CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 173 enrolled
Drug / intervention
Capecitabine (Xeloda) +3 moredrug
Likely dose
Capecitabine (Xeloda) 825 mg/m2from record
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Search/NCT01308190
NCT01308190Phase 3Completed

Prospective Randomized Clinical Trial for no Inferiority With Preoperative Chemoradiotherapy and Transanal Endoscopic Microsurgery (TEM) Versus Total Mesorectal Excision in T2-T3s N0, M0 Rectal Cancer

Corporacion Parc Tauli·interventional·Posted Mar 4, 2011·Updated Nov 23, 2021

In Brief

A Phase 3 clinical trial evaluating Capecitabine (Xeloda), 50.4 Gy, and 2 other interventions for Rectal Cancer. Completed, enrolled 173 participants across 1 site.

Detailed Summary

The standard treatment of rectal adenocarcinoma is total mesorectal excision (TME). The technique involves a low anterior rectal or colo-anal resection, very often associated with a protective stoma or abdominal-perineal resection with permanent colostomy. Transanal endoscopic microsurgery (TEM) allows access to tumors up to 20 cm from the anal margin, with minimal postoperative morbidity and mortality. Recent studies of T1 rectal adenocarcinomas consider TEM to be the technique of choice. However the treatment of T2 rectal cancers remains controversial. Chemotherapy and radiotherapy (CT/RT) has achieved a concomitant reduction in local recurrence and an increase in survival. Hypothesis: Patients with rectal adenocarcinoma less than 10 cm from the anal margin and up to 4 cm in size, staged after endorectal ultrasound and MRI as T2 or superficial T3 N0-M0-N0-M0, who underwent surgery after preoperative local chemoradiotherapy (TEM), achieve effective results in terms of local recurrence similar to radical surgery (TME). OBJECTIVES: Primary: To compare the results of local recurrence at 2 years in patients treated with preoperative chemoradiotherapy and TEM and in patients treated with conventional radical surgery (TME). Secondary: To analyse the 3-year survival results in patients treated with CT/RT. Methodology: Multicenter clinical trial in a calculated sample of 173 patients.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRectal Cancer
CountriesSpain

Timeline

Phase 3CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedMar 4, 2011
Enrollment StartAug 1, 2010
Primary CompletionDec 1, 2017
Study CompletionOct 1, 2021
TodayJul 2, 2026
Enrollment to primary: 7.3 yearsPosted 15.3 years ago

Interventions

Capecitabine (Xeloda)drug

Capecitabine 825 mg/m2 every 12 hours orally on days of radiotherapy

50.4 Gyradiation

Radiotherapy was administered in daily fractions of 1.8 Gy 5 days a week according to standard schema. The total dose is 45 Gy plus a boost of 5.4 Gy to the tumor area

Transanal Endoscopic Microsurgeryprocedure

6-8 weeks after Chemoradiotherapy

Total Mesorectal Excisionprocedure

Standard surgical treatment of T2 , T3s, N0, M0 rectal cancer. Early after diagnosis