Actively Recruiting

Age: 18Years +
All Genders
NCT06361043

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

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-04-25

30

Participants Needed

1

Research Sites

149 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent
  • Histologically confirmed adenocarcinoma or squamous cell carcinoma of the thoracic esophagus or gastroesophageal junction (Siewert I-II)
  • Clinical stage cT2-4b cN0 cM0 or cTany cN+ cM0, or early-stage esophageal cancer not eligible for upfront surgery
  • Age 18 years or older
  • Karnofsky Performance Status (KPS) at least 70 or ECOG score 0-1
  • No psychological, familial, sociological, or geographical conditions that could prevent compliance with the study and follow-up
Not Eligible

You will not qualify if you...

  • Cervical esophageal cancers (15-18 cm from the incisors)
  • Clinical or radiologic evidence of metastatic disease
  • Any active cancer within 2 years before study registration that could affect treatment
  • Prior thoracic radiotherapy causing overlapping radiation fields
  • Pregnant or breastfeeding females
  • Induction chemotherapy for current cancer allowed only if last dose was between 10 and 90 days before registration

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Inselspital, University of Berne, Deparftment of Radio-Oncology

Bern, Switzerland, 3010

Actively Recruiting

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Research Team

H

Hossein Hemmatazad, MD

CONTACT

T

Timo Nannen

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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