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The Safety and Effects of Gefitinib in Triple-negative,EGFR Positive Metastatic Breast Cancer

Primary Purpose

Breast Cancer

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
gefitinib
Sponsored by
Jiangmen Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring Triple-negative breast cancer, Epidermal growth factor receptor, Gefitinib

Eligibility Criteria

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

Inclusion Criteria:

  • ≥18 years of age
  • ≥1 measurable or assessable lesion
  • Eastern Cooperative Oncology Group(ECOG)performance status of 0-2
  • adequate renal,hepatic and hematological function
  • a life expectancy of >12 weeks
  • histologically proven EGFR positive metastatic TNBC

Exclusion Criteria:

  • brain metastasis

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    gefitinib

    Arm Description

    gefitinib tablet 250mg/day by mouth until disease progression

    Outcomes

    Primary Outcome Measures

    clinical benefit rate
    The primary end point is objective clinical benefit rate defined as objective response or stable disease for≥24wk

    Secondary Outcome Measures

    progress-free survival(PFS)
    Progress-free survival(PFS)is defined as the time from start of treatment to progression or death.

    Full Information

    First Posted
    November 19, 2012
    Last Updated
    November 30, 2012
    Sponsor
    Jiangmen Central Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01732276
    Brief Title
    The Safety and Effects of Gefitinib in Triple-negative,EGFR Positive Metastatic Breast Cancer
    Official Title
    Phase Ⅱ Study of Gefitinib in Triple-negative,EGFR Positive Metastatic Breast Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2012
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2013 (undefined)
    Primary Completion Date
    April 2015 (Anticipated)
    Study Completion Date
    October 2015 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Jiangmen Central Hospital

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Breast cancer is a heterogeneous disease and can be classified into several distinctive subgroups. Triple-negative breast cancer(TNBC) is defined by lack of estrogen(ER), progesterone(PR) immunoreactivity and lack of human epidermal receptor-2(HER2) overexpression. TNBC comprises around 15% of all breast cancer and is characterized by its aggressive clinical behavior and insensitivity toward available targeted treatment strategies such as endocrine and anti-HER2 therapies.Although TNBC is sensitive to chemotherapy,early relapse with metastatic disease is common and the prognosis is poor. Development Of novel treatment strategies is,therefore,needed and the study of other potential targets in TNBC,like tyrosine kinase receptors,is a topic of interest. Epidermal Growth Factor Receptor(EGFR) is a transmembrane receptor tyrosine kinase that encoded by cell erythroblastosis virus oncogene B1(C-erbB1) and belongs to the HER/Erythroblastosis virus oncogene B(ErbB) family. By several signal pathways,EGFR regulates cell proliferation, differentiation, apoptosis, invasion,and angiogenesis,and serves as a poor prognostic factor.EGFR is overexpressed in a variety of malignancies including TNBC.Gene expression profiling and immunohistochemical studies have indicated that 40 to 60% of TNBCs exhibit EGFR expression and gene amplification was found in 18% of this subgroup,but EGFR mutation was rare in TNBC. By far,the role of gefitinib, an EGFR tyrosine kinase inhibitor(TKI),in the metastatic TNBC has not been identified. Most clinical trials about EGFR TKIs in the breast cancer have one or more limitations including:1) the study population had received heavily pretreatment; 2)the enrolled patients included several subgroups of breast cancer; 3)the expression of EGFR was not clear in the enrolled patients. Here, the investigators launch a prospective clinical trial, and about 50 patients with triple-negative,EGFR positive metastatic breast cancer that have received at least second line therapy will be enrolled. these patients will be treated with gefitinib, the toxicity and effects of gefitinib will be recorded prospectively to evaluate the role of gefitinib in the metastatic TNBC.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Breast Cancer
    Keywords
    Triple-negative breast cancer, Epidermal growth factor receptor, Gefitinib

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    50 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    gefitinib
    Arm Type
    Experimental
    Arm Description
    gefitinib tablet 250mg/day by mouth until disease progression
    Intervention Type
    Drug
    Intervention Name(s)
    gefitinib
    Other Intervention Name(s)
    IRRESA
    Primary Outcome Measure Information:
    Title
    clinical benefit rate
    Description
    The primary end point is objective clinical benefit rate defined as objective response or stable disease for≥24wk
    Time Frame
    one month
    Secondary Outcome Measure Information:
    Title
    progress-free survival(PFS)
    Description
    Progress-free survival(PFS)is defined as the time from start of treatment to progression or death.
    Time Frame
    every 4 weeks
    Other Pre-specified Outcome Measures:
    Title
    Toxicity
    Description
    Toxicity is assessed twice weekly and adverse effects(AEs) are classified according to the National Cancer Institute Common Toxicity Criteria(NCI-CTC).
    Time Frame
    twice weekly

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: ≥18 years of age ≥1 measurable or assessable lesion Eastern Cooperative Oncology Group(ECOG)performance status of 0-2 adequate renal,hepatic and hematological function a life expectancy of >12 weeks histologically proven EGFR positive metastatic TNBC Exclusion Criteria: brain metastasis
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    gengsheng yu
    Phone
    0086-0750-3165915
    Email
    gengsheng_yu@hotmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    gengsheng yu
    Organizational Affiliation
    Department of oncology, Jiangmen central hospital, Jiangmen, China
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    The Safety and Effects of Gefitinib in Triple-negative,EGFR Positive Metastatic Breast Cancer

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