The main objective is to provide original research results that may change clinical practice related to metastatic colorectal cancer. The study will evaluate treatment and patient care at different stages of the disease trajectory and the use of health care for this large group of patients. It will be possible to compare the effectiveness of chemotherapy, radiotherapy and symptomatic treatment given to "real life" patients with the efficacy reported in randomised clinical trials. By using longitudinal information on imaging, biomarkers, clinical staging and place of care it will be possible to improve patient classification at various stages of the disease. Based on this, a more appropriate, individualized treatment for colorectal cancer may be recommended during the phases of the disease trajectory. Participation in this project will not influence the treatment for colorectal cancer. All patients will be treated and followed-up according to current regional and national guidelines.
The available evidence-based knowledge of patient management is translated into regularly updated clinical guidelines for diagnosis, staging and treatment. The guidelines represent the basis for oncology care in Norway, and health care providers are expected to follow these guidelines. Current guidelines are derived from studies where patients are highly selected and not representative for the whole cohort of patients with metastatic disease. One can speculate if the results of trials conducted in regional centers can be generalized to whole populations in a region. In this respect it will be valuable to study advanced colorectal cancer in the whole population of Middle-Norway, with both one regional center and all other hospitals in the area. More knowledge is needed for the optimal selection of treatment for individual patients. In relation to symptom relief, physical and psychological functioning and overall quality of life, there is clearly a lack of high quality research. A longitudinal follow-up of a large number of metastatic colorectal cancer patients with regular assessments has not been previously launched. The existing infrastructure in Norway makes the study feasible and will provide high internal and external validity related to clinical outcomes. The study will constitute a unique platform for comprehensive research aimed at this patient group. It also provides a concept that can be transferred to other major diseases, and it can be extended to other health regions of Norway.
Study Type
OBSERVATIONAL
Enrollment
354
Ålesund Hospital
Ålesund, Norway
Kristiansund Hospital
Kristiansund, Norway
Levanger Hospital
Levanger, Norway
Molde hospital
Molde, Norway
Namsos Hospital
Namsos, Norway
St Olavs Hospital
Trondheim, Norway
Volda Hospital HF
Volda, Norway
survival
Cancer-specific and overall survival according to treatment, age, sex, biological markers
Time frame: 3 years or until death
Nutritional status
reported on PG-SGA, patient version
Time frame: 3 years or until death
Patient expectations
patient expectations about effects of chemotherapy and satisfaction with treatment
Time frame: 3 years or until death
WHO performance status
Time frame: 3 years or until death
Toxicity of therapy
Number of dose reductions and treatment delays
Time frame: 3 years or until death
Toxicity of therapy
Common Terminology Criteria for Adverse Events (CTCAE) v4.0; grade 3-4 for the following items: Hematology, infectious, gastrointestinal, neurological and thromboembolism
Time frame: 3 years or until death
Health related quality of life
reported on EORTC QLQ-C30
Time frame: 3 years or until death
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