ID

34179

Descripción

Phase I/II Trial of Stereotactic Body Radiotherapy With Concurrent Fixed Dose Tyrosine Kinase Inhibitors in Metastatic Renal Cell Carcinoma: Dose Limiting Toxicity and Abscopal Effect.; ODM derived from: https://clinicaltrials.gov/show/NCT02334709

Link

https://clinicaltrials.gov/show/NCT02334709

Palabras clave

  1. 15/1/19 15/1/19 -
Titular de derechos de autor

GSK group of companies

Subido en

15 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Carcinoma, Renal Cell NCT02334709

Eligibility Carcinoma, Renal Cell NCT02334709

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Descripción

ID.1

Tipo de datos

boolean

diagnosis of rcc with clear-cell component histology
Descripción

ID.2

Tipo de datos

boolean

at least 3 extracranial measurable metastatic lesions per recist
Descripción

ID.3

Tipo de datos

boolean

karnofsky performance score >60
Descripción

ID.4

Tipo de datos

boolean

patients should have undergone cytoreductive treatment of their rcc at least 6 weeks prior to inclusion
Descripción

ID.5

Tipo de datos

boolean

patients should have adequate organ function for tki treatment.
Descripción

ID.6

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior systemic treatment for rcc
Descripción

ID.7

Tipo de datos

boolean

uncontrolled central nervous metastases
Descripción

ID.8

Tipo de datos

boolean

prior radiotherapy interfering with sbrt
Descripción

ID.9

Tipo de datos

boolean

any disorder precluding understanding of trial information.
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Carcinoma, Renal Cell NCT02334709

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
signed informed consent
boolean
ID.2
Item
diagnosis of rcc with clear-cell component histology
boolean
ID.3
Item
at least 3 extracranial measurable metastatic lesions per recist
boolean
ID.4
Item
karnofsky performance score >60
boolean
ID.5
Item
patients should have undergone cytoreductive treatment of their rcc at least 6 weeks prior to inclusion
boolean
ID.6
Item
patients should have adequate organ function for tki treatment.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
prior systemic treatment for rcc
boolean
ID.8
Item
uncontrolled central nervous metastases
boolean
ID.9
Item
prior radiotherapy interfering with sbrt
boolean
ID.10
Item
any disorder precluding understanding of trial information.
boolean

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