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Capecitabine, Oxaliplatin and Trastuzumab in Treating Patients With HER2 Positive Metastatic Breast Cancer

Primary Purpose

Metastatic Breast Cancer

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Capecitabine
Oxaliplatin
Trastuzumab
Sponsored by
Hoosier Cancer Research Network
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Breast Cancer focused on measuring Breast Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Histologic or cytologic diagnosis of breast cancer with evidence of (1) unresectable, locally recurrent, or (2) metastatic disease.· HER2 gene amplification by FISH. HER protein overexpression by immunohistochemistry will not be sufficient for entry.· At least one measurable lesion as defined by the RECIST. Prior hormonal therapy for metastatic disease is allowed. Maximum of one prior chemotherapy regimen or trastuzumab-containing regimen for unresectable, locally recurrent or metastatic disease Prior radiation therapy is allowed as long as the irradiated area is not the only source of measurable disease. Exclusion Criteria: No prior therapy with capecitabine or oxaliplatin in any setting No prior therapy with other platinum compounds· No other forms of cancer therapy including radiation, chemotherapy and hormonal therapy within 21 days prior to beginning protocol therapy.· No prior unanticipated severe reaction to fluoropyrimidine therapy, or known sensitivity to 5-fluorouracil.· No prior fluoropyrimidine therapy for metastatic disease is allowed. Prior adjuvant fluoropyrimidine therapy is allowed if completed > 12 months from study entry.· No symptomatic brain metastasis. · No evidence of serious concomitant systemic disorders incompatible with the study · No peripheral neuropathy · No major surgery within 28 days prior to beginning protocol therapy.· Negative pregnancy test· No current breastfeeding· No malabsorption syndrome· No evidence of serious concomitant systemic disorders incompatible with the study· Patients must not be treated with any of the following while on protocol therapy or within 28 days prior to beginning protocol therapy: sorivudine, brivudine, cimetidine, allopurinol.

Sites / Locations

  • Medical & Surgical Specialists, LLC
  • Cancer Care Center of Southern Indiana
  • Elkhart Clinic
  • Fort Wayne Oncology & Hematology, Inc
  • Indiana University Cancer Center
  • Quality Cancer Center (MCGOP)
  • Community Regional Cancer Center
  • Medical Consultants, P.C.
  • Northern Indiana Cancer Research Consortium
  • AP&S Clinic
  • Center for Hematology/Oncology of S. Michigan

Arms of the Study

Arm 1

Arm Type

Active Comparator

Arm Label

1

Arm Description

Capecitabine + Oxaliplatin + trastuzumab. Patients must be HER2 positive.

Outcomes

Primary Outcome Measures

- · To determine the objective response rate (CR+PR) of capecitabine, oxaliplatin and trastuzumab(CAPOX-T) in patients with HER2 positive metastatic breast cancer.

Secondary Outcome Measures

To measure time to progression
To determine rate of clinical benefit response (CR + PR + SD > 6 months)
To determine toxicity rate of CAPOX-T in this patient population
To explore potential correlations between changes in HER2 circulating extracellular domain in the primary tumor with response

Full Information

First Posted
September 9, 2005
Last Updated
April 29, 2011
Sponsor
Hoosier Cancer Research Network
Collaborators
Sanofi, Hoffmann-La Roche, Walther Cancer Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00216073
Brief Title
Capecitabine, Oxaliplatin and Trastuzumab in Treating Patients With HER2 Positive Metastatic Breast Cancer
Official Title
A Phase II Trial of Capecitabine, Oxaliplatin and Trastuzumab (CAPOX-T) in Patients With HER-2 Positive Metastatic Breast Cancer: Hoosier Oncology Group BRE03-61
Study Type
Interventional

2. Study Status

Record Verification Date
April 2011
Overall Recruitment Status
Terminated
Why Stopped
Lack of patient accrual
Study Start Date
March 2004 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
October 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Hoosier Cancer Research Network
Collaborators
Sanofi, Hoffmann-La Roche, Walther Cancer Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In vitro data suggest synergy between oxaliplatin and 5-FU. The combination of oxaliplatin with 5-fluorouracil produced objective response rates ranging from 27-34% in two studies of patients with prior chemotherapy. Capecitabine was designed as an orally administered, tumor selective fluoropyrimidine, preferentially converted to 5-FU at the tumor site by the higher levels of pyrimidine nucleoside phosphorylase (PyNPase) in tumor tissues compared to normal tissues. The end result is higher concentrations of 5-fluorouracil in tumor relative to surrounding normal tissue. Trastuzumab is synergistic in vitro with multiple chemotherapeutic agents including the platinum compounds. Studies have shown the efficacy of trastuzumab combined with chemotherapy in patients with HER2 overexpressing metastatic breast cancer. This trial will investigate the activity of capecitabine and oxaliplatin administered with trastuzumab (CAPOX-T) in patients with HER2 overexpressing in patients with advanced disease.
Detailed Description
OUTLINE: This is a multi-center study. CAPOX-T (21 day cycle):Capecitabine 825 mg/m2 orally twice daily Days 1-14Oxaliplatin 100 mg/m2 intravenously Day 1 Trastuzumab : 6 mg/kg intravenously Day 1.8mg/kg loading dose should be given in cycle 1 for patients without previous trastuzumab therapy only. Patients may continue combination therapy until progression or toxicity intervenes. Patients who discontinue either or both cytotoxic agents due to toxicity may, at the investigators discretion, continue therapy with the remaining agents on study until progressive disease ECOG performance status 0 or 1 Hematopoietic:· ANC > 1,200/mm3· Platelets > 100,000/mm3 Hepatic:· Total bilirubin < 1.5 x ULN· AST < 2 x ULN (up to 5 x ULN in patients with known liver involvement) Renal:· Serum creatinine < 1.5 x ULN and estimated creatinine clearance >50ml/min as calculated with Cockroft-Gault equation Cardiovascular:· No clinically significant cardiac disease (e.g. congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmias not well controlled with medication) or myocardial infarction within the last 12 months.· LVEF > LLN by MUGA or ECHO

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Breast Cancer
Keywords
Breast Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Capecitabine + Oxaliplatin + trastuzumab. Patients must be HER2 positive.
Intervention Type
Drug
Intervention Name(s)
Capecitabine
Intervention Description
Capecitabine 825 mg/m2 po bid, days 1-14
Intervention Type
Drug
Intervention Name(s)
Oxaliplatin
Intervention Description
Oxaliplatin 100 mg/m2 IV, day 1
Intervention Type
Drug
Intervention Name(s)
Trastuzumab
Intervention Description
Trastuzumab 6mg/kg IV, day 1. 8 mg/kg loading dose given in cycle 1 for patients without previous trastuzumab therapy only.
Primary Outcome Measure Information:
Title
- · To determine the objective response rate (CR+PR) of capecitabine, oxaliplatin and trastuzumab(CAPOX-T) in patients with HER2 positive metastatic breast cancer.
Time Frame
18 months
Secondary Outcome Measure Information:
Title
To measure time to progression
Time Frame
18 months
Title
To determine rate of clinical benefit response (CR + PR + SD > 6 months)
Time Frame
18 months
Title
To determine toxicity rate of CAPOX-T in this patient population
Time Frame
18 months
Title
To explore potential correlations between changes in HER2 circulating extracellular domain in the primary tumor with response
Time Frame
18 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologic or cytologic diagnosis of breast cancer with evidence of (1) unresectable, locally recurrent, or (2) metastatic disease.· HER2 gene amplification by FISH. HER protein overexpression by immunohistochemistry will not be sufficient for entry.· At least one measurable lesion as defined by the RECIST. Prior hormonal therapy for metastatic disease is allowed. Maximum of one prior chemotherapy regimen or trastuzumab-containing regimen for unresectable, locally recurrent or metastatic disease Prior radiation therapy is allowed as long as the irradiated area is not the only source of measurable disease. Exclusion Criteria: No prior therapy with capecitabine or oxaliplatin in any setting No prior therapy with other platinum compounds· No other forms of cancer therapy including radiation, chemotherapy and hormonal therapy within 21 days prior to beginning protocol therapy.· No prior unanticipated severe reaction to fluoropyrimidine therapy, or known sensitivity to 5-fluorouracil.· No prior fluoropyrimidine therapy for metastatic disease is allowed. Prior adjuvant fluoropyrimidine therapy is allowed if completed > 12 months from study entry.· No symptomatic brain metastasis. · No evidence of serious concomitant systemic disorders incompatible with the study · No peripheral neuropathy · No major surgery within 28 days prior to beginning protocol therapy.· Negative pregnancy test· No current breastfeeding· No malabsorption syndrome· No evidence of serious concomitant systemic disorders incompatible with the study· Patients must not be treated with any of the following while on protocol therapy or within 28 days prior to beginning protocol therapy: sorivudine, brivudine, cimetidine, allopurinol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathy Miller, M.D.
Organizational Affiliation
Hoosier Oncology Group, LLC
Official's Role
Study Chair
Facility Information:
Facility Name
Medical & Surgical Specialists, LLC
City
Galesburg
State/Province
Illinois
ZIP/Postal Code
61401
Country
United States
Facility Name
Cancer Care Center of Southern Indiana
City
Bloomington
State/Province
Indiana
ZIP/Postal Code
47403
Country
United States
Facility Name
Elkhart Clinic
City
Elkhart
State/Province
Indiana
ZIP/Postal Code
46515
Country
United States
Facility Name
Fort Wayne Oncology & Hematology, Inc
City
Fort Wayne
State/Province
Indiana
ZIP/Postal Code
46815
Country
United States
Facility Name
Indiana University Cancer Center
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Quality Cancer Center (MCGOP)
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Community Regional Cancer Center
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46256
Country
United States
Facility Name
Medical Consultants, P.C.
City
Muncie
State/Province
Indiana
ZIP/Postal Code
47303
Country
United States
Facility Name
Northern Indiana Cancer Research Consortium
City
South Bend
State/Province
Indiana
ZIP/Postal Code
46601
Country
United States
Facility Name
AP&S Clinic
City
Terre Haute
State/Province
Indiana
ZIP/Postal Code
47804
Country
United States
Facility Name
Center for Hematology/Oncology of S. Michigan
City
Jackson
State/Province
Michigan
ZIP/Postal Code
49201
Country
United States

12. IPD Sharing Statement

Links:
URL
http://hoosieroncologygroup.org/
Description
Hoosier Oncology Group Home Page

Learn more about this trial

Capecitabine, Oxaliplatin and Trastuzumab in Treating Patients With HER2 Positive Metastatic Breast Cancer

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