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Clinical Trials in Switzerland / NCT06361043
Recruiting Observational

Conebeam CT-based Online Adaptive Radio-Therapy for Esophageal Cancer (ARTEC)

NCT06361043 · tracked via the Priya Life Science Switzerland tracker
Phase
Observational
Started
2024-04-20
Last updated
2024-04-25

Condition(s) studied

Esophageal Cancer

Study summary

Despite multimodal therapy, patients with esophageal cancer have poor prognosis with 5-year overall survival around 25%. Considering tumor-related death as main reason for high mortality rate in those patients, treatment-related cardio-pulmonary toxicities could also play a role in this regard. Online adaptive radiotherapy offers the possibility for daily re-planning and therefore helps radiation oncologists to better spare the organs at risk and reduce radiation-induced toxicity. Tha aim of ARTEC is to assess the pulmonary toxicity in patients with esophageal cancer treated with online adaptive radiotherapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Written informed consent * Histologically confirmed diagnosis of AC (Adenocarcinoma) or SCC (squamos cell carcinoma) of the thoracic esophagus or gastroesophageal junction (Siewert I-II) * Patients with cT2-4b cN0 cM0 or cTany cN+ cM0 or any patient with early stage EC ineligible for upfront surgery * Age \>= 18 years old * Karnofsky Performance Status (KPS) \>= 70 or ECOG (Eastern Cooperative Oncology Group) 0 - 1 * Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with patients before registration in the trial Exclusion Criteria: * Cervical esophageal cancers (15-18 cm from the incisors) * Definitive clinical or radiologic evidence of metastatic disease * Any active malignancy within 2 years of study registration that may alter the course of esophageal cancer treatment * Prior thoracic radiotherapy that would result in overlap of radiation therapy fields * Induction chemotherapy for the current malignancy prior to RCHT is allowed if last dose is no more than 90 days and no less than 10 days prior to registration * Pregnant and/or breast-feeding females

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Inselspital, University of Berne, Deparftment of Radio-Oncology Bern Switzerland Recruiting

More Insel Gruppe AG, University Hospital Bern trials in Switzerland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06361043 on ClinicalTrials.gov ↗ ← All trials in Switzerland