ID

34204

Beskrivning

RAS Switch in Patients With Metastatic RAS Native Colorectal Tumors Treated With 1st Line FOLFIRI-Cetuximab; ODM derived from: https://clinicaltrials.gov/show/NCT01943786

Länk

https://clinicaltrials.gov/show/NCT01943786

Nyckelord

  1. 2019-01-15 2019-01-15 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

15 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Colorectal Cancer Metastatic NCT01943786

Eligibility Colorectal Cancer Metastatic NCT01943786

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of stage iv colorectal adenocarcinoma.
Beskrivning

ID.1

Datatyp

boolean

patient ≥ 18 years of age.
Beskrivning

ID.2

Datatyp

boolean

ecog ps 0-1
Beskrivning

ID.3

Datatyp

boolean

life expectancy ≥ 6 months
Beskrivning

ID.4

Datatyp

boolean

candidate for first-line systemic chemotherapy according to regular clinical practice.
Beskrivning

ID.5

Datatyp

boolean

measurable disease.
Beskrivning

ID.6

Datatyp

boolean

wild-type kras
Beskrivning

ID.7

Datatyp

boolean

signed informed consent form.
Beskrivning

ID.8

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient who has received prior chemotherapy for metastatic crc, except for adjuvant treatment completed at least six months before entering study.
Beskrivning

ID.9

Datatyp

boolean

patient in whom there is a contraindication for the use of any of the drugs used in first-line treatment of colorectal cancer: 5-fluorouracil,, irinotecan or cetuximab
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Colorectal Cancer Metastatic NCT01943786

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosis of stage iv colorectal adenocarcinoma.
boolean
ID.2
Item
patient ≥ 18 years of age.
boolean
ID.3
Item
ecog ps 0-1
boolean
ID.4
Item
life expectancy ≥ 6 months
boolean
ID.5
Item
candidate for first-line systemic chemotherapy according to regular clinical practice.
boolean
ID.6
Item
measurable disease.
boolean
ID.7
Item
wild-type kras
boolean
ID.8
Item
signed informed consent form.
boolean
Item Group
C0680251 (UMLS CUI)
ID.9
Item
patient who has received prior chemotherapy for metastatic crc, except for adjuvant treatment completed at least six months before entering study.
boolean
ID.10
Item
patient in whom there is a contraindication for the use of any of the drugs used in first-line treatment of colorectal cancer: 5-fluorouracil,, irinotecan or cetuximab
boolean

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