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Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients

BACKGROUND: Nivolumab combined with ipilimumab have shown activity in melanoma brain metastasis (MBM). However, in most of the clinical trials investigating immunotherapy in this subgroup, patients with symptomatic MBM and/or prior local brain radiotherapy were excluded. We studied the efficacy of n...

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Autores principales: Amaral, Teresa, Kiecker, Felix, Schaefer, Sarah, Stege, Henner, Kaehler, Katharina, Terheyden, Patrick, Gesierich, Anja, Gutzmer, Ralf, Haferkamp, Sebastian, Uttikal, Jochen, Berking, Carola, Rafei-Shamsabadi, David, Reinhardt, Lydia, Meier, Friedegund, Karoglan, Ante, Posch, Christian, Gambichler, Thilo, Pfoehler, Claudia, Thoms, Kai, Tietze, Julia, Debus, Dirk, Herbst, Rudolf, Emmert, Steffen, Loquai, Carmen, Hassel, Jessica C, Meiss, Frank, Tueting, Thomas, Heinrich, Vanessa, Eigentler, Thomas, Garbe, Claus, Zimmer, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206917/
https://www.ncbi.nlm.nih.gov/pubmed/32221017
http://dx.doi.org/10.1136/jitc-2019-000333
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author Amaral, Teresa
Kiecker, Felix
Schaefer, Sarah
Stege, Henner
Kaehler, Katharina
Terheyden, Patrick
Gesierich, Anja
Gutzmer, Ralf
Haferkamp, Sebastian
Uttikal, Jochen
Berking, Carola
Rafei-Shamsabadi, David
Reinhardt, Lydia
Meier, Friedegund
Karoglan, Ante
Posch, Christian
Gambichler, Thilo
Pfoehler, Claudia
Thoms, Kai
Tietze, Julia
Debus, Dirk
Herbst, Rudolf
Emmert, Steffen
Loquai, Carmen
Hassel, Jessica C
Meiss, Frank
Tueting, Thomas
Heinrich, Vanessa
Eigentler, Thomas
Garbe, Claus
Zimmer, Lisa
author_facet Amaral, Teresa
Kiecker, Felix
Schaefer, Sarah
Stege, Henner
Kaehler, Katharina
Terheyden, Patrick
Gesierich, Anja
Gutzmer, Ralf
Haferkamp, Sebastian
Uttikal, Jochen
Berking, Carola
Rafei-Shamsabadi, David
Reinhardt, Lydia
Meier, Friedegund
Karoglan, Ante
Posch, Christian
Gambichler, Thilo
Pfoehler, Claudia
Thoms, Kai
Tietze, Julia
Debus, Dirk
Herbst, Rudolf
Emmert, Steffen
Loquai, Carmen
Hassel, Jessica C
Meiss, Frank
Tueting, Thomas
Heinrich, Vanessa
Eigentler, Thomas
Garbe, Claus
Zimmer, Lisa
author_sort Amaral, Teresa
collection PubMed
description BACKGROUND: Nivolumab combined with ipilimumab have shown activity in melanoma brain metastasis (MBM). However, in most of the clinical trials investigating immunotherapy in this subgroup, patients with symptomatic MBM and/or prior local brain radiotherapy were excluded. We studied the efficacy of nivolumab plus ipilimumab alone or in combination with local therapies regardless of treatment line in patients with asymptomatic and symptomatic MBM. METHODS: Patients with MBM treated with nivolumab plus ipilimumab in 23 German Skin Cancer Centers between April 2015 and October 2018 were investigated. Overall survival (OS) was evaluated by Kaplan-Meier estimator and univariate and multivariate Cox proportional hazard analyses were performed to determine prognostic factors associated with OS. RESULTS: Three hundred and eighty patients were included in this study and 31% had symptomatic MBM (60/193 with data available) at the time of start nivolumab plus ipilimumab. The median follow-up was 18 months and the 2 years and 3 years OS rates were 41% and 30%, respectively. We identified the following independently significant prognostic factors for OS: elevated serum lactate dehydrogenase and protein S100B levels, number of MBM and Eastern Cooperative Oncology Group performance status. In these patients treated with checkpoint inhibition first-line or later, in the subgroup of patients with BRAFV600-mutated melanoma we found no differences in terms of OS when receiving first-line either BRAF and MEK inhibitors or nivolumab plus ipilimumab (p=0.085). In BRAF wild-type patients treated with nivolumab plus ipilimumab in first-line or later there was also no difference in OS (p=0.996). Local therapy with stereotactic radiosurgery or surgery led to an improvement in OS compared with not receiving local therapy (p=0.009), regardless of the timepoint of the local therapy. Receiving combined immunotherapy for MBM in first-line or at a later time point made no difference in terms of OS in this study population (p=0.119). CONCLUSION: Immunotherapy with nivolumab plus ipilimumab, particularly in combination with stereotactic radiosurgery or surgery improves OS in asymptomatic and symptomatic MBM.
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spelling pubmed-72069172020-05-12 Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients Amaral, Teresa Kiecker, Felix Schaefer, Sarah Stege, Henner Kaehler, Katharina Terheyden, Patrick Gesierich, Anja Gutzmer, Ralf Haferkamp, Sebastian Uttikal, Jochen Berking, Carola Rafei-Shamsabadi, David Reinhardt, Lydia Meier, Friedegund Karoglan, Ante Posch, Christian Gambichler, Thilo Pfoehler, Claudia Thoms, Kai Tietze, Julia Debus, Dirk Herbst, Rudolf Emmert, Steffen Loquai, Carmen Hassel, Jessica C Meiss, Frank Tueting, Thomas Heinrich, Vanessa Eigentler, Thomas Garbe, Claus Zimmer, Lisa J Immunother Cancer Clinical/Translational Cancer Immunotherapy BACKGROUND: Nivolumab combined with ipilimumab have shown activity in melanoma brain metastasis (MBM). However, in most of the clinical trials investigating immunotherapy in this subgroup, patients with symptomatic MBM and/or prior local brain radiotherapy were excluded. We studied the efficacy of nivolumab plus ipilimumab alone or in combination with local therapies regardless of treatment line in patients with asymptomatic and symptomatic MBM. METHODS: Patients with MBM treated with nivolumab plus ipilimumab in 23 German Skin Cancer Centers between April 2015 and October 2018 were investigated. Overall survival (OS) was evaluated by Kaplan-Meier estimator and univariate and multivariate Cox proportional hazard analyses were performed to determine prognostic factors associated with OS. RESULTS: Three hundred and eighty patients were included in this study and 31% had symptomatic MBM (60/193 with data available) at the time of start nivolumab plus ipilimumab. The median follow-up was 18 months and the 2 years and 3 years OS rates were 41% and 30%, respectively. We identified the following independently significant prognostic factors for OS: elevated serum lactate dehydrogenase and protein S100B levels, number of MBM and Eastern Cooperative Oncology Group performance status. In these patients treated with checkpoint inhibition first-line or later, in the subgroup of patients with BRAFV600-mutated melanoma we found no differences in terms of OS when receiving first-line either BRAF and MEK inhibitors or nivolumab plus ipilimumab (p=0.085). In BRAF wild-type patients treated with nivolumab plus ipilimumab in first-line or later there was also no difference in OS (p=0.996). Local therapy with stereotactic radiosurgery or surgery led to an improvement in OS compared with not receiving local therapy (p=0.009), regardless of the timepoint of the local therapy. Receiving combined immunotherapy for MBM in first-line or at a later time point made no difference in terms of OS in this study population (p=0.119). CONCLUSION: Immunotherapy with nivolumab plus ipilimumab, particularly in combination with stereotactic radiosurgery or surgery improves OS in asymptomatic and symptomatic MBM. BMJ Publishing Group 2020-03-26 /pmc/articles/PMC7206917/ /pubmed/32221017 http://dx.doi.org/10.1136/jitc-2019-000333 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Clinical/Translational Cancer Immunotherapy
Amaral, Teresa
Kiecker, Felix
Schaefer, Sarah
Stege, Henner
Kaehler, Katharina
Terheyden, Patrick
Gesierich, Anja
Gutzmer, Ralf
Haferkamp, Sebastian
Uttikal, Jochen
Berking, Carola
Rafei-Shamsabadi, David
Reinhardt, Lydia
Meier, Friedegund
Karoglan, Ante
Posch, Christian
Gambichler, Thilo
Pfoehler, Claudia
Thoms, Kai
Tietze, Julia
Debus, Dirk
Herbst, Rudolf
Emmert, Steffen
Loquai, Carmen
Hassel, Jessica C
Meiss, Frank
Tueting, Thomas
Heinrich, Vanessa
Eigentler, Thomas
Garbe, Claus
Zimmer, Lisa
Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients
title Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients
title_full Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients
title_fullStr Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients
title_full_unstemmed Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients
title_short Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients
title_sort combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a decog* study in 380 patients
topic Clinical/Translational Cancer Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206917/
https://www.ncbi.nlm.nih.gov/pubmed/32221017
http://dx.doi.org/10.1136/jitc-2019-000333
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