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
Hauptverfasser: 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.
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container_issue
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container_title European journal of cancer (1990)
container_volume 114
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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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><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 &amp; 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. 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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 &amp; 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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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identifier ISSN: 0959-8049
ispartof European journal of cancer (1990), 2019-06, Vol.114, p.67-75
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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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