ID

36386

Description

Study of ESR1 Mutations in Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02473120

Lien

https://clinicaltrials.gov/show/NCT02473120

Mots-clés

  1. 09/05/2019 09/05/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

9 mai 2019

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.

Groupe Item commentaires pour :

Item commentaires pour :

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

Eligibility Metastatic Breast Cancer NCT02473120

Eligibility Metastatic Breast Cancer NCT02473120

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
woman aged superior to 18 years old
Description

Gender | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
inform consent signed
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
metastatic breast cancer or loco-regionnaly advanced breast cancer
Description

Secondary malignant neoplasm of female breast | Advanced breast cancer Local-Regional

Type de données

boolean

Alias
UMLS CUI [1]
C0346993
UMLS CUI [2,1]
C3495917
UMLS CUI [2,2]
C1947913
inoperable
Description

Inoperable

Type de données

boolean

Alias
UMLS CUI [1]
C0205187
with an indication to treat with aromatase inhibitor
Description

Indication Aromatase Inhibitors

Type de données

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0593802
treatment with aromatase inhibitors innitiated at the inclusion or at least 6 months before inclusion with a stable disease
Description

Aromatase Inhibitors Initiation | Stable Disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C0593802
UMLS CUI [1,2]
C1704686
UMLS CUI [2]
C0677946
without precedent treatment or with treatment by chemotherapy/tamoxifen/faslodex or aromatase inhibitors in a adjuvant treatment and with a time frame of 2 years between last treatment with aromatase inhibitors and metastatic evolution
Description

Prior Therapy Absent | Chemotherapy | Tamoxifen | Faslodex | Aromatase Inhibitors | Adjuvant therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0332197
UMLS CUI [2]
C0392920
UMLS CUI [3]
C0039286
UMLS CUI [4]
C0701491
UMLS CUI [5]
C0593802
UMLS CUI [6]
C0677850
treatment by aromatase inhibitors alone or in combination with a targeted therapy (trastuzumab +/- pertuzumab, bevacizumab, everolimus)
Description

Aromatase Inhibitors alone | Aromatase Inhibitors Combination Targeted Therapy | trastuzumab | pertuzumab | bevacizumab | everolimus

Type de données

boolean

Alias
UMLS CUI [1,1]
C0593802
UMLS CUI [1,2]
C0205171
UMLS CUI [2,1]
C0593802
UMLS CUI [2,2]
C0205195
UMLS CUI [2,3]
C2985566
UMLS CUI [3]
C0728747
UMLS CUI [4]
C1328025
UMLS CUI [5]
C0796392
UMLS CUI [6]
C0541315
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
no inform consent signed
Description

Informed Consent Lacking

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
patient under guardianship, curatorship
Description

Patient Guardianship

Type de données

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0870627
psychosocial disorder
Description

Psychosocial problem

Type de données

boolean

Alias
UMLS CUI [1]
C0740697
no affiliated or beneficiary of a social benefit system
Description

Social insurance Lacking

Type de données

boolean

Alias
UMLS CUI [1,1]
C0037435
UMLS CUI [1,2]
C0332268

Similar models

Eligibility Metastatic Breast Cancer NCT02473120

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
woman aged superior to 18 years old
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Informed Consent
Item
inform consent signed
boolean
C0021430 (UMLS CUI [1])
Secondary malignant neoplasm of female breast | Advanced breast cancer Local-Regional
Item
metastatic breast cancer or loco-regionnaly advanced breast cancer
boolean
C0346993 (UMLS CUI [1])
C3495917 (UMLS CUI [2,1])
C1947913 (UMLS CUI [2,2])
Inoperable
Item
inoperable
boolean
C0205187 (UMLS CUI [1])
Indication Aromatase Inhibitors
Item
with an indication to treat with aromatase inhibitor
boolean
C3146298 (UMLS CUI [1,1])
C0593802 (UMLS CUI [1,2])
Aromatase Inhibitors Initiation | Stable Disease
Item
treatment with aromatase inhibitors innitiated at the inclusion or at least 6 months before inclusion with a stable disease
boolean
C0593802 (UMLS CUI [1,1])
C1704686 (UMLS CUI [1,2])
C0677946 (UMLS CUI [2])
Prior Therapy Absent | Chemotherapy | Tamoxifen | Faslodex | Aromatase Inhibitors | Adjuvant therapy
Item
without precedent treatment or with treatment by chemotherapy/tamoxifen/faslodex or aromatase inhibitors in a adjuvant treatment and with a time frame of 2 years between last treatment with aromatase inhibitors and metastatic evolution
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2])
C0039286 (UMLS CUI [3])
C0701491 (UMLS CUI [4])
C0593802 (UMLS CUI [5])
C0677850 (UMLS CUI [6])
Aromatase Inhibitors alone | Aromatase Inhibitors Combination Targeted Therapy | trastuzumab | pertuzumab | bevacizumab | everolimus
Item
treatment by aromatase inhibitors alone or in combination with a targeted therapy (trastuzumab +/- pertuzumab, bevacizumab, everolimus)
boolean
C0593802 (UMLS CUI [1,1])
C0205171 (UMLS CUI [1,2])
C0593802 (UMLS CUI [2,1])
C0205195 (UMLS CUI [2,2])
C2985566 (UMLS CUI [2,3])
C0728747 (UMLS CUI [3])
C1328025 (UMLS CUI [4])
C0796392 (UMLS CUI [5])
C0541315 (UMLS CUI [6])
Item Group
C0680251 (UMLS CUI)
Informed Consent Lacking
Item
no inform consent signed
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Patient Guardianship
Item
patient under guardianship, curatorship
boolean
C0030705 (UMLS CUI [1,1])
C0870627 (UMLS CUI [1,2])
Psychosocial problem
Item
psychosocial disorder
boolean
C0740697 (UMLS CUI [1])
Social insurance Lacking
Item
no affiliated or beneficiary of a social benefit system
boolean
C0037435 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])

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

Les champs marqués d’un * sont obligatoires.

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