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Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial)

BACKGROUND: Irreversible electroporation (IRE) is a novel image-guided tumor ablation technique that has shown promise for the ablation of lesions in proximity to vital structures such as blood vessels and bile ducts. The primary aim of the COLDFIRE-2 trial is to investigate the efficacy of IRE for...

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Autores principales: Scheffer, Hester J., Vroomen, Laurien G P H, Nielsen, Karin, van Tilborg, Aukje A J M, Comans, Emile F I, van Kuijk, Cornelis, van der Meijs, Bram B., van den Bergh, Janneke, van den Tol, Petrousjka M P, Meijerink, Martijn R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619419/
https://www.ncbi.nlm.nih.gov/pubmed/26497813
http://dx.doi.org/10.1186/s12885-015-1736-5
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author Scheffer, Hester J.
Vroomen, Laurien G P H
Nielsen, Karin
van Tilborg, Aukje A J M
Comans, Emile F I
van Kuijk, Cornelis
van der Meijs, Bram B.
van den Bergh, Janneke
van den Tol, Petrousjka M P
Meijerink, Martijn R.
author_facet Scheffer, Hester J.
Vroomen, Laurien G P H
Nielsen, Karin
van Tilborg, Aukje A J M
Comans, Emile F I
van Kuijk, Cornelis
van der Meijs, Bram B.
van den Bergh, Janneke
van den Tol, Petrousjka M P
Meijerink, Martijn R.
author_sort Scheffer, Hester J.
collection PubMed
description BACKGROUND: Irreversible electroporation (IRE) is a novel image-guided tumor ablation technique that has shown promise for the ablation of lesions in proximity to vital structures such as blood vessels and bile ducts. The primary aim of the COLDFIRE-2 trial is to investigate the efficacy of IRE for unresectable, centrally located colorectal liver metastases (CRLM). Secondary outcomes are safety, technical success, and the accuracy of contrast-enhanced (ce)CT and (18)F-FDG PET-CT in the detection of local tumor progression (LTP). METHODS/DESIGN: In this single-arm, multicenter phase II clinical trial, twenty-nine patients with (18)F-FDG PET-avid CRLM ≤ 3,5 cm will be prospectively included to undergo IRE of the respective lesion. All lesions must be unresectable and unsuitable for thermal ablation due to vicinity of vital structures. Technical success is based on ceMRI one day post-IRE. All complications related to the IRE procedure are registered. Follow-up consists of (18)F-FDG PET-CT and 4-phase liver CT at 3-monthly intervals during the first year of follow-up. Treatment efficacy is defined as the percentage of tumors successfully eradicated 12 months after the initial IRE procedure based on clinical follow-up using both imaging modalities, tumor marker and (if available) histopathology. To determine the accuracy of (18)F-FDG PET-CT and ceCT, both imaging modalities will be individually scored by two reviewers that are blinded for the final oncologic outcome. DISCUSSION: To date, patients with a central CRLM unsuitable for resection or thermal ablation have no curative treatment option and are given palliative chemotherapy. For these patients, IRE may prove a life-saving treatment option. The results of the proposed trial may represent an important step towards the implementation of IRE for central liver tumors in the clinical setting. TRIAL REGISTRATION: Trial registration number: NCT02082782.
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spelling pubmed-46194192015-10-26 Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial) Scheffer, Hester J. Vroomen, Laurien G P H Nielsen, Karin van Tilborg, Aukje A J M Comans, Emile F I van Kuijk, Cornelis van der Meijs, Bram B. van den Bergh, Janneke van den Tol, Petrousjka M P Meijerink, Martijn R. BMC Cancer Study Protocol BACKGROUND: Irreversible electroporation (IRE) is a novel image-guided tumor ablation technique that has shown promise for the ablation of lesions in proximity to vital structures such as blood vessels and bile ducts. The primary aim of the COLDFIRE-2 trial is to investigate the efficacy of IRE for unresectable, centrally located colorectal liver metastases (CRLM). Secondary outcomes are safety, technical success, and the accuracy of contrast-enhanced (ce)CT and (18)F-FDG PET-CT in the detection of local tumor progression (LTP). METHODS/DESIGN: In this single-arm, multicenter phase II clinical trial, twenty-nine patients with (18)F-FDG PET-avid CRLM ≤ 3,5 cm will be prospectively included to undergo IRE of the respective lesion. All lesions must be unresectable and unsuitable for thermal ablation due to vicinity of vital structures. Technical success is based on ceMRI one day post-IRE. All complications related to the IRE procedure are registered. Follow-up consists of (18)F-FDG PET-CT and 4-phase liver CT at 3-monthly intervals during the first year of follow-up. Treatment efficacy is defined as the percentage of tumors successfully eradicated 12 months after the initial IRE procedure based on clinical follow-up using both imaging modalities, tumor marker and (if available) histopathology. To determine the accuracy of (18)F-FDG PET-CT and ceCT, both imaging modalities will be individually scored by two reviewers that are blinded for the final oncologic outcome. DISCUSSION: To date, patients with a central CRLM unsuitable for resection or thermal ablation have no curative treatment option and are given palliative chemotherapy. For these patients, IRE may prove a life-saving treatment option. The results of the proposed trial may represent an important step towards the implementation of IRE for central liver tumors in the clinical setting. TRIAL REGISTRATION: Trial registration number: NCT02082782. BioMed Central 2015-10-24 /pmc/articles/PMC4619419/ /pubmed/26497813 http://dx.doi.org/10.1186/s12885-015-1736-5 Text en © Scheffer et al. 2015 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 Study Protocol
Scheffer, Hester J.
Vroomen, Laurien G P H
Nielsen, Karin
van Tilborg, Aukje A J M
Comans, Emile F I
van Kuijk, Cornelis
van der Meijs, Bram B.
van den Bergh, Janneke
van den Tol, Petrousjka M P
Meijerink, Martijn R.
Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial)
title Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial)
title_full Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial)
title_fullStr Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial)
title_full_unstemmed Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial)
title_short Colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase II clinical trial (COLDFIRE-2 trial)
title_sort colorectal liver metastatic disease: efficacy of irreversible electroporation—a single-arm phase ii clinical trial (coldfire-2 trial)
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619419/
https://www.ncbi.nlm.nih.gov/pubmed/26497813
http://dx.doi.org/10.1186/s12885-015-1736-5
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