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Local Excision in Downstaged Rectal Cancer

Phase III Randomized Trial of Local Excision Versus Total Mesorectal Excision in Downstaged T2T3 Low Rectal Cancer After Radiochemotherapy

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00427375
Acronym
GRECCAR 2
Enrollment
148
Registered
2007-01-29
Start date
2007-03-05
Completion date
2018-02-08
Last updated
2018-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal Neoplasms

Keywords

Rectal cancer surgery, Neoadjuvant radiochemotherapy, Randomized clinical trial, Multicenter study

Brief summary

Patients with T2T3 low rectal cancer (size =\< 4 cm) received neoadjuvant treatment (50Gy in 5 weeks with concomitant chemotherapy. Good responders (residual tumour =\< 2 cm) are randomised in local vs rectal excision, 6-8 weeks after treatment. The composite end point evaluates the rate of patients with death, recurrence, major morbidity or severe after effects at two years.

Detailed description

Rectal excision is the standard surgical treatment of rectal cancer. The risk of mortality and major short and long term morbidity induced by rectal excision justifies new treatments. Local excision is a conservative alternative approach associated with low mortality and morbidity. The purpose of this prospective randomised multicenter study is to compare local vs rectal excision in good responders after radiochemotherapy for low rectal cancer. Patients with T2T3 low rectal cancer, less than 8 cm from the anal verge, size =\< 4 cm, received neoadjuvant treatment, included radiotherapy between 45-55Gy in 5 weeks with concomitant chemotherapy consist of at least, one fluoropyrimidine. Good clinical responders (residual tumour =\< 2 cm) are randomised in local vs rectal excision, 6-8 weeks after treatment. In case of not confirmed pathological response following local excision, complementary rectal excision is required. Bad responders (residual tumour \> 2cm) are treated by primary rectal excision. Follow-up includes digital rectal examination, CT-scan and endorectal ultrasound (if local excision) every 4 months for 2 years, then every 6 months for 3 years.

Interventions

PROCEDURElocal rectal excision

New surgical option in good responders after neoadjuvant treatment for low rectal cancer

PROCEDUREtotal mesorectal excision

standard surgery

Sponsors

Sanofi
CollaboratorINDUSTRY
Roche Pharma AG
CollaboratorINDUSTRY
University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* T2T3 low adenocarcinoma of the rectum * Tumour size =\< 4cm * Less than 8 cm from the anal verge * No metastatic disease * Patient is at least 18 years of age * ECOG performance status score =\< 2 * Patient and doctor have signed informed consent * inclusion criteria : Residual clinical tumour size =\< 2cm after radiochemotherapy

Exclusion criteria

* T1, T4 tumour or anal sphincter invasion * Metastatic disease (M1) * Contra indication for radiotherapy and/or fluoropyrimidine use in chemotherapy * History of cancer * Symptomatic cardiac or coronary insufficiency * Severe renal insufficiency * Peripheral neuropathy * Patient included in a trial

Design outcomes

Primary

MeasureTime frame
Compare the proportion of patients presenting at least 1 component of the composite outcome (4 components: death, recurrence, major morbidity and severe after effects) at 2 years after24 months

Secondary

MeasureTime frame
Compare the incidence at 2 years of each component separately: death, recurrence, major morbidity and severe after effect24 months
5-year survival.5 years
Quality of life (QLQ C30 - CR38)at 0, 4, 8 and 12 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026