Randomised Study Evaluating Adjuvant Chemotherapy After Resection of Stage III Colonic Adenocarcinoma in Patients of 70 and Over

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age75+
SponsorFederation Francophone de Cancerologie Digestive

About this trial

Colorectal cancer occurs mainly in elderly patients. Recent estimation showed that in France more than 50% of the patients diagnosed with a colorectal cancer are 70 years old or more. Adjuvant chemotherapy has demonstrated a benefit on disease-free survival and overall survival after a stage III colon cancer resection. Nevertheless adjuvant chemotherapy is poorly used in elderly patients. Prognostic improvement with chemotherapy based on 5FU is suggested by a post-hoc analysis of randomized prospective clinical trial. But elderly patients in this study were highly selected and patients older than 80 represented only 0.7% of the total population. Thus, there is still a concern about the benefit of adjuvant 5FU-based chemotherapy in very elderly unselected patients.

The recommended treatment for stage III adjuvant chemotherapy is a combination of fuoropyrimidine and oxaliplatin. Nevertheless oxaliplatin did not demonstrated survival advantage in elderly patients.

Altogether there are still two matters of debate:

* First, is there a benefit of fluoropyrimidine-based adjuvant chemotherapy for unfit elderly patients? * Second, is there a benefit of oxaliplatin-based adjuvant chemotherapy for fit elderly patients? The aim of this randomized phase III study is to evaluate the benefit for disease-free survival of adjuvant chemotherapy in elderly patient and which chemotherapy.

The elderly patient population will be dichotomized into two groups according to physician's choice after a multidisciplinary evaluation involving a geriatrician, with two different randomization assignments. The patients with an expected life-expectancy below 4 years according Lee score are excluded of this study.

Some biological tumour abnormalities are more frequently observed in elderly (i.e. mismatch repair deficiency), therefore an evaluation of specific biological prognostic factors is needed in elderly population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 70 years

Patient considered able to receive chemotherapy

Lee score detailed faxed to CRGA

Stage III colon adenocarcinoma

Disqualifiers

Other progressive disease (cancer uncontrolled for less than 2 years)

Rectal Cancer (located less than 15 cm from the anal verge endoscopy or sub-peritoneal)

ANC <2000 / mm3 for group 1 and ANC <1500 / mm3 for group 2 and platelets <100,000 / mm3 or hemoglobin <9 g / dL

Neuropathy for patients in group 1

Trial design

Design model

Parallel

Treatments tested in this trial

  • LV5FU2 or capectitabine

    Drug
  • FOLFOX4 or XELOX

    Drug
  • Observation

    Other intervention
  • LV5FU2 or capecitabine

    Drug

Treatment groups

774 Participants
are divided into 4 treatment groups
Group A: GROUP1 -ARM AExperimental treatment 1 intervention
Group B: GROUP1-ARMBExperimental treatment 1 intervention
Group C: GROUP2- ARM CExperimental treatment 1 intervention
Group D: GROUP2-ARM DExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The 3-year disease-free survival

Time frame
3 years after last patient in

Secondary outcomes

1

Overal survival

Time frame
5 years after last patient in
2

Observed toxicities, graded according to NCI-CTC v4

Time frame
3 years after last patient in

Other outcomes

Sponsors and contacts

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