Expression level of vascular endothelial growth factor receptor-2 in radical nephrectomy specimens as a prognostic predictor in patients with metastatic renal cell carcinoma treated with sunitinib

Abstract Objectives To investigate the expression levels of multiple molecular markers in radical nephrectomy specimens from patients with metastatic renal cell carcinoma (RCC) treated with sunitinib in order to identify factors predicting susceptibility to this agent. Materials and methods This stu...

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Veröffentlicht in:Urologic oncology 2013-05, Vol.31 (4), p.493-498
Hauptverfasser: Terakawa, Tomoaki, M.D., Ph.D, Miyake, Hideaki, M.D., Ph.D, Kusuda, Yuji, M.D, Fujisawa, Masato, M.D., Ph.D
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container_issue 4
container_start_page 493
container_title Urologic oncology
container_volume 31
creator Terakawa, Tomoaki, M.D., Ph.D
Miyake, Hideaki, M.D., Ph.D
Kusuda, Yuji, M.D
Fujisawa, Masato, M.D., Ph.D
description Abstract Objectives To investigate the expression levels of multiple molecular markers in radical nephrectomy specimens from patients with metastatic renal cell carcinoma (RCC) treated with sunitinib in order to identify factors predicting susceptibility to this agent. Materials and methods This study included a total of 40 consecutive patients undergoing radical nephrectomy, who were diagnosed as having metastatic RCC and subsequently treated with sunitinib. Expression levels of 10 molecular markers, including Bcl-2, Bcl-xL, Bax, phosphorylated Akt, p44/42 mitogen-activated protein kinase, and signal transducers and activation of transcription 3, vascular endothelial growth factor receptor (VEGFR)-1 and -2, and platelet-derived growth factor receptor-α and -β, in primary RCC specimens were assessed by immunohistochemical staining. Results Of several factors examined, tumor grade and the expression level of VEGFR-2 were shown to have significant impacts on response to sunitinib in these 40 patients. Progression-free survival (PFS) was significantly associated with the expression levels of VEGFR-2 in addition to tumor grade, performance status, Memorial Sloan-Kettering Cancer Center risk classification and pretreatment c-reactive protein level on univariate analysis. Of these significant factors, only VEGFR-2 expression appeared to be independently related to PFS on multivariate analysis. In fact, PFS in patients with strong expression of VEGFR-2 was significantly favorable compared with that in those with weak expression of VEGFR-2. Conclusions Collectively, these findings suggest that it would be useful to consider expression levels of potential molecular markers, particularly VEGFR-2, as well as conventional clinical parameters to select metastatic RCC patients likely to benefit from treatment with sunitinib.
doi_str_mv 10.1016/j.urolonc.2011.02.012
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Materials and methods This study included a total of 40 consecutive patients undergoing radical nephrectomy, who were diagnosed as having metastatic RCC and subsequently treated with sunitinib. Expression levels of 10 molecular markers, including Bcl-2, Bcl-xL, Bax, phosphorylated Akt, p44/42 mitogen-activated protein kinase, and signal transducers and activation of transcription 3, vascular endothelial growth factor receptor (VEGFR)-1 and -2, and platelet-derived growth factor receptor-α and -β, in primary RCC specimens were assessed by immunohistochemical staining. Results Of several factors examined, tumor grade and the expression level of VEGFR-2 were shown to have significant impacts on response to sunitinib in these 40 patients. Progression-free survival (PFS) was significantly associated with the expression levels of VEGFR-2 in addition to tumor grade, performance status, Memorial Sloan-Kettering Cancer Center risk classification and pretreatment c-reactive protein level on univariate analysis. Of these significant factors, only VEGFR-2 expression appeared to be independently related to PFS on multivariate analysis. In fact, PFS in patients with strong expression of VEGFR-2 was significantly favorable compared with that in those with weak expression of VEGFR-2. Conclusions Collectively, these findings suggest that it would be useful to consider expression levels of potential molecular markers, particularly VEGFR-2, as well as conventional clinical parameters to select metastatic RCC patients likely to benefit from treatment with sunitinib.</description><identifier>ISSN: 1078-1439</identifier><identifier>EISSN: 1873-2496</identifier><identifier>DOI: 10.1016/j.urolonc.2011.02.012</identifier><identifier>PMID: 21478036</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antineoplastic Agents - therapeutic use ; Biomarkers, Tumor - metabolism ; Carcinoma, Renal Cell - metabolism ; Carcinoma, Renal Cell - mortality ; Carcinoma, Renal Cell - secondary ; Carcinoma, Renal Cell - therapy ; Combined Modality Therapy ; Female ; Follow-Up Studies ; Humans ; Immunoenzyme Techniques ; Indoles - therapeutic use ; Kidney Neoplasms - metabolism ; Kidney Neoplasms - mortality ; Kidney Neoplasms - pathology ; Kidney Neoplasms - therapy ; Male ; Middle Aged ; Neoplasm Grading ; Neoplasm Metastasis ; Neoplasm Staging ; Nephrectomy - mortality ; Prognosis ; Progression-free survival ; Pyrroles - therapeutic use ; Renal cell carcinoma ; Sunitinib ; Survival Rate ; Urology ; Vascular Endothelial Growth Factor Receptor-2 - metabolism ; VEGFR-2</subject><ispartof>Urologic oncology, 2013-05, Vol.31 (4), p.493-498</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-e55ff004d4f24d9bdb9e7b896a97af264297bbdeb163d22f768d67cf88cfadfe3</citedby><cites>FETCH-LOGICAL-c420t-e55ff004d4f24d9bdb9e7b896a97af264297bbdeb163d22f768d67cf88cfadfe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.urolonc.2011.02.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21478036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Terakawa, Tomoaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Miyake, Hideaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Kusuda, Yuji, M.D</creatorcontrib><creatorcontrib>Fujisawa, Masato, M.D., Ph.D</creatorcontrib><title>Expression level of vascular endothelial growth factor receptor-2 in radical nephrectomy specimens as a prognostic predictor in patients with metastatic renal cell carcinoma treated with sunitinib</title><title>Urologic oncology</title><addtitle>Urol Oncol</addtitle><description>Abstract Objectives To investigate the expression levels of multiple molecular markers in radical nephrectomy specimens from patients with metastatic renal cell carcinoma (RCC) treated with sunitinib in order to identify factors predicting susceptibility to this agent. Materials and methods This study included a total of 40 consecutive patients undergoing radical nephrectomy, who were diagnosed as having metastatic RCC and subsequently treated with sunitinib. Expression levels of 10 molecular markers, including Bcl-2, Bcl-xL, Bax, phosphorylated Akt, p44/42 mitogen-activated protein kinase, and signal transducers and activation of transcription 3, vascular endothelial growth factor receptor (VEGFR)-1 and -2, and platelet-derived growth factor receptor-α and -β, in primary RCC specimens were assessed by immunohistochemical staining. Results Of several factors examined, tumor grade and the expression level of VEGFR-2 were shown to have significant impacts on response to sunitinib in these 40 patients. Progression-free survival (PFS) was significantly associated with the expression levels of VEGFR-2 in addition to tumor grade, performance status, Memorial Sloan-Kettering Cancer Center risk classification and pretreatment c-reactive protein level on univariate analysis. Of these significant factors, only VEGFR-2 expression appeared to be independently related to PFS on multivariate analysis. In fact, PFS in patients with strong expression of VEGFR-2 was significantly favorable compared with that in those with weak expression of VEGFR-2. Conclusions Collectively, these findings suggest that it would be useful to consider expression levels of potential molecular markers, particularly VEGFR-2, as well as conventional clinical parameters to select metastatic RCC patients likely to benefit from treatment with sunitinib.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Carcinoma, Renal Cell - metabolism</subject><subject>Carcinoma, Renal Cell - mortality</subject><subject>Carcinoma, Renal Cell - secondary</subject><subject>Carcinoma, Renal Cell - therapy</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Indoles - therapeutic use</subject><subject>Kidney Neoplasms - metabolism</subject><subject>Kidney Neoplasms - mortality</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kidney Neoplasms - therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Grading</subject><subject>Neoplasm Metastasis</subject><subject>Neoplasm Staging</subject><subject>Nephrectomy - mortality</subject><subject>Prognosis</subject><subject>Progression-free survival</subject><subject>Pyrroles - therapeutic use</subject><subject>Renal cell carcinoma</subject><subject>Sunitinib</subject><subject>Survival Rate</subject><subject>Urology</subject><subject>Vascular Endothelial Growth Factor Receptor-2 - metabolism</subject><subject>VEGFR-2</subject><issn>1078-1439</issn><issn>1873-2496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUsuOFCEUrRiNM45-goalmyqBol4bjZmMj2QSF-qaUHCZpq2CEqie6f_zw7yVbl24MSFwE845l3sORfGS0YpR1r7ZV2sMU_C64pSxivKKMv6ouGR9V5dcDO1jrGnXl0zUw0XxLKU9pUz0jD0tLjgTXU_r9rL4dfOwREjJBU8mOMBEgiUHlfQ6qUjAm5B3MDk1kbsY7vOOWKVziCSChgWLkhPnSVTGacR4WHZ4k8N8JGkB7WbwiShcZInhzoeUncYSEL6pIHVR2YHPidw7VJ8hq5TVhorgUVHDhJuK2vkwK5IjqAzmBE6rd9l5Nz4vnlg1JXhxPq-K7x9uvl1_Km-_fPx8_f621ILTXELTWEupMMJyYYbRjAN0Yz-0auiU5a3gQzeOBkbW1oZz27W9aTtt-15bZSzUV8Xrky4O83OFlOXs0vZC5SGsSbJaNA3rWUsR2pygOoaUIli5RDereJSMyi1AuZfnAOUWoKRcYoDIe3VusY4zmL-sP4kh4N0JADjowUGUSaOBGi3dnJcmuP-2ePuPgp7QRczvBxwh7cMa0XmcRiYkyK_bL9o-EWOU0o629W_-wsth</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>Terakawa, Tomoaki, M.D., Ph.D</creator><creator>Miyake, Hideaki, M.D., Ph.D</creator><creator>Kusuda, Yuji, M.D</creator><creator>Fujisawa, Masato, M.D., Ph.D</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20130501</creationdate><title>Expression level of vascular endothelial growth factor receptor-2 in radical nephrectomy specimens as a prognostic predictor in patients with metastatic renal cell carcinoma treated with sunitinib</title><author>Terakawa, Tomoaki, M.D., Ph.D ; Miyake, Hideaki, M.D., Ph.D ; Kusuda, Yuji, M.D ; Fujisawa, Masato, M.D., Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-e55ff004d4f24d9bdb9e7b896a97af264297bbdeb163d22f768d67cf88cfadfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Carcinoma, Renal Cell - metabolism</topic><topic>Carcinoma, Renal Cell - mortality</topic><topic>Carcinoma, Renal Cell - secondary</topic><topic>Carcinoma, Renal Cell - therapy</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Indoles - therapeutic use</topic><topic>Kidney Neoplasms - metabolism</topic><topic>Kidney Neoplasms - mortality</topic><topic>Kidney Neoplasms - pathology</topic><topic>Kidney Neoplasms - therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Grading</topic><topic>Neoplasm Metastasis</topic><topic>Neoplasm Staging</topic><topic>Nephrectomy - mortality</topic><topic>Prognosis</topic><topic>Progression-free survival</topic><topic>Pyrroles - therapeutic use</topic><topic>Renal cell carcinoma</topic><topic>Sunitinib</topic><topic>Survival Rate</topic><topic>Urology</topic><topic>Vascular Endothelial Growth Factor Receptor-2 - metabolism</topic><topic>VEGFR-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Terakawa, Tomoaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Miyake, Hideaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Kusuda, Yuji, M.D</creatorcontrib><creatorcontrib>Fujisawa, Masato, M.D., Ph.D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Urologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Terakawa, Tomoaki, M.D., Ph.D</au><au>Miyake, Hideaki, M.D., Ph.D</au><au>Kusuda, Yuji, M.D</au><au>Fujisawa, Masato, M.D., Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression level of vascular endothelial growth factor receptor-2 in radical nephrectomy specimens as a prognostic predictor in patients with metastatic renal cell carcinoma treated with sunitinib</atitle><jtitle>Urologic oncology</jtitle><addtitle>Urol Oncol</addtitle><date>2013-05-01</date><risdate>2013</risdate><volume>31</volume><issue>4</issue><spage>493</spage><epage>498</epage><pages>493-498</pages><issn>1078-1439</issn><eissn>1873-2496</eissn><abstract>Abstract Objectives To investigate the expression levels of multiple molecular markers in radical nephrectomy specimens from patients with metastatic renal cell carcinoma (RCC) treated with sunitinib in order to identify factors predicting susceptibility to this agent. Materials and methods This study included a total of 40 consecutive patients undergoing radical nephrectomy, who were diagnosed as having metastatic RCC and subsequently treated with sunitinib. Expression levels of 10 molecular markers, including Bcl-2, Bcl-xL, Bax, phosphorylated Akt, p44/42 mitogen-activated protein kinase, and signal transducers and activation of transcription 3, vascular endothelial growth factor receptor (VEGFR)-1 and -2, and platelet-derived growth factor receptor-α and -β, in primary RCC specimens were assessed by immunohistochemical staining. Results Of several factors examined, tumor grade and the expression level of VEGFR-2 were shown to have significant impacts on response to sunitinib in these 40 patients. Progression-free survival (PFS) was significantly associated with the expression levels of VEGFR-2 in addition to tumor grade, performance status, Memorial Sloan-Kettering Cancer Center risk classification and pretreatment c-reactive protein level on univariate analysis. Of these significant factors, only VEGFR-2 expression appeared to be independently related to PFS on multivariate analysis. In fact, PFS in patients with strong expression of VEGFR-2 was significantly favorable compared with that in those with weak expression of VEGFR-2. Conclusions Collectively, these findings suggest that it would be useful to consider expression levels of potential molecular markers, particularly VEGFR-2, as well as conventional clinical parameters to select metastatic RCC patients likely to benefit from treatment with sunitinib.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21478036</pmid><doi>10.1016/j.urolonc.2011.02.012</doi><tpages>6</tpages></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Antineoplastic Agents - therapeutic use
Biomarkers, Tumor - metabolism
Carcinoma, Renal Cell - metabolism
Carcinoma, Renal Cell - mortality
Carcinoma, Renal Cell - secondary
Carcinoma, Renal Cell - therapy
Combined Modality Therapy
Female
Follow-Up Studies
Humans
Immunoenzyme Techniques
Indoles - therapeutic use
Kidney Neoplasms - metabolism
Kidney Neoplasms - mortality
Kidney Neoplasms - pathology
Kidney Neoplasms - therapy
Male
Middle Aged
Neoplasm Grading
Neoplasm Metastasis
Neoplasm Staging
Nephrectomy - mortality
Prognosis
Progression-free survival
Pyrroles - therapeutic use
Renal cell carcinoma
Sunitinib
Survival Rate
Urology
Vascular Endothelial Growth Factor Receptor-2 - metabolism
VEGFR-2
title Expression level of vascular endothelial growth factor receptor-2 in radical nephrectomy specimens as a prognostic predictor in patients with metastatic renal cell carcinoma treated with sunitinib
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