The clinical benefit of resection of the primary tumour in patients with synchronous unresectable metastases is not known. In the literature studies usually describe retrospective selected patients with synchronous metastases treated with or without resection of the primary tumour. All these studies are biased in patient selection and there are no prospective randomized studies on this topic. In patients with few or absent symptoms of the primary tumour, arguments both in favour and against initial resection have been presented, and therefore a randomized trial is warranted. Although recent publications suggest that resection of the primary tumour in synchronous metastasized colon cancer patients might not be necessary, this appears to be based on feasibility and not on clinical outcome. Several studies comparing large groups of patients with or without resection of the primary tumour suggest an improved survival when the primary tumour is resected. A potential benefit of resection of the primary tumour is to prevent complications of the primary tumour during chemotherapy treatment or during later stages of the disease. A recent analysis of the CAIRO and CAIRO2 data showed that metastatic colon cancer patients who had a resection of the primary tumour prior to study entry, had an improved survival compared to patients without a resection of the primary tumour. However, these patients were selected after the primary tumour was resected and therefore these results are not corrected for surgical morbidity and mortality. The investigators here propose a randomized trial in order to demonstrate that resection of the primary tumour does improve overall survival.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
206
Surgical resection of the colon tumour
First line fluoropyrimidine-based chemotherapy with bevacizumab. The chemotherapy regimen is to the discretion of the local investigator, who may choose between: 5FU/LV or capecitabine or capecitabine + oxaliplatin(CAPOX)or 5FU + oxaliplatin(FOLFOX 4 or FOLFOX 7)or 5FU + irinotecan (FOLFIRI) or capecitabine + irinotecan(CAPIRI)
University Hospital Aalborg
Aalborg, Denmark
Rigshospitalet
Copenhagen, Denmark
Herlev Hospital
Herlev, Denmark
Regionshospital Herning
Herning, Denmark
Roskilde hospital
Roskilde, Denmark
Jeroen Bosch
's-Hertogenbosch, Netherlands
Overall survival
Overall survival of the intent-to-treat population
Time frame: Time from randomisation until death, assessed up to 5 years
Progression-free survival
Time frame: Time from randomisation until first progression or death whichever comes first, asessed up to 5 years
Response to chemotherapy
Response rate according to RECIST 1.1
Time frame: Fist-line chemotherapy, assessed until progression
Systemic therapy related toxicity
Adverse events grade 3-4 according to NCI-CTC 4.0
Time frame: Every 3 weeks during first-line treatment
Surgery related morbidity and mortality
Time frame: 30 days
Quality of life
EORTC QLQ-C30 and CR38
Time frame: Every 6 months from randomisation until first progression
Interval between randomization and initiation of systemic treatment
Time frame: Number of days between randomization and initiation of systemic treatment
Cost-benefit analyses
Time frame: Until end of first-line systemic treatment
Patients requiring resection of the primary tumour in the non-resection arm
Number of patients requiring resection of the primary tumour in the non-resection arm
Time frame: Time from randomisation until death, assessed up to 5 years
Overall survival in patients in whom treatment according to protocol was initiated
Having received at least one cycle of systemic treatment in arm A and surgery in arm B
Time frame: Time form randomisation until death, assessed up to 5 years
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Medisch Centrum Alkmaar
Alkmaar, Netherlands
Ziekenhuisgroep Twente
Almelo, Netherlands
Flevoziekenhuis
Almere Stad, Netherlands
Ziekenhuis Amstelland
Amstelveen, Netherlands
...and 36 more locations