ID

20437

Description

Blood Levels of Tumor Cells in Predicting Response in Patients Receiving First-Line Chemotherapy for Stage IV Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00898014

Lien

https://clinicaltrials.gov/show/NCT00898014

Mots-clés

  1. 22/02/2017 22/02/2017 -
Téléchargé le

22 février 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00898014

Eligibility Breast Cancer NCT00898014

Criteria
Description

Criteria

diagnosis of stage iv breast cancer
Description

breast carcinoma, tumor stage

Type de données

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C1300072
measurable or evaluable disease
Description

measurable or evaluable disease

Type de données

boolean

Alias
UMLS CUI [1]
C1513041
UMLS CUI [2]
C1516986
scheduled to receive first-line chemotherapy with or without trastuzumab (herceptin®), depending on her-2 status
Description

First line treatment; Chemotherapy Regimen | Breast Carcinoma; HER2/Neu Status | trastuzumab

Type de données

boolean

Alias
UMLS CUI [1,1]
C1708063
UMLS CUI [1,2]
C0392920
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C1512413
UMLS CUI [3]
C0728747
histologic block available for confirming pathologic diagnosis and measuring her-2 status via fish
Description

histological diagnosis, her2 status

Type de données

boolean

Alias
UMLS CUI [1]
C0679557
UMLS CUI [2]
C1512413
patient characteristics:
Description

characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C1521970
life expectancy > 3 months
Description

life expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
no other cancer in the past 5 years except for basal cell skin cancer or epithelial in situ cancer of the cervix
Description

History of neoplastic disease | Basal cell carcinoma | Carcinoma in situ of uterine cervix

Type de données

boolean

Alias
UMLS CUI [1]
C2735088
UMLS CUI [2]
C0007117
UMLS CUI [3]
C0851140
no geographic, social, or psychiatric reasons that would make treatment impossible
Description

Protocol Compliance; Limited (extensiveness)

Type de données

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0439801
prior concurrent therapy:
Description

prior concurrent therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0009429
no prior chemotherapy for metastatic disease
Description

prior chemotherapy for metastatic disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C2939420

Similar models

Eligibility Breast Cancer NCT00898014

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
breast carcinoma, tumor stage
Item
diagnosis of stage iv breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
measurable or evaluable disease
Item
measurable or evaluable disease
boolean
C1513041 (UMLS CUI [1])
C1516986 (UMLS CUI [2])
First line treatment; Chemotherapy Regimen | Breast Carcinoma; HER2/Neu Status | trastuzumab
Item
scheduled to receive first-line chemotherapy with or without trastuzumab (herceptin®), depending on her-2 status
boolean
C1708063 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C1512413 (UMLS CUI [2,2])
C0728747 (UMLS CUI [3])
histological diagnosis, her2 status
Item
histologic block available for confirming pathologic diagnosis and measuring her-2 status via fish
boolean
C0679557 (UMLS CUI [1])
C1512413 (UMLS CUI [2])
characteristics
Item
patient characteristics:
boolean
C1521970 (UMLS CUI [1])
life expectancy
Item
life expectancy > 3 months
boolean
C0023671 (UMLS CUI [1])
History of neoplastic disease | Basal cell carcinoma | Carcinoma in situ of uterine cervix
Item
no other cancer in the past 5 years except for basal cell skin cancer or epithelial in situ cancer of the cervix
boolean
C2735088 (UMLS CUI [1])
C0007117 (UMLS CUI [2])
C0851140 (UMLS CUI [3])
Protocol Compliance; Limited (extensiveness)
Item
no geographic, social, or psychiatric reasons that would make treatment impossible
boolean
C0525058 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
prior concurrent therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1,1])
C0009429 (UMLS CUI [1,2])
prior chemotherapy for metastatic disease
Item
no prior chemotherapy for metastatic disease
boolean
C1514457 (UMLS CUI [1,1])
C2939420 (UMLS CUI [1,2])

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