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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6048048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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