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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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. |
doi_str_mv | 10.1200/JCO.2017.74.7352 |
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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? Subgroup Analysis of the METEOR Trial</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-7fe7276b365ec4849e611d288040bccd183c24e40d34522bf8ace596034f90553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anilides - pharmacology</topic><topic>Anilides - therapeutic use</topic><topic>Bone Neoplasms - pathology</topic><topic>Bone Neoplasms - secondary</topic><topic>Carcinoma, Renal Cell - drug therapy</topic><topic>Carcinoma, Renal Cell - mortality</topic><topic>Carcinoma, Renal Cell - pathology</topic><topic>Humans</topic><topic>Kidney Neoplasms - drug therapy</topic><topic>Kidney Neoplasms - mortality</topic><topic>Kidney Neoplasms - pathology</topic><topic>Male</topic><topic>Neoplasm Metastasis</topic><topic>ORIGINAL REPORTS</topic><topic>Pyridines - pharmacology</topic><topic>Pyridines - therapeutic use</topic><topic>Receptor Protein-Tyrosine Kinases - pharmacology</topic><topic>Receptor Protein-Tyrosine Kinases - therapeutic use</topic><topic>Standard of Care - standards</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Escudier, Bernard</au><au>Powles, Thomas</au><au>Motzer, Robert J</au><au>Olencki, Thomas</au><au>Arén Frontera, Osvaldo</au><au>Oudard, Stephane</au><au>Rolland, Frederic</au><au>Tomczak, Piotr</au><au>Castellano, Daniel</au><au>Appleman, Leonard J</au><au>Drabkin, Harry</au><au>Vaena, Daniel</au><au>Milwee, Steven</au><au>Youkstetter, Jillian</au><au>Lougheed, Julie C</au><au>Bracarda, Sergio</au><au>Choueiri, Toni K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cabozantinib, a New Standard of Care for Patients With Advanced Renal Cell Carcinoma and Bone Metastases? 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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