0 Evaluaciones

ID

16428

Descripción

A Study of Pertuzumab in Participants With Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02491892

Link

https://clinicaltrials.gov/show/NCT02491892

Palabras clave

  1. 16/7/16 16/7/16 -
  2. 17/9/21 17/9/21 -
Subido en

16 de julio de 2016

DOI

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Licencia

Creative Commons BY 4.0

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    Eligibility Breast Cancer NCT02491892

    Eligibility Breast Cancer NCT02491892

    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    females at least 18 years of age
    Descripción

    Gender | Age

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2]
    C0001779
    histologically-confirmed metastatic breast cancer with low her2 expression and at least one measurable lesion according to response evaluation criteria in solid tumors (recist)
    Descripción

    Carcinoma breast stage IV | HER-2 protein overexpression low | Measurable lesion

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0278488
    UMLS CUI [2,1]
    C3888504
    UMLS CUI [2,2]
    C0205251
    UMLS CUI [3]
    C1513041
    karnofsky performance status at least 80%
    Descripción

    Karnofsky Performance Status

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0206065
    disease progression on/after up to 2 different chemotherapy regimens, including an anthracycline-containing therapy
    Descripción

    Chemotherapy Quantity | Anthracycline Antibiotics | Disease Progression

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0392920
    UMLS CUI [1,2]
    C1265611
    UMLS CUI [2]
    C0003234
    UMLS CUI [3]
    C0242656
    left ventricular ejection fraction (lvef) at least 50%
    Descripción

    Left ventricular ejection fraction

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0428772
    adequate liver function
    Descripción

    Liver function

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0232741
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    pleural effusions, ascites, or bone lesions as the only manifestation(s) of cancer
    Descripción

    Malignant Neoplasm Manifestation of | Pleural effusion disorder | Ascites | Bone lesion

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0006826
    UMLS CUI [1,2]
    C1280464
    UMLS CUI [2]
    C0032227
    UMLS CUI [3]
    C0003962
    UMLS CUI [4]
    C0238792
    pulmonary or central nervous system (cns) metastases
    Descripción

    Secondary malignant neoplasm of lung | CNS metastases

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0153676
    UMLS CUI [2]
    C0686377
    chemotherapy, radiotherapy, or immunotherapy within 4 weeks; or hormone therapy within 2 weeks of day 1
    Descripción

    Chemotherapy | Therapeutic radiology procedure | Immunotherapy | Hormone Therapy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0392920
    UMLS CUI [2]
    C1522449
    UMLS CUI [3]
    C0021083
    UMLS CUI [4]
    C0279025
    previous treatment with any drug that targets the her2 receptor family
    Descripción

    Pharmaceutical Preparation Targeting erbB-2 Receptor

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C1521840
    UMLS CUI [1,3]
    C0069515
    previous treatment with corticosteroids as cancer therapy
    Descripción

    cancer treatment | Adrenal Cortex Hormones

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0920425
    UMLS CUI [2]
    C0001617
    history of significant cardiac disease
    Descripción

    Heart Disease Significant

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0018799
    UMLS CUI [1,2]
    C0750502
    major surgery or trauma within 4 weeks of day 1
    Descripción

    major surgery | Major trauma

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0679637
    UMLS CUI [2]
    C0332677
    pregnant or lactating women
    Descripción

    Pregnancy | Breast Feeding

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147

    Similar models

    Eligibility Breast Cancer NCT02491892

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Gender | Age
    Item
    females at least 18 years of age
    boolean
    C0079399 (UMLS CUI [1])
    C0001779 (UMLS CUI [2])
    Carcinoma breast stage IV | HER-2 protein overexpression low | Measurable lesion
    Item
    histologically-confirmed metastatic breast cancer with low her2 expression and at least one measurable lesion according to response evaluation criteria in solid tumors (recist)
    boolean
    C0278488 (UMLS CUI [1])
    C3888504 (UMLS CUI [2,1])
    C0205251 (UMLS CUI [2,2])
    C1513041 (UMLS CUI [3])
    Karnofsky Performance Status
    Item
    karnofsky performance status at least 80%
    boolean
    C0206065 (UMLS CUI [1])
    Chemotherapy Quantity | Anthracycline Antibiotics | Disease Progression
    Item
    disease progression on/after up to 2 different chemotherapy regimens, including an anthracycline-containing therapy
    boolean
    C0392920 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    C0003234 (UMLS CUI [2])
    C0242656 (UMLS CUI [3])
    Left ventricular ejection fraction
    Item
    left ventricular ejection fraction (lvef) at least 50%
    boolean
    C0428772 (UMLS CUI [1])
    Liver function
    Item
    adequate liver function
    boolean
    C0232741 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Malignant Neoplasm Manifestation of | Pleural effusion disorder | Ascites | Bone lesion
    Item
    pleural effusions, ascites, or bone lesions as the only manifestation(s) of cancer
    boolean
    C0006826 (UMLS CUI [1,1])
    C1280464 (UMLS CUI [1,2])
    C0032227 (UMLS CUI [2])
    C0003962 (UMLS CUI [3])
    C0238792 (UMLS CUI [4])
    Secondary malignant neoplasm of lung | CNS metastases
    Item
    pulmonary or central nervous system (cns) metastases
    boolean
    C0153676 (UMLS CUI [1])
    C0686377 (UMLS CUI [2])
    Chemotherapy | Therapeutic radiology procedure | Immunotherapy | Hormone Therapy
    Item
    chemotherapy, radiotherapy, or immunotherapy within 4 weeks; or hormone therapy within 2 weeks of day 1
    boolean
    C0392920 (UMLS CUI [1])
    C1522449 (UMLS CUI [2])
    C0021083 (UMLS CUI [3])
    C0279025 (UMLS CUI [4])
    Pharmaceutical Preparation Targeting erbB-2 Receptor
    Item
    previous treatment with any drug that targets the her2 receptor family
    boolean
    C0013227 (UMLS CUI [1,1])
    C1521840 (UMLS CUI [1,2])
    C0069515 (UMLS CUI [1,3])
    cancer treatment | Adrenal Cortex Hormones
    Item
    previous treatment with corticosteroids as cancer therapy
    boolean
    C0920425 (UMLS CUI [1])
    C0001617 (UMLS CUI [2])
    Heart Disease Significant
    Item
    history of significant cardiac disease
    boolean
    C0018799 (UMLS CUI [1,1])
    C0750502 (UMLS CUI [1,2])
    major surgery | Major trauma
    Item
    major surgery or trauma within 4 weeks of day 1
    boolean
    C0679637 (UMLS CUI [1])
    C0332677 (UMLS CUI [2])
    Pregnancy | Breast Feeding
    Item
    pregnant or lactating women
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])

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