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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03699111
Other study ID # CTRIAL-IE 17-26
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 19, 2018
Est. completion date April 3, 2022

Study information

Verified date November 2022
Source Cancer Trials Ireland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a translational, multicentre and multinational study. The aim of this study is to identify new patient stratification tools in microsatellite stable RAS mutant metastatic Colorectal Cancer


Description:

The rational of COLOSSUS is to provide new and more effective stratification tools and therapeutic interventions, specifically tailored to MSS RAS mt mCRC patients


Recruitment information / eligibility

Status Completed
Enrollment 29
Est. completion date April 3, 2022
Est. primary completion date April 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria Patient Status 1. Ability to give signed informed consent prior to any study specific procedures and willing and able to comply with the protocol, 2. Age = 18 years, 3. ECOG status of = 2, 4. At least 16 weeks of life expectancy at time of entry into the study. Disease-related 5. Histologically confirmed stage IV MSS RAS mt mCRC as per standard diagnostic tests, 6. Unresectable and measurable disease (at least one measurable target lesion) as per clinical and radiologic criteria (RECIST v.1.1), 7. No prior chemotherapy and/or radiation therapy for CRC administered in the metastatic setting, 8. Scheduled to receive or receiving SOC chemotherapy with fluoropyrimidines and oxaliplatin +/- bevacizumab (baseline blood sample should be collected and questionnaires completed during pre-screening and before chemotherapy initiation), 9. Availability of archival formalin-fixed paraffin-embedded (FFPE) tissue from: 1. Preferred: surgical resection of the primary or metastatic tumour or 2. Biopsy samples (biopsy taken at endoscope, needle core or surgical incision or excision) obtained from the primary or metastatic tumour. The archival FFPE tissue blocks must be obtained during initial diagnosis (before patient was exposed to any chemotherapy and/or radiation therapy). Exclusion Criteria 1. Patient with CRC that has received any therapy for CRC before: 1. surgical resection of tissue that would be utilised in this study or 2. biopsy procedure for tissue that would be utilised in this study, 2. Patient who has received any investigational product within 28 days of the first day of palliative chemotherapy administration, 3. Patient with any significant history of non-compliance to medical treatments or with inability to grant reliable informed consent, 4. Patient with clinical or laboratory contraindication to receive SOC chemotherapy with fluoropyrimidines and oxaliplatin.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Private Practice Oncology, Heidelberg Heidelberg
Germany University Hospital, Mannheim Mannheim
Germany Private Practice Oncology, Speyer Speyer
Ireland Bon Secours Hospital, Cork Cork
Ireland Beaumont Hospital Dublin
Ireland St Vincent's University Hospital Dublin
Ireland Tallaght University Hospital Dublin
Ireland University Hospital Galway Galway
Spain Hospital Universitari Vall d'Hebron Barcelona
Spain Institut Catala d'Oncologia Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Cancer Trials Ireland

Countries where clinical trial is conducted

Germany,  Ireland,  Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stratification Tools Identification and technical (analytical) validation of new patient stratification tools (COLOSSUS subtypes) in MSS RAS mt mCRC using a novel integrative systems biomedicine multi-omics discovery framework. 4 years
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