A Phase II trial of Higher RadiOtherapy Dose In The Eradication of early rectal cancer.

Study ID: 41422
Short Title: APHRODITE
Trust Name: UHS
Recruitment Site: Southampton General Hospital
Disease Area: Colorectal cancer
Phase: N/A
Expected End Date: 30/04/2025
Postcode: SO16 6YD
Contact Name: Amanda Pattie
Contact Email: studysupport1and3.crnwessex@nihr.ac.uk
Active: Yes

Inclusion criteria, exclusion criteria and study summary

- Biopsy confirmed adenocarcinoma of the rectum - Age 18 or over - Able to provide written informed consent - MDT deems patient unsuitable for radical TME surgical resection of their tumour either because they are considered to be at increased surgical risk from TME (for example due to general frailty or due to specific co-morbidities which make anaesthetic or surgery hazardous, such as cardiac disease, pulmonary disease, renal failure, previous anaesthetic problems or previous pelvic surgery), or they have marked anxiety at the prospect of a stoma, or because of anticipated difficulty managing a stoma post-operatively (including physical causes such as arthritis, Dupuytren’s contracture and visual problems). - Patient is suitable for either pelvic radiotherapy or chemoradiation in the opinion of the treating oncologist - ECOG PS 0-2 - Primary tumour is < = 4 cm in maximum diameter - Primary tumour is staged at T1-T3b. (TNM staging as per UICC 8th Edition (Appendix B), with additional T3 subdivisions) - Tumour is visible on MRI - Superior aspect of tumour is at or below a horizontal line drawn from the anterior aspect of the S2/3 junction on pre-treatment MRI - No unequivocally involved lymph nodes, i.e. NX (nodes too small to characterise as to say equivocal nodes) and N0 are both eligible - For low rectal tumours superior to the puborectalis sling, patients are eligible if the mesorectal fascia or levator are: o Clear (> 1 mm from disease to levator ani or mesorectal fascia) o or threatened (< = 1mm from disease to levator ani or mesorectal fascia) o or mesorectal fascia is involved but not breached - Estimated creatinine clearance > = 50 mls/min (estimated using a validated creatinine clearance calculation e.g. Cockroft and Gault (Appendix D) or Wright formula) - Absolute neutrophil count > 1.5 x 109/l; platelets > 100 x 109/l - Serum transaminase concentration < 3 x Upper Limit Normal (ULN) - Bilirubin concentration < 1.5 x ULN

- Nodal involvement identified by nodes showing irregular margins and or heterogeneous signal on the high resolution MRI (i.e. N1-N2) - The presence of EMVI discontinuous with the primary tumour - Discontinuous tumour deposits (N1c) - Dominant mucinous tumour on MRI - Signet ring carcinoma or tumours histopathologically containing a neuroendocrine component - Tumour has grown through and breached mesorectal fascia - Tumour involves or breaches the levator ani (as this would be T4b disease) - Involvement of anal intersphincteric plane or external anal sphincter or adjacent organs (If the participant has a low rectal tumour extending inferior to the puborectalis sling, involvement of the internal anal sphincter is permitted) - Undergone an attempt at complete local resection of their cancer - Previous pelvic radiotherapy - Definite distant metastases (equivocal distant metastases on the CT scan are permitted, e.g. indeterminate lung modules, sub-centimetre retroperitoneal nodes or indeterminate liver lesion) - Defunctioning colostomy or ileostomy has been fashioned - Prior invasive malignancy unless disease free for a minimum of 3 years (excluding basal cell carcinoma of the skin or other in situ carcinomas) - Prior systemic chemotherapy for colorectal cancer - Women who are pregnant, breastfeeding or a women of child bearing potential who are unwilling to use effective contraceptive methods

An increasing number of patients with early rectal cancer in the UK are being identified through the bowel screening programme. There is a growing number of patients who may not be suitable for surgery, due to other medical comorbidities and factors. These patients may suffer from symptoms as their cancer grows, including pain, diarrhoea and the need for a stoma (bowel bag). For these patients, radiotherapy combined with chemotherapy, or radiotherapy only is used. A standard dose of radiotherapy given over 5.5 weeks can lead to the cancer disappearing in about one third of patients. In this trial we want to find out if a higher radiotherapy dose given over the same time will give greater benefit to patients with acceptable side effects. This could lead to better treatment and improved quality of life.

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