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Novel risk scoring system for metastatic renal cell carcinoma patients treated with cabozantinib
•We created a comprehensive risk scoring system specific for mRCC patients treated with cabozantinib which includes sites of metastasis, histology, monocyte-to-lymphocyte ratio, and ECOG performance status which may aid medical oncologists with treatment decisions for mRCC patients.•High-risk and in...
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Published in: | Cancer treatment and research communications 2021, Vol.28, p.100393-100393, Article 100393 |
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creator | Martini, Dylan J. Kline, Meredith R. Liu, Yuan Shabto, Julie M. Carthon, Bradley C. Russler, Greta Anne Yantorni, Lauren Hitron, Emilie Elise Caulfield, Sarah Goldman, Jamie M. Harris, Wayne B. Kucuk, Omer Master, Viraj A Bilen, Mehmet Asim |
description | •We created a comprehensive risk scoring system specific for mRCC patients treated with cabozantinib which includes sites of metastasis, histology, monocyte-to-lymphocyte ratio, and ECOG performance status which may aid medical oncologists with treatment decisions for mRCC patients.•High-risk and intermediate-risk patients had significantly worse OS and PFS compared to low-risk patients in multivariate analysis.•These factors are readily available and easily assessed in the clinical setting for the stratification of patients prior to initiating treatment with cabozantinib, which could make this risk scoring system a helpful tool to use in conjunction with the IMDC criteria.
Cabozantinib is an effective treatment for metastatic renal cell carcinoma (mRCC). The international mRCC database consortium (IMDC) criteria is the gold standard for risk stratification in mRCC. We created a risk scoring system specific for mRCC patients treated with cabozantinib.
We conducted a retrospective review of 87 patients with mRCC treated with cabozantinib at Winship Cancer Institute from 2015 to 2019. Overall survival (OS) and progression free survival (PFS) were used to measure clinical outcomes. Upon variable selection in multivariable analysis (MVA), elevated baseline monocyte-to-lymphocyte ratio (MLR), sarcomatoid histologic component, ECOG PS > 1, and absence of bone metastases were each assigned 1 point. A three-group risk scoring system was then created: low (score=0–1), intermediate (score=2), and high risk (score=3–4). The Cox proportional hazard model and Kaplan-Meier method were used for survival analyses.
The median age was 62 years-old and the majority were males (71%) with clear-cell RCC (75%). Most (67%) received at least 1 prior line of systemic therapy. High risk and intermediate risk pts had significantly shorter OS (high risk HR: 13.84, p |
doi_str_mv | 10.1016/j.ctarc.2021.100393 |
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Cabozantinib is an effective treatment for metastatic renal cell carcinoma (mRCC). The international mRCC database consortium (IMDC) criteria is the gold standard for risk stratification in mRCC. We created a risk scoring system specific for mRCC patients treated with cabozantinib.
We conducted a retrospective review of 87 patients with mRCC treated with cabozantinib at Winship Cancer Institute from 2015 to 2019. Overall survival (OS) and progression free survival (PFS) were used to measure clinical outcomes. Upon variable selection in multivariable analysis (MVA), elevated baseline monocyte-to-lymphocyte ratio (MLR), sarcomatoid histologic component, ECOG PS > 1, and absence of bone metastases were each assigned 1 point. A three-group risk scoring system was then created: low (score=0–1), intermediate (score=2), and high risk (score=3–4). The Cox proportional hazard model and Kaplan-Meier method were used for survival analyses.
The median age was 62 years-old and the majority were males (71%) with clear-cell RCC (75%). Most (67%) received at least 1 prior line of systemic therapy. High risk and intermediate risk pts had significantly shorter OS (high risk HR: 13.84, p<0.001; intermediate risk HR: 3.50, p = 0.004) and PFS (high risk HR: 7.31, p<0.001; intermediate risk HR: 1.87, p = 0.053) compared to low risk patients in MVA.
RCC patients treated with cabozantinib may benefit from specific risk stratification criteria using RCC histology, ECOG PS, sites of metastatic disease, and MLR. These variables are easily accessible in the clinical setting and may be helpful to determine which mRCC patients may benefit from treatment with cabozantinib.</description><identifier>ISSN: 2468-2942</identifier><identifier>EISSN: 2468-2942</identifier><identifier>DOI: 10.1016/j.ctarc.2021.100393</identifier><identifier>PMID: 34029879</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Anilides - therapeutic use ; Antineoplastic Agents - therapeutic use ; Carcinoma, Renal Cell - drug therapy ; Carcinoma, Renal Cell - immunology ; Carcinoma, Renal Cell - mortality ; Carcinoma, Renal Cell - pathology ; Female ; Humans ; Inflammation ; Kaplan-Meier Estimate ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - immunology ; Kidney Neoplasms - mortality ; Kidney Neoplasms - pathology ; Leukocyte Count ; Male ; Middle Aged ; Prognostic biomarkers ; Proportional Hazards Models ; Protein Kinase Inhibitors - therapeutic use ; Pyridines - therapeutic use ; Renal cell carcinoma ; Retrospective Studies ; Risk Factors ; Sites of metastasis ; Targeted therapy</subject><ispartof>Cancer treatment and research communications, 2021, Vol.28, p.100393-100393, Article 100393</ispartof><rights>2021 The Author(s)</rights><rights>Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4073-90b51a0d7425211315c23d2937649f633306e8f095db76356dcecce4161fe4303</citedby><cites>FETCH-LOGICAL-c4073-90b51a0d7425211315c23d2937649f633306e8f095db76356dcecce4161fe4303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4023,27922,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34029879$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martini, Dylan J.</creatorcontrib><creatorcontrib>Kline, Meredith R.</creatorcontrib><creatorcontrib>Liu, Yuan</creatorcontrib><creatorcontrib>Shabto, Julie M.</creatorcontrib><creatorcontrib>Carthon, Bradley C.</creatorcontrib><creatorcontrib>Russler, Greta Anne</creatorcontrib><creatorcontrib>Yantorni, Lauren</creatorcontrib><creatorcontrib>Hitron, Emilie Elise</creatorcontrib><creatorcontrib>Caulfield, Sarah</creatorcontrib><creatorcontrib>Goldman, Jamie M.</creatorcontrib><creatorcontrib>Harris, Wayne B.</creatorcontrib><creatorcontrib>Kucuk, Omer</creatorcontrib><creatorcontrib>Master, Viraj A</creatorcontrib><creatorcontrib>Bilen, Mehmet Asim</creatorcontrib><title>Novel risk scoring system for metastatic renal cell carcinoma patients treated with cabozantinib</title><title>Cancer treatment and research communications</title><addtitle>Cancer Treat Res Commun</addtitle><description>•We created a comprehensive risk scoring system specific for mRCC patients treated with cabozantinib which includes sites of metastasis, histology, monocyte-to-lymphocyte ratio, and ECOG performance status which may aid medical oncologists with treatment decisions for mRCC patients.•High-risk and intermediate-risk patients had significantly worse OS and PFS compared to low-risk patients in multivariate analysis.•These factors are readily available and easily assessed in the clinical setting for the stratification of patients prior to initiating treatment with cabozantinib, which could make this risk scoring system a helpful tool to use in conjunction with the IMDC criteria.
Cabozantinib is an effective treatment for metastatic renal cell carcinoma (mRCC). The international mRCC database consortium (IMDC) criteria is the gold standard for risk stratification in mRCC. We created a risk scoring system specific for mRCC patients treated with cabozantinib.
We conducted a retrospective review of 87 patients with mRCC treated with cabozantinib at Winship Cancer Institute from 2015 to 2019. Overall survival (OS) and progression free survival (PFS) were used to measure clinical outcomes. Upon variable selection in multivariable analysis (MVA), elevated baseline monocyte-to-lymphocyte ratio (MLR), sarcomatoid histologic component, ECOG PS > 1, and absence of bone metastases were each assigned 1 point. A three-group risk scoring system was then created: low (score=0–1), intermediate (score=2), and high risk (score=3–4). The Cox proportional hazard model and Kaplan-Meier method were used for survival analyses.
The median age was 62 years-old and the majority were males (71%) with clear-cell RCC (75%). Most (67%) received at least 1 prior line of systemic therapy. High risk and intermediate risk pts had significantly shorter OS (high risk HR: 13.84, p<0.001; intermediate risk HR: 3.50, p = 0.004) and PFS (high risk HR: 7.31, p<0.001; intermediate risk HR: 1.87, p = 0.053) compared to low risk patients in MVA.
RCC patients treated with cabozantinib may benefit from specific risk stratification criteria using RCC histology, ECOG PS, sites of metastatic disease, and MLR. These variables are easily accessible in the clinical setting and may be helpful to determine which mRCC patients may benefit from treatment with cabozantinib.</description><subject>Anilides - therapeutic use</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Carcinoma, Renal Cell - immunology</subject><subject>Carcinoma, Renal Cell - mortality</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Kaplan-Meier Estimate</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - immunology</subject><subject>Kidney Neoplasms - mortality</subject><subject>Kidney Neoplasms - pathology</subject><subject>Leukocyte Count</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prognostic biomarkers</subject><subject>Proportional Hazards Models</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Pyridines - therapeutic use</subject><subject>Renal cell carcinoma</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Sites of metastasis</subject><subject>Targeted therapy</subject><issn>2468-2942</issn><issn>2468-2942</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9UctOHDEQtCKigAhfECnyD-zi99iHRIpQIEgILsnZ8dg9izcz45XtLCJfH8MkCC5c3FZXV5W6C6EPlKwpoep0u_bVZb9mhNHWIdzwN-iICaVXzAh28Ox_iE5K2RJCqGa0E-YdOuSCMKM7c4R-Xqc9jDjH8gsXn3KcN7jclwoTHlLGE1RXqqvR4wyzG7GHsT3NOc5pcnjXIJhrwTWDqxDwXay3De_THzfXOMf-PXo7uLHAyb96jH6cf_1-9m11dXNxefblauUF6fjKkF5SR0InmGSUcio944EZ3ilhBsU5Jwr0QIwMfae4VMGD9yCoogMITvgxulx0Q3Jbu8txcvneJhftYyPljXW57TGC1doPXhsllWHCUWkgSKDGq0GyYGjftD4vWrvf_QTNaa7ZjS9EXyJzvLWbtLdaECmFbgJ8EfA5lZJheOJSYh_ys1v7mJ99yM8u-TXWx-e2T5z_abWBT8sAtEPuI2RbfDu_hxAz-No2ja8a_AV6Ma3Y</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Martini, Dylan J.</creator><creator>Kline, Meredith R.</creator><creator>Liu, Yuan</creator><creator>Shabto, Julie M.</creator><creator>Carthon, Bradley C.</creator><creator>Russler, Greta Anne</creator><creator>Yantorni, Lauren</creator><creator>Hitron, Emilie Elise</creator><creator>Caulfield, Sarah</creator><creator>Goldman, Jamie M.</creator><creator>Harris, Wayne B.</creator><creator>Kucuk, Omer</creator><creator>Master, Viraj A</creator><creator>Bilen, Mehmet Asim</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>5PM</scope><scope>DOA</scope></search><sort><creationdate>2021</creationdate><title>Novel risk scoring system for metastatic renal cell carcinoma patients treated with cabozantinib</title><author>Martini, Dylan J. ; Kline, Meredith R. ; Liu, Yuan ; Shabto, Julie M. ; Carthon, Bradley C. ; Russler, Greta Anne ; Yantorni, Lauren ; Hitron, Emilie Elise ; Caulfield, Sarah ; Goldman, Jamie M. ; Harris, Wayne B. ; Kucuk, Omer ; Master, Viraj A ; Bilen, Mehmet Asim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4073-90b51a0d7425211315c23d2937649f633306e8f095db76356dcecce4161fe4303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anilides - therapeutic use</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Carcinoma, Renal Cell - drug therapy</topic><topic>Carcinoma, Renal Cell - immunology</topic><topic>Carcinoma, Renal Cell - mortality</topic><topic>Carcinoma, Renal Cell - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Kaplan-Meier Estimate</topic><topic>Kidney Neoplasms - drug therapy</topic><topic>Kidney Neoplasms - immunology</topic><topic>Kidney Neoplasms - mortality</topic><topic>Kidney Neoplasms - pathology</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prognostic biomarkers</topic><topic>Proportional Hazards Models</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Pyridines - therapeutic use</topic><topic>Renal cell carcinoma</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Sites of metastasis</topic><topic>Targeted therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martini, Dylan J.</creatorcontrib><creatorcontrib>Kline, Meredith R.</creatorcontrib><creatorcontrib>Liu, Yuan</creatorcontrib><creatorcontrib>Shabto, Julie M.</creatorcontrib><creatorcontrib>Carthon, Bradley C.</creatorcontrib><creatorcontrib>Russler, Greta Anne</creatorcontrib><creatorcontrib>Yantorni, Lauren</creatorcontrib><creatorcontrib>Hitron, Emilie Elise</creatorcontrib><creatorcontrib>Caulfield, Sarah</creatorcontrib><creatorcontrib>Goldman, Jamie M.</creatorcontrib><creatorcontrib>Harris, Wayne B.</creatorcontrib><creatorcontrib>Kucuk, Omer</creatorcontrib><creatorcontrib>Master, Viraj A</creatorcontrib><creatorcontrib>Bilen, Mehmet Asim</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Cancer treatment and research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martini, Dylan J.</au><au>Kline, Meredith R.</au><au>Liu, Yuan</au><au>Shabto, Julie M.</au><au>Carthon, Bradley C.</au><au>Russler, Greta Anne</au><au>Yantorni, Lauren</au><au>Hitron, Emilie Elise</au><au>Caulfield, Sarah</au><au>Goldman, Jamie M.</au><au>Harris, Wayne B.</au><au>Kucuk, Omer</au><au>Master, Viraj A</au><au>Bilen, Mehmet Asim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel risk scoring system for metastatic renal cell carcinoma patients treated with cabozantinib</atitle><jtitle>Cancer treatment and research communications</jtitle><addtitle>Cancer Treat Res Commun</addtitle><date>2021</date><risdate>2021</risdate><volume>28</volume><spage>100393</spage><epage>100393</epage><pages>100393-100393</pages><artnum>100393</artnum><issn>2468-2942</issn><eissn>2468-2942</eissn><abstract>•We created a comprehensive risk scoring system specific for mRCC patients treated with cabozantinib which includes sites of metastasis, histology, monocyte-to-lymphocyte ratio, and ECOG performance status which may aid medical oncologists with treatment decisions for mRCC patients.•High-risk and intermediate-risk patients had significantly worse OS and PFS compared to low-risk patients in multivariate analysis.•These factors are readily available and easily assessed in the clinical setting for the stratification of patients prior to initiating treatment with cabozantinib, which could make this risk scoring system a helpful tool to use in conjunction with the IMDC criteria.
Cabozantinib is an effective treatment for metastatic renal cell carcinoma (mRCC). The international mRCC database consortium (IMDC) criteria is the gold standard for risk stratification in mRCC. We created a risk scoring system specific for mRCC patients treated with cabozantinib.
We conducted a retrospective review of 87 patients with mRCC treated with cabozantinib at Winship Cancer Institute from 2015 to 2019. Overall survival (OS) and progression free survival (PFS) were used to measure clinical outcomes. Upon variable selection in multivariable analysis (MVA), elevated baseline monocyte-to-lymphocyte ratio (MLR), sarcomatoid histologic component, ECOG PS > 1, and absence of bone metastases were each assigned 1 point. A three-group risk scoring system was then created: low (score=0–1), intermediate (score=2), and high risk (score=3–4). The Cox proportional hazard model and Kaplan-Meier method were used for survival analyses.
The median age was 62 years-old and the majority were males (71%) with clear-cell RCC (75%). Most (67%) received at least 1 prior line of systemic therapy. High risk and intermediate risk pts had significantly shorter OS (high risk HR: 13.84, p<0.001; intermediate risk HR: 3.50, p = 0.004) and PFS (high risk HR: 7.31, p<0.001; intermediate risk HR: 1.87, p = 0.053) compared to low risk patients in MVA.
RCC patients treated with cabozantinib may benefit from specific risk stratification criteria using RCC histology, ECOG PS, sites of metastatic disease, and MLR. These variables are easily accessible in the clinical setting and may be helpful to determine which mRCC patients may benefit from treatment with cabozantinib.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>34029879</pmid><doi>10.1016/j.ctarc.2021.100393</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anilides - therapeutic use Antineoplastic Agents - therapeutic use Carcinoma, Renal Cell - drug therapy Carcinoma, Renal Cell - immunology Carcinoma, Renal Cell - mortality Carcinoma, Renal Cell - pathology Female Humans Inflammation Kaplan-Meier Estimate Kidney Neoplasms - drug therapy Kidney Neoplasms - immunology Kidney Neoplasms - mortality Kidney Neoplasms - pathology Leukocyte Count Male Middle Aged Prognostic biomarkers Proportional Hazards Models Protein Kinase Inhibitors - therapeutic use Pyridines - therapeutic use Renal cell carcinoma Retrospective Studies Risk Factors Sites of metastasis Targeted therapy |
title | Novel risk scoring system for metastatic renal cell carcinoma patients treated with cabozantinib |
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