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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
Main Authors: 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
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container_title Cancer treatment and research communications
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creator Martini, Dylan J.
Kline, Meredith R.
Liu, Yuan
Shabto, Julie M.
Carthon, Bradley C.
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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
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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 &gt; 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&lt;0.001; intermediate risk HR: 3.50, p = 0.004) and PFS (high risk HR: 7.31, p&lt;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). 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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 &gt; 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&lt;0.001; intermediate risk HR: 3.50, p = 0.004) and PFS (high risk HR: 7.31, p&lt;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. 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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 &gt; 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&lt;0.001; intermediate risk HR: 3.50, p = 0.004) and PFS (high risk HR: 7.31, p&lt;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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