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The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma

BACKGROUND: The outcome of patients who progress on front-line immune-based combination regimens (IC) including immune checkpoint inhibitors (CPI) and receive subsequent systemic therapy is unknown. METHODS: Retrospective analysis of consecutive patients with clear-cell mRCC who progressed on one of...

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Autores principales: Barata, Pedro Coelho, De Liano, Alfonso Gomez, Mendiratta, Prateek, Crolley, Valerie, Szabados, Bernadett, Morrison, Laura, Wood, Laura, Allman, Kimberly, Tyler, Allison, Martin, Allison, Gilligan, Timothy, Grivas, Petros, Ornstein, Moshe, Garcia, Jorge A., Powles, Thomas, Rini, Brian I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048048/
https://www.ncbi.nlm.nih.gov/pubmed/29795307
http://dx.doi.org/10.1038/s41416-018-0104-z
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author Barata, Pedro Coelho
De Liano, Alfonso Gomez
Mendiratta, Prateek
Crolley, Valerie
Szabados, Bernadett
Morrison, Laura
Wood, Laura
Allman, Kimberly
Tyler, Allison
Martin, Allison
Gilligan, Timothy
Grivas, Petros
Ornstein, Moshe
Garcia, Jorge A.
Powles, Thomas
Rini, Brian I.
author_facet Barata, Pedro Coelho
De Liano, Alfonso Gomez
Mendiratta, Prateek
Crolley, Valerie
Szabados, Bernadett
Morrison, Laura
Wood, Laura
Allman, Kimberly
Tyler, Allison
Martin, Allison
Gilligan, Timothy
Grivas, Petros
Ornstein, Moshe
Garcia, Jorge A.
Powles, Thomas
Rini, Brian I.
author_sort Barata, Pedro Coelho
collection PubMed
description BACKGROUND: The outcome of patients who progress on front-line immune-based combination regimens (IC) including immune checkpoint inhibitors (CPI) and receive subsequent systemic therapy is unknown. METHODS: Retrospective analysis of consecutive patients with clear-cell mRCC who progressed on one of seven clinical trials investigating an IC and received ≥1 line of subsequent VEGFR TKI therapy. RESULTS: Thirty-three patients [median age 57 (37–77), 85% male, 73% ECOG 0] were included. For evaluable patients (N = 28), the best response to first subsequent therapy was 29% partial response, 54% stable disease, and 18% progressive disease. The median PFS (mPFS) for first subsequent therapy was 6.4 months (95% CI, 4.4–8.4); no difference in mPFS by prior type of IC (VEGFR TKI-CPI vs. CPI-CPI) was noted (p = 0.310). Significant AEs were observed in 30% of patients, more frequently transaminitis (9%). CONCLUSIONS: VEGFR TKIs have clinical activity in mRCC refractory to IC therapy, possibly impacted by the mechanism of prior combination therapy.
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spelling pubmed-60480482019-07-17 The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma Barata, Pedro Coelho De Liano, Alfonso Gomez Mendiratta, Prateek Crolley, Valerie Szabados, Bernadett Morrison, Laura Wood, Laura Allman, Kimberly Tyler, Allison Martin, Allison Gilligan, Timothy Grivas, Petros Ornstein, Moshe Garcia, Jorge A. Powles, Thomas Rini, Brian I. Br J Cancer Article BACKGROUND: The outcome of patients who progress on front-line immune-based combination regimens (IC) including immune checkpoint inhibitors (CPI) and receive subsequent systemic therapy is unknown. METHODS: Retrospective analysis of consecutive patients with clear-cell mRCC who progressed on one of seven clinical trials investigating an IC and received ≥1 line of subsequent VEGFR TKI therapy. RESULTS: Thirty-three patients [median age 57 (37–77), 85% male, 73% ECOG 0] were included. For evaluable patients (N = 28), the best response to first subsequent therapy was 29% partial response, 54% stable disease, and 18% progressive disease. The median PFS (mPFS) for first subsequent therapy was 6.4 months (95% CI, 4.4–8.4); no difference in mPFS by prior type of IC (VEGFR TKI-CPI vs. CPI-CPI) was noted (p = 0.310). Significant AEs were observed in 30% of patients, more frequently transaminitis (9%). CONCLUSIONS: VEGFR TKIs have clinical activity in mRCC refractory to IC therapy, possibly impacted by the mechanism of prior combination therapy. Nature Publishing Group UK 2018-05-24 2018-07-17 /pmc/articles/PMC6048048/ /pubmed/29795307 http://dx.doi.org/10.1038/s41416-018-0104-z Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by/4.0/Note: This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Barata, Pedro Coelho
De Liano, Alfonso Gomez
Mendiratta, Prateek
Crolley, Valerie
Szabados, Bernadett
Morrison, Laura
Wood, Laura
Allman, Kimberly
Tyler, Allison
Martin, Allison
Gilligan, Timothy
Grivas, Petros
Ornstein, Moshe
Garcia, Jorge A.
Powles, Thomas
Rini, Brian I.
The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma
title The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma
title_full The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma
title_fullStr The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma
title_full_unstemmed The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma
title_short The efficacy of VEGFR TKI therapy after progression on immune combination therapy in metastatic renal cell carcinoma
title_sort efficacy of vegfr tki therapy after progression on immune combination therapy in metastatic renal cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048048/
https://www.ncbi.nlm.nih.gov/pubmed/29795307
http://dx.doi.org/10.1038/s41416-018-0104-z
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