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ocal ablation of liver and lung metastases in patients with colorectal cancer after failure of first- or later-line systemic chemotherapy – a prospective trial

Conditions
C18
C19
C20
Malignant neoplasm of colon
Malignant neoplasm of rectosigmoid junction
Malignant neoplasm of rectum
Registration Number
DRKS00006295
Lead Sponsor
niversitätsklinikum Magdeburg
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
152
Inclusion Criteria

• Histologically confirmed colorectal cancer with liver, lung and / or lymph node metastases
• progression after chemotherapy
• No more than 2 members with active disease
• primary tumor resected, no evidence of local recurrence
• diameter of the largest liver lesion max. 5 cm, not more than five liver metastases
OR
Diameter of the largest lesion 15cm, not more than three liver metastases
(Satellite metastases near the target lesion excluded)
• No more than three lung metastases with a diameter of max. 5cm
OR
not more than five lesions up to 3 cm diameter
• No more than two distant metastases outside the lung and liver (except bone metastases)
• ECOG performance status = 1
• Karnofsky Index = 70%

Exclusion Criteria

• Cerebral metastasis
• Symptomatic bone metastasis
• peritoneal, pleural carcinosis
• Other malignant diseases
• Life expectancy <6 months
• violation of an inclusion criterion

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Progression-free survival after local percutaneous ablation of colorectal liver and lung metastases in patients with progression under first-line (second/thrid line) chemotherapy compared to survival without progression of systemically treated patients group as part of a matched-pair analysis<br><br>(diagnostic imaging, clinical data and questionnaire)
Secondary Outcome Measures
NameTimeMethod
- Effectiveness/local tumor control (follow up CT and/or MRI every 3 months)<br>- Overall survival and quality of life (EQ-5D) of patients (clinical data, questionnaire every 3 months)<br>- these results will be associated with results from collected blood and tissue samples to identify prognostic factors (e.g. microsatellite instability, mutation status: kras/nras/braf, micro-RNA in blodd and tissue)
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