ID

43593

Description

Epirubicin and Cyclophosphamide Followed By Docetaxel and Trastuzumab in Treating Women With HER2-Positive Stage III or Stage IV Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00379015

Lien

https://clinicaltrials.gov/show/NCT00379015

Mots-clés

Versions (2)
  1. 13/01/2017 13/01/2017 -
  2. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

  • Plus récent
  • Plus ancien
  • Favori
  • Plus récent
    • Plus récent
    • Plus ancien
    • Favori

Aucun commentaire

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Breast Cancer NCT00379015

Anglais

Eligibility Breast Cancer NCT00379015

1 Formulaires  
Criteria
Description

Criteria

diagnosis of primary breast cancer
Description

Breast Carcinoma Primary

Type de données

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205225
stage iiib, iiic, or iv disease
Description

Disease TNM clinical staging

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3258246
no inflammatory disease
Description

Inflammatory disorder

Type de données

boolean

Alias
UMLS CUI [1]
C1290884
her2 over-expressing tumor as assessed by immunohistochemistry and/or fluorescent in situ hybridization
Description

Malignant Neoplasm ERBB2 Protein Overexpression Immunohistochemistry | Fluorescent in Situ Hybridization

Type de données

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C1515560
UMLS CUI [1,3]
C0021044
UMLS CUI [2]
C0162789
hormone receptor status known
Description

Hormone Receptor Status Known

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205309
patient characteristics:
Description

Client Characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
female
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
menopausal status not specified
Description

Menopausal Status Unspecified

Type de données

boolean

Alias
UMLS CUI [1,1]
C3829127
UMLS CUI [1,2]
C0205370
performance status 0-1
Description

performance status

Type de données

boolean

Alias
UMLS CUI [1]
C1518965
wbc ≤ 10,000/mm³
Description

White Blood Cell Count procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0023508
absolute neutrophil count ≥ 2,000/mm³
Description

Absolute neutrophil count

Type de données

boolean

Alias
UMLS CUI [1]
C0948762
platelet count ≥ 100,000/mm³
Description

Platelet Count measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0032181
hemoglobin ≥ 9.5 g/dl
Description

Hemoglobin measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0518015
sgot/sgpt ≤ 60 iu/l
Description

Aspartate aminotransferase measurement | Alanine aminotransferase measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0201899
UMLS CUI [2]
C0201836
bilirubin ≤ 1.5 mg/dl
Description

Serum total bilirubin measurement

Type de données

boolean

Alias
UMLS CUI [1]
C1278039
creatinine ≤ 1.5 mg/dl
Description

Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
lvef ≥ 55%
Description

Left ventricular ejection fraction

Type de données

boolean

Alias
UMLS CUI [1]
C0428772
no signs of pneumonitis
Description

Pneumonitis signs

Type de données

boolean

Alias
UMLS CUI [1,1]
C3714636
UMLS CUI [1,2]
C0220912
prior concurrent therapy:
Description

Therapeutic procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
no prior surgery except for biopsy
Description

Operative Surgical Procedure | Biopsy

Type de données

boolean

Alias
UMLS CUI [1]
C0543467
UMLS CUI [2]
C0005558
no prior or concurrent chemotherapy and/or hormonal therapy
Description

Chemotherapy | Hormone Therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C0279025
no prior or concurrent biological therapy
Description

Biological treatment

Type de données

boolean

Alias
UMLS CUI [1]
C1531518
no prior or concurrent radiotherapy except postoperative radiotherapy
Description

Therapeutic radiology procedure | Postoperative course of radiotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C1522449
UMLS CUI [2]
C0436206
Retour au début de la page

Similar models

Eligibility Breast Cancer NCT00379015

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Breast Carcinoma Primary
Item
diagnosis of primary breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Disease TNM clinical staging
Item
stage iiib, iiic, or iv disease
boolean
C0012634 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Inflammatory disorder
Item
no inflammatory disease
boolean
C1290884 (UMLS CUI [1])
Malignant Neoplasm ERBB2 Protein Overexpression Immunohistochemistry | Fluorescent in Situ Hybridization
Item
her2 over-expressing tumor as assessed by immunohistochemistry and/or fluorescent in situ hybridization
boolean
C0006826 (UMLS CUI [1,1])
C1515560 (UMLS CUI [1,2])
C0021044 (UMLS CUI [1,3])
C0162789 (UMLS CUI [2])
Hormone Receptor Status Known
Item
hormone receptor status known
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205309 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
performance status
Item
performance status 0-1
boolean
C1518965 (UMLS CUI [1])
White Blood Cell Count procedure
Item
wbc ≤ 10,000/mm³
boolean
C0023508 (UMLS CUI [1])
Absolute neutrophil count
Item
absolute neutrophil count ≥ 2,000/mm³
boolean
C0948762 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count ≥ 100,000/mm³
boolean
C0032181 (UMLS CUI [1])
Hemoglobin measurement
Item
hemoglobin ≥ 9.5 g/dl
boolean
C0518015 (UMLS CUI [1])
Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
sgot/sgpt ≤ 60 iu/l
boolean
C0201899 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
Serum total bilirubin measurement
Item
bilirubin ≤ 1.5 mg/dl
boolean
C1278039 (UMLS CUI [1])
Creatinine measurement, serum
Item
creatinine ≤ 1.5 mg/dl
boolean
C0201976 (UMLS CUI [1])
Left ventricular ejection fraction
Item
lvef ≥ 55%
boolean
C0428772 (UMLS CUI [1])
Pneumonitis signs
Item
no signs of pneumonitis
boolean
C3714636 (UMLS CUI [1,1])
C0220912 (UMLS CUI [1,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Operative Surgical Procedure | Biopsy
Item
no prior surgery except for biopsy
boolean
C0543467 (UMLS CUI [1])
C0005558 (UMLS CUI [2])
Chemotherapy | Hormone Therapy
Item
no prior or concurrent chemotherapy and/or hormonal therapy
boolean
C0392920 (UMLS CUI [1])
C0279025 (UMLS CUI [2])
Biological treatment
Item
no prior or concurrent biological therapy
boolean
C1531518 (UMLS CUI [1])
Therapeutic radiology procedure | Postoperative course of radiotherapy
Item
no prior or concurrent radiotherapy except postoperative radiotherapy
boolean
C1522449 (UMLS CUI [1])
C0436206 (UMLS CUI [2])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial