ID

34147

Beskrivning

A Combined GWAS and miRNA for the Identification of Bevacizumab Response Predictors in Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01598285

Länk

https://clinicaltrials.gov/show/NCT01598285

Nyckelord

  1. 2019-01-14 2019-01-14 -
Rättsinnehavare

GSK group of companies

Uppladdad den

14 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer Invasive Nos NCT01598285

Eligibility Breast Cancer Invasive Nos NCT01598285

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with breast cancer, at a disseminated stage
Beskrivning

ID.1

Datatyp

boolean

patients treated with bevacizumab in combination with weekly paclitaxel as first line chemotherapy and who have progressed
Beskrivning

ID.2

Datatyp

boolean

alive patients authorizing the extraction and analysis of their biological samples.
Beskrivning

ID.3

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a second neoplasia
Beskrivning

ID.4

Datatyp

boolean

deceased patients
Beskrivning

ID.5

Datatyp

boolean

patients who have not agreed to participate in the study
Beskrivning

ID.6

Datatyp

boolean

her2 positive patients
Beskrivning

ID.7

Datatyp

boolean

patients with cns metastases when first treated with bevacizumab in combination with paclitaxel
Beskrivning

ID.8

Datatyp

boolean

patients with local-regional recurrence only and
Beskrivning

ID.9

Datatyp

boolean

patients with status ned (resected metastases)
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Breast Cancer Invasive Nos NCT01598285

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients with breast cancer, at a disseminated stage
boolean
ID.2
Item
patients treated with bevacizumab in combination with weekly paclitaxel as first line chemotherapy and who have progressed
boolean
ID.3
Item
alive patients authorizing the extraction and analysis of their biological samples.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
patients with a second neoplasia
boolean
ID.5
Item
deceased patients
boolean
ID.6
Item
patients who have not agreed to participate in the study
boolean
ID.7
Item
her2 positive patients
boolean
ID.8
Item
patients with cns metastases when first treated with bevacizumab in combination with paclitaxel
boolean
ID.9
Item
patients with local-regional recurrence only and
boolean
ID.10
Item
patients with status ned (resected metastases)
boolean

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