Outcomes of patients with metastatic clear-cell renal cell carcinoma treated with second-line VEGFR-TKI after first-line immune checkpoint inhibitors
Immune checkpoint inhibitors (ICIs) are being increasingly utilised in the front-line (1L) setting of metastatic clear-cell renal cell carcinoma (mccRCC). Limited data exist on responses and survival on second-line (2L) vascular endothelial growth factor–receptor tyrosine kinase inhibitor (VEGFR-TKI...
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Veröffentlicht in: | European journal of cancer (1990) 2019-06, Vol.114, p.67-75 |
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creator | Shah, A.Y. Kotecha, R.R. Lemke, E.A. Chandramohan, A. Chaim, J.L. Msaouel, P. Xiao, L. Gao, J. Campbell, M.T. Zurita, A.J. Wang, J. Corn, P.G. Jonasch, E. Motzer, R.J. Sharma, P. Voss, M.H. Tannir, N.M. |
description | Immune checkpoint inhibitors (ICIs) are being increasingly utilised in the front-line (1L) setting of metastatic clear-cell renal cell carcinoma (mccRCC). Limited data exist on responses and survival on second-line (2L) vascular endothelial growth factor–receptor tyrosine kinase inhibitor (VEGFR-TKI) therapy after 1L ICI therapy.
This is a retrospective study of mccRCC patients treated with 2L VEGFR-TKI after progressive disease (PD) with 1L ICI. Patients were treated at MD Anderson Cancer Center or Memorial Sloan Kettering Cancer Center between December 2015 and February 2018. Objective response was assessed by blinded radiologists' review using Response Evaluation Criteria in Solid Tumours v1.1. Descriptive statistics and Kaplan–Meier method were used.
Seventy patients were included in the analysis. Median age at mccRCC diagnosis was 59 years; 8 patients (11%) had international metastatic database consortium favourable-risk disease, 48 (69%) had intermediate-risk disease and 14 (20%) had poor-risk disease. As 1L therapy, 12 patients (17%) received anti–programmed death ligand-1 (PD-(L)1) monotherapy with nivolumab or atezolizumab, 33 (47%) received nivolumab plus ipilimumab and 25 (36%) received combination anti–PD-(L)1 plus bevacizumab. 2L TKI therapies included pazopanib, sunitinib, axitinib and cabozantinib. On 2L TKI therapy, one patient (1.5%) achieved a complete response, 27 patients (39.7%) a partial response and 36 patients (52.9%) stable disease. Median progression-free survival (mPFS) was 13.2 months (95% confidence interval: 10.1, NA). Forty-five percent of subjects required a dose reduction, and twenty-seven percent of patients discontinued treatment because of toxicity.
In this retrospective study of patients with mccRCC receiving 2L TKI monotherapy after 1L ICI, we observed 2L antitumour activity and tolerance comparable to historical data for 1L TKI.
•Immunotherapy (ICI) is moving to front-line treatment in metastatic RCC for intermediate- and poor-risk patients.•Little data exists on responses to second-line (2L) TKI after front-line (1L) ICI.•Our data showed that 2L VEGFR-TKI have ORR 41% and DCR 94% after 1L ICI–containing regimen.•Median PFS on 2L VEGFR-TKI after 1L ICI in metastatic clear-cell RCC was 13.2 mo.•Safety and tolerability of 2L VEGFR-TKI after 1L ICI is typical of class effects. |
doi_str_mv | 10.1016/j.ejca.2019.04.003 |
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This is a retrospective study of mccRCC patients treated with 2L VEGFR-TKI after progressive disease (PD) with 1L ICI. Patients were treated at MD Anderson Cancer Center or Memorial Sloan Kettering Cancer Center between December 2015 and February 2018. Objective response was assessed by blinded radiologists' review using Response Evaluation Criteria in Solid Tumours v1.1. Descriptive statistics and Kaplan–Meier method were used.
Seventy patients were included in the analysis. Median age at mccRCC diagnosis was 59 years; 8 patients (11%) had international metastatic database consortium favourable-risk disease, 48 (69%) had intermediate-risk disease and 14 (20%) had poor-risk disease. As 1L therapy, 12 patients (17%) received anti–programmed death ligand-1 (PD-(L)1) monotherapy with nivolumab or atezolizumab, 33 (47%) received nivolumab plus ipilimumab and 25 (36%) received combination anti–PD-(L)1 plus bevacizumab. 2L TKI therapies included pazopanib, sunitinib, axitinib and cabozantinib. On 2L TKI therapy, one patient (1.5%) achieved a complete response, 27 patients (39.7%) a partial response and 36 patients (52.9%) stable disease. Median progression-free survival (mPFS) was 13.2 months (95% confidence interval: 10.1, NA). Forty-five percent of subjects required a dose reduction, and twenty-seven percent of patients discontinued treatment because of toxicity.
In this retrospective study of patients with mccRCC receiving 2L TKI monotherapy after 1L ICI, we observed 2L antitumour activity and tolerance comparable to historical data for 1L TKI.
•Immunotherapy (ICI) is moving to front-line treatment in metastatic RCC for intermediate- and poor-risk patients.•Little data exists on responses to second-line (2L) TKI after front-line (1L) ICI.•Our data showed that 2L VEGFR-TKI have ORR 41% and DCR 94% after 1L ICI–containing regimen.•Median PFS on 2L VEGFR-TKI after 1L ICI in metastatic clear-cell RCC was 13.2 mo.•Safety and tolerability of 2L VEGFR-TKI after 1L ICI is typical of class effects.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2019.04.003</identifier><identifier>PMID: 31075726</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Anticancer properties ; Apoptosis ; Bevacizumab ; Cancer ; Carcinoma, Renal Cell - drug therapy ; Carcinoma, Renal Cell - mortality ; Carcinoma, Renal Cell - pathology ; ccRCC ; Clear cell renal cell carcinoma ; Clear cell-type renal cell carcinoma ; Confidence intervals ; Consortia ; Enzyme inhibitors ; Female ; Growth factors ; Health risks ; Humans ; Immune checkpoint inhibitor ; Immune checkpoint inhibitors ; Immunological tolerance ; Immunotherapy ; Immunotherapy - methods ; Immunotherapy refractory ; Inhibitors ; Kidney cancer ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - mortality ; Kidney Neoplasms - pathology ; Kinases ; Male ; Median (statistics) ; Metastases ; Metastasis ; Metastatic kidney cancer ; Middle Aged ; Monoclonal antibodies ; Protein Kinase Inhibitors - pharmacology ; Protein Kinase Inhibitors - therapeutic use ; Protein-tyrosine kinase receptors ; RCC ; Renal cell carcinoma ; Retrospective Studies ; Risk ; Solid tumors ; Statistical analysis ; Survival ; Survival Analysis ; Targeted cancer therapy ; Therapy ; Therapy sequence ; Toxicity ; Treatment Outcome ; Tumors ; Tyrosine ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - antagonists & inhibitors ; Vascular endothelial growth factor receptors ; VEGFR-TKI</subject><ispartof>European journal of cancer (1990), 2019-06, Vol.114, p.67-75</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Jun 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-d4e9bfed457c717e4df3506aeaea37c942d9024011c9290bc59287e1ec824db03</citedby><cites>FETCH-LOGICAL-c483t-d4e9bfed457c717e4df3506aeaea37c942d9024011c9290bc59287e1ec824db03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0959804919302369$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31075726$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shah, A.Y.</creatorcontrib><creatorcontrib>Kotecha, R.R.</creatorcontrib><creatorcontrib>Lemke, E.A.</creatorcontrib><creatorcontrib>Chandramohan, A.</creatorcontrib><creatorcontrib>Chaim, J.L.</creatorcontrib><creatorcontrib>Msaouel, P.</creatorcontrib><creatorcontrib>Xiao, L.</creatorcontrib><creatorcontrib>Gao, J.</creatorcontrib><creatorcontrib>Campbell, M.T.</creatorcontrib><creatorcontrib>Zurita, A.J.</creatorcontrib><creatorcontrib>Wang, J.</creatorcontrib><creatorcontrib>Corn, P.G.</creatorcontrib><creatorcontrib>Jonasch, E.</creatorcontrib><creatorcontrib>Motzer, R.J.</creatorcontrib><creatorcontrib>Sharma, P.</creatorcontrib><creatorcontrib>Voss, M.H.</creatorcontrib><creatorcontrib>Tannir, N.M.</creatorcontrib><title>Outcomes of patients with metastatic clear-cell renal cell carcinoma treated with second-line VEGFR-TKI after first-line immune checkpoint inhibitors</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Immune checkpoint inhibitors (ICIs) are being increasingly utilised in the front-line (1L) setting of metastatic clear-cell renal cell carcinoma (mccRCC). Limited data exist on responses and survival on second-line (2L) vascular endothelial growth factor–receptor tyrosine kinase inhibitor (VEGFR-TKI) therapy after 1L ICI therapy.
This is a retrospective study of mccRCC patients treated with 2L VEGFR-TKI after progressive disease (PD) with 1L ICI. Patients were treated at MD Anderson Cancer Center or Memorial Sloan Kettering Cancer Center between December 2015 and February 2018. Objective response was assessed by blinded radiologists' review using Response Evaluation Criteria in Solid Tumours v1.1. Descriptive statistics and Kaplan–Meier method were used.
Seventy patients were included in the analysis. Median age at mccRCC diagnosis was 59 years; 8 patients (11%) had international metastatic database consortium favourable-risk disease, 48 (69%) had intermediate-risk disease and 14 (20%) had poor-risk disease. As 1L therapy, 12 patients (17%) received anti–programmed death ligand-1 (PD-(L)1) monotherapy with nivolumab or atezolizumab, 33 (47%) received nivolumab plus ipilimumab and 25 (36%) received combination anti–PD-(L)1 plus bevacizumab. 2L TKI therapies included pazopanib, sunitinib, axitinib and cabozantinib. On 2L TKI therapy, one patient (1.5%) achieved a complete response, 27 patients (39.7%) a partial response and 36 patients (52.9%) stable disease. Median progression-free survival (mPFS) was 13.2 months (95% confidence interval: 10.1, NA). Forty-five percent of subjects required a dose reduction, and twenty-seven percent of patients discontinued treatment because of toxicity.
In this retrospective study of patients with mccRCC receiving 2L TKI monotherapy after 1L ICI, we observed 2L antitumour activity and tolerance comparable to historical data for 1L TKI.
•Immunotherapy (ICI) is moving to front-line treatment in metastatic RCC for intermediate- and poor-risk patients.•Little data exists on responses to second-line (2L) TKI after front-line (1L) ICI.•Our data showed that 2L VEGFR-TKI have ORR 41% and DCR 94% after 1L ICI–containing regimen.•Median PFS on 2L VEGFR-TKI after 1L ICI in metastatic clear-cell RCC was 13.2 mo.•Safety and tolerability of 2L VEGFR-TKI after 1L ICI is typical of class effects.</description><subject>Anticancer properties</subject><subject>Apoptosis</subject><subject>Bevacizumab</subject><subject>Cancer</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Carcinoma, Renal Cell - mortality</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>ccRCC</subject><subject>Clear cell renal cell carcinoma</subject><subject>Clear cell-type renal cell carcinoma</subject><subject>Confidence intervals</subject><subject>Consortia</subject><subject>Enzyme inhibitors</subject><subject>Female</subject><subject>Growth factors</subject><subject>Health risks</subject><subject>Humans</subject><subject>Immune checkpoint inhibitor</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunological tolerance</subject><subject>Immunotherapy</subject><subject>Immunotherapy - methods</subject><subject>Immunotherapy refractory</subject><subject>Inhibitors</subject><subject>Kidney cancer</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - mortality</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kinases</subject><subject>Male</subject><subject>Median (statistics)</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Metastatic kidney cancer</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Protein Kinase Inhibitors - pharmacology</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Protein-tyrosine kinase receptors</subject><subject>RCC</subject><subject>Renal cell carcinoma</subject><subject>Retrospective Studies</subject><subject>Risk</subject><subject>Solid tumors</subject><subject>Statistical analysis</subject><subject>Survival</subject><subject>Survival Analysis</subject><subject>Targeted cancer therapy</subject><subject>Therapy</subject><subject>Therapy sequence</subject><subject>Toxicity</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tyrosine</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - antagonists & inhibitors</subject><subject>Vascular endothelial growth factor receptors</subject><subject>VEGFR-TKI</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UcFu1DAQjRCILoUf4IAsceGSZew461hCSFXVlopKlVDhanknE9ZLEi-2U8SH8L84pFTAAfkwlue9N573iuI5hzUHvnm9X9Me7VoA12uQa4DqQbHijdIlNLV4WKxA17psQOqj4kmMewBQjYTHxVHFQdVKbFbFj-spoR8oMt-xg02OxhTZN5d2bKBkY8pPyLAnG0qkvmeBRtuzX1e0Ad3oB8tSIJuoXXiR0I9t2buR2Kezi_MP5c37S2a7RIF1LsS0tNwwTLngjvDLwbsxMTfu3NYlH-LT4lFn-0jP7upx8fH87Ob0XXl1fXF5enJVomyqVLaS9LajVtYKFVck266qYWMpn0qhlqLVICRwjlpo2GKtRaOIEzZCtluojou3i-5h2g7UYl4-2N4cghts-G68debvzuh25rO_NaqulNQ8C7y6Ewj-60QxmcHF2Rw7kp-iEaLiGhou5lkv_4Hu_RSymTNKalUJ0DqjxILC4GMM1N1_hoOZUzd7M6du5tQNSJNTz6QXf65xT_kdcwa8WQCUzbx1FEzEnDRS6wJhMq13_9P_CQa2wT0</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>Shah, A.Y.</creator><creator>Kotecha, R.R.</creator><creator>Lemke, E.A.</creator><creator>Chandramohan, A.</creator><creator>Chaim, J.L.</creator><creator>Msaouel, P.</creator><creator>Xiao, L.</creator><creator>Gao, J.</creator><creator>Campbell, M.T.</creator><creator>Zurita, A.J.</creator><creator>Wang, J.</creator><creator>Corn, P.G.</creator><creator>Jonasch, E.</creator><creator>Motzer, R.J.</creator><creator>Sharma, P.</creator><creator>Voss, M.H.</creator><creator>Tannir, N.M.</creator><general>Elsevier Ltd</general><general>Elsevier Science Ltd</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>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190601</creationdate><title>Outcomes of patients with metastatic clear-cell renal cell carcinoma treated with second-line VEGFR-TKI after first-line immune checkpoint inhibitors</title><author>Shah, A.Y. ; Kotecha, R.R. ; Lemke, E.A. ; Chandramohan, A. ; Chaim, J.L. ; Msaouel, P. ; Xiao, L. ; Gao, J. ; Campbell, M.T. ; Zurita, A.J. ; Wang, J. ; Corn, P.G. ; Jonasch, E. ; Motzer, R.J. ; Sharma, P. ; Voss, M.H. ; Tannir, N.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-d4e9bfed457c717e4df3506aeaea37c942d9024011c9290bc59287e1ec824db03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anticancer properties</topic><topic>Apoptosis</topic><topic>Bevacizumab</topic><topic>Cancer</topic><topic>Carcinoma, Renal Cell - drug therapy</topic><topic>Carcinoma, Renal Cell - mortality</topic><topic>Carcinoma, Renal Cell - pathology</topic><topic>ccRCC</topic><topic>Clear cell renal cell carcinoma</topic><topic>Clear cell-type renal cell carcinoma</topic><topic>Confidence intervals</topic><topic>Consortia</topic><topic>Enzyme inhibitors</topic><topic>Female</topic><topic>Growth factors</topic><topic>Health risks</topic><topic>Humans</topic><topic>Immune checkpoint inhibitor</topic><topic>Immune checkpoint inhibitors</topic><topic>Immunological tolerance</topic><topic>Immunotherapy</topic><topic>Immunotherapy - methods</topic><topic>Immunotherapy refractory</topic><topic>Inhibitors</topic><topic>Kidney cancer</topic><topic>Kidney Neoplasms - drug therapy</topic><topic>Kidney Neoplasms - mortality</topic><topic>Kidney Neoplasms - pathology</topic><topic>Kinases</topic><topic>Male</topic><topic>Median (statistics)</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Metastatic kidney cancer</topic><topic>Middle Aged</topic><topic>Monoclonal antibodies</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Protein-tyrosine kinase receptors</topic><topic>RCC</topic><topic>Renal cell carcinoma</topic><topic>Retrospective Studies</topic><topic>Risk</topic><topic>Solid tumors</topic><topic>Statistical analysis</topic><topic>Survival</topic><topic>Survival Analysis</topic><topic>Targeted cancer therapy</topic><topic>Therapy</topic><topic>Therapy sequence</topic><topic>Toxicity</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tyrosine</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - antagonists & inhibitors</topic><topic>Vascular endothelial growth factor receptors</topic><topic>VEGFR-TKI</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shah, A.Y.</creatorcontrib><creatorcontrib>Kotecha, R.R.</creatorcontrib><creatorcontrib>Lemke, E.A.</creatorcontrib><creatorcontrib>Chandramohan, A.</creatorcontrib><creatorcontrib>Chaim, J.L.</creatorcontrib><creatorcontrib>Msaouel, P.</creatorcontrib><creatorcontrib>Xiao, L.</creatorcontrib><creatorcontrib>Gao, J.</creatorcontrib><creatorcontrib>Campbell, M.T.</creatorcontrib><creatorcontrib>Zurita, A.J.</creatorcontrib><creatorcontrib>Wang, J.</creatorcontrib><creatorcontrib>Corn, P.G.</creatorcontrib><creatorcontrib>Jonasch, E.</creatorcontrib><creatorcontrib>Motzer, R.J.</creatorcontrib><creatorcontrib>Sharma, P.</creatorcontrib><creatorcontrib>Voss, M.H.</creatorcontrib><creatorcontrib>Tannir, N.M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shah, A.Y.</au><au>Kotecha, R.R.</au><au>Lemke, E.A.</au><au>Chandramohan, A.</au><au>Chaim, J.L.</au><au>Msaouel, P.</au><au>Xiao, L.</au><au>Gao, J.</au><au>Campbell, M.T.</au><au>Zurita, A.J.</au><au>Wang, J.</au><au>Corn, P.G.</au><au>Jonasch, E.</au><au>Motzer, R.J.</au><au>Sharma, P.</au><au>Voss, M.H.</au><au>Tannir, N.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcomes of patients with metastatic clear-cell renal cell carcinoma treated with second-line VEGFR-TKI after first-line immune checkpoint inhibitors</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>114</volume><spage>67</spage><epage>75</epage><pages>67-75</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Immune checkpoint inhibitors (ICIs) are being increasingly utilised in the front-line (1L) setting of metastatic clear-cell renal cell carcinoma (mccRCC). Limited data exist on responses and survival on second-line (2L) vascular endothelial growth factor–receptor tyrosine kinase inhibitor (VEGFR-TKI) therapy after 1L ICI therapy.
This is a retrospective study of mccRCC patients treated with 2L VEGFR-TKI after progressive disease (PD) with 1L ICI. Patients were treated at MD Anderson Cancer Center or Memorial Sloan Kettering Cancer Center between December 2015 and February 2018. Objective response was assessed by blinded radiologists' review using Response Evaluation Criteria in Solid Tumours v1.1. Descriptive statistics and Kaplan–Meier method were used.
Seventy patients were included in the analysis. Median age at mccRCC diagnosis was 59 years; 8 patients (11%) had international metastatic database consortium favourable-risk disease, 48 (69%) had intermediate-risk disease and 14 (20%) had poor-risk disease. As 1L therapy, 12 patients (17%) received anti–programmed death ligand-1 (PD-(L)1) monotherapy with nivolumab or atezolizumab, 33 (47%) received nivolumab plus ipilimumab and 25 (36%) received combination anti–PD-(L)1 plus bevacizumab. 2L TKI therapies included pazopanib, sunitinib, axitinib and cabozantinib. On 2L TKI therapy, one patient (1.5%) achieved a complete response, 27 patients (39.7%) a partial response and 36 patients (52.9%) stable disease. Median progression-free survival (mPFS) was 13.2 months (95% confidence interval: 10.1, NA). Forty-five percent of subjects required a dose reduction, and twenty-seven percent of patients discontinued treatment because of toxicity.
In this retrospective study of patients with mccRCC receiving 2L TKI monotherapy after 1L ICI, we observed 2L antitumour activity and tolerance comparable to historical data for 1L TKI.
•Immunotherapy (ICI) is moving to front-line treatment in metastatic RCC for intermediate- and poor-risk patients.•Little data exists on responses to second-line (2L) TKI after front-line (1L) ICI.•Our data showed that 2L VEGFR-TKI have ORR 41% and DCR 94% after 1L ICI–containing regimen.•Median PFS on 2L VEGFR-TKI after 1L ICI in metastatic clear-cell RCC was 13.2 mo.•Safety and tolerability of 2L VEGFR-TKI after 1L ICI is typical of class effects.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31075726</pmid><doi>10.1016/j.ejca.2019.04.003</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7537491 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Anticancer properties Apoptosis Bevacizumab Cancer Carcinoma, Renal Cell - drug therapy Carcinoma, Renal Cell - mortality Carcinoma, Renal Cell - pathology ccRCC Clear cell renal cell carcinoma Clear cell-type renal cell carcinoma Confidence intervals Consortia Enzyme inhibitors Female Growth factors Health risks Humans Immune checkpoint inhibitor Immune checkpoint inhibitors Immunological tolerance Immunotherapy Immunotherapy - methods Immunotherapy refractory Inhibitors Kidney cancer Kidney Neoplasms - drug therapy Kidney Neoplasms - mortality Kidney Neoplasms - pathology Kinases Male Median (statistics) Metastases Metastasis Metastatic kidney cancer Middle Aged Monoclonal antibodies Protein Kinase Inhibitors - pharmacology Protein Kinase Inhibitors - therapeutic use Protein-tyrosine kinase receptors RCC Renal cell carcinoma Retrospective Studies Risk Solid tumors Statistical analysis Survival Survival Analysis Targeted cancer therapy Therapy Therapy sequence Toxicity Treatment Outcome Tumors Tyrosine Vascular endothelial growth factor Vascular Endothelial Growth Factor A - antagonists & inhibitors Vascular endothelial growth factor receptors VEGFR-TKI |
title | Outcomes of patients with metastatic clear-cell renal cell carcinoma treated with second-line VEGFR-TKI after first-line immune checkpoint inhibitors |
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