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Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis
BACKGROUND: There is limited data on the use of targeted or immunotherapy (TT/IT) in combination with single fraction stereotactic radiosurgery (SRS) in patients with melanoma brain metastasis (MBM). Therefore, we analyzed the outcome and toxicity of SRS alone compared to SRS in combination with TT/...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023694/ https://www.ncbi.nlm.nih.gov/pubmed/32059731 http://dx.doi.org/10.1186/s13014-020-1485-8 |
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author | Hadi, Indrawati Roengvoraphoj, Olarn Bodensohn, Raphael Hofmaier, Jan Niyazi, Maximilian Belka, Claus Nachbichler, Silke Birgit |
author_facet | Hadi, Indrawati Roengvoraphoj, Olarn Bodensohn, Raphael Hofmaier, Jan Niyazi, Maximilian Belka, Claus Nachbichler, Silke Birgit |
author_sort | Hadi, Indrawati |
collection | PubMed |
description | BACKGROUND: There is limited data on the use of targeted or immunotherapy (TT/IT) in combination with single fraction stereotactic radiosurgery (SRS) in patients with melanoma brain metastasis (MBM). Therefore, we analyzed the outcome and toxicity of SRS alone compared to SRS in combination with TT/IT. METHODS: Patients with MBM treated with single session SRS at our department between 2014 and 2017 with a minimum follow-up of 3 months after first SRS were included. The primary endpoint of this study was local control (LC). Secondary endpoints were distant intracranial control, radiation necrosis-free survival (RNFS), and overall survival (OS). The local/ distant intracranial control rates, RNFS and OS were analyzed using the Kaplan-Meier method. The log-rank test was used to test differences between groups. Cox proportional hazard model was performed for univariate continuous variables and multivariate analyses. RESULTS: Twenty-eight patients (17 male and 11 female) with 52 SRS-lesions were included. The median follow-up was 19 months (range 14–24 months) after first SRS. Thirty-six lesions (69.2%) were treated with TT/IT simultaneously (4 weeks before and 4 weeks after SRS), while 16 lesions (30.8%) were treated with SRS alone or with sequential TT/IT. The 1-year local control rate was 100 and 83.3% for SRS with TT/IT and SRS alone (p = 0.023), respectively. The estimated 1-year RNFS was 90.0 and 82.1% for SRS in combination with TT/IT and SRS alone (p = 0.935). The distant intracranial control rate after 1 year was 47.7 and 50% for SRS in combination with TT/IT and SRS alone (p = 0.933). On univariate analysis, the diagnosis-specific Graded Prognostic Assessment including the BRAF status (Melanoma-molGPA) was associated with a significantly improved LC. Neither gender nor SRS-PTV margin had a prognostic impact on LC. V10 and V12 were significantly associated with RNFS (p < 0.001 and p = 0.004). CONCLUSION: SRS with simultaneous TT/IT significantly improved LC with no significant difference in radiation necrosis rate. The therapy combination appears to be effective and safe. However, prospective studies on SRS with simultaneous TT/IT are necessary and ongoing. TRIAL REGISTRATION: The institutional review board approved this analysis on 10th of February 2015 and all patients signed informed consent (UE nr. 128–14). |
format | Online Article Text |
id | pubmed-7023694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70236942020-02-20 Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis Hadi, Indrawati Roengvoraphoj, Olarn Bodensohn, Raphael Hofmaier, Jan Niyazi, Maximilian Belka, Claus Nachbichler, Silke Birgit Radiat Oncol Research BACKGROUND: There is limited data on the use of targeted or immunotherapy (TT/IT) in combination with single fraction stereotactic radiosurgery (SRS) in patients with melanoma brain metastasis (MBM). Therefore, we analyzed the outcome and toxicity of SRS alone compared to SRS in combination with TT/IT. METHODS: Patients with MBM treated with single session SRS at our department between 2014 and 2017 with a minimum follow-up of 3 months after first SRS were included. The primary endpoint of this study was local control (LC). Secondary endpoints were distant intracranial control, radiation necrosis-free survival (RNFS), and overall survival (OS). The local/ distant intracranial control rates, RNFS and OS were analyzed using the Kaplan-Meier method. The log-rank test was used to test differences between groups. Cox proportional hazard model was performed for univariate continuous variables and multivariate analyses. RESULTS: Twenty-eight patients (17 male and 11 female) with 52 SRS-lesions were included. The median follow-up was 19 months (range 14–24 months) after first SRS. Thirty-six lesions (69.2%) were treated with TT/IT simultaneously (4 weeks before and 4 weeks after SRS), while 16 lesions (30.8%) were treated with SRS alone or with sequential TT/IT. The 1-year local control rate was 100 and 83.3% for SRS with TT/IT and SRS alone (p = 0.023), respectively. The estimated 1-year RNFS was 90.0 and 82.1% for SRS in combination with TT/IT and SRS alone (p = 0.935). The distant intracranial control rate after 1 year was 47.7 and 50% for SRS in combination with TT/IT and SRS alone (p = 0.933). On univariate analysis, the diagnosis-specific Graded Prognostic Assessment including the BRAF status (Melanoma-molGPA) was associated with a significantly improved LC. Neither gender nor SRS-PTV margin had a prognostic impact on LC. V10 and V12 were significantly associated with RNFS (p < 0.001 and p = 0.004). CONCLUSION: SRS with simultaneous TT/IT significantly improved LC with no significant difference in radiation necrosis rate. The therapy combination appears to be effective and safe. However, prospective studies on SRS with simultaneous TT/IT are necessary and ongoing. TRIAL REGISTRATION: The institutional review board approved this analysis on 10th of February 2015 and all patients signed informed consent (UE nr. 128–14). BioMed Central 2020-02-14 /pmc/articles/PMC7023694/ /pubmed/32059731 http://dx.doi.org/10.1186/s13014-020-1485-8 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hadi, Indrawati Roengvoraphoj, Olarn Bodensohn, Raphael Hofmaier, Jan Niyazi, Maximilian Belka, Claus Nachbichler, Silke Birgit Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis |
title | Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis |
title_full | Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis |
title_fullStr | Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis |
title_full_unstemmed | Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis |
title_short | Stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis |
title_sort | stereotactic radiosurgery combined with targeted/ immunotherapy in patients with melanoma brain metastasis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023694/ https://www.ncbi.nlm.nih.gov/pubmed/32059731 http://dx.doi.org/10.1186/s13014-020-1485-8 |
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