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OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma

BACKGROUND: Preclinical studies suggest that skull remodeling surgery (SR-surgery) increases the dose of tumor treating fields (TTFields) in glioblastoma (GBM) and prevents wasteful current shunting through the skin. SR-surgery introduces minor skull defects to focus the cancer-inhibiting currents t...

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Autores principales: Korshoej, Anders Rosendal, Lukacova, Slavka, Lassen-Ramshad, Yasmin, Rahbek, Christian, Severinsen, Kåre Eg, Guldberg, Trine Lignell, Mikic, Nikola, Jensen, Mette Haldrup, Cortnum, Søren Ole Stigaard, von Oettingen, Gorm, Sørensen, Jens Christian Hedemann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660275/
https://www.ncbi.nlm.nih.gov/pubmed/33215088
http://dx.doi.org/10.1093/noajnl/vdaa121
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author Korshoej, Anders Rosendal
Lukacova, Slavka
Lassen-Ramshad, Yasmin
Rahbek, Christian
Severinsen, Kåre Eg
Guldberg, Trine Lignell
Mikic, Nikola
Jensen, Mette Haldrup
Cortnum, Søren Ole Stigaard
von Oettingen, Gorm
Sørensen, Jens Christian Hedemann
author_facet Korshoej, Anders Rosendal
Lukacova, Slavka
Lassen-Ramshad, Yasmin
Rahbek, Christian
Severinsen, Kåre Eg
Guldberg, Trine Lignell
Mikic, Nikola
Jensen, Mette Haldrup
Cortnum, Søren Ole Stigaard
von Oettingen, Gorm
Sørensen, Jens Christian Hedemann
author_sort Korshoej, Anders Rosendal
collection PubMed
description BACKGROUND: Preclinical studies suggest that skull remodeling surgery (SR-surgery) increases the dose of tumor treating fields (TTFields) in glioblastoma (GBM) and prevents wasteful current shunting through the skin. SR-surgery introduces minor skull defects to focus the cancer-inhibiting currents toward the tumor and increase the treatment dose. This study aimed to test the safety and feasibility of this concept in a phase I setting. METHODS: Fifteen adult patients with the first recurrence of GBM were treated with personalized SR-surgery, TTFields, and physician’s choice oncological therapy. The primary endpoint was toxicity and secondary endpoints included standard efficacy outcomes. RESULTS: SR-surgery resulted in a mean skull defect area of 10.6 cm(2) producing a median TTFields enhancement of 32% (range 25–59%). The median TTFields treatment duration was 6.8 months and the median compliance rate 90%. Patients received either bevacizumab, bevacizumab/irinotecan, or temozolomide rechallenge. We observed 71 adverse events (AEs) of grades 1 (52%), 2 (35%), and 3 (13%). There were no grade 4 or 5 AEs or intervention-related serious AEs. Six patients experienced minor TTFields-induced skin rash. The median progression-free survival (PFS) was 4.6 months and the PFS rate at 6 months was 36%. The median overall survival (OS) was 15.5 months and the OS rate at 12 months was 55%. CONCLUSIONS: TTFields therapy combined with SR-surgery and medical oncological treatment is safe and nontoxic and holds the potential to improve the outcome for GBM patients through focal dose enhancement in the tumor.
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spelling pubmed-76602752020-11-18 OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma Korshoej, Anders Rosendal Lukacova, Slavka Lassen-Ramshad, Yasmin Rahbek, Christian Severinsen, Kåre Eg Guldberg, Trine Lignell Mikic, Nikola Jensen, Mette Haldrup Cortnum, Søren Ole Stigaard von Oettingen, Gorm Sørensen, Jens Christian Hedemann Neurooncol Adv Clinical Investigations BACKGROUND: Preclinical studies suggest that skull remodeling surgery (SR-surgery) increases the dose of tumor treating fields (TTFields) in glioblastoma (GBM) and prevents wasteful current shunting through the skin. SR-surgery introduces minor skull defects to focus the cancer-inhibiting currents toward the tumor and increase the treatment dose. This study aimed to test the safety and feasibility of this concept in a phase I setting. METHODS: Fifteen adult patients with the first recurrence of GBM were treated with personalized SR-surgery, TTFields, and physician’s choice oncological therapy. The primary endpoint was toxicity and secondary endpoints included standard efficacy outcomes. RESULTS: SR-surgery resulted in a mean skull defect area of 10.6 cm(2) producing a median TTFields enhancement of 32% (range 25–59%). The median TTFields treatment duration was 6.8 months and the median compliance rate 90%. Patients received either bevacizumab, bevacizumab/irinotecan, or temozolomide rechallenge. We observed 71 adverse events (AEs) of grades 1 (52%), 2 (35%), and 3 (13%). There were no grade 4 or 5 AEs or intervention-related serious AEs. Six patients experienced minor TTFields-induced skin rash. The median progression-free survival (PFS) was 4.6 months and the PFS rate at 6 months was 36%. The median overall survival (OS) was 15.5 months and the OS rate at 12 months was 55%. CONCLUSIONS: TTFields therapy combined with SR-surgery and medical oncological treatment is safe and nontoxic and holds the potential to improve the outcome for GBM patients through focal dose enhancement in the tumor. Oxford University Press 2020-09-15 /pmc/articles/PMC7660275/ /pubmed/33215088 http://dx.doi.org/10.1093/noajnl/vdaa121 Text en © The Author(s) 2020. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Korshoej, Anders Rosendal
Lukacova, Slavka
Lassen-Ramshad, Yasmin
Rahbek, Christian
Severinsen, Kåre Eg
Guldberg, Trine Lignell
Mikic, Nikola
Jensen, Mette Haldrup
Cortnum, Søren Ole Stigaard
von Oettingen, Gorm
Sørensen, Jens Christian Hedemann
OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma
title OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma
title_full OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma
title_fullStr OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma
title_full_unstemmed OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma
title_short OptimalTTF-1: Enhancing tumor treating fields therapy with skull remodeling surgery. A clinical phase I trial in adult recurrent glioblastoma
title_sort optimalttf-1: enhancing tumor treating fields therapy with skull remodeling surgery. a clinical phase i trial in adult recurrent glioblastoma
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660275/
https://www.ncbi.nlm.nih.gov/pubmed/33215088
http://dx.doi.org/10.1093/noajnl/vdaa121
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