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Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma

BACKGROUND: Cytotoxic chemotherapy (CC) is currently used in metastatic melanoma after patients have developed resistance to immune checkpoint inhibitors (ICI) and/or Mitogen‐Activated Protein Kinase inhibitors (MAPKi). We sought to evaluate if a previous treatment by ICI or MAPKi influences clinica...

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Autores principales: Mangin, Marie‐Alix, Boespflug, Amélie, Maucort Boulch, Delphine, Vacheron, Charles‐Hervé, Carpentier, Isabelle, Thomas, Luc, Dalle, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124115/
https://www.ncbi.nlm.nih.gov/pubmed/33932099
http://dx.doi.org/10.1002/cam4.3760
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author Mangin, Marie‐Alix
Boespflug, Amélie
Maucort Boulch, Delphine
Vacheron, Charles‐Hervé
Carpentier, Isabelle
Thomas, Luc
Dalle, Stéphane
author_facet Mangin, Marie‐Alix
Boespflug, Amélie
Maucort Boulch, Delphine
Vacheron, Charles‐Hervé
Carpentier, Isabelle
Thomas, Luc
Dalle, Stéphane
author_sort Mangin, Marie‐Alix
collection PubMed
description BACKGROUND: Cytotoxic chemotherapy (CC) is currently used in metastatic melanoma after patients have developed resistance to immune checkpoint inhibitors (ICI) and/or Mitogen‐Activated Protein Kinase inhibitors (MAPKi). We sought to evaluate if a previous treatment by ICI or MAPKi influences clinical outcomes in patients treated by CC in metastatic melanoma. METHODS: Eighty‐eight patients with a metastatic melanoma, treated by CC after a previous treatment by ICI or MAPKi between January 2009 and October 2019, were retrospectively analyzed. Progression‐Free‐Survival (PFS), Overall Survival (OS), Overall Response Rate (ORR), and Disease Control Rate (DCR) were evaluated in patients treated by CC according to their prior treatment by ICI or MAPKi. RESULTS: Patients treated by CC after ICI tended to have a better median PFS (2.81 months (2.39–5.30) versus 2.40 months (0.91–2.75), p = 0.023), median OS (6.03 months (3.54–11.54) versus 4.44 months (1.54–8.59), p = 0.27), DCR (26.0% vs. 10.5%, p = 0.121) and ORR (22.0% vs. 7.9% p = 0.134) than those previously treated by MAPKi. CONCLUSIONS: A prior treatment by an MAPKi may be associated with a worse response to CC than ICI, and further investigations should be performed to confirm if there is a clinical benefit to propose CC in this setting.
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spelling pubmed-81241152021-05-21 Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma Mangin, Marie‐Alix Boespflug, Amélie Maucort Boulch, Delphine Vacheron, Charles‐Hervé Carpentier, Isabelle Thomas, Luc Dalle, Stéphane Cancer Med Clinical Cancer Research BACKGROUND: Cytotoxic chemotherapy (CC) is currently used in metastatic melanoma after patients have developed resistance to immune checkpoint inhibitors (ICI) and/or Mitogen‐Activated Protein Kinase inhibitors (MAPKi). We sought to evaluate if a previous treatment by ICI or MAPKi influences clinical outcomes in patients treated by CC in metastatic melanoma. METHODS: Eighty‐eight patients with a metastatic melanoma, treated by CC after a previous treatment by ICI or MAPKi between January 2009 and October 2019, were retrospectively analyzed. Progression‐Free‐Survival (PFS), Overall Survival (OS), Overall Response Rate (ORR), and Disease Control Rate (DCR) were evaluated in patients treated by CC according to their prior treatment by ICI or MAPKi. RESULTS: Patients treated by CC after ICI tended to have a better median PFS (2.81 months (2.39–5.30) versus 2.40 months (0.91–2.75), p = 0.023), median OS (6.03 months (3.54–11.54) versus 4.44 months (1.54–8.59), p = 0.27), DCR (26.0% vs. 10.5%, p = 0.121) and ORR (22.0% vs. 7.9% p = 0.134) than those previously treated by MAPKi. CONCLUSIONS: A prior treatment by an MAPKi may be associated with a worse response to CC than ICI, and further investigations should be performed to confirm if there is a clinical benefit to propose CC in this setting. John Wiley and Sons Inc. 2021-05-01 /pmc/articles/PMC8124115/ /pubmed/33932099 http://dx.doi.org/10.1002/cam4.3760 Text en © 2021 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 Clinical Cancer Research
Mangin, Marie‐Alix
Boespflug, Amélie
Maucort Boulch, Delphine
Vacheron, Charles‐Hervé
Carpentier, Isabelle
Thomas, Luc
Dalle, Stéphane
Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma
title Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma
title_full Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma
title_fullStr Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma
title_full_unstemmed Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma
title_short Decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma
title_sort decreased survival in patients treated by chemotherapy after targeted therapy compared to immunotherapy in metastatic melanoma
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124115/
https://www.ncbi.nlm.nih.gov/pubmed/33932099
http://dx.doi.org/10.1002/cam4.3760
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