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ID

43829

Description

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

Lien

https://clinicaltrials.gov/show/NCT00632723

Mots-clés

  1. 05/05/2016 05/05/2016 -
  2. 18/06/2016 18/06/2016 -
  3. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

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Licence

Creative Commons BY 4.0

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    Eligibility Breast Cancer NCT00632723

    Eligibility Breast Cancer NCT00632723

    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    histological or cytological confirmation of breast cancer that is either
    Description

    diagnosis of breast cancer

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0019638 (Histology)
    a primary tumor in a patient unfit for or who has declined surgery
    Description

    patient with primary tumor

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0677930 (Primary Neoplasm)
    UMLS CUI [1,2]
    C0677930 (Primary Neoplasm)
    UMLS CUI [2]
    C0749192 (Surgery Declined)
    LOINC
    LA4388-0
    advanced (locally or metastatic) disease
    Description

    advanced disease

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0679246 (advanced disease)
    acquired resistance to tamoxifen or er negative tumour
    Description

    resistance to tamoxifen or ER negative tumour

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0332325 (Resistant (qualifier value))
    SNOMED
    30714006
    UMLS CUI [1,2]
    C0039286 (tamoxifen)
    SNOMED
    75959001
    UMLS CUI [2]
    C2584629 (Estrogen receptor negative neoplasm)
    SNOMED
    441117001
    at least one measurable or assessable lesion
    Description

    measurable disease

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1513041 (Measurable Disease)
    who performance status 0 - 2
    Description

    who performance status

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1520224 (ECOG performance status)
    SNOMED
    423740007
    life expectancy of 12 weeks or more
    Description

    life expectancy

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0023671 (Life Expectancy)
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    more than one previous chemotherapy regimens for advanced disease
    Description

    previous chemotherapy regimens

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0205156 (Previous)
    SNOMED
    9130008
    LOINC
    LP21061-4
    UMLS CUI [1,2]
    C0392920 (Chemotherapy Regimen)
    SNOMED
    716872004
    prior anthracycline chemotherapy (> 250 mg/m2 adriamycin)
    Description

    prior anthracycline chemotherapy

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0003234 (Anthracycline Antibiotics)
    SNOMED
    108787006
    radiotherapy completed within 14 days prior to day 1 of treatment
    Description

    radiotherapy completed

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1522449 (Therapeutic radiology procedure)
    SNOMED
    53438000
    LOINC
    LA4351-8
    incomplete healing from prior oncologic or other major surgery
    Description

    incomplete healing from prior surgery

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0543478 (Residual Tumor)
    signs of neurological symptoms consistent with spinal cord compression
    Description

    neurological symptoms with spinal cord compression

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0235031 (Neurologic Symptoms)
    SNOMED
    267070008
    UMLS CUI [1,2]
    C0037926 (Compression of spinal cord)
    SNOMED
    71286001
    any evidence of clinically active interstitial lung disease (patients with chronic stable
    Description

    active interstitial lung disease

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0206062 (Lung Diseases, Interstitial)
    SNOMED
    233703007

    Similar models

    Eligibility Breast Cancer NCT00632723

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    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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