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Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO)
BACKGROUND: This study was conducted to investigate a new short-course radiotherapy regimen for patients with metastatic hormone refractory prostate cancer (HRPC) presenting with a dominant debilitating symptom. METHODS / DESIGN: This is an international, multi-center single arm prospective feasibil...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327575/ https://www.ncbi.nlm.nih.gov/pubmed/30630502 http://dx.doi.org/10.1186/s13014-019-1209-0 |
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author | Carl, Jesper Rades, Dirk Doemer, Claudia Setter, Cornelia Dunst, Jürgen Holländer, Niels Henrik |
author_facet | Carl, Jesper Rades, Dirk Doemer, Claudia Setter, Cornelia Dunst, Jürgen Holländer, Niels Henrik |
author_sort | Carl, Jesper |
collection | PubMed |
description | BACKGROUND: This study was conducted to investigate a new short-course radiotherapy regimen for patients with metastatic hormone refractory prostate cancer (HRPC) presenting with a dominant debilitating symptom. METHODS / DESIGN: This is an international, multi-center single arm prospective feasibility study that aims to include 34 patients with HRPC and a dominant debilitating symptom. The dominant symptomatic lesion will receive 4 × 5 Gy of high-precision radiotherapy, and the most aggressive part of the lesion 4 × 7 Gy using a simultaneous integrated boost technique. Based on advanced magnetic resonance imaging (MRI), an apparent diffusion coefficient (ADC) map will be calculated for the lesion using diffusion weighted imaging sequences. The dominant symptomatic lesion (GTV1) is drawn manually using the information from T2w-MRI and computed tomography scans. The most aggressive part of the dominant lesion (GTV2) is defined by using the ADC map. An auxiliary volume is created including only voxels in the GTV1 that presents with ADC values below 1200 × 10(− 6) mm(2)/s. The most aggressive part is defined as voxels with an ADC value below the median ADC value. Primary endpoint is feasibility, i.e. proportion of patients who complete radiotherapy with ≥90% of the prescribed dose. Secondary endpoints include dominant symptom score, progression-free survival (freedom from symptoms), overall survival, acute toxicity, quality of life, change in ADC from baseline to end of treatment and 6 months following treatment. DISCUSSION: If this new radiotherapy regimen proves to be feasible, a prospective randomized phase II/III dose escalation study will be designed in order to improve the outcomes of palliative radiotherapy of symptomatic metastatic HRPC. STUDY STATUS: The study is ongoing and will be recruiting patients soon. TRIAL REGISTRATION: clinicaltrials.gov NCT03658434. Initially registered on 30th of July, 2018 |
format | Online Article Text |
id | pubmed-6327575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63275752019-01-15 Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO) Carl, Jesper Rades, Dirk Doemer, Claudia Setter, Cornelia Dunst, Jürgen Holländer, Niels Henrik Radiat Oncol Study Protocol BACKGROUND: This study was conducted to investigate a new short-course radiotherapy regimen for patients with metastatic hormone refractory prostate cancer (HRPC) presenting with a dominant debilitating symptom. METHODS / DESIGN: This is an international, multi-center single arm prospective feasibility study that aims to include 34 patients with HRPC and a dominant debilitating symptom. The dominant symptomatic lesion will receive 4 × 5 Gy of high-precision radiotherapy, and the most aggressive part of the lesion 4 × 7 Gy using a simultaneous integrated boost technique. Based on advanced magnetic resonance imaging (MRI), an apparent diffusion coefficient (ADC) map will be calculated for the lesion using diffusion weighted imaging sequences. The dominant symptomatic lesion (GTV1) is drawn manually using the information from T2w-MRI and computed tomography scans. The most aggressive part of the dominant lesion (GTV2) is defined by using the ADC map. An auxiliary volume is created including only voxels in the GTV1 that presents with ADC values below 1200 × 10(− 6) mm(2)/s. The most aggressive part is defined as voxels with an ADC value below the median ADC value. Primary endpoint is feasibility, i.e. proportion of patients who complete radiotherapy with ≥90% of the prescribed dose. Secondary endpoints include dominant symptom score, progression-free survival (freedom from symptoms), overall survival, acute toxicity, quality of life, change in ADC from baseline to end of treatment and 6 months following treatment. DISCUSSION: If this new radiotherapy regimen proves to be feasible, a prospective randomized phase II/III dose escalation study will be designed in order to improve the outcomes of palliative radiotherapy of symptomatic metastatic HRPC. STUDY STATUS: The study is ongoing and will be recruiting patients soon. TRIAL REGISTRATION: clinicaltrials.gov NCT03658434. Initially registered on 30th of July, 2018 BioMed Central 2019-01-10 /pmc/articles/PMC6327575/ /pubmed/30630502 http://dx.doi.org/10.1186/s13014-019-1209-0 Text en © The Author(s). 2019 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 Carl, Jesper Rades, Dirk Doemer, Claudia Setter, Cornelia Dunst, Jürgen Holländer, Niels Henrik Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO) |
title | Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO) |
title_full | Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO) |
title_fullStr | Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO) |
title_full_unstemmed | Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO) |
title_short | Palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (PRADO) |
title_sort | palliative radiotherapy to dominant symptomatic lesion in patients with hormone refractory prostate cancer (prado) |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327575/ https://www.ncbi.nlm.nih.gov/pubmed/30630502 http://dx.doi.org/10.1186/s13014-019-1209-0 |
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