ID

43829

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00632723

Trefwoorden

  1. 05-05-16 05-05-16 -
  2. 18-06-16 18-06-16 -
  3. 20-09-21 20-09-21 -
Geüploaded op

20 september 2021

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00632723

Eligibility Breast Cancer NCT00632723

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

diagnosis of breast cancer

Datatype

boolean

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

patient with primary tumor

Datatype

boolean

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

advanced disease

Datatype

boolean

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

resistance to tamoxifen or ER negative tumour

Datatype

boolean

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

measurable disease

Datatype

boolean

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

who performance status

Datatype

boolean

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

life expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

previous chemotherapy regimens

Datatype

boolean

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

prior anthracycline chemotherapy

Datatype

boolean

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

radiotherapy completed

Datatype

boolean

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

incomplete healing from prior surgery

Datatype

boolean

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

neurological symptoms with spinal cord compression

Datatype

boolean

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

active interstitial lung disease

Datatype

boolean

Alias
UMLS CUI [1]
C0206062

Similar models

Eligibility Breast Cancer NCT00632723

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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