doi_str_mv | 10.3233/CBM-230159 |
format | Article |
fullrecord | <record><control><sourceid>proquest_AFRWT</sourceid><recordid>TN_cdi_proquest_miscellaneous_2866109781</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.3233_CBM-230159</sage_id><sourcerecordid>2866109781</sourcerecordid><originalsourceid>FETCH-LOGICAL-c306t-dd69e7089ee26cb4deea89fd713ec55f191255cb0cf25499b5e6ae0f393564a03</originalsourceid><addsrcrecordid>eNpt0U1rFTEUBuAgiq3VjT9AAi4UYWo-JjOTZXvVWmhxo-vhTObMbepMcs3JVPrvTbnVgnSVEB7e5ORl7LUUx1pp_XFzelkpLaSxT9ih7FpTdcaqp2Vv2roq5_qAvSC6FqLWUtnn7EC3bXGdPGS3J0RI5MOW5yvkuxS3IVL2jt_AvCKPEz-__LThydNPTi4m5FNMPPibOK8LDFVOCBlHvoPsMWTiv32-4gkDzNxBcJg4hJEvMPttgJD5gjOEuMBL9myCmfDV_XrEfnz5_H3ztbr4dna-ObmonBZNrsaxsdiKziKqxg31iAidncZWanTGTNJKZYwbhJuUqa0dDDaAYtJWm6YGoY_Y-31ume3XipT7xZPDubwC40q96ppGClt-o9C3_9HruKYyyZ3qbFOrTtZFfdgrlyJRwqnfJb9Auu2l6O8K6Ush_b6Qgt_cR67DguM_-reBAt7tAcEWH-57JOoPdyOSsw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2889642814</pqid></control><display><type>article</type><title>Assessing the prognostic value of IMDC risk score for nivolumab-treated patients with renal cancer and malignant melanoma</title><source>Sage Journals GOLD Open Access 2024</source><creator>Beypınar, Ismail ; Sözel, Yıldız ; Önder, Arif Hakan</creator><creatorcontrib>Beypınar, Ismail ; Sözel, Yıldız ; Önder, Arif Hakan</creatorcontrib><description>BACKGROUND:
The response of Renal Cell Cancer (RCC) to tyrosine kinase inhibitors (TKI) has been well established. Although these stratifications have been established for TKI response and prognosis, these parameters have recently been used to predict immunotherapy response in RCC. We aimed to use a combination of clinical parameters of International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk groups and metastatic sites at the time of diagnosis to predict the effectiveness of immune checkpoint inhibitors in malignant melanoma (MM).
METHOD:
In this cross-sectional study, we retrospectively analyzed the demographic information, metastatic sites, and IMDC risk group data. The blood parameters were included in the first cycle of nivolumab treatment.
RESULTS:
The OS was statistically different between the RCC and MM groups in terms of the IMDC. In univariate analysis of stage at diagnosis, CRP levels and bone and bone marrow metastases were confirmed to be prognostic factors in the MM population in terms of OS. Brain metastasis was a prognostic factor for RCC, whereas sex, line of treatment, LDH, bone, and splenic metastasis remained significant in patients with MM in terms of OS. Brain metastasis was prognostic in both cancer types in multivariate analysis in terms of PFS. In addition to brain metastasis, LDH levels and lung, liver, and splenic metastases also affect PFS in patients with MM undergoing nivolumab treatment.
CONCLUSION:
In our study, the IMDC was confirmed to be a prognostic factor for MM. The IMDC groups were similar, except for the favorable RCC and MM groups. Different metastatic sites were prognostic, similar to the IMDC risk group in the MM group.</description><identifier>ISSN: 1574-0153</identifier><identifier>EISSN: 1875-8592</identifier><identifier>DOI: 10.3233/CBM-230159</identifier><identifier>PMID: 37718781</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Bone marrow ; Brain ; Brain cancer ; Brain Neoplasms ; Cancer ; Carcinoma, Renal Cell - drug therapy ; Cross-Sectional Studies ; Diagnosis ; Humans ; Immune checkpoint inhibitors ; Immunotherapy ; Kidney cancer ; Kidney Neoplasms - drug therapy ; Kinases ; Medical prognosis ; Melanoma ; Melanoma - drug therapy ; Melanoma, Cutaneous Malignant ; Metastases ; Metastasis ; Monoclonal antibodies ; Multivariate analysis ; Nivolumab - therapeutic use ; Parameters ; Patients ; Prognosis ; Protein-tyrosine kinase ; Renal cell carcinoma ; Retrospective Studies ; Risk ; Risk groups ; Skin cancer ; Spleen ; Targeted cancer therapy ; Tyrosine</subject><ispartof>Cancer biomarkers : section A of Disease markers, 2023-01, Vol.38 (3), p.367-377</ispartof><rights>2023 – IOS Press. All rights reserved.</rights><rights>Copyright IOS Press BV 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c306t-dd69e7089ee26cb4deea89fd713ec55f191255cb0cf25499b5e6ae0f393564a03</cites><orcidid>0000-0002-0853-4096 ; 0000-0001-6406-7309 ; 0000-0002-0121-5228</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.3233/CBM-230159$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.3233/CBM-230159$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21946,27832,27903,27904,44924,45312</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.3233/CBM-230159?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37718781$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beypınar, Ismail</creatorcontrib><creatorcontrib>Sözel, Yıldız</creatorcontrib><creatorcontrib>Önder, Arif Hakan</creatorcontrib><title>Assessing the prognostic value of IMDC risk score for nivolumab-treated patients with renal cancer and malignant melanoma</title><title>Cancer biomarkers : section A of Disease markers</title><addtitle>Cancer Biomark</addtitle><description>BACKGROUND:
The response of Renal Cell Cancer (RCC) to tyrosine kinase inhibitors (TKI) has been well established. Although these stratifications have been established for TKI response and prognosis, these parameters have recently been used to predict immunotherapy response in RCC. We aimed to use a combination of clinical parameters of International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk groups and metastatic sites at the time of diagnosis to predict the effectiveness of immune checkpoint inhibitors in malignant melanoma (MM).
METHOD:
In this cross-sectional study, we retrospectively analyzed the demographic information, metastatic sites, and IMDC risk group data. The blood parameters were included in the first cycle of nivolumab treatment.
RESULTS:
The OS was statistically different between the RCC and MM groups in terms of the IMDC. In univariate analysis of stage at diagnosis, CRP levels and bone and bone marrow metastases were confirmed to be prognostic factors in the MM population in terms of OS. Brain metastasis was a prognostic factor for RCC, whereas sex, line of treatment, LDH, bone, and splenic metastasis remained significant in patients with MM in terms of OS. Brain metastasis was prognostic in both cancer types in multivariate analysis in terms of PFS. In addition to brain metastasis, LDH levels and lung, liver, and splenic metastases also affect PFS in patients with MM undergoing nivolumab treatment.
CONCLUSION:
In our study, the IMDC was confirmed to be a prognostic factor for MM. The IMDC groups were similar, except for the favorable RCC and MM groups. Different metastatic sites were prognostic, similar to the IMDC risk group in the MM group.</description><subject>Bone marrow</subject><subject>Brain</subject><subject>Brain cancer</subject><subject>Brain Neoplasms</subject><subject>Cancer</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Cross-Sectional Studies</subject><subject>Diagnosis</subject><subject>Humans</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunotherapy</subject><subject>Kidney cancer</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kinases</subject><subject>Medical prognosis</subject><subject>Melanoma</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma, Cutaneous Malignant</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Monoclonal antibodies</subject><subject>Multivariate analysis</subject><subject>Nivolumab - therapeutic use</subject><subject>Parameters</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Protein-tyrosine kinase</subject><subject>Renal cell carcinoma</subject><subject>Retrospective Studies</subject><subject>Risk</subject><subject>Risk groups</subject><subject>Skin cancer</subject><subject>Spleen</subject><subject>Targeted cancer therapy</subject><subject>Tyrosine</subject><issn>1574-0153</issn><issn>1875-8592</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0U1rFTEUBuAgiq3VjT9AAi4UYWo-JjOTZXvVWmhxo-vhTObMbepMcs3JVPrvTbnVgnSVEB7e5ORl7LUUx1pp_XFzelkpLaSxT9ih7FpTdcaqp2Vv2roq5_qAvSC6FqLWUtnn7EC3bXGdPGS3J0RI5MOW5yvkuxS3IVL2jt_AvCKPEz-__LThydNPTi4m5FNMPPibOK8LDFVOCBlHvoPsMWTiv32-4gkDzNxBcJg4hJEvMPttgJD5gjOEuMBL9myCmfDV_XrEfnz5_H3ztbr4dna-ObmonBZNrsaxsdiKziKqxg31iAidncZWanTGTNJKZYwbhJuUqa0dDDaAYtJWm6YGoY_Y-31ume3XipT7xZPDubwC40q96ppGClt-o9C3_9HruKYyyZ3qbFOrTtZFfdgrlyJRwqnfJb9Auu2l6O8K6Ush_b6Qgt_cR67DguM_-reBAt7tAcEWH-57JOoPdyOSsw</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Beypınar, Ismail</creator><creator>Sözel, Yıldız</creator><creator>Önder, Arif Hakan</creator><general>SAGE Publications</general><general>IOS Press BV</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>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0853-4096</orcidid><orcidid>https://orcid.org/0000-0001-6406-7309</orcidid><orcidid>https://orcid.org/0000-0002-0121-5228</orcidid></search><sort><creationdate>20230101</creationdate><title>Assessing the prognostic value of IMDC risk score for nivolumab-treated patients with renal cancer and malignant melanoma</title><author>Beypınar, Ismail ; Sözel, Yıldız ; Önder, Arif Hakan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-dd69e7089ee26cb4deea89fd713ec55f191255cb0cf25499b5e6ae0f393564a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Bone marrow</topic><topic>Brain</topic><topic>Brain cancer</topic><topic>Brain Neoplasms</topic><topic>Cancer</topic><topic>Carcinoma, Renal Cell - drug therapy</topic><topic>Cross-Sectional Studies</topic><topic>Diagnosis</topic><topic>Humans</topic><topic>Immune checkpoint inhibitors</topic><topic>Immunotherapy</topic><topic>Kidney cancer</topic><topic>Kidney Neoplasms - drug therapy</topic><topic>Kinases</topic><topic>Medical prognosis</topic><topic>Melanoma</topic><topic>Melanoma - drug therapy</topic><topic>Melanoma, Cutaneous Malignant</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Monoclonal antibodies</topic><topic>Multivariate analysis</topic><topic>Nivolumab - therapeutic use</topic><topic>Parameters</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Protein-tyrosine kinase</topic><topic>Renal cell carcinoma</topic><topic>Retrospective Studies</topic><topic>Risk</topic><topic>Risk groups</topic><topic>Skin cancer</topic><topic>Spleen</topic><topic>Targeted cancer therapy</topic><topic>Tyrosine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beypınar, Ismail</creatorcontrib><creatorcontrib>Sözel, Yıldız</creatorcontrib><creatorcontrib>Önder, Arif Hakan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer biomarkers : section A of Disease markers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Beypınar, Ismail</au><au>Sözel, Yıldız</au><au>Önder, Arif Hakan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessing the prognostic value of IMDC risk score for nivolumab-treated patients with renal cancer and malignant melanoma</atitle><jtitle>Cancer biomarkers : section A of Disease markers</jtitle><addtitle>Cancer Biomark</addtitle><date>2023-01-01</date><risdate>2023</risdate><volume>38</volume><issue>3</issue><spage>367</spage><epage>377</epage><pages>367-377</pages><issn>1574-0153</issn><eissn>1875-8592</eissn><abstract>BACKGROUND:
The response of Renal Cell Cancer (RCC) to tyrosine kinase inhibitors (TKI) has been well established. Although these stratifications have been established for TKI response and prognosis, these parameters have recently been used to predict immunotherapy response in RCC. We aimed to use a combination of clinical parameters of International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk groups and metastatic sites at the time of diagnosis to predict the effectiveness of immune checkpoint inhibitors in malignant melanoma (MM).
METHOD:
In this cross-sectional study, we retrospectively analyzed the demographic information, metastatic sites, and IMDC risk group data. The blood parameters were included in the first cycle of nivolumab treatment.
RESULTS:
The OS was statistically different between the RCC and MM groups in terms of the IMDC. In univariate analysis of stage at diagnosis, CRP levels and bone and bone marrow metastases were confirmed to be prognostic factors in the MM population in terms of OS. Brain metastasis was a prognostic factor for RCC, whereas sex, line of treatment, LDH, bone, and splenic metastasis remained significant in patients with MM in terms of OS. Brain metastasis was prognostic in both cancer types in multivariate analysis in terms of PFS. In addition to brain metastasis, LDH levels and lung, liver, and splenic metastases also affect PFS in patients with MM undergoing nivolumab treatment.
CONCLUSION:
In our study, the IMDC was confirmed to be a prognostic factor for MM. The IMDC groups were similar, except for the favorable RCC and MM groups. Different metastatic sites were prognostic, similar to the IMDC risk group in the MM group.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>37718781</pmid><doi>10.3233/CBM-230159</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-0853-4096</orcidid><orcidid>https://orcid.org/0000-0001-6406-7309</orcidid><orcidid>https://orcid.org/0000-0002-0121-5228</orcidid></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | ISSN: 1574-0153 |
ispartof | Cancer biomarkers : section A of Disease markers, 2023-01, Vol.38 (3), p.367-377 |
issn | 1574-0153 1875-8592 |
language | eng |
recordid | cdi_proquest_miscellaneous_2866109781 |
source | Sage Journals GOLD Open Access 2024 |
subjects | Bone marrow Brain Brain cancer Brain Neoplasms Cancer Carcinoma, Renal Cell - drug therapy Cross-Sectional Studies Diagnosis Humans Immune checkpoint inhibitors Immunotherapy Kidney cancer Kidney Neoplasms - drug therapy Kinases Medical prognosis Melanoma Melanoma - drug therapy Melanoma, Cutaneous Malignant Metastases Metastasis Monoclonal antibodies Multivariate analysis Nivolumab - therapeutic use Parameters Patients Prognosis Protein-tyrosine kinase Renal cell carcinoma Retrospective Studies Risk Risk groups Skin cancer Spleen Targeted cancer therapy Tyrosine |
title | Assessing the prognostic value of IMDC risk score for nivolumab-treated patients with renal cancer and malignant melanoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T22%3A53%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_AFRWT&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Assessing%20the%20prognostic%20value%20of%20IMDC%20risk%20score%20for%20nivolumab-treated%20patients%20with%20renal%20cancer%20and%20malignant%20melanoma&rft.jtitle=Cancer%20biomarkers%20:%20section%20A%20of%20Disease%20markers&rft.au=Beyp%C4%B1nar,%20Ismail&rft.date=2023-01-01&rft.volume=38&rft.issue=3&rft.spage=367&rft.epage=377&rft.pages=367-377&rft.issn=1574-0153&rft.eissn=1875-8592&rft_id=info:doi/10.3233/CBM-230159&rft_dat=%3Cproquest_AFRWT%3E2866109781%3C/proquest_AFRWT%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2889642814&rft_id=info:pmid/37718781&rft_sage_id=10.3233_CBM-230159&rfr_iscdi=true |