ID

34147

Descripción

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

Link

https://clinicaltrials.gov/show/NCT01598285

Palabras clave

  1. 14/1/19 14/1/19 -
Titular de derechos de autor

GSK group of companies

Subido en

14 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer Invasive Nos NCT01598285

Eligibility Breast Cancer Invasive Nos NCT01598285

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

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

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a second neoplasia
Descripción

ID.4

Tipo de datos

boolean

deceased patients
Descripción

ID.5

Tipo de datos

boolean

patients who have not agreed to participate in the study
Descripción

ID.6

Tipo de datos

boolean

her2 positive patients
Descripción

ID.7

Tipo de datos

boolean

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

ID.8

Tipo de datos

boolean

patients with local-regional recurrence only and
Descripción

ID.9

Tipo de datos

boolean

patients with status ned (resected metastases)
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Breast Cancer Invasive Nos NCT01598285

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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