ID

14812

Descrição

Gemcitabine Plus Cisplatin Versus Gemcitabine Plus Carboplatin in Triple Negative Breast Cancer (TNBC); ODM derived from: https://clinicaltrials.gov/show/NCT02341911

Link

https://clinicaltrials.gov/show/NCT02341911

Palavras-chave

Versões (1)
  1. 29/04/2016 29/04/2016 -
Transferido a

29 de abril de 2016

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Breast Cancer NCT02341911

Inglês

Eligibility Breast Cancer NCT02341911

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. histological proven unresectable recurrent or advanced breast cancer, including de novo stage iv disease.
Descrição

Breast Carcinoma unresectable | Carcinoma breast stage IV de novo

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C1519810
UMLS CUI [2,1]
C0278488
UMLS CUI [2,2]
C1515568
2. triple-negative for estrogen receptor (er), progestogen receptor (pr), and human epithelial receptor-2 (her2) by immunohistochemistry (er <1%, pr <1% and her2 negative). a negative her2 gene amplification should be verified by fish test for those patients with her2 (2+). for those with her2 (1+), fish test might be considered by the investigator.
Descrição

Triple-Negative Breast Cancer Finding | Status of estrogen receptors of neoplasm | Status of progesterone receptors of neoplasm | erbB-2 Receptor | Immunohistochemistry | Human epidermal growth factor 2 negative carcinoma of breast | Human epidermal growth factor 2 gene amplification negative | Fluorescent in Situ Hybridization

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348819
UMLS CUI [2]
C2919271
UMLS CUI [3]
C2919590
UMLS CUI [4]
C0069515
UMLS CUI [5]
C0021044
UMLS CUI [6]
C2316304
UMLS CUI [7]
C3874302
UMLS CUI [8]
C0162789
3. no prior chemotherapy for metastatic breast cancer is permitted. prior administration of chemotherapy in the adjuvant/neoadjuvant setting is acceptable if completed 6 months before the enrollment.
Descrição

Prior Chemotherapy Carcinoma breast stage IV | Adjuvant therapy | Neoadjuvant Therapy

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0278488
UMLS CUI [2]
C0677850
UMLS CUI [3]
C0600558
4. at least one measurable disease according to the response evaluation criteria in solid tumor (recist 1.1)
Descrição

Measurable Disease Response Evaluation Criteria in Solid Tumors

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1709926
5. performance status no more than 1
Descrição

ECOG performance status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1520224
6. all patients enrolled are required to have adequate hematologic, hepatic, and renal function
Descrição

Hematologic function | Liver function | Renal function

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0221130
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232804
7. life expectancy longer than 12 weeks
Descrição

Life Expectancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023671
8. no serious medical history of heart, lung, liver and kidney
Descrição

Heart Diseases | Lung diseases | Liver diseases | Kidney Diseases

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0018799
UMLS CUI [2]
C0024115
UMLS CUI [3]
C0023895
UMLS CUI [4]
C0022658
9. be able to understand the study procedures and sign informed consent.
Descrição

Comprehension Study Protocol Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [1,3]
C0021430
10. patients with good compliance
Descrição

Compliance behavior Good

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0205170
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. pregnant or lactating women (female patients of child-bearing potential must have a negative serum pregnancy test within 14 days before the first day of drug dosing, or, if positive, a pregnancy should be ruled out by ultrasound)
Descrição

Pregnancy | Breast Feeding | Childbearing Potential Serum pregnancy test negative Ultrasonics (sound)

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0430061
UMLS CUI [3,3]
C1456803
2. women of child-bearing potential, unwilling to use adequate contraceptive protection during the process of the study
Descrição

Childbearing Potential | Unwilling Contraceptive methods

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3831118
UMLS CUI [2,1]
C0558080
UMLS CUI [2,2]
C0700589
3. treatment with radiotherapy at the axial skeleton within 4 weeks before the first treatment or has not recovered from all toxicities of previous radiotherapy
Descrição

Therapeutic radiology procedure Entire axial skeleton | Toxic effect Prior radiation therapy

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C1321508
UMLS CUI [2,1]
C0600688
UMLS CUI [2,2]
C0279134
4. treatment with an investigational product within 4 weeks before the first treatment
Descrição

Therapeutic procedure Investigational New Drugs

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0013230
5. patients with symptomatic central nervous system metastases are not permitted, except for those with stable and asymptomatic brain metastases who have completed cranial irradiation, and have at least one measurable lesion outside the brain. radiotherapy should be completed within 4 weeks prior to the registration
Descrição

CNS metastases | Metastatic malignant neoplasm to brain | Cranial Irradiation | Measurable Disease | Therapeutic radiology procedure

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0686377
UMLS CUI [2]
C0220650
UMLS CUI [3]
C0079172
UMLS CUI [4]
C1513041
UMLS CUI [5]
C1522449
6. other active malignancies (including other hematologic malignancies) or other malignancies within the last 5 years, except for cured nonmelanoma skin cancer or cervical intraepithelial neoplasia.
Descrição

Malignant Neoplasms | Hematologic Neoplasms | Skin carcinoma | Cervical Intraepithelial Neoplasia

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0376545
UMLS CUI [3]
C0699893
UMLS CUI [4]
C0206708
7. patients having a history of clinically significant cardiovascular, hepatic, respiratory or renal diseases, clinically significant hematological and endocrinal abnormalities, clinically significant neurological or psychiatric conditions
Descrição

Cardiovascular Diseases | Liver diseases | Respiration Disorders | Kidney Diseases | Abnormality of blood and blood-forming tissues | Abnormality of the endocrine system | nervous system disorder | Mental disorders

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0007222
UMLS CUI [2]
C0023895
UMLS CUI [3]
C0035204
UMLS CUI [4]
C0022658
UMLS CUI [5]
C0850715
UMLS CUI [6]
C4025823
UMLS CUI [7]
C0027765
UMLS CUI [8]
C0004936
8. uncontrolled serious infection
Descrição

Communicable Diseases Uncontrolled

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205318
Voltar ao início da página

Similar models

Eligibility Breast Cancer NCT02341911

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma unresectable | Carcinoma breast stage IV de novo
Item
1. histological proven unresectable recurrent or advanced breast cancer, including de novo stage iv disease.
boolean
C0678222 (UMLS CUI [1,1])
C1519810 (UMLS CUI [1,2])
C0278488 (UMLS CUI [2,1])
C1515568 (UMLS CUI [2,2])
Triple-Negative Breast Cancer Finding | Status of estrogen receptors of neoplasm | Status of progesterone receptors of neoplasm | erbB-2 Receptor | Immunohistochemistry | Human epidermal growth factor 2 negative carcinoma of breast | Human epidermal growth factor 2 gene amplification negative | Fluorescent in Situ Hybridization
Item
2. triple-negative for estrogen receptor (er), progestogen receptor (pr), and human epithelial receptor-2 (her2) by immunohistochemistry (er <1%, pr <1% and her2 negative). a negative her2 gene amplification should be verified by fish test for those patients with her2 (2+). for those with her2 (1+), fish test might be considered by the investigator.
boolean
C2348819 (UMLS CUI [1])
C2919271 (UMLS CUI [2])
C2919590 (UMLS CUI [3])
C0069515 (UMLS CUI [4])
C0021044 (UMLS CUI [5])
C2316304 (UMLS CUI [6])
C3874302 (UMLS CUI [7])
C0162789 (UMLS CUI [8])
Prior Chemotherapy Carcinoma breast stage IV | Adjuvant therapy | Neoadjuvant Therapy
Item
3. no prior chemotherapy for metastatic breast cancer is permitted. prior administration of chemotherapy in the adjuvant/neoadjuvant setting is acceptable if completed 6 months before the enrollment.
boolean
C1514457 (UMLS CUI [1,1])
C0278488 (UMLS CUI [1,2])
C0677850 (UMLS CUI [2])
C0600558 (UMLS CUI [3])
Measurable Disease Response Evaluation Criteria in Solid Tumors
Item
4. at least one measurable disease according to the response evaluation criteria in solid tumor (recist 1.1)
boolean
C1513041 (UMLS CUI [1,1])
C1709926 (UMLS CUI [1,2])
ECOG performance status
Item
5. performance status no more than 1
boolean
C1520224 (UMLS CUI [1])
Hematologic function | Liver function | Renal function
Item
6. all patients enrolled are required to have adequate hematologic, hepatic, and renal function
boolean
C0221130 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Life Expectancy
Item
7. life expectancy longer than 12 weeks
boolean
C0023671 (UMLS CUI [1])
Heart Diseases | Lung diseases | Liver diseases | Kidney Diseases
Item
8. no serious medical history of heart, lung, liver and kidney
boolean
C0018799 (UMLS CUI [1])
C0024115 (UMLS CUI [2])
C0023895 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
Comprehension Study Protocol Informed Consent
Item
9. be able to understand the study procedures and sign informed consent.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
Compliance behavior Good
Item
10. patients with good compliance
boolean
C1321605 (UMLS CUI [1,1])
C0205170 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding | Childbearing Potential Serum pregnancy test negative Ultrasonics (sound)
Item
1. pregnant or lactating women (female patients of child-bearing potential must have a negative serum pregnancy test within 14 days before the first day of drug dosing, or, if positive, a pregnancy should be ruled out by ultrasound)
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0430061 (UMLS CUI [3,2])
C1456803 (UMLS CUI [3,3])
Childbearing Potential | Unwilling Contraceptive methods
Item
2. women of child-bearing potential, unwilling to use adequate contraceptive protection during the process of the study
boolean
C3831118 (UMLS CUI [1])
C0558080 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Therapeutic radiology procedure Entire axial skeleton | Toxic effect Prior radiation therapy
Item
3. treatment with radiotherapy at the axial skeleton within 4 weeks before the first treatment or has not recovered from all toxicities of previous radiotherapy
boolean
C1522449 (UMLS CUI [1,1])
C1321508 (UMLS CUI [1,2])
C0600688 (UMLS CUI [2,1])
C0279134 (UMLS CUI [2,2])
Therapeutic procedure Investigational New Drugs
Item
4. treatment with an investigational product within 4 weeks before the first treatment
boolean
C0087111 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
CNS metastases | Metastatic malignant neoplasm to brain | Cranial Irradiation | Measurable Disease | Therapeutic radiology procedure
Item
5. patients with symptomatic central nervous system metastases are not permitted, except for those with stable and asymptomatic brain metastases who have completed cranial irradiation, and have at least one measurable lesion outside the brain. radiotherapy should be completed within 4 weeks prior to the registration
boolean
C0686377 (UMLS CUI [1])
C0220650 (UMLS CUI [2])
C0079172 (UMLS CUI [3])
C1513041 (UMLS CUI [4])
C1522449 (UMLS CUI [5])
Malignant Neoplasms | Hematologic Neoplasms | Skin carcinoma | Cervical Intraepithelial Neoplasia
Item
6. other active malignancies (including other hematologic malignancies) or other malignancies within the last 5 years, except for cured nonmelanoma skin cancer or cervical intraepithelial neoplasia.
boolean
C0006826 (UMLS CUI [1])
C0376545 (UMLS CUI [2])
C0699893 (UMLS CUI [3])
C0206708 (UMLS CUI [4])
Cardiovascular Diseases | Liver diseases | Respiration Disorders | Kidney Diseases | Abnormality of blood and blood-forming tissues | Abnormality of the endocrine system | nervous system disorder | Mental disorders
Item
7. patients having a history of clinically significant cardiovascular, hepatic, respiratory or renal diseases, clinically significant hematological and endocrinal abnormalities, clinically significant neurological or psychiatric conditions
boolean
C0007222 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
C0035204 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
C0850715 (UMLS CUI [5])
C4025823 (UMLS CUI [6])
C0027765 (UMLS CUI [7])
C0004936 (UMLS CUI [8])
Communicable Diseases Uncontrolled
Item
8. uncontrolled serious infection
boolean
C0009450 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial