Intra-hepatic Chemotherapy in Patients With Liver Metastases From Breast Cancer and Limited Extrahepatic Disease
This study is currently recruiting participants.
Verified September 2012 by Herlev Hospital
Sponsor:
Herlev Hospital
Collaborators:
Odense University Hospital
Aarhus University Hospital
Information provided by:
Herlev Hospital
ClinicalTrials.gov Identifier:
NCT01387295
First received: May 31, 2011
Last updated: September 27, 2012
Last verified: September 2012
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Purpose
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 with limited extrahepatic disease are included.
| Condition | Intervention | Phase |
|---|---|---|
|
Metastatic Breast Cancer Liver Metastases |
Drug: oxaliplatin, capecitabine, trastuzumab |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | 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 in Patients With Limited Extrahepatic Disease |
Resource links provided by NLM:
Further study details as provided by Herlev Hospital:
Primary Outcome Measures:
- Response rate [ Time Frame: 6 months after last patient included ] [ Designated as safety issue: No ]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
Secondary Outcome Measures:
- Number of patients suitable for local therapy (radiofrequency) [ Time Frame: 6 months after last patient included ] [ Designated as safety issue: No ]Total number of patients receiving RF treatment or surgical treatment
- Survival [ Time Frame: 6 months after last patient included ] [ Designated as safety issue: No ]All patients in intent-to-treat population , calculated from start of treatment to death of any course
- toxicity [ Time Frame: 28 days after last treatment of last patient ] [ Designated as safety issue: Yes ]All patients who received at least one dose of study drug are evaluable for toxicity. CTC version 3.0 will be used.
- PFS [ Time Frame: 6 months after last patient included ] [ Designated as safety issue: No ]From start of therapy to progression or death of any cause.
| Estimated Enrollment: | 100 |
| Study Start Date: | April 2010 |
| Estimated Study Completion Date: | April 2014 |
| Estimated Primary Completion Date: | April 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: chemotherapy |
Drug: oxaliplatin, capecitabine, trastuzumab
Oxaliplatin intrahepatic capecitabine and trastuzumab systemic
Other Name: HAI
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:• Informed consent
- Age > 18 years
- Performance status 0-1; expected survival ≥ 3 months
- Patient with histologically or cytologically confirmed locally advanced or metastatic adenocarcinoma of the breast
- Liver metastases not suitable for local treatment
- Extrahepatic disease should be determined by PET-CT-scan.
- No progression on treatment with capecitabine.
- Prior treatment with taxane (adjuvant or for metastatic disease)
- Metastases < 70 % of the liver
- Neutrophile granulocytes > 1.5 x 109/l og thrombocytes > 100 x 109/l
- Bilirubin < 2.0 x UNL (upper normal limit).
- Creatinine-clearance > 30 ml/min.
- INR < 1.6.
- If the patient is HER2-positive:Baseline LVEF ≥ 50 %
Exclusion Criteria:
- History of chemotherapy within the 4-week period prior to the start of trial medication
- Other current or prior malignant disease except adequately treated and cured carcinoma in situ of the cervix or squamous cell carcinoma of the skin.
- Previous treatment with oxaliplatin
- Cytotoxic or experimental treatment within a 14 days period before start of trial medication
- The patient is not allowed to participate in other clinical trials.
- Any clinical symptoms suggesting peripheral neuropathy < or equal to grade 2 or CNS metastases (In case of clinical suspicion on CNS metastases a MR or CT scan should be performed within 4 weeks before inclusion
- Other severe medical conditions e.g. severe cardial disease or AMI < 1 year
- Presence of diseases which prevent oral therapy.
- Patients with uncontrolled infection
- Pregnant or lactating women
- Women capable of childbearing not using a sufficient non—hormonal method of birth control
- Patients not able to understand the treatment or to collaborate.
- Prior serious or unsuspected reaction after treatment with fluoropyrimidine
- Known prior hypersensitivity reactions to the agents
If the patient is HER2-positive:
- Dyspnoea in due to complication related to malignant disease e.g.lung metastases with lymphangitis or other conditions with need of supportive oxygen.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01387295
Contacts
| Contact: Dorte Nielsen, Professor | +4544884000 ext 82344 | dornie01@heh.regionh.dk |
| Contact: Birgitte Krogh Jensen, Study nurse | +4544884000 ext 89562 | bikrje01@heh.regionh.dk |
Locations
| Denmark | |
| Herlev Hospital | Recruiting |
| Herlev, Denmark, DK-2730 | |
| Contact: Dorte Nielsen, Professor +4544884000 ext 82344 dornie01@heh.regionh.dk | |
| Contact: Birgitte Krogh Jensen, Study nurse +454488000 ext 89562 bikrje01@heh.regionh.dk | |
| Principal Investigator: Dorte Nielsen, professor | |
Sponsors and Collaborators
Herlev Hospital
Odense University Hospital
Aarhus University Hospital
Investigators
| Principal Investigator: | Dorte Nielsen, Professor | professor |
More Information
No publications provided
| Responsible Party: | Dorte Nielsen, professor DMSci, Department of Oncology, Herlev Hospital |
| ClinicalTrials.gov Identifier: | NCT01387295 History of Changes |
| Other Study ID Numbers: | MA 0918 |
| Study First Received: | May 31, 2011 |
| Last Updated: | September 27, 2012 |
| Health Authority: | Denmark: Danish Medicines Agency |
Keywords provided by Herlev Hospital:
|
breast cancer liver metastases intrahepatic chemotherapy |
Additional relevant MeSH terms:
|
Breast Neoplasms Neoplasm Metastasis Neoplasms, Second Primary Liver Neoplasms Neoplasms by Site Neoplasms Breast Diseases Skin Diseases Neoplastic Processes Pathologic Processes Digestive System Neoplasms |
Digestive System Diseases Liver Diseases Oxaliplatin Trastuzumab Capecitabine Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Antimetabolites, Antineoplastic Antimetabolites Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 23, 2013