Combination Gemcitabine, Carboplatin With or Without Trastuzumab in Patients With Metastatic Breast Cancer

Last updated: May 2, 2011
Sponsor: SCRI Development Innovations, LLC
Overall Status: Completed

Phase

2

Condition

Breast Cancer

Cancer

Treatment

N/A

Clinical Study ID

NCT00193076
SCRI BRE 63
H3036S
B9E-US-S324
  • Ages > 18
  • Female

Study Summary

Pre-clinical data suggests that combination therapy with gemcitabine and carboplatin is synergistic, and both drugs may be synergistic with trastuzumab. Additionally, recent clinical data suggest that the combination of gemcitabine with platinum is an active regimen in metastatic breast cancer. This study will test the combination of gemcitabine with carboplatin in patients with metastatic breast cancer. Patients with Her2/neu overexpression will be stratified to receive trastuzumab in addition to gemcitabine and carboplatin.

Eligibility Criteria

Inclusion

Inclusion Criteria: To be included in this study, you must meet the following criteria:

  • Locally advanced or metastatic breast cancer

  • Measurable disease as per RECIST criteria

  • No prior chemotherapy in the metastatic breast setting

  • Prior chemotherapy and/or hormonal therapy for early stage breast cancer

  • Adjuvant Herceptin is allowed

  • Prior radiation therapy in either the metastatic or early stage setting

  • Patients may have received any number of hormonal therapies

  • Age >18 years

  • Only women are eligible for the study

  • Able to perform activities of daily living with minimal assistance

  • Normal organ and bone marrow function

  • Patients who will be receiving Trastuzumab must have normal heart function

  • Sign a written informed consent document

Exclusion

Exclusion Criteria: You cannot participate in this study if any of the following apply to you:

  • Received prior chemotherapy for metastatic breast cancer

  • Known leptomeningeal carcinomatosis

  • Uncontrolled brain metastasis

  • Uncontrolled intercurrent illness

  • Pregnant or lactating

  • History of other non-breast cancer malignancy

  • Received prior chemotherapy for early stage breast cancer within 6 months Please note: There are additional inclusion/exclusion criteria. The study center willdetermine if you meet all of the criteria. If you do not qualify for the trial, studypersonnel will explain the reasons. If you do qualify, study personnel will explain thetrial in detail and answer any questions you may have.

Study Design

Total Participants: 96
Study Start date:
November 01, 2003
Estimated Completion Date:
October 31, 2008

Study Description

Upon determination of eligibility, all patients will receive the following treatment:

Gemcitabine + Carboplatin

Connect with a study center

  • Tennessee Oncology

    Nashville, Tennessee 37203
    United States

    Site Not Available

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