ID

43829

Descrizione

IRESSA™ (Gefitinib) in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00632723

collegamento

https://clinicaltrials.gov/show/NCT00632723

Keywords

  1. 05/05/16 05/05/16 -
  2. 18/06/16 18/06/16 -
  3. 20/09/21 20/09/21 -
Caricato su

20 settembre 2021

DOI

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Licenza

Creative Commons BY 4.0

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    Eligibility Breast Cancer NCT00632723

    Eligibility Breast Cancer NCT00632723

    Inclusion Criteria
    Descrizione

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    histological or cytological confirmation of breast cancer that is either
    Descrizione

    diagnosis of breast cancer

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0019638
    a primary tumor in a patient unfit for or who has declined surgery
    Descrizione

    patient with primary tumor

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0677930
    UMLS CUI [1,2]
    C0677930
    UMLS CUI [2]
    C0749192
    advanced (locally or metastatic) disease
    Descrizione

    advanced disease

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0679246
    acquired resistance to tamoxifen or er negative tumour
    Descrizione

    resistance to tamoxifen or ER negative tumour

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0332325
    UMLS CUI [1,2]
    C0039286
    UMLS CUI [2]
    C2584629
    at least one measurable or assessable lesion
    Descrizione

    measurable disease

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1513041
    who performance status 0 - 2
    Descrizione

    who performance status

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1520224
    life expectancy of 12 weeks or more
    Descrizione

    life expectancy

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0023671
    Exclusion Criteria
    Descrizione

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    more than one previous chemotherapy regimens for advanced disease
    Descrizione

    previous chemotherapy regimens

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0205156
    UMLS CUI [1,2]
    C0392920
    prior anthracycline chemotherapy (> 250 mg/m2 adriamycin)
    Descrizione

    prior anthracycline chemotherapy

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0003234
    radiotherapy completed within 14 days prior to day 1 of treatment
    Descrizione

    radiotherapy completed

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    incomplete healing from prior oncologic or other major surgery
    Descrizione

    incomplete healing from prior surgery

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0543478
    signs of neurological symptoms consistent with spinal cord compression
    Descrizione

    neurological symptoms with spinal cord compression

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0235031
    UMLS CUI [1,2]
    C0037926
    any evidence of clinically active interstitial lung disease (patients with chronic stable
    Descrizione

    active interstitial lung disease

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0206062

    Similar models

    Eligibility Breast Cancer NCT00632723

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    C1512693 (UMLS CUI)
    diagnosis of breast cancer
    Item
    histological or cytological confirmation of breast cancer that is either
    boolean
    C0019638 (UMLS CUI [1])
    patient with primary tumor
    Item
    a primary tumor in a patient unfit for or who has declined surgery
    boolean
    C0677930 (UMLS CUI [1,1])
    C0677930 (UMLS CUI [1,2])
    C0749192 (UMLS CUI [2])
    advanced disease
    Item
    advanced (locally or metastatic) disease
    boolean
    C0679246 (UMLS CUI [1])
    resistance to tamoxifen or ER negative tumour
    Item
    acquired resistance to tamoxifen or er negative tumour
    boolean
    C0332325 (UMLS CUI [1,1])
    C0039286 (UMLS CUI [1,2])
    C2584629 (UMLS CUI [2])
    measurable disease
    Item
    at least one measurable or assessable lesion
    boolean
    C1513041 (UMLS CUI [1])
    who performance status
    Item
    who performance status 0 - 2
    boolean
    C1520224 (UMLS CUI [1])
    life expectancy
    Item
    life expectancy of 12 weeks or more
    boolean
    C0023671 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    previous chemotherapy regimens
    Item
    more than one previous chemotherapy regimens for advanced disease
    boolean
    C0205156 (UMLS CUI [1,1])
    C0392920 (UMLS CUI [1,2])
    prior anthracycline chemotherapy
    Item
    prior anthracycline chemotherapy (> 250 mg/m2 adriamycin)
    boolean
    C0003234 (UMLS CUI [1])
    radiotherapy completed
    Item
    radiotherapy completed within 14 days prior to day 1 of treatment
    boolean
    C1522449 (UMLS CUI [1])
    incomplete healing from prior surgery
    Item
    incomplete healing from prior oncologic or other major surgery
    boolean
    C0543478 (UMLS CUI [1])
    neurological symptoms with spinal cord compression
    Item
    signs of neurological symptoms consistent with spinal cord compression
    boolean
    C0235031 (UMLS CUI [1,1])
    C0037926 (UMLS CUI [1,2])
    active interstitial lung disease
    Item
    any evidence of clinically active interstitial lung disease (patients with chronic stable
    boolean
    C0206062 (UMLS CUI [1])

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