ID

21229

Descripción

Study of DNA Mutations in Predicting the Effect of External-Beam Radiation Therapy in Patients With Early Breast Cancer, Localized Prostate Cancer, or Gynecological Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00601406

Link

https://clinicaltrials.gov/show/NCT00601406

Palabras clave

  1. 13/4/17 13/4/17 -
Subido en

13 de abril de 2017

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00601406

Eligibility Breast Cancer NCT00601406

Criteria
Descripción

Criteria

patients must have received curative external-beam radiotherapy within the context of a formal clinical study for any of the following:
Descripción

curative radiotherapy in clinical study

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0008972
UMLS CUI [1,2]
C1522449
early breast cancer after breast-conserving surgery
Descripción

early breast cancer after breast-conserving surgery

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C4016951
UMLS CUI [1,2]
C0917927
localized prostate cancer
Descripción

prostate cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0600139
gynecological cancer (may have also received brachytherapy)
Descripción

gynecological cancer, brachytherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0017411
UMLS CUI [1,3]
C0006098
venous blood samples must be available
Descripción

venous blood samples available

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0444255
UMLS CUI [1,2]
C0470187
patients will be identified from the following clinical studies:
Descripción

patient identification studies

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0008972
UMLS CUI [1,2]
C1269815
cambridge intensity-modulated radiotherapy breast randomized trial
Descripción

radiotherapy to breast trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0008972
UMLS CUI [1,2]
C0948310
rt01 prostate radiotherapy randomized trial/other prostate trials
Descripción

radiotherapy to prostate trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0008972
UMLS CUI [1,2]
C0948317
christie hospital breast, prostate, and gynecological cancer radiotherapy patients
Descripción

radiotherapy to breast, prostate, gynecological cancer trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0008972
UMLS CUI [1,2]
C0948310
UMLS CUI [1,3]
C0948317
UMLS CUI [1,4]
C1522449
UMLS CUI [1,5]
C0017411
UMLS CUI [1,6]
C0006826
must have minimum follow up with late normal tissue effect scoring for two years available
Descripción

follow up available

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0589120
patient characteristics:
Descripción

patient characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
no other malignancy prior to treatment for the specified tumor types except basal cell or squamous cell carcinoma of the skin or in situ carcinoma
Descripción

other malignancies

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0006826
prior concurrent therapy:
Descripción

concurrent therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009429
see disease characteristics
Descripción

disease characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1705348

Similar models

Eligibility Breast Cancer NCT00601406

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
curative radiotherapy in clinical study
Item
patients must have received curative external-beam radiotherapy within the context of a formal clinical study for any of the following:
boolean
C0008972 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
early breast cancer after breast-conserving surgery
Item
early breast cancer after breast-conserving surgery
boolean
C4016951 (UMLS CUI [1,1])
C0917927 (UMLS CUI [1,2])
prostate cancer
Item
localized prostate cancer
boolean
C0600139 (UMLS CUI [1])
gynecological cancer, brachytherapy
Item
gynecological cancer (may have also received brachytherapy)
boolean
C0006826 (UMLS CUI [1,1])
C0017411 (UMLS CUI [1,2])
C0006098 (UMLS CUI [1,3])
venous blood samples available
Item
venous blood samples must be available
boolean
C0444255 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
patient identification studies
Item
patients will be identified from the following clinical studies:
boolean
C0008972 (UMLS CUI [1,1])
C1269815 (UMLS CUI [1,2])
radiotherapy to breast trial
Item
cambridge intensity-modulated radiotherapy breast randomized trial
boolean
C0008972 (UMLS CUI [1,1])
C0948310 (UMLS CUI [1,2])
radiotherapy to prostate trial
Item
rt01 prostate radiotherapy randomized trial/other prostate trials
boolean
C0008972 (UMLS CUI [1,1])
C0948317 (UMLS CUI [1,2])
radiotherapy to breast, prostate, gynecological cancer trial
Item
christie hospital breast, prostate, and gynecological cancer radiotherapy patients
boolean
C0008972 (UMLS CUI [1,1])
C0948310 (UMLS CUI [1,2])
C0948317 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,4])
C0017411 (UMLS CUI [1,5])
C0006826 (UMLS CUI [1,6])
follow up available
Item
must have minimum follow up with late normal tissue effect scoring for two years available
boolean
C0589120 (UMLS CUI [1])
patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
other malignancies
Item
no other malignancy prior to treatment for the specified tumor types except basal cell or squamous cell carcinoma of the skin or in situ carcinoma
boolean
C0009488 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
disease characteristics
Item
see disease characteristics
boolean
C1705348 (UMLS CUI [1])

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