ID

23693

Description

Treatment of Larotaxel/Docetaxel, +/- Trastuzumab, After Anthracycline-cyclophosphamide in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00485979

Link

https://clinicaltrials.gov/show/NCT00485979

Keywords

Versions (1)
  1. 7/10/17 7/10/17 -
Uploaded on

July 10, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT00485979

English

Eligibility Breast Neoplasms NCT00485979

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven invasive breast adenocarcinoma
Description

Breast adenocarcinoma Invasive

Data type

boolean

Alias
UMLS CUI [1,1]
C0858252
UMLS CUI [1,2]
C0205281
localized breast cancer: stage ii and iii
Description

Breast Carcinoma Localized TNM Breast tumor staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0392752
UMLS CUI [1,3]
C0474926
tumors clinically palpable and ineligible for breast conservative surgery: unifocal tumor with diameter ≥ 3cm (clinical examination) or central unifocal tumor, or whose characteristics make pre-operative chemotherapy mandatory due to high risk factors (i.e. ipsilateral lymph nodes involvement, rapid growth rate)
Description

Malignant Neoplasms Clinical Palpable | Malignant Neoplasms Inappropriate Breast-Conserving Surgery | Unifocal tumor Diameter Size Physical Examination | Unifocal tumor Central | Preoperative Chemotherapy Due to High risk factors | Lymph Node Involvement Ipsilateral | Unifocal tumor Growth rate Rapid

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0205210
UMLS CUI [1,3]
C0522499
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C1548788
UMLS CUI [2,3]
C0917927
UMLS CUI [3,1]
C1302361
UMLS CUI [3,2]
C1301886
UMLS CUI [3,3]
C0456389
UMLS CUI [3,4]
C0031809
UMLS CUI [4,1]
C1302361
UMLS CUI [4,2]
C0205099
UMLS CUI [5,1]
C2347669
UMLS CUI [5,2]
C0678226
UMLS CUI [5,3]
C1830377
UMLS CUI [6,1]
C0806692
UMLS CUI [6,2]
C0441989
UMLS CUI [7,1]
C1302361
UMLS CUI [7,2]
C0449249
UMLS CUI [7,3]
C0456962
after 30 june 2008, known status for her2neu by immunohistochemistry (ihc) or by fluorescent in situ hybridization (fish)
Description

HER2/Neu Status Immunohistochemistry | HER2/Neu Status Fluorescent in Situ Hybridization

Data type

boolean

Alias
UMLS CUI [1,1]
C1512413
UMLS CUI [1,2]
C0021044
UMLS CUI [2,1]
C1512413
UMLS CUI [2,2]
C0162789
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
bilateral and inflammatory breast cancer
Description

Inflammatory Breast Carcinoma Bilateral

Data type

boolean

Alias
UMLS CUI [1,1]
C0278601
UMLS CUI [1,2]
C0238767
abnormal left ventricular ejection fraction
Description

Left ventricular ejection fraction Abnormal

Data type

boolean

Alias
UMLS CUI [1,1]
C0428772
UMLS CUI [1,2]
C0205161
distant metastases or locoregional relapse
Description

Distant metastasis | Relapse Local-Regional

Data type

boolean

Alias
UMLS CUI [1]
C1269798
UMLS CUI [2,1]
C0277556
UMLS CUI [2,2]
C1947913
inadequate organ functions
Description

Organ function Inadequate

Data type

boolean

Alias
UMLS CUI [1,1]
C0678852
UMLS CUI [1,2]
C0205412
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Breast Neoplasms NCT00485979

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Breast adenocarcinoma Invasive
Item
histologically proven invasive breast adenocarcinoma
boolean
C0858252 (UMLS CUI [1,1])
C0205281 (UMLS CUI [1,2])
Breast Carcinoma Localized TNM Breast tumor staging
Item
localized breast cancer: stage ii and iii
boolean
C0678222 (UMLS CUI [1,1])
C0392752 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
Malignant Neoplasms Clinical Palpable | Malignant Neoplasms Inappropriate Breast-Conserving Surgery | Unifocal tumor Diameter Size Physical Examination | Unifocal tumor Central | Preoperative Chemotherapy Due to High risk factors | Lymph Node Involvement Ipsilateral | Unifocal tumor Growth rate Rapid
Item
tumors clinically palpable and ineligible for breast conservative surgery: unifocal tumor with diameter ≥ 3cm (clinical examination) or central unifocal tumor, or whose characteristics make pre-operative chemotherapy mandatory due to high risk factors (i.e. ipsilateral lymph nodes involvement, rapid growth rate)
boolean
C0006826 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C0522499 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C1548788 (UMLS CUI [2,2])
C0917927 (UMLS CUI [2,3])
C1302361 (UMLS CUI [3,1])
C1301886 (UMLS CUI [3,2])
C0456389 (UMLS CUI [3,3])
C0031809 (UMLS CUI [3,4])
C1302361 (UMLS CUI [4,1])
C0205099 (UMLS CUI [4,2])
C2347669 (UMLS CUI [5,1])
C0678226 (UMLS CUI [5,2])
C1830377 (UMLS CUI [5,3])
C0806692 (UMLS CUI [6,1])
C0441989 (UMLS CUI [6,2])
C1302361 (UMLS CUI [7,1])
C0449249 (UMLS CUI [7,2])
C0456962 (UMLS CUI [7,3])
HER2/Neu Status Immunohistochemistry | HER2/Neu Status Fluorescent in Situ Hybridization
Item
after 30 june 2008, known status for her2neu by immunohistochemistry (ihc) or by fluorescent in situ hybridization (fish)
boolean
C1512413 (UMLS CUI [1,1])
C0021044 (UMLS CUI [1,2])
C1512413 (UMLS CUI [2,1])
C0162789 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Inflammatory Breast Carcinoma Bilateral
Item
bilateral and inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
Left ventricular ejection fraction Abnormal
Item
abnormal left ventricular ejection fraction
boolean
C0428772 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
Distant metastasis | Relapse Local-Regional
Item
distant metastases or locoregional relapse
boolean
C1269798 (UMLS CUI [1])
C0277556 (UMLS CUI [2,1])
C1947913 (UMLS CUI [2,2])
Organ function Inadequate
Item
inadequate organ functions
boolean
C0678852 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
Study Subject Participation Status
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean
C2348568 (UMLS CUI [1])
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