This is a observational, prospective, single arm, proof of concept study to assess safety, feasibility, and potential efficacy of combining Yttrium-90 transarterial radioembolization(TARE) with standard systemic therapy in clinical practice for potentially resectable patients with colorectal liver metastases (CRLM). Alternatively, resectability will also be evaluated. The investigators hypothesize that by applying this approach, higher local control and resection rates can be achieved (typically below 13% for patients who are initially deemed unresectable). Additionally, this treatment option is expected to help delay or reduce the need for (a switch in) systemic treatment and eventually improve survival in patients with liver metastases that are not resectable. All studies reporting the results of TARE at ablative doses are retrospective cohort studies or cases series. Prospective data is needed to expand the indications and reimbursement of radioembolization. Other objectives of the study are: * To calculate the resection rate in patients undergoing the combined approach. * To evaluate immune markers in peripheral blood and resected metastases. * To formulate the first concept of an algorithm, enable to deliver personalized AI assisted dosimetry. * To assess potential role of circulating tumor DNA (ctDNA) in evaluation of patient prognosis and follow up. * To determine the grade of necrosis at the time of resection and correlate with the absorbed dose.
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Monitoring for adverse events related to the procedure.
Timeframe: From 90Y radioembolization (week 2-4) to the end of study at 30 weeks
Evaluate the safety related to the procedure by measuring changes in Liver function values in blood.
Timeframe: From 90Y radioembolization (week 2-4) to the end of study at 30 weeks
Evaluate the safety related to the procedure by measuring changes in Liver function values in blood.
Timeframe: From 90Y radioembolization (week 2-4) to the end of study at 30 weeks
Evaluate the safety related to the procedure by measuring changes in Liver function values in blood.
Timeframe: From 90Y radioembolization (week 2-4) to the end of study at 30 weeks
Evaluate the safety related to the procedure by measuring changes in tumor markers in blood.
Timeframe: From 90Y radioembolization (week 2-4) to the end of study at 30 weeks
Evaluate the quality of Life After Liver Resection Assessed by FACT-C (Version 4) Following 90Y Radioembolization
Timeframe: From 90Y radioembolization (week 2-4) to the end of study at 30 weeks
Evaluate the efficacy of the procedure by tumor response rate assessed by means of RECIST 1.1
Timeframe: From week 0 to resection, progression or week 26-28
Evaluate the efficacy of the procedure: pathologic response assessment on the resected specimens.
Timeframe: From week 0 to resection, progression or week 26-28