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Non-OpeRative MANagement of Rectal Cancer Patients — NORMANDY  

Rectal Cancer Clinical Trial

Official title:
Non-OpeRative MANagement of Rectal Cancer Patients Who Had Clinical Complete Response After Pre-operative Chemo-raDiotherapY

Clinical Trial Summary

This study is a single-center, open, prospective, single-treatment trial (pilot study). This study aims to analyze the treatment results after receiving capecitabine adjuvant chemotherapy for 4 months after non-surgical treatment in patients who had completed and could have clinical complete remission with capecitabine preoperative chemoradiotherapy with capecitabine for mid-to-lower rectal cancer and to investigate the feasibility of non-surgical treatment.

Clinical Trial Description

Indication: 1. mid-to-lower rectal cancer was diagnosed histologically as adenocarcinoma in preoperative examination, 2. the tumor was located at the lower boundary of the tumor spans the anorectal junction, and the clinical stage is stage 2 or 3, and 3. clinical complete remission was confirmed after the treatment response evaluation at 8 weeks after completion of preoperative chemoradiotherapy according to MR/SFS and biopsy. Aim: 1. to analyze the treatment results after receiving capecitabine adjuvant chemotherapy for 4 months after non-surgical treatment in patients who had completed and could have clinical complete remission with capecitabine preoperative chemoradiotherapy with capecitabine for mid-to-lower rectal cancer 2. to investigate the feasibility of non-surgical treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04696757
Study type Interventional
Source Kangbuk Samsung Hospital
Contact Dong-Hoe Koo
Phone +82-2001-8330
Email dhkoo.smc@gmail.com
Status Recruiting
Phase Early Phase 1
Start date February 1, 2018
Completion date December 31, 2024
View Details
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