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Taking people in GermanyNo phase

Adjusting Radiotherapy Daily Using a New Machine for Several Cancers

Studies daily-adjusted radiation treatment for several cancers in adults 18 and older.

Plain-language title generated from the registry record
Registry title: Online Adaptive Radiotherapy Using a Novel Linear Accelerator (ETHOS)

Key facts

Where
Berlin, GermanySee the site

Where in Germany

  • Charité - UniversitätsmedizinBerlin, GermanyTaking people

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Trial details

Who runs it
Charite University, Berlin, Germany
Trial code
NCT06116019
Record updated
3 November 2023
Original description
The study focuses on the scientific and clinical evaluation of online adaptive radiotherapy (ART) using the Varian/SHS ETHOS treatment system. In this study, radiation treatment plans are dynamically adjusted on a daily basis over several weeks of therapy to account for anatomical shifts in either the tumour or adjacent normal tissue - a capability that has been difficult to achieve due to technical limitations. With the ETHOS accelerator, such real-time adjustments can be made based on cone beam computed tomography (CBCT). This is a prospective observational study with the primary objective of investigating the feasibility and acceptability of performing ART with ETHOS for different tumour entities. The study will also evaluate the feasibility of integrating multi-parametric data sets into the ART workflow, such as standardised electronic feedback on treatment toxicity from both patients (ePROMS) and physicians (ePRT).Read full original descriptionShow less

A Prospective Study on Online Adaptive Radiotherapy (ART) Using the ETHOS Linear Accelerator for Various Tumor Entities and the Feasibility of Integrating Multi-Parametric Patient Data Into the Adaptive Workflow

The study focuses on the scientific and clinical evaluation of online adaptive radiotherapy (ART) using the Varian/SHS ETHOS treatment system. In this study, radiation treatment plans are dynamically adjusted on a daily basis over several weeks of therapy to account for anatomical shifts in either the tumour or adjacent normal tissue - a capability that has been difficult to achieve due to technical limitations. With the ETHOS accelerator, such real-time adjustments can be made based on cone beam computed tomography (CBCT). This is a prospective observational study with the primary objective of investigating the feasibility and acceptability of performing ART with ETHOS for different tumour entities. The study will also evaluate the feasibility of integrating multi-parametric data sets into the ART workflow, such as standardised electronic feedback on treatment toxicity from both patients (ePROMS) and physicians (ePRT).

Inclusion: Adult patients (>18 years); All tumor entities with an indication for radiotherapy and/or chemoradiotherapy; Signed informed consent.

Exclusion: Pregnancy; Patients who are not capable of giving consent.

ClinicalTrials.gov NCT06116019