CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 920 enrolled
Drug / intervention
M1 scheme +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01558921
NCT01558921Phase 3Active

Randomized Multicentre Phase III Study of Short Course Radiation Therapy Followed by Prolonged Pre-operative Chemotherapy and Surgery in Primary High Risk Rectal Cancer Compared to Standard Chemoradiotherapy and Surgery and Optional Adjuvant Chemotherapy.

University Medical Center Groningen·interventional·Posted Mar 20, 2012·Updated May 1, 2026

In Brief

A Phase 3 clinical trial evaluating M1 scheme and standard long course chemoradiotherapy for Rectal Cancer. Active but no longer recruiting, targeting 920 participants across 56 sites in 7 countries.

Detailed Summary

Currently the 3-year disease free survival of patients with locally advanced rectal cancer is about 50%. Current standard treatment for patients at high risk of failing locally and/or systemically includes pre-operative long course radiotherapy (5 weeks) in combination with chemotherapy (so called neoadjuvant chemoradiotherapy). The neoadjuvant chemoradiotherapy has been demonstrated to improve local control, but had no effect on the overall survival. Different studies in patients with rectal cancer studying the effect of adjuvant post operative chemotherapy did not result in an improved survival. This may be due the fact that rectal cancer surgery (TME) is associated with a high complication rate so substantial proportion of patients cannot receive chemotherapy postoperatively. An alternative approach is to administer the systemic therapy preoperative. To guarantee control of the rectum tumor short-course radiotherapy (5 days) is given, as different studies showed local control of the tumor for a long time. During this waiting period the patient is in a good condition to receive an optimal dose of chemotherapy. The investigators hypothesize that with this proposed protocol both the local tumour and possible micrometastases are effectively treated and that this will result in an increased survival. The investigators will compare this with the standard treatment of neoadjuvant chemoradiation followed by TME surgery and optional adjuvant chemotherapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRectal Cancer
CountriesDenmark, Netherlands, Norway, Slovenia, Spain, Sweden, United States

Timeline

Phase 3Active
2012201320142015201620172018201920202021202220232024202520262027
First PostedMar 20, 2012
Enrollment StartJun 21, 2011
Primary CompletionMar 8, 2020
Study CompletionDec 31, 2026
TodayJul 2, 2026
Enrollment to primary: 8.7 yearsPosted 14.3 years ago

Interventions

M1 schemeother

short course 5x5Gy radiation scheme is followed by six cycles of combination chemotherapy (capecitabine and oxaliplatin (CAPOX)) and surgery. FOLFOX4 may be given as alternative for CAPOX

standard long course chemoradiotherapyother

long course chemoradiotherapy followed by surgery. Optional adjuvant chemotherapy (CAPOX or FOLFOX) is allowed in the control group.