Hilar fat infiltration: A new prognostic factor in metastatic clear cell renal cell carcinoma with first-line sunitinib treatment
Abstract Introduction The selection of patients with metastatic clear cell renal cell carcinoma (ccRCC) who may benefit from targeted tyrosine kinase inhibitors has been a challenge, even more so now with the advent of new therapies. Hilar fat infiltration (HFI) is a validated prognostic factor in n...
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creator | Kammerer-Jacquet, Solène-Florence, MD, PhD Brunot, Angelique, MD Bensalah, Karim, MD, PhD Campillo-Gimenez, Boris, MD Lefort, Mathilde, PhD Bayat, Sahar, MD, PhD Ravaud, Alain, MD, PhD Dupuis, Frantz, MD Yacoub, Mokrane, MD Verhoest, Gregory, MD, PhD Peyronnet, Benoit, MD Mathieu, Romain, MD Lespagnol, Alexandra, PhD Mosser, Jean, PharmD, PhD Edeline, Julien, MD, PhD Laguerre, Brigitte, MD Bernhard, Jean-Christophe, MD, PhD Rioux-Leclercq, Nathalie, MD, PhD |
description | Abstract Introduction The selection of patients with metastatic clear cell renal cell carcinoma (ccRCC) who may benefit from targeted tyrosine kinase inhibitors has been a challenge, even more so now with the advent of new therapies. Hilar fat infiltration (HFI) is a validated prognostic factor in nonmetastatic ccRCC (TNM 2009 staging system) but has never been studied in metastatic patients. We aimed to assess its phenotype and prognostic effect in patients with metastatic ccRCC treated with first-line sunitinib. Materials and methods In a multicentric study, we retrospectively included 90 patients and studied the corresponding ccRCC at the pathological, immunohistochemical, and molecular levels. Patient and tumor characteristics were compared using univariate and multivariate analysis. All the features were then studied by Cox models for prognostic effect. Results HFI was found in 42 patients (46.7%), who had worse prognosis (Heng criteria) ( P = 0.003), liver metastases ( P = 0.036), and progressive diseases at first radiological evaluation ( P = 0.024). The corresponding ccRCC was associated with poor pathological prognostic factors that are well known in nonmetastatic ccRCC. For these patients, median progression-free survival was 4 months vs. 13 months ( P = 0.02), and median overall survival was 14 months vs. 29 months ( P = 0.006). In a multivariate Cox model integrating all the variables, only poor prognosis, according to the Heng criteria and HFI, remained independently associated with both progression-free survival and overall survival. Conclusion HFI was demonstrated for the first time to be an independent poor prognostic factor. Its potential role in predicting resistance to antiangiogenic therapy warrants further investigation. |
doi_str_mv | 10.1016/j.urolonc.2017.05.015 |
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fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_01632553v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1078143917302326</els_id><sourcerecordid>1910792817</sourcerecordid><originalsourceid>FETCH-LOGICAL-c501t-a05fe6e64402a6dfde4c1bb2104a4ea3028c59125e4151438df24038398c343d3</originalsourceid><addsrcrecordid>eNqFkk1v1DAQhiMEoqXwE0A-wiHBn9mEA9WqAhZpJQ7A2fI6EzqLYxfbadUj_xxHWXrgwmlGo2dm9M47VfWS0YZR1r49NnMMLnjbcMo2DVUNZepRdc66jai57NvHJaebrmZS9GfVs5SOlDLZMfa0OuNdy_pW0PPq9w6diWQ0maAf0eVoMgb_jmyJhztyE8MPH1JGWxCbQywUmSCblM1StA5KtwXnSARv3JpaEy36MBlyh_majBhTrh16IGn2mNHjgeQIJk_g8_PqyWhcgheneFF9__jh29Wu3n_59Plqu6-toizXhqoRWmilpNy0wziAtOxw4IxKI8EIyjuresYVSKaK5m4YuaSiE31nhRSDuKjerHOvjdM3EScT73UwqHfbvV5q5aqCKyVuWWFfr2zR_2uGlPWEaZFmPIQ5adaX0_a8Y5uCqhW1MaQUYXyYzahenNJHfXJKL05pqsomVfpenVbMhwmGh66_1hTgcgWgHOUWIepkEbyFASPYrIeA_13x_p8JtpiA1rifcA_pGOZYLCtqdOKa6q_LuyzfUlRRLngr_gBQz7zt</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1910792817</pqid></control><display><type>article</type><title>Hilar fat infiltration: A new prognostic factor in metastatic clear cell renal cell carcinoma with first-line sunitinib treatment</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Kammerer-Jacquet, Solène-Florence, MD, PhD ; Brunot, Angelique, MD ; Bensalah, Karim, MD, PhD ; Campillo-Gimenez, Boris, MD ; Lefort, Mathilde, PhD ; Bayat, Sahar, MD, PhD ; Ravaud, Alain, MD, PhD ; Dupuis, Frantz, MD ; Yacoub, Mokrane, MD ; Verhoest, Gregory, MD, PhD ; Peyronnet, Benoit, MD ; Mathieu, Romain, MD ; Lespagnol, Alexandra, PhD ; Mosser, Jean, PharmD, PhD ; Edeline, Julien, MD, PhD ; Laguerre, Brigitte, MD ; Bernhard, Jean-Christophe, MD, PhD ; Rioux-Leclercq, Nathalie, MD, PhD</creator><creatorcontrib>Kammerer-Jacquet, Solène-Florence, MD, PhD ; Brunot, Angelique, MD ; Bensalah, Karim, MD, PhD ; Campillo-Gimenez, Boris, MD ; Lefort, Mathilde, PhD ; Bayat, Sahar, MD, PhD ; Ravaud, Alain, MD, PhD ; Dupuis, Frantz, MD ; Yacoub, Mokrane, MD ; Verhoest, Gregory, MD, PhD ; Peyronnet, Benoit, MD ; Mathieu, Romain, MD ; Lespagnol, Alexandra, PhD ; Mosser, Jean, PharmD, PhD ; Edeline, Julien, MD, PhD ; Laguerre, Brigitte, MD ; Bernhard, Jean-Christophe, MD, PhD ; Rioux-Leclercq, Nathalie, MD, PhD</creatorcontrib><description>Abstract Introduction The selection of patients with metastatic clear cell renal cell carcinoma (ccRCC) who may benefit from targeted tyrosine kinase inhibitors has been a challenge, even more so now with the advent of new therapies. Hilar fat infiltration (HFI) is a validated prognostic factor in nonmetastatic ccRCC (TNM 2009 staging system) but has never been studied in metastatic patients. We aimed to assess its phenotype and prognostic effect in patients with metastatic ccRCC treated with first-line sunitinib. Materials and methods In a multicentric study, we retrospectively included 90 patients and studied the corresponding ccRCC at the pathological, immunohistochemical, and molecular levels. Patient and tumor characteristics were compared using univariate and multivariate analysis. All the features were then studied by Cox models for prognostic effect. Results HFI was found in 42 patients (46.7%), who had worse prognosis (Heng criteria) ( P = 0.003), liver metastases ( P = 0.036), and progressive diseases at first radiological evaluation ( P = 0.024). The corresponding ccRCC was associated with poor pathological prognostic factors that are well known in nonmetastatic ccRCC. For these patients, median progression-free survival was 4 months vs. 13 months ( P = 0.02), and median overall survival was 14 months vs. 29 months ( P = 0.006). In a multivariate Cox model integrating all the variables, only poor prognosis, according to the Heng criteria and HFI, remained independently associated with both progression-free survival and overall survival. Conclusion HFI was demonstrated for the first time to be an independent poor prognostic factor. Its potential role in predicting resistance to antiangiogenic therapy warrants further investigation.</description><identifier>ISSN: 1078-1439</identifier><identifier>EISSN: 1873-2496</identifier><identifier>DOI: 10.1016/j.urolonc.2017.05.015</identifier><identifier>PMID: 28619630</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adipocytes - pathology ; Adult ; Aged ; Aged, 80 and over ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Cancer ; Carcinoma, Renal Cell - drug therapy ; Carcinoma, Renal Cell - mortality ; Carcinoma, Renal Cell - pathology ; Clear cell renal cell carcinoma ; Female ; Hilar fat infiltration ; Human health and pathology ; Humans ; Indoles - administration & dosage ; Indoles - pharmacology ; Indoles - therapeutic use ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - mortality ; Kidney Neoplasms - pathology ; Life Sciences ; Male ; Middle Aged ; Prognosis ; Prognostic ; Pyrroles - administration & dosage ; Pyrroles - pharmacology ; Pyrroles - therapeutic use ; Retrospective Studies ; Sunitinib ; Survival Analysis ; Urology ; Urology and Nephrology</subject><ispartof>Urologic oncology, 2017-10, Vol.35 (10), p.603.e7-603.e14</ispartof><rights>Elsevier Inc.</rights><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-a05fe6e64402a6dfde4c1bb2104a4ea3028c59125e4151438df24038398c343d3</citedby><cites>FETCH-LOGICAL-c501t-a05fe6e64402a6dfde4c1bb2104a4ea3028c59125e4151438df24038398c343d3</cites><orcidid>0000-0002-2329-5265 ; 0000-0001-8157-2825 ; 0000-0001-9455-6744 ; 0000-0003-2775-8703 ; 0000-0002-6623-741X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.urolonc.2017.05.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28619630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-rennes.hal.science/hal-01632553$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Kammerer-Jacquet, Solène-Florence, MD, PhD</creatorcontrib><creatorcontrib>Brunot, Angelique, MD</creatorcontrib><creatorcontrib>Bensalah, Karim, MD, PhD</creatorcontrib><creatorcontrib>Campillo-Gimenez, Boris, MD</creatorcontrib><creatorcontrib>Lefort, Mathilde, PhD</creatorcontrib><creatorcontrib>Bayat, Sahar, MD, PhD</creatorcontrib><creatorcontrib>Ravaud, Alain, MD, PhD</creatorcontrib><creatorcontrib>Dupuis, Frantz, MD</creatorcontrib><creatorcontrib>Yacoub, Mokrane, MD</creatorcontrib><creatorcontrib>Verhoest, Gregory, MD, PhD</creatorcontrib><creatorcontrib>Peyronnet, Benoit, MD</creatorcontrib><creatorcontrib>Mathieu, Romain, MD</creatorcontrib><creatorcontrib>Lespagnol, Alexandra, PhD</creatorcontrib><creatorcontrib>Mosser, Jean, PharmD, PhD</creatorcontrib><creatorcontrib>Edeline, Julien, MD, PhD</creatorcontrib><creatorcontrib>Laguerre, Brigitte, MD</creatorcontrib><creatorcontrib>Bernhard, Jean-Christophe, MD, PhD</creatorcontrib><creatorcontrib>Rioux-Leclercq, Nathalie, MD, PhD</creatorcontrib><title>Hilar fat infiltration: A new prognostic factor in metastatic clear cell renal cell carcinoma with first-line sunitinib treatment</title><title>Urologic oncology</title><addtitle>Urol Oncol</addtitle><description>Abstract Introduction The selection of patients with metastatic clear cell renal cell carcinoma (ccRCC) who may benefit from targeted tyrosine kinase inhibitors has been a challenge, even more so now with the advent of new therapies. Hilar fat infiltration (HFI) is a validated prognostic factor in nonmetastatic ccRCC (TNM 2009 staging system) but has never been studied in metastatic patients. We aimed to assess its phenotype and prognostic effect in patients with metastatic ccRCC treated with first-line sunitinib. Materials and methods In a multicentric study, we retrospectively included 90 patients and studied the corresponding ccRCC at the pathological, immunohistochemical, and molecular levels. Patient and tumor characteristics were compared using univariate and multivariate analysis. All the features were then studied by Cox models for prognostic effect. Results HFI was found in 42 patients (46.7%), who had worse prognosis (Heng criteria) ( P = 0.003), liver metastases ( P = 0.036), and progressive diseases at first radiological evaluation ( P = 0.024). The corresponding ccRCC was associated with poor pathological prognostic factors that are well known in nonmetastatic ccRCC. For these patients, median progression-free survival was 4 months vs. 13 months ( P = 0.02), and median overall survival was 14 months vs. 29 months ( P = 0.006). In a multivariate Cox model integrating all the variables, only poor prognosis, according to the Heng criteria and HFI, remained independently associated with both progression-free survival and overall survival. Conclusion HFI was demonstrated for the first time to be an independent poor prognostic factor. Its potential role in predicting resistance to antiangiogenic therapy warrants further investigation.</description><subject>Adipocytes - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Cancer</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Carcinoma, Renal Cell - mortality</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>Clear cell renal cell carcinoma</subject><subject>Female</subject><subject>Hilar fat infiltration</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Indoles - administration & dosage</subject><subject>Indoles - pharmacology</subject><subject>Indoles - therapeutic use</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - mortality</subject><subject>Kidney Neoplasms - pathology</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Prognostic</subject><subject>Pyrroles - administration & dosage</subject><subject>Pyrroles - pharmacology</subject><subject>Pyrroles - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Sunitinib</subject><subject>Survival Analysis</subject><subject>Urology</subject><subject>Urology and Nephrology</subject><issn>1078-1439</issn><issn>1873-2496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1v1DAQhiMEoqXwE0A-wiHBn9mEA9WqAhZpJQ7A2fI6EzqLYxfbadUj_xxHWXrgwmlGo2dm9M47VfWS0YZR1r49NnMMLnjbcMo2DVUNZepRdc66jai57NvHJaebrmZS9GfVs5SOlDLZMfa0OuNdy_pW0PPq9w6diWQ0maAf0eVoMgb_jmyJhztyE8MPH1JGWxCbQywUmSCblM1StA5KtwXnSARv3JpaEy36MBlyh_majBhTrh16IGn2mNHjgeQIJk_g8_PqyWhcgheneFF9__jh29Wu3n_59Plqu6-toizXhqoRWmilpNy0wziAtOxw4IxKI8EIyjuresYVSKaK5m4YuaSiE31nhRSDuKjerHOvjdM3EScT73UwqHfbvV5q5aqCKyVuWWFfr2zR_2uGlPWEaZFmPIQ5adaX0_a8Y5uCqhW1MaQUYXyYzahenNJHfXJKL05pqsomVfpenVbMhwmGh66_1hTgcgWgHOUWIepkEbyFASPYrIeA_13x_p8JtpiA1rifcA_pGOZYLCtqdOKa6q_LuyzfUlRRLngr_gBQz7zt</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Kammerer-Jacquet, Solène-Florence, MD, PhD</creator><creator>Brunot, Angelique, MD</creator><creator>Bensalah, Karim, MD, PhD</creator><creator>Campillo-Gimenez, Boris, MD</creator><creator>Lefort, Mathilde, PhD</creator><creator>Bayat, Sahar, MD, PhD</creator><creator>Ravaud, Alain, MD, PhD</creator><creator>Dupuis, Frantz, MD</creator><creator>Yacoub, Mokrane, MD</creator><creator>Verhoest, Gregory, MD, PhD</creator><creator>Peyronnet, Benoit, MD</creator><creator>Mathieu, Romain, MD</creator><creator>Lespagnol, Alexandra, PhD</creator><creator>Mosser, Jean, PharmD, PhD</creator><creator>Edeline, Julien, MD, PhD</creator><creator>Laguerre, Brigitte, MD</creator><creator>Bernhard, Jean-Christophe, MD, PhD</creator><creator>Rioux-Leclercq, Nathalie, MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier</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><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-2329-5265</orcidid><orcidid>https://orcid.org/0000-0001-8157-2825</orcidid><orcidid>https://orcid.org/0000-0001-9455-6744</orcidid><orcidid>https://orcid.org/0000-0003-2775-8703</orcidid><orcidid>https://orcid.org/0000-0002-6623-741X</orcidid></search><sort><creationdate>20171001</creationdate><title>Hilar fat infiltration: A new prognostic factor in metastatic clear cell renal cell carcinoma with first-line sunitinib treatment</title><author>Kammerer-Jacquet, Solène-Florence, MD, PhD ; Brunot, Angelique, MD ; Bensalah, Karim, MD, PhD ; Campillo-Gimenez, Boris, MD ; Lefort, Mathilde, PhD ; Bayat, Sahar, MD, PhD ; Ravaud, Alain, MD, PhD ; Dupuis, Frantz, MD ; Yacoub, Mokrane, MD ; Verhoest, Gregory, MD, PhD ; Peyronnet, Benoit, MD ; Mathieu, Romain, MD ; Lespagnol, Alexandra, PhD ; Mosser, Jean, PharmD, PhD ; Edeline, Julien, MD, PhD ; Laguerre, Brigitte, MD ; Bernhard, Jean-Christophe, MD, PhD ; Rioux-Leclercq, Nathalie, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-a05fe6e64402a6dfde4c1bb2104a4ea3028c59125e4151438df24038398c343d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adipocytes - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Cancer</topic><topic>Carcinoma, Renal Cell - drug therapy</topic><topic>Carcinoma, Renal Cell - mortality</topic><topic>Carcinoma, Renal Cell - pathology</topic><topic>Clear cell renal cell carcinoma</topic><topic>Female</topic><topic>Hilar fat infiltration</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Indoles - administration & dosage</topic><topic>Indoles - pharmacology</topic><topic>Indoles - therapeutic use</topic><topic>Kidney Neoplasms - drug therapy</topic><topic>Kidney Neoplasms - mortality</topic><topic>Kidney Neoplasms - pathology</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Prognostic</topic><topic>Pyrroles - administration & dosage</topic><topic>Pyrroles - pharmacology</topic><topic>Pyrroles - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Sunitinib</topic><topic>Survival Analysis</topic><topic>Urology</topic><topic>Urology and Nephrology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kammerer-Jacquet, Solène-Florence, MD, PhD</creatorcontrib><creatorcontrib>Brunot, Angelique, MD</creatorcontrib><creatorcontrib>Bensalah, Karim, MD, PhD</creatorcontrib><creatorcontrib>Campillo-Gimenez, Boris, MD</creatorcontrib><creatorcontrib>Lefort, Mathilde, PhD</creatorcontrib><creatorcontrib>Bayat, Sahar, MD, PhD</creatorcontrib><creatorcontrib>Ravaud, Alain, MD, PhD</creatorcontrib><creatorcontrib>Dupuis, Frantz, MD</creatorcontrib><creatorcontrib>Yacoub, Mokrane, MD</creatorcontrib><creatorcontrib>Verhoest, Gregory, MD, PhD</creatorcontrib><creatorcontrib>Peyronnet, Benoit, MD</creatorcontrib><creatorcontrib>Mathieu, Romain, MD</creatorcontrib><creatorcontrib>Lespagnol, Alexandra, PhD</creatorcontrib><creatorcontrib>Mosser, Jean, PharmD, PhD</creatorcontrib><creatorcontrib>Edeline, Julien, MD, PhD</creatorcontrib><creatorcontrib>Laguerre, Brigitte, MD</creatorcontrib><creatorcontrib>Bernhard, Jean-Christophe, MD, PhD</creatorcontrib><creatorcontrib>Rioux-Leclercq, Nathalie, MD, PhD</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><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Urologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kammerer-Jacquet, Solène-Florence, MD, PhD</au><au>Brunot, Angelique, MD</au><au>Bensalah, Karim, MD, PhD</au><au>Campillo-Gimenez, Boris, MD</au><au>Lefort, Mathilde, PhD</au><au>Bayat, Sahar, MD, PhD</au><au>Ravaud, Alain, MD, PhD</au><au>Dupuis, Frantz, MD</au><au>Yacoub, Mokrane, MD</au><au>Verhoest, Gregory, MD, PhD</au><au>Peyronnet, Benoit, MD</au><au>Mathieu, Romain, MD</au><au>Lespagnol, Alexandra, PhD</au><au>Mosser, Jean, PharmD, PhD</au><au>Edeline, Julien, MD, PhD</au><au>Laguerre, Brigitte, MD</au><au>Bernhard, Jean-Christophe, MD, PhD</au><au>Rioux-Leclercq, Nathalie, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hilar fat infiltration: A new prognostic factor in metastatic clear cell renal cell carcinoma with first-line sunitinib treatment</atitle><jtitle>Urologic oncology</jtitle><addtitle>Urol Oncol</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>35</volume><issue>10</issue><spage>603.e7</spage><epage>603.e14</epage><pages>603.e7-603.e14</pages><issn>1078-1439</issn><eissn>1873-2496</eissn><abstract>Abstract Introduction The selection of patients with metastatic clear cell renal cell carcinoma (ccRCC) who may benefit from targeted tyrosine kinase inhibitors has been a challenge, even more so now with the advent of new therapies. Hilar fat infiltration (HFI) is a validated prognostic factor in nonmetastatic ccRCC (TNM 2009 staging system) but has never been studied in metastatic patients. We aimed to assess its phenotype and prognostic effect in patients with metastatic ccRCC treated with first-line sunitinib. Materials and methods In a multicentric study, we retrospectively included 90 patients and studied the corresponding ccRCC at the pathological, immunohistochemical, and molecular levels. Patient and tumor characteristics were compared using univariate and multivariate analysis. All the features were then studied by Cox models for prognostic effect. Results HFI was found in 42 patients (46.7%), who had worse prognosis (Heng criteria) ( P = 0.003), liver metastases ( P = 0.036), and progressive diseases at first radiological evaluation ( P = 0.024). The corresponding ccRCC was associated with poor pathological prognostic factors that are well known in nonmetastatic ccRCC. For these patients, median progression-free survival was 4 months vs. 13 months ( P = 0.02), and median overall survival was 14 months vs. 29 months ( P = 0.006). In a multivariate Cox model integrating all the variables, only poor prognosis, according to the Heng criteria and HFI, remained independently associated with both progression-free survival and overall survival. Conclusion HFI was demonstrated for the first time to be an independent poor prognostic factor. Its potential role in predicting resistance to antiangiogenic therapy warrants further investigation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28619630</pmid><doi>10.1016/j.urolonc.2017.05.015</doi><orcidid>https://orcid.org/0000-0002-2329-5265</orcidid><orcidid>https://orcid.org/0000-0001-8157-2825</orcidid><orcidid>https://orcid.org/0000-0001-9455-6744</orcidid><orcidid>https://orcid.org/0000-0003-2775-8703</orcidid><orcidid>https://orcid.org/0000-0002-6623-741X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adipocytes - pathology Adult Aged Aged, 80 and over Antineoplastic Agents - administration & dosage Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Cancer Carcinoma, Renal Cell - drug therapy Carcinoma, Renal Cell - mortality Carcinoma, Renal Cell - pathology Clear cell renal cell carcinoma Female Hilar fat infiltration Human health and pathology Humans Indoles - administration & dosage Indoles - pharmacology Indoles - therapeutic use Kidney Neoplasms - drug therapy Kidney Neoplasms - mortality Kidney Neoplasms - pathology Life Sciences Male Middle Aged Prognosis Prognostic Pyrroles - administration & dosage Pyrroles - pharmacology Pyrroles - therapeutic use Retrospective Studies Sunitinib Survival Analysis Urology Urology and Nephrology |
title | Hilar fat infiltration: A new prognostic factor in metastatic clear cell renal cell carcinoma with first-line sunitinib treatment |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T20%3A58%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hilar%20fat%20infiltration:%20A%20new%20prognostic%20factor%20in%20metastatic%20clear%20cell%20renal%20cell%20carcinoma%20with%20first-line%20sunitinib%20treatment&rft.jtitle=Urologic%20oncology&rft.au=Kammerer-Jacquet,%20Sol%C3%A8ne-Florence,%20MD,%20PhD&rft.date=2017-10-01&rft.volume=35&rft.issue=10&rft.spage=603.e7&rft.epage=603.e14&rft.pages=603.e7-603.e14&rft.issn=1078-1439&rft.eissn=1873-2496&rft_id=info:doi/10.1016/j.urolonc.2017.05.015&rft_dat=%3Cproquest_hal_p%3E1910792817%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1910792817&rft_id=info:pmid/28619630&rft_els_id=S1078143917302326&rfr_iscdi=true |