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Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study
Gemcitabine has shown clinical activity against angiosarcoma in small series, alone, or combined with taxanes. We aimed to evaluate its activity as a single‐agent in a larger series of patients with advanced angiosarcoma. We retrospectively reviewed the electronic medical records of consecutive adul...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939156/ https://www.ncbi.nlm.nih.gov/pubmed/35971325 http://dx.doi.org/10.1002/cam4.5147 |
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author | Watson, Sarah Verret, Benjamin Ropert, Stanislas Adam, Julien Bahleda, Rastislav Briand, Sylvain Cavalcanti, Andrea Chamseddine, Ali N. Court, Charles Fadel, Elie Faron, Matthieu Haddag‐Miliani, Leila Henon, Clémence Pechoux, Cécile Le Levy, Antonin Mercier, Olaf Ngo, Carine Honoré, Charles Cesne, Axel Le Mir, Olivier |
author_facet | Watson, Sarah Verret, Benjamin Ropert, Stanislas Adam, Julien Bahleda, Rastislav Briand, Sylvain Cavalcanti, Andrea Chamseddine, Ali N. Court, Charles Fadel, Elie Faron, Matthieu Haddag‐Miliani, Leila Henon, Clémence Pechoux, Cécile Le Levy, Antonin Mercier, Olaf Ngo, Carine Honoré, Charles Cesne, Axel Le Mir, Olivier |
author_sort | Watson, Sarah |
collection | PubMed |
description | Gemcitabine has shown clinical activity against angiosarcoma in small series, alone, or combined with taxanes. We aimed to evaluate its activity as a single‐agent in a larger series of patients with advanced angiosarcoma. We retrospectively reviewed the electronic medical records of consecutive adult patients with advanced angiosarcoma treated with single‐agent gemcitabine at our institutions from January 2010 to January 2021. Response was evaluated according to RECIST 1.1, and toxicity was graded according to NCI‐CTC v5.0. 42 patients were identified. 38 patients (90%) had received prior anthracyclines and weekly paclitaxel, and 9 (21%) had received pazopanib. The best tumor response was partial response (PR) in 16 patients (38%), or stable disease (10 patients, 24%). All 8 patients with cardiac angiosarcoma experienced a PR. Median PFS was 5.4 months (95%CI: 3.1–6.5), and median OS was 9.9 months (95%CI: 6.6–13.4). Single‐agent gemcitabine has clinically meaningful activity in advanced, heavily pre‐treated angiosarcoma. |
format | Online Article Text |
id | pubmed-9939156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99391562023-02-20 Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study Watson, Sarah Verret, Benjamin Ropert, Stanislas Adam, Julien Bahleda, Rastislav Briand, Sylvain Cavalcanti, Andrea Chamseddine, Ali N. Court, Charles Fadel, Elie Faron, Matthieu Haddag‐Miliani, Leila Henon, Clémence Pechoux, Cécile Le Levy, Antonin Mercier, Olaf Ngo, Carine Honoré, Charles Cesne, Axel Le Mir, Olivier Cancer Med BRIEF COMMUNICATION Gemcitabine has shown clinical activity against angiosarcoma in small series, alone, or combined with taxanes. We aimed to evaluate its activity as a single‐agent in a larger series of patients with advanced angiosarcoma. We retrospectively reviewed the electronic medical records of consecutive adult patients with advanced angiosarcoma treated with single‐agent gemcitabine at our institutions from January 2010 to January 2021. Response was evaluated according to RECIST 1.1, and toxicity was graded according to NCI‐CTC v5.0. 42 patients were identified. 38 patients (90%) had received prior anthracyclines and weekly paclitaxel, and 9 (21%) had received pazopanib. The best tumor response was partial response (PR) in 16 patients (38%), or stable disease (10 patients, 24%). All 8 patients with cardiac angiosarcoma experienced a PR. Median PFS was 5.4 months (95%CI: 3.1–6.5), and median OS was 9.9 months (95%CI: 6.6–13.4). Single‐agent gemcitabine has clinically meaningful activity in advanced, heavily pre‐treated angiosarcoma. John Wiley and Sons Inc. 2022-08-15 /pmc/articles/PMC9939156/ /pubmed/35971325 http://dx.doi.org/10.1002/cam4.5147 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | BRIEF COMMUNICATION Watson, Sarah Verret, Benjamin Ropert, Stanislas Adam, Julien Bahleda, Rastislav Briand, Sylvain Cavalcanti, Andrea Chamseddine, Ali N. Court, Charles Fadel, Elie Faron, Matthieu Haddag‐Miliani, Leila Henon, Clémence Pechoux, Cécile Le Levy, Antonin Mercier, Olaf Ngo, Carine Honoré, Charles Cesne, Axel Le Mir, Olivier Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study |
title | Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study |
title_full | Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study |
title_fullStr | Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study |
title_full_unstemmed | Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study |
title_short | Single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: A multicenter, retrospective study |
title_sort | single‐agent gemcitabine in patients with advanced, pre‐treated angiosarcoma: a multicenter, retrospective study |
topic | BRIEF COMMUNICATION |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939156/ https://www.ncbi.nlm.nih.gov/pubmed/35971325 http://dx.doi.org/10.1002/cam4.5147 |
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