search
Back to results

ROCS (Radiotherapy After Oesophageal Cancer Stenting) Study (ROCS)

Primary Purpose

Oesophageal Cancer

Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
Radiotherapy
Sponsored by
Lisette Nixon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Oesophageal Cancer focused on measuring Radiotherapy, stent, quality of life

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Histological confirmation of oesophageal carcinoma excluding small cell histology
  2. Not suitable for radical treatment (oesophagectomy or radical chemoradiotherapy) either because of patient choice or medical reasons
  3. Dysphagia clinically assessed as needing stent as primary treatment of the dysphagia
  4. Age 16 years or over
  5. Discussion and treatment decision for stent placement made by an upper GI multi-disciplinary team
  6. Clinician assessment of ability to attend for radiotherapy
  7. Expected survival of at least 12 weeks
  8. Written informed consent
  9. Patient has completed baseline Quality of Life Questionnaires (please note, as a minimum patients must have completed OG25)

Exclusion Criteria:

  1. Histology of small cell carcinoma type
  2. Tumour length of greater than 12 cm
  3. Tumour growth within 2 cm of the upper oesophageal sphincter
  4. Endoscopic treatment of the tumour, other than dilatation, planned in the peri-stent period
  5. Presence of a tracheo-oesophageal fistula
  6. Presence of a pacemaker in proposed radiotherapy field
  7. Previous radiotherapy to the area of the proposed radiotherapy field
  8. Planned endoscopic treatment of the tumour (e.g. laser) in the immediate peri-stenting period
  9. 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

Arm Type

No Intervention

Experimental

Arm Label

Arm A: Self-expanding metal stents (SEMS) (Control Arm)

Arm B: SEMS plus external beam radiotherapy (Intervention Arm)

Arm Description

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.

Outcomes

Primary Outcome Measures

patient-reported dysphagia
Assess the impact of radiotherapy in addition to self-expanding metal stent (SEMS) placement on time to progression of patient-reported dysphagia in a patient population unable to undergo surgery.

Secondary Outcome Measures

quality of life
Assess the impact of combination treatment on core components of health related quality of life
overall survival
Assess the impact of radiotherapy in addition to SEMS placement on overall survival
morbidity
Measure morbidity associated with the interventions
re-intervention rate
Measure re-intervention rates
cost
Assess the cost of the addition of radiotherapy to SEMS placement

Full Information

First Posted
July 31, 2013
Last Updated
June 3, 2019
Sponsor
Lisette Nixon
search

1. Study Identification

Unique Protocol Identification Number
NCT01915693
Brief Title
ROCS (Radiotherapy After Oesophageal Cancer Stenting) Study
Acronym
ROCS
Official Title
Palliative Radiotherapy in Addition to Self-expanding Metal Stent for Improving Dysphagia and Survival in Advanced Oesophageal Cancer: ROCS (Radiotherapy After Oesophageal Cancer Stenting) Study.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
October 2013 (Actual)
Primary Completion Date
November 2018 (Actual)
Study Completion Date
November 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Lisette Nixon

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The single most distressing symptom for more than 70% of patients with oesophageal cancer is difficulty in swallowing (dysphagia) caused by blockage of the gullet by a tumour. This causes severe restrictions on food intake, physical activity, social functioning and overall quality of life. Amongst the more effective treatments for improving swallowing, is the insertion of a metal stent across the blocked part, which then self-expands to open up the gullet (Self Expanding Metal Stent or SEMS). The addition of radiotherapy may help to improve the problems caused by dysphagia and provide an additional survival benefit. The purpose of this study is to test the impact of adding radiotherapy to SEMS on: the length of time swallow remains improved for quality of life survival
Detailed Description
The primary objective of the study is to assess the impact of radiotherapy in addition to self-expanding metal stent (SEMS) placement on time to progression of patient-reported dysphagia in a patient population unable to undergo surgery. Patients will be eligible to take part in the trial if they have oesophageal cancer, are in need of SEMS because of dysphagia, are aged 16 years or older, have been clinically assessed to be able to receive radiotherapy, have an expected survival of at least 12 weeks and are able to give written informed consent. 496 patients will be randomised to receive either SEMS alone or SEMS with radiotherapy. The radiotherapy will be given as an outpatient either as five treatments (one per day) over one week, or ten treatments over two weeks. Questionnaires will be completed before treatment, and at weeks two and four and then monthly for up to one year to assess quality of life and cost effectiveness. Interviews will be held with trial participants at three time points to explore their experiences while on the trial. Interviews will also be held with patients who do not consent to take part in the trial to explore their reasons for non-consent. Treatments: Arm A: Self-expanding metal stents (SEMS) (Control 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. Arm B: SEMS plus external beam radiotherapy (Intervention Arm) 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. There will also be a qualitative component of the trial will have two aims: i) to explore the feasibility of patients' recruitment to the trial and ii) to explore participants' experience of the trial interventions. It will examine their experience of consent and recruitment including reasons for declining, and examine patients' motivation to accept randomisation to an intervention which may include extra radiotherapy. This is an optional component and will require separate consent. Patients who do not consent to the trial, but who do consent to the qualitative component, will be interviewed about their reasons for not-consenting as soon as possible after the approach to participate. Trial participants who consent to the qualitative component will be interviewed three times: at weeks one and four to capture initial decision-making thoughts and then after the interventions (week 8) to explore patients' experience of interventions and perceptions of benefit or detriment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oesophageal Cancer
Keywords
Radiotherapy, stent, quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
220 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm A: Self-expanding metal stents (SEMS) (Control Arm)
Arm Type
No Intervention
Arm Description
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.
Arm Title
Arm B: SEMS plus external beam radiotherapy (Intervention Arm)
Arm Type
Experimental
Arm Description
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.
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
External beam radiotherapy (EBRT) delivering a tumour absorbed dose of 20Gy in 5 fractions or 30Gy in 10 fractions.
Primary Outcome Measure Information:
Title
patient-reported dysphagia
Description
Assess the impact of radiotherapy in addition to self-expanding metal stent (SEMS) placement on time to progression of patient-reported dysphagia in a patient population unable to undergo surgery.
Time Frame
within one year
Secondary Outcome Measure Information:
Title
quality of life
Description
Assess the impact of combination treatment on core components of health related quality of life
Time Frame
within one year
Title
overall survival
Description
Assess the impact of radiotherapy in addition to SEMS placement on overall survival
Time Frame
one year
Title
morbidity
Description
Measure morbidity associated with the interventions
Time Frame
one year
Title
re-intervention rate
Description
Measure re-intervention rates
Time Frame
one year
Title
cost
Description
Assess the cost of the addition of radiotherapy to SEMS placement
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
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
Facility Information:
Facility Name
Bristol Haematology and Oncology Centre
City
Bristol
State/Province
England
ZIP/Postal Code
BS2 8ED
Country
United Kingdom
Facility Name
Doncaster Royal Infirmary
City
Doncaster
State/Province
England
ZIP/Postal Code
DN2 5LT
Country
United Kingdom
Facility Name
James Cook University Hospital
City
Middlesbrough
State/Province
England
ZIP/Postal Code
TS4 3BW
Country
United Kingdom
Facility Name
George Eliot Hospital
City
Nuneaton
State/Province
England
ZIP/Postal Code
CV10 7DJ
Country
United Kingdom
Facility Name
Conquest Hospital
City
Saint Leonards-on-Sea
State/Province
England
ZIP/Postal Code
TN37 7RD
Country
United Kingdom
Facility Name
Cancer Research Centre at Weston Park Hospital
City
Sheffield
State/Province
England
ZIP/Postal Code
S1O 2SJ
Country
United Kingdom
Facility Name
Musgrove Park Hospital
City
Taunton
State/Province
England
ZIP/Postal Code
TA1 5DA
Country
United Kingdom
Facility Name
Southend University Hospital NHS Foundation Trust
City
Westcliff-On-Sea
State/Province
England
ZIP/Postal Code
SS0 0RY
Country
United Kingdom
Facility Name
Weston General Hospital
City
Weston-super-Mare
State/Province
England
ZIP/Postal Code
BS23 4TQ
Country
United Kingdom
Facility Name
Ninewells Hospital
City
Dundee
State/Province
Scotland
ZIP/Postal Code
DD1 9SY
Country
United Kingdom
Facility Name
Ysbyty Gwynedd
City
Bangor
State/Province
Wales
ZIP/Postal Code
LL57 2PW
Country
United Kingdom
Facility Name
Velindre Cancer Center at Velindre Hospital
City
Cardiff
State/Province
Wales
ZIP/Postal Code
CF14 2TL
Country
United Kingdom
Facility Name
Royal Gwent Hospital
City
Newport Gwent
State/Province
Wales
ZIP/Postal Code
NP9 2UB
Country
United Kingdom
Facility Name
Glan Clwyd Hospital
City
Rhyl, Denbighshire
State/Province
Wales
ZIP/Postal Code
LL 18 5UJ
Country
United Kingdom
Facility Name
Wrexham Maelor Hospital
City
Wrexham
State/Province
Wales
ZIP/Postal Code
LL13 7TD
Country
United Kingdom
Facility Name
Weston Park Hospital
City
Sheffield
Country
United Kingdom
Facility Name
Southampton General Hospital
City
Southampton
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
34042566
Citation
Adamson D, Blazeby J, Porter C, Hurt C, Griffiths G, Nelson A, Sewell B, Jones M, Svobodova M, Fitzsimmons D, Nixon L, Fitzgibbon J, Thomas S, Millin A, Crosby T, Staffurth J, Byrne A. Palliative radiotherapy combined with stent insertion to reduce recurrent dysphagia in oesophageal cancer patients: the ROCS RCT. Health Technol Assess. 2021 May;25(31):1-144. doi: 10.3310/hta25310.
Results Reference
derived
PubMed Identifier
33610215
Citation
Adamson D, Byrne A, Porter C, Blazeby J, Griffiths G, Nelson A, Sewell B, Jones M, Svobodova M, Fitzsimmons D, Nixon L, Fitzgibbon J, Thomas S, Millin A, Crosby T, Staffurth J, Hurt C. Palliative radiotherapy after oesophageal cancer stenting (ROCS): a multicentre, open-label, phase 3 randomised controlled trial. Lancet Gastroenterol Hepatol. 2021 Apr;6(4):292-303. doi: 10.1016/S2468-1253(21)00004-2. Epub 2021 Feb 19. Erratum In: Lancet Gastroenterol Hepatol. 2021 Apr;6(4):e3.
Results Reference
derived

Learn more about this trial

ROCS (Radiotherapy After Oesophageal Cancer Stenting) Study

We'll reach out to this number within 24 hrs