Cabozantinib, a New Standard of Care for Patients With Advanced Renal Cell Carcinoma and Bone Metastases? Subgroup Analysis of the METEOR Trial

Purpose Cabozantinib, an inhibitor of tyrosine kinases including MET, vascular endothelial growth factor receptors, and AXL, increased progression-free survival (PFS), overall survival (OS), and objective response rate (ORR) in patients with advanced renal cell carcinoma (RCC) after previous vascula...

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Veröffentlicht in:Journal of clinical oncology 2018-03, Vol.36 (8), p.765-772
Hauptverfasser: Escudier, Bernard, Powles, Thomas, Motzer, Robert J, Olencki, Thomas, Arén Frontera, Osvaldo, Oudard, Stephane, Rolland, Frederic, Tomczak, Piotr, Castellano, Daniel, Appleman, Leonard J, Drabkin, Harry, Vaena, Daniel, Milwee, Steven, Youkstetter, Jillian, Lougheed, Julie C, Bracarda, Sergio, Choueiri, Toni K
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container_end_page 772
container_issue 8
container_start_page 765
container_title Journal of clinical oncology
container_volume 36
creator Escudier, Bernard
Powles, Thomas
Motzer, Robert J
Olencki, Thomas
Arén Frontera, Osvaldo
Oudard, Stephane
Rolland, Frederic
Tomczak, Piotr
Castellano, Daniel
Appleman, Leonard J
Drabkin, Harry
Vaena, Daniel
Milwee, Steven
Youkstetter, Jillian
Lougheed, Julie C
Bracarda, Sergio
Choueiri, Toni K
description Purpose Cabozantinib, an inhibitor of tyrosine kinases including MET, vascular endothelial growth factor receptors, and AXL, increased progression-free survival (PFS), overall survival (OS), and objective response rate (ORR) in patients with advanced renal cell carcinoma (RCC) after previous vascular endothelial growth factor receptor-targeted therapy in the phase III METEOR trial. Because bone metastases are associated with increased morbidity in patients with RCC, bone-related outcomes were analyzed in METEOR. Patients and Methods Six hundred fifty-eight patients were randomly assigned 1:1 to receive 60 mg cabozantinib or 10 mg everolimus. Prespecified subgroup analyses of PFS, OS, and ORR were conducted in patients grouped by baseline bone metastases status per independent radiology committee (IRC). Additional end points included bone scan response per IRC, skeletal-related events, and changes in bone biomarkers. Results For patients with bone metastases at baseline (cabozantinib [n = 77]; everolimus [n = 65]), median PFS was 7.4 months for cabozantinib versus 2.7 months for everolimus (hazard ratio, 0.33 [95% CI, 0.21 to 0.51]). Median OS was also longer with cabozantinib (20.1 months v 12.1 months; hazard ratio, 0.54 [95% CI, 0.34 to 0.84]), and ORR per IRC was higher (17% v 0%). The rate of skeletal-related events was 23% with cabozantinib and 29% with everolimus, and bone scan response per IRC was 20% versus 10%, respectively. PFS, OS, and ORR were also improved with cabozantinib in patients without bone metastases. Changes in bone biomarkers were greater with cabozantinib than with everolimus. The overall safety profiles of cabozantinib and everolimus in patients with bone metastases were consistent with those observed in patients without bone metastases. Conclusion Cabozantinib treatment was associated with improved PFS, OS, and ORR when compared with everolimus treatment in patients with advanced RCC and bone metastases and represents a good treatment option for these patients.
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Subgroup Analysis of the METEOR Trial</title><source>MEDLINE</source><source>American Society of Clinical Oncology Online Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Escudier, Bernard ; Powles, Thomas ; Motzer, Robert J ; Olencki, Thomas ; Arén Frontera, Osvaldo ; Oudard, Stephane ; Rolland, Frederic ; Tomczak, Piotr ; Castellano, Daniel ; Appleman, Leonard J ; Drabkin, Harry ; Vaena, Daniel ; Milwee, Steven ; Youkstetter, Jillian ; Lougheed, Julie C ; Bracarda, Sergio ; Choueiri, Toni K</creator><creatorcontrib>Escudier, Bernard ; Powles, Thomas ; Motzer, Robert J ; Olencki, Thomas ; Arén Frontera, Osvaldo ; Oudard, Stephane ; Rolland, Frederic ; Tomczak, Piotr ; Castellano, Daniel ; Appleman, Leonard J ; Drabkin, Harry ; Vaena, Daniel ; Milwee, Steven ; Youkstetter, Jillian ; Lougheed, Julie C ; Bracarda, Sergio ; Choueiri, Toni K</creatorcontrib><description>Purpose Cabozantinib, an inhibitor of tyrosine kinases including MET, vascular endothelial growth factor receptors, and AXL, increased progression-free survival (PFS), overall survival (OS), and objective response rate (ORR) in patients with advanced renal cell carcinoma (RCC) after previous vascular endothelial growth factor receptor-targeted therapy in the phase III METEOR trial. Because bone metastases are associated with increased morbidity in patients with RCC, bone-related outcomes were analyzed in METEOR. Patients and Methods Six hundred fifty-eight patients were randomly assigned 1:1 to receive 60 mg cabozantinib or 10 mg everolimus. Prespecified subgroup analyses of PFS, OS, and ORR were conducted in patients grouped by baseline bone metastases status per independent radiology committee (IRC). Additional end points included bone scan response per IRC, skeletal-related events, and changes in bone biomarkers. Results For patients with bone metastases at baseline (cabozantinib [n = 77]; everolimus [n = 65]), median PFS was 7.4 months for cabozantinib versus 2.7 months for everolimus (hazard ratio, 0.33 [95% CI, 0.21 to 0.51]). Median OS was also longer with cabozantinib (20.1 months v 12.1 months; hazard ratio, 0.54 [95% CI, 0.34 to 0.84]), and ORR per IRC was higher (17% v 0%). The rate of skeletal-related events was 23% with cabozantinib and 29% with everolimus, and bone scan response per IRC was 20% versus 10%, respectively. PFS, OS, and ORR were also improved with cabozantinib in patients without bone metastases. Changes in bone biomarkers were greater with cabozantinib than with everolimus. The overall safety profiles of cabozantinib and everolimus in patients with bone metastases were consistent with those observed in patients without bone metastases. Conclusion Cabozantinib treatment was associated with improved PFS, OS, and ORR when compared with everolimus treatment in patients with advanced RCC and bone metastases and represents a good treatment option for these patients.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2017.74.7352</identifier><identifier>PMID: 29309249</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject>Anilides - pharmacology ; Anilides - therapeutic use ; Bone Neoplasms - pathology ; Bone Neoplasms - secondary ; Carcinoma, Renal Cell - drug therapy ; Carcinoma, Renal Cell - mortality ; Carcinoma, Renal Cell - pathology ; Humans ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - mortality ; Kidney Neoplasms - pathology ; Male ; Neoplasm Metastasis ; ORIGINAL REPORTS ; Pyridines - pharmacology ; Pyridines - therapeutic use ; Receptor Protein-Tyrosine Kinases - pharmacology ; Receptor Protein-Tyrosine Kinases - therapeutic use ; Standard of Care - standards ; Survival Analysis</subject><ispartof>Journal of clinical oncology, 2018-03, Vol.36 (8), p.765-772</ispartof><rights>2018 by American Society of Clinical Oncology 2018 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-7fe7276b365ec4849e611d288040bccd183c24e40d34522bf8ace596034f90553</citedby><cites>FETCH-LOGICAL-c443t-7fe7276b365ec4849e611d288040bccd183c24e40d34522bf8ace596034f90553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3716,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29309249$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Escudier, Bernard</creatorcontrib><creatorcontrib>Powles, Thomas</creatorcontrib><creatorcontrib>Motzer, Robert J</creatorcontrib><creatorcontrib>Olencki, Thomas</creatorcontrib><creatorcontrib>Arén Frontera, Osvaldo</creatorcontrib><creatorcontrib>Oudard, Stephane</creatorcontrib><creatorcontrib>Rolland, Frederic</creatorcontrib><creatorcontrib>Tomczak, Piotr</creatorcontrib><creatorcontrib>Castellano, Daniel</creatorcontrib><creatorcontrib>Appleman, Leonard J</creatorcontrib><creatorcontrib>Drabkin, Harry</creatorcontrib><creatorcontrib>Vaena, Daniel</creatorcontrib><creatorcontrib>Milwee, Steven</creatorcontrib><creatorcontrib>Youkstetter, Jillian</creatorcontrib><creatorcontrib>Lougheed, Julie C</creatorcontrib><creatorcontrib>Bracarda, Sergio</creatorcontrib><creatorcontrib>Choueiri, Toni K</creatorcontrib><title>Cabozantinib, a New Standard of Care for Patients With Advanced Renal Cell Carcinoma and Bone Metastases? Subgroup Analysis of the METEOR Trial</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Purpose Cabozantinib, an inhibitor of tyrosine kinases including MET, vascular endothelial growth factor receptors, and AXL, increased progression-free survival (PFS), overall survival (OS), and objective response rate (ORR) in patients with advanced renal cell carcinoma (RCC) after previous vascular endothelial growth factor receptor-targeted therapy in the phase III METEOR trial. Because bone metastases are associated with increased morbidity in patients with RCC, bone-related outcomes were analyzed in METEOR. Patients and Methods Six hundred fifty-eight patients were randomly assigned 1:1 to receive 60 mg cabozantinib or 10 mg everolimus. Prespecified subgroup analyses of PFS, OS, and ORR were conducted in patients grouped by baseline bone metastases status per independent radiology committee (IRC). Additional end points included bone scan response per IRC, skeletal-related events, and changes in bone biomarkers. Results For patients with bone metastases at baseline (cabozantinib [n = 77]; everolimus [n = 65]), median PFS was 7.4 months for cabozantinib versus 2.7 months for everolimus (hazard ratio, 0.33 [95% CI, 0.21 to 0.51]). Median OS was also longer with cabozantinib (20.1 months v 12.1 months; hazard ratio, 0.54 [95% CI, 0.34 to 0.84]), and ORR per IRC was higher (17% v 0%). The rate of skeletal-related events was 23% with cabozantinib and 29% with everolimus, and bone scan response per IRC was 20% versus 10%, respectively. PFS, OS, and ORR were also improved with cabozantinib in patients without bone metastases. Changes in bone biomarkers were greater with cabozantinib than with everolimus. The overall safety profiles of cabozantinib and everolimus in patients with bone metastases were consistent with those observed in patients without bone metastases. Conclusion Cabozantinib treatment was associated with improved PFS, OS, and ORR when compared with everolimus treatment in patients with advanced RCC and bone metastases and represents a good treatment option for these patients.</description><subject>Anilides - pharmacology</subject><subject>Anilides - therapeutic use</subject><subject>Bone Neoplasms - pathology</subject><subject>Bone Neoplasms - secondary</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Carcinoma, Renal Cell - mortality</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>Humans</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - mortality</subject><subject>Kidney Neoplasms - pathology</subject><subject>Male</subject><subject>Neoplasm Metastasis</subject><subject>ORIGINAL REPORTS</subject><subject>Pyridines - pharmacology</subject><subject>Pyridines - therapeutic use</subject><subject>Receptor Protein-Tyrosine Kinases - pharmacology</subject><subject>Receptor Protein-Tyrosine Kinases - therapeutic use</subject><subject>Standard of Care - standards</subject><subject>Survival Analysis</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUtv1DAUhS0EokNhzwp5yYIMfsbJBjSNhgIqDGoHwc5ynJuOUcYe7KRV-RP8ZRy1VCBZugufc-7jQ-g5JUvKCHn9sdksGaFqqcRScckeoAWVTBVKSfkQLYjirKAV_36EnqT0gxAqKi4foyNWc1IzUS_Q78a04Zfxo_OufYUN_gzX-GI0vjOxw6HHjYmA-xDxFzM68GPC39y4w6vuyngLHT4HbwbcwDDMUut82Buc7fgkeMCfYDQpP0hv8cXUXsYwHfAqO26SS3P8uMui9Xa9Ocfb6MzwFD3qzZDg2V09Rl_frbfN--Jsc_qhWZ0VVgg-FqoHxVTZ8lKCFZWooaS0Y1VFBGmt7fLSlgkQpONCMtb2lbEg65Jw0ddESn6M3tzmHqZ2D53Nm0Uz6EN0exNvdDBO___j3U5fhitd5haVIDng5V1ADD8nSKPeu2TzGYyHMCVN66qWQlSSZSm5ldoYUorQ37ehRM8cdeaoZ45aCT1zzJYX_453b_gLjv8ByDCZXA</recordid><startdate>20180310</startdate><enddate>20180310</enddate><creator>Escudier, Bernard</creator><creator>Powles, Thomas</creator><creator>Motzer, Robert J</creator><creator>Olencki, Thomas</creator><creator>Arén Frontera, Osvaldo</creator><creator>Oudard, Stephane</creator><creator>Rolland, Frederic</creator><creator>Tomczak, Piotr</creator><creator>Castellano, Daniel</creator><creator>Appleman, Leonard J</creator><creator>Drabkin, Harry</creator><creator>Vaena, Daniel</creator><creator>Milwee, Steven</creator><creator>Youkstetter, Jillian</creator><creator>Lougheed, Julie C</creator><creator>Bracarda, Sergio</creator><creator>Choueiri, Toni K</creator><general>American Society of Clinical Oncology</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>5PM</scope></search><sort><creationdate>20180310</creationdate><title>Cabozantinib, a New Standard of Care for Patients With Advanced Renal Cell Carcinoma and Bone Metastases? 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Subgroup Analysis of the METEOR Trial</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2018-03-10</date><risdate>2018</risdate><volume>36</volume><issue>8</issue><spage>765</spage><epage>772</epage><pages>765-772</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Purpose Cabozantinib, an inhibitor of tyrosine kinases including MET, vascular endothelial growth factor receptors, and AXL, increased progression-free survival (PFS), overall survival (OS), and objective response rate (ORR) in patients with advanced renal cell carcinoma (RCC) after previous vascular endothelial growth factor receptor-targeted therapy in the phase III METEOR trial. Because bone metastases are associated with increased morbidity in patients with RCC, bone-related outcomes were analyzed in METEOR. Patients and Methods Six hundred fifty-eight patients were randomly assigned 1:1 to receive 60 mg cabozantinib or 10 mg everolimus. Prespecified subgroup analyses of PFS, OS, and ORR were conducted in patients grouped by baseline bone metastases status per independent radiology committee (IRC). Additional end points included bone scan response per IRC, skeletal-related events, and changes in bone biomarkers. Results For patients with bone metastases at baseline (cabozantinib [n = 77]; everolimus [n = 65]), median PFS was 7.4 months for cabozantinib versus 2.7 months for everolimus (hazard ratio, 0.33 [95% CI, 0.21 to 0.51]). Median OS was also longer with cabozantinib (20.1 months v 12.1 months; hazard ratio, 0.54 [95% CI, 0.34 to 0.84]), and ORR per IRC was higher (17% v 0%). The rate of skeletal-related events was 23% with cabozantinib and 29% with everolimus, and bone scan response per IRC was 20% versus 10%, respectively. PFS, OS, and ORR were also improved with cabozantinib in patients without bone metastases. Changes in bone biomarkers were greater with cabozantinib than with everolimus. The overall safety profiles of cabozantinib and everolimus in patients with bone metastases were consistent with those observed in patients without bone metastases. Conclusion Cabozantinib treatment was associated with improved PFS, OS, and ORR when compared with everolimus treatment in patients with advanced RCC and bone metastases and represents a good treatment option for these patients.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>29309249</pmid><doi>10.1200/JCO.2017.74.7352</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Anilides - pharmacology
Anilides - therapeutic use
Bone Neoplasms - pathology
Bone Neoplasms - secondary
Carcinoma, Renal Cell - drug therapy
Carcinoma, Renal Cell - mortality
Carcinoma, Renal Cell - pathology
Humans
Kidney Neoplasms - drug therapy
Kidney Neoplasms - mortality
Kidney Neoplasms - pathology
Male
Neoplasm Metastasis
ORIGINAL REPORTS
Pyridines - pharmacology
Pyridines - therapeutic use
Receptor Protein-Tyrosine Kinases - pharmacology
Receptor Protein-Tyrosine Kinases - therapeutic use
Standard of Care - standards
Survival Analysis
title Cabozantinib, a New Standard of Care for Patients With Advanced Renal Cell Carcinoma and Bone Metastases? Subgroup Analysis of the METEOR Trial
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