Physical Activity in Patients With Metastatic Colorectal Cancer Who Receive Palliative First-line Chemotherapy. A Multicenter Open Label Randomized Controlled Trial
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Metastatic Colorectal Cancer
- Sponsor
- Swiss Group for Clinical Cancer Research
- Enrollment
- 100
- Locations
- 24
- Primary Endpoint
- Change in Patient-reported symptoms as measured by ESAS-r
- Status
- Terminated
- Last Updated
- 3 years ago
Overview
Brief Summary
The purpose of this study is to assess whether a structured physical activity program (PA) during palliative chemotherapy improves progression-free survival (PFS) and/or patient-reported outcomes (ESAS-r) in patients with metastatic colorectal cancer.
Detailed Description
While safety and feasibility as well as some improvements in fitness, fatigue and certain aspects of quality of life have been shown for physical activity in cancer patients during treatment, none of the pre-requisites above (i-iv) is fulfilled in the setting of patients with advanced colon cancer. However, evidence, primarily from the adjuvant setting, that physical activity impacts on treatment tolerability and tumor progression is a strong enough rationale to now embark on this prospective trial. By assessing in a large randomized controlled trial whether a 12-week structured physical activity program during chemotherapy in patients with newly diagnosed colorectal cancer undergoing standard first-line chemotherapy improves progression-free survival as compared to standard first-line chemotherapy alone, all pre-requisites for a practice-changing intervention are met. The physical exercise ACTIVE-program describes a 12-week exercise program consisting of a combination of a bi-weekly aerobic exercise (cycle ergometer) supervised by a physical therapist and a self-paced increase in physical activity during daily life using a pedometer with a daily step goal as a motivational tool. In addition to the supervised exercise program twice a week, patients of the intervention group are recommended to be physically active at home. All patients will undergo standard systemic therapy for metastatic colorectal cancer. Patients in the care-as-usual group are not actively encouraged to change their physical activity level e.g. to start a fitness program during chemotherapy.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Written informed consent according to ICH/GCP regulations before randomization.
- •Patient with histologically or cytologically confirmed colorectal carcinoma (CRC) who start palliative first-line systemic therapy for inoperable or metastatic disease.
- •Note: Patients can be included before the start or within the first three weeks of first-line systemic treatment.
- •Patients with histologically or cytologically confirmed colorectal carcinoma (CRC), who start first-line "conversion"-therapy for borderline resectable metastatic disease and will be reassessed for metastasectomy after 3-4 months of systemic treatment.
- •Note: Patients can be included before the start or within the first three weeks of first-line systemic treatment.
- •Patients who are diagnosed with metastatic disease and were initially treated with surgery and/or radiochemotherapy to the primary tumor are eligible (except if all disease sites/metastases have been removed) Patients who have been curatively treated with histologically or cytologically confirmed nonmetastatic CRC previously and now relapse with metastatic disease are also eligible, irrespective of previous radiochemotherapy and/or adjuvant chemotherapy
- •Patients must have measurable disease on CT scan or MRI to be performed within 6 weeks before randomization (measurability criteria according to RECIST 1.1, non-nodal lesions ≥10 mm, lymph nodes ≥15mm) OR evaluable disease i.e. patient with nonmeasurable metastases but elevated serum tumor-marker (CEA at least \>2xULN).
- •Command of written and spoken language allowing for informed consent and for filling in trial questionnaires.
- •Baseline patient-reported outcomes (PROs) have been completed.
- •WHO performance status 0-
Exclusion Criteria
- •Pre-existing severe medical conditions precluding participation in a physical activity program as determined by the local investigator. Such conditions include: chronic heart failure (greater than NYHA II), recent myocardial infarction (less than 3 months ago), unstable angina pectoris, clinically significant arrhythmias, uncontrolled hypertension with repeated systolic blood pressure above 160mmHg, and COPD (requiring oxygen supply or GOLD stadium greater than 2).
- •Inability to ride a cycle ergometer e.g. for musculoskeletal reasons.
- •Patients in whom all CRC metastases have been removed surgically. It is allowed to include patients for whom metastasectomy might be an option if chemotherapy induces a significant response.
- •Any serious underlying medical condition (at the judgment of the investigator) which could impair the ability of the patient to participate in the trial (e.g. active autoimmune disease, uncontrolled diabetes).
- •Concurrent treatment in a trial with experimental drugs or other anti-cancer therapy, which are hypothesized to alter tumor progression. Participation in an observational trial or a translational trial is allowed. Palliative radiotherapy is allowed.
- •Psychiatric disorder precluding understanding of trial information, giving informed consent, filling out PRO forms, or interfering with compliance.
- •Any psychological, familial, sociological or geographical condition potentially hampering proper compliance with the trial protocol.
Outcomes
Primary Outcomes
Change in Patient-reported symptoms as measured by ESAS-r
Time Frame: in at week 6, 12, 18, 24, 48
The ESAS-r is a summary score ranging from 0 to 100 with lower scores representing better quality of life of the patients.
Progression-free survival (PFS)
Time Frame: every 8 or 9 weeks during one year
Change between 2 tumor assessments
Secondary Outcomes
- Overall survival(after progression (expected 1 year) lifelong follow-up)
- Chemotherapy-completion-rate(week 6, 12, 18, and 24)
- Best Objective Response(at week 8 or 9 during one year)
- Selected adverse events(day 1 of each cycle (every 8 or 9 weeks))
- Initiation or increase of anti-hypertensive drugs(day 1 of each cycle (every 8 or 9 weeks) for one year)