Herlev Hospital
Herlev, DK-2730, Denmark
NCT Number: NCT01387373
This is a phase II trial evaluating intra-hepatic chemotherapy with oxaliplatin every second week in combination with systemic capecitabine and in patients with a HER2-positive tumour in combination with trastuzumab (Herceptin®) in patient with non-resectable liver metastases from breast cancer.
Only patients without extrahepatic disease are included.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Herlev, DK-2730, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
-
If the patient is HER2-positive:
Oxaliplatin intrahepatic capecitabine + trastuzumab systemic
Other names: HAI
Time frame: 6 months after inclusion of last patient
Number of patients with complete or partial response in the liver (RECIST version 1.1)Only patients with measurable disease are included in the protocol. Response rate number of patients with CR + PR divided with total number
Time frame: 6 months after inclusion of last patient
Time from treatment start to progression of disease or death of any cause.
Time frame: 6 months after inclusion of last patient
Total number of patients receiving RF treatment or surgical treatment
Time frame: 6 months after inclusion of last patient
All patients in intent-to-treat population , calculated from start of treatment to death of any cause
Time frame: 28 days after last patient last dose
All patients who received at least one dose of study drug are evaluable for toxicity. CTC version 3.0 will be used.
Dorte Nielsen
Other
Intra-hepatic Chemotherapy With Oxaliplatin Every Second Week in Combination With Systemic Capecitabine in Patient With Non-resectable Liver Metastases From Breast Cancer. A Phase II Trial
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