Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Pelican Cancer Foundation | OTHER |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Extramural venous invasion (EMVI) is the spread of microscopic tumour cells into the veins around the tumour. Rectal cancer treatment has improved greatly over recent years. However, it is important for us to learn as much about the tumours as possible in order to develop newer therapies. Current treatments may benefit from new genetic information relating to the cancer. We hope to identify genetic differences in certain types of rectal cancer which will allow future treatments.
Neoadjuvant chemoradiotherapy (CRT) is widely accepted as beneficial to selected patients in terms of decreased risk of local recurrence and overall survival. Current management of rectal cancer involves risk stratification through pre-operative staging leading to formulation of treatment strategy. Very little is known about the long-term outcomes and response to CRT on MRI detected extramural venous invasion (mrEMVI). Although mrEMVI is accepted as a marker of poor prognosis, whether it has a predictive value and should be specifically treated is not known.
Molecular and genetic profiling provides us with an opportunity to understand the underlying mechanisms which govern clinical behaviour in rectal cancer. Using high-throughput technology such as tissue microarray analysis allows large-scale analysis of specimens in a relatively short amount of time. It offers the ability to compare the molecular profiles of different subtypes of rectal cancer such as mrEMVI-positive and -negative tumours and whether any changes are observed following CRT. This can then be correlated with clinical behaviour over the medium and long-term with regards to local recurrence, distant metastases and overall survival.
This study will identify important differences between key rectal cancer tumour subtypes. Identification of reliable pathological markers of EMVI pathways (from both the primary tumour sample, but more importantly from the pre-operative biopsies) has real potential for taking us a step closer to more personalised management of rectal cancer by establishing prognostic biomarkers reflective of disease type, but also through the underlying biology that may be highlighted (with its promise of therapeutic translation).
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1 | Patients with mrEMVI positive rectal cancer | ||
| Group 2 | Patients with mrEMVI negative rectal cancer |
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| The primary endpoint will be time to relapse pertaining to the primary objective of relapse rate at 1 year and 3 years. | 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| Response rates (in terms of mrTstage, mrN stage, involvement of CRM (circumferential resection margin) and mrTRG (tumour regression grade)) in addition to recurrence rates at 1 year and 3 years. | 3 years | |
| Measurement of the change in mrEMVI from pre to post pre-operative therapy, will be based on a new proposed EMVI-TRG classification (EMVI TRG 1-5). |
Not provided
Inclusion Criteria:
Exclusion Criteria
Not provided
Not provided
Not provided
Patients aged over 18 years of age presenting with adenocarcinoma of the rectum. This will be diagnosed on colonoscopy and/or biopsy and MRI, and treatment strategy will include pre-operative CRT followed by surgery.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Gina Brown | Royal Marsden NHS Foundation Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Peterborough City Hospital | Peterborough | Cambridgeshire | PE3 9GZ | United Kingdom | ||
| Leighton Hospital |
Not provided
Not provided
Not provided
Not provided
Histopathology samples taken after rectal tumour removal surgery will be analysed using micrarray techniques. The pathological tissue microarrays (TMAs) will be generated using the Alphelys Tissue Arrayer Minicore®3 system. Markers that will be evaluated will be initially directed at epithelial to mesenchymal (EMT) transition pathways, as our preliminary studies suggest that this phylogenetically conserved molecular program has important roles in tumour dissemination and resistance to conventional chemotherapy.
mrEMVI Regression Grade Scoring Table: Grade 5 - No response (intermediate signal intensity, same appearances as original tumour) Grade 4 - Slight response (little areas of fibrosis or mucin but mostly tumour) Grade 3 - Moderate response (>50% fibrosis or mucin, and visible intermediate signal) Grade 2 - Good response (dense fibrosis; no obvious residual tumour, signifying minimal residual disease or no tumour) Grade 1 - Radiological complete response (rCR) (linear/crescentic 1-2mm scar in mucosa or submucosa only.) |
| 5 months |
| Crewe |
| Cheshire |
| CW1 4QJ |
| United Kingdom |
| Royal Cornwall Hospital | Truro | Cornwall | TR1 3LQ | United Kingdom |
| Derriford Hospital | Plymouth | Devon | PL6 8DH | United Kingdom |
| Poole Hospital | Poole | Dorset | BH15 2JB | United Kingdom |
| University Hospital Southampton NHS Foundation Trust | Southampton | Hampshire | SO16 6YD | United Kingdom |
| North Manchester General Hospital | Crumpsall | Manchester | M8 5RB | United Kingdom |
| University Hospital of South Manchester | Wythenshawe | Manchester | M23 9LT | United Kingdom |
| Kings Mill Hospital | Sutton in Ashfield | Nottinghamshire | NG17 4JL | United Kingdom |
| Queen's Hospital, Burton Upon Trent | Burton-on-Trent | Staffordshire | Burton-on-Trent | United Kingdom |
| Royal Surrey County Hospital | Guildford | Surrey | GU2 7XX | United Kingdom |
| Homerton University Hospital | London | Surrey | E9 6SR | United Kingdom |
| Croydon University Hospital | Thornton Heath | Surrey | CR7 7YE | United Kingdom |
| University Hospital Coventry | Coventry | West Midlands | CV2 2DX | United Kingdom |
| Salisbury District Hospital | Salisbury | Wiltshire | SP2 8BJ | United Kingdom |
| Royal Marsden Hospital | London and Surrey | United Kingdom |
| George Eliot Hospital | Nuneaton | CV10 7DJ | United Kingdom |
| Alexandra Hospital | Redditch | B98 7UB | United Kingdom |
| South Warwickshire NHS Foundation Trust (Warwick Hospital) | Warwick | CV34 5BW | United Kingdom |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D012002 | Rectal Diseases |
| D015179 | Colorectal Neoplasms |
| D002288 | Adenocarcinoma, Mucinous |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D018297 | Neoplasms, Cystic, Mucinous, and Serous |
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D007410 | Intestinal Diseases |
| D012004 | Rectal Neoplasms |
| ID | Term |
|---|---|
| D003108 | Colonic Diseases |
Not provided
Not provided