Phase II Study to Assess the Safety of Non-operative Management for Low Rectal Cancer

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a 5 year Phase II study to evaluate the safety of non-operative management (NOM) in patients with low rectal cancer (LRC) who achieve a complete clinical response (cCR) following chemoradiotherapy (CRT). The safety of NOM will be evaluated by assessing (i) rate of local re-growth and (ii) rate of macroscopically positive resection margin (R2) when surgery is required due to local re-growth. NOM will be considered safe or as effective as surgery to achieve local control if the rate of local re-growth is equal to or less than 30% and the rate of a macroscopically positive margin is 0%.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Completed chemoradiotherapy (CRT) as standard of care \[Stage II and Stage III (T3-T4N0, AnyTN1-2)\]; \[50 Gy (2 Gy x 25 fractions) with 5-FU or capecitabine\]

• Planned or probable APR

• ALL criteria for complete clinical response are met between 8 and 10 weeks following completion of CRT

• 18 years or older

• Provides written consent

Locations
Other Locations
Canada
Sinai Health System
RECRUITING
Toronto
Contact Information
Primary
Erin Kennedy
erin.kennedy@sinaihealthsystem.ca
416-586-4800
Backup
Selina Schmocker
selina.schmocker@sinaihealthsystem.ca
416-586-4800
Time Frame
Start Date: 2018-03-16
Estimated Completion Date: 2026-12
Participants
Target number of participants: 90
Treatments
Experimental: non-operative management
Patients with low rectal cancer who have achieved a complete clinical response following chemoradiotherapy will undergo active follow-up with regular clinical visits, physical exam, endoscopy and imaging assessments at regular intervals for 2 years to assess for tumour re-growth or spread to the liver and lungs
Related Therapeutic Areas
Sponsors
Leads: Mount Sinai Hospital, Canada

This content was sourced from clinicaltrials.gov