ROCS (Radiotherapy After Oesophageal Cancer Stenting) Study (ROCS)
Oesophageal Cancer
About this trial
This is an interventional treatment trial for Oesophageal Cancer focused on measuring Radiotherapy, stent, quality of life
Eligibility Criteria
Inclusion Criteria:
- Histological confirmation of oesophageal carcinoma excluding small cell histology
- Not suitable for radical treatment (oesophagectomy or radical chemoradiotherapy) either because of patient choice or medical reasons
- Dysphagia clinically assessed as needing stent as primary treatment of the dysphagia
- Age 16 years or over
- Discussion and treatment decision for stent placement made by an upper GI multi-disciplinary team
- Clinician assessment of ability to attend for radiotherapy
- Expected survival of at least 12 weeks
- Written informed consent
- Patient has completed baseline Quality of Life Questionnaires (please note, as a minimum patients must have completed OG25)
Exclusion Criteria:
- Histology of small cell carcinoma type
- Tumour length of greater than 12 cm
- Tumour growth within 2 cm of the upper oesophageal sphincter
- Endoscopic treatment of the tumour, other than dilatation, planned in the peri-stent period
- Presence of a tracheo-oesophageal fistula
- Presence of a pacemaker in proposed radiotherapy field
- Previous radiotherapy to the area of the proposed radiotherapy field
- Planned endoscopic treatment of the tumour (e.g. laser) in the immediate peri-stenting period
- Female patient who is pregnant
Sites / Locations
- Bristol Haematology and Oncology Centre
- Doncaster Royal Infirmary
- James Cook University Hospital
- George Eliot Hospital
- Conquest Hospital
- Cancer Research Centre at Weston Park Hospital
- Musgrove Park Hospital
- Southend University Hospital NHS Foundation Trust
- Weston General Hospital
- Ninewells Hospital
- Ysbyty Gwynedd
- Velindre Cancer Center at Velindre Hospital
- Royal Gwent Hospital
- Glan Clwyd Hospital
- Wrexham Maelor Hospital
- Weston Park Hospital
- Southampton General Hospital
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Arm A: Self-expanding metal stents (SEMS) (Control Arm)
Arm B: SEMS plus external beam radiotherapy (Intervention Arm)
SEMS insertion will be undertaken in accordance with standard local protocols. Covered or partially covered metal stents will be used and the length type and mode of stent placement will be selected by the clinician. Insertion will occur within two weeks of randomisation.
External beam radiotherapy (EBRT) is routinely available at regional cancer centres across the UK. For palliation of dysphagia in oesophageal cancer, a radiotherapy course delivering a tumour absorbed dose of 20Gy in 5 fractions or 30Gy in 10 fractions within 4 weeks of SEMS insertion.