ID

36405

Descrição

Efficacy and Safety of Bevacizumab Plus Sorafenib for the Third-line Treatment in Metastatic Renal Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02330783

Link

https://clinicaltrials.gov/show/NCT02330783

Palavras-chave

Versões (1)
  1. 11/05/2019 11/05/2019 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

11 de maio de 2019

DOI

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Licença

Creative Commons BY 4.0
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Eligibility Metastatic Renal Cell Carcinoma NCT02330783

Inglês

Eligibility Metastatic Renal Cell Carcinoma NCT02330783

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
age≥18 years, ≤75 years, male or female
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
advanced renal cellcarcinoma is diagnosed histologically or pathologically
Descrição

Renal Cell Carcinoma Advanced

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0007134
UMLS CUI [1,2]
C0205179
1st line treatment of sunitinib and 2nd line treatment of everolimus and no more systemic anti-angiogenesis targeted drug therapy
Descrição

First line treatment Sunitinib | Second line treatment Everolimus | Antiangiogenesis therapy Systemic

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1708063
UMLS CUI [1,2]
C1176020
UMLS CUI [2,1]
C1710038
UMLS CUI [2,2]
C0541315
UMLS CUI [3,1]
C0281318
UMLS CUI [3,2]
C0205373
have at least one measurable tumor lesion (response evaluation criteria in solid tumors)
Descrição

Measurable lesion Quantity

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1265611
eastern cooperative oncology group（ecog) performance scale is 0 or 1
Descrição

ECOG performance status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1520224
the expected life span is ≥12 weeks
Descrição

Life Expectancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023671
no contraindications for chemotherapy, with enough liver function and renal function and normal ecg recording peripheral hemogram: neutrophil≥1.5×109/l, plt≥100×109/l, hgb≥90g/l renal function: serum creatinine≤1.5 folds the upper limit of normal (uln) for patients with non-metastatic liver dysfunction:alanine aminotransferase and aspartate aminotransferase≤2.5 uln, for patients with metastatic liver dysfunction: alanine aminotransferase and aspartate aminotransferase≤5 uln
Descrição

Medical contraindication Absent Chemotherapy | Liver function | Renal function | Hematologic function | Neutrophil count | Platelet Count measurement | Hemoglobin measurement | Creatinine measurement, serum | Liver Dysfunction Without Neoplasm Metastasis | Alanine aminotransferase measurement | Aspartate aminotransferase measurement | Liver Dysfunction metastatic

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0392920
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232804
UMLS CUI [4]
C0221130
UMLS CUI [5]
C0200633
UMLS CUI [6]
C0032181
UMLS CUI [7]
C0518015
UMLS CUI [8]
C0201976
UMLS CUI [9,1]
C0086565
UMLS CUI [9,2]
C0332288
UMLS CUI [9,3]
C0027627
UMLS CUI [10]
C0201836
UMLS CUI [11]
C0201899
UMLS CUI [12,1]
C0086565
UMLS CUI [12,2]
C1522484
the patients participate voluntarily and have signed the informed consent form
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant and lactating women, or female patients of child-bearing age without taking contraceptive measures
Descrição

Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0700589
UMLS CUI [3,3]
C0332197
patients with severe acute infection without being controlled effectively or having pyogenic and chronic infections with persistently unhealed wounds
Descrição

Communicable Disease Severe Poorly controlled | Infection pyogenic | Chronic infectious disease | Non-healed wound Persistent

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C3853134
UMLS CUI [2]
C0858906
UMLS CUI [3]
C0151317
UMLS CUI [4,1]
C0750433
UMLS CUI [4,2]
C0205322
past history of serious heart diseases, including: cardiac function classification ≥nyha class ii, unstable angina pectoris, myocardial infarction, arrhythmia requiring anti-arrhythmic drug therapy (excluding β-blockers or digoxin), and uncontrolled hypertension
Descrição

Heart Disease Serious | Cardiac function New York Heart Association Classification | Angina, Unstable | Myocardial Infarction | Cardiac Arrhythmia Requirement Anti-Arrhythmia Agents | Exception Adrenergic beta-1 Receptor Antagonists | Exception Digoxin | Uncontrolled hypertension

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205404
UMLS CUI [2,1]
C0232164
UMLS CUI [2,2]
C1275491
UMLS CUI [3]
C0002965
UMLS CUI [4]
C0027051
UMLS CUI [5,1]
C0003811
UMLS CUI [5,2]
C1514873
UMLS CUI [5,3]
C0003195
UMLS CUI [6,1]
C1705847
UMLS CUI [6,2]
C0304516
UMLS CUI [7,1]
C1705847
UMLS CUI [7,2]
C0012265
UMLS CUI [8]
C1868885
patients with a history of hiv infection or active phase of chronic hepatitis b/c
Descrição

HIV Infection | Hepatitis B, Chronic | Hepatitis C, Chronic

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0524909
UMLS CUI [3]
C0524910
negative imaging examination result 4 weeks prior to enrollment)
Descrição

Imaging Negative

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0011923
UMLS CUI [1,2]
C1513916
epilepsy patients requiring drug therapy (e.g. steroids or antiepileptic drugs)
Descrição

Epilepsy Requirement Pharmacotherapy | Steroids | Antiepileptic Agents

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0014544
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0013216
UMLS CUI [2]
C0038317
UMLS CUI [3]
C0003299
a history of allogeneic organ transplantation
Descrição

Organ Transplantation Allogeneic

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0029216
UMLS CUI [1,2]
C1515895
patients with evidence of hemorrhagic constitution or a past history of hemorrhage
Descrição

Patient constitution Hemorrhagic | Hemorrhage In the past

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0683521
UMLS CUI [1,2]
C0333275
UMLS CUI [2,1]
C0019080
UMLS CUI [2,2]
C1444637
patients currently receiving renal dialysis
Descrição

Dialysis renal

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0011946
UMLS CUI [1,2]
C0022646
past or present concomitant tumors with the primary lesions or histological characteristics different from the tumors evaluated in this study, excluding other tumor cured longer than 3 years before enrollment
Descrição

Cancer Other | Exception Neoplasm Cured

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1707251
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0027651
UMLS CUI [2,3]
C1880198
patients participating in other clinical trials simultaneously
Descrição

Study Subject Participation Status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568
other conditions unsatisfying the inclusion criteria in the investigator's opinions
Descrição

Condition Inconsistent Inclusion criteria

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0442809
UMLS CUI [1,3]
C1512693
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Similar models

Eligibility Metastatic Renal Cell Carcinoma NCT02330783

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age≥18 years, ≤75 years, male or female
boolean
C0001779 (UMLS CUI [1])
Renal Cell Carcinoma Advanced
Item
advanced renal cellcarcinoma is diagnosed histologically or pathologically
boolean
C0007134 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
First line treatment Sunitinib | Second line treatment Everolimus | Antiangiogenesis therapy Systemic
Item
1st line treatment of sunitinib and 2nd line treatment of everolimus and no more systemic anti-angiogenesis targeted drug therapy
boolean
C1708063 (UMLS CUI [1,1])
C1176020 (UMLS CUI [1,2])
C1710038 (UMLS CUI [2,1])
C0541315 (UMLS CUI [2,2])
C0281318 (UMLS CUI [3,1])
C0205373 (UMLS CUI [3,2])
Measurable lesion Quantity
Item
have at least one measurable tumor lesion (response evaluation criteria in solid tumors)
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
ECOG performance status
Item
eastern cooperative oncology group（ecog) performance scale is 0 or 1
boolean
C1520224 (UMLS CUI [1])
Life Expectancy
Item
the expected life span is ≥12 weeks
boolean
C0023671 (UMLS CUI [1])
Medical contraindication Absent Chemotherapy | Liver function | Renal function | Hematologic function | Neutrophil count | Platelet Count measurement | Hemoglobin measurement | Creatinine measurement, serum | Liver Dysfunction Without Neoplasm Metastasis | Alanine aminotransferase measurement | Aspartate aminotransferase measurement | Liver Dysfunction metastatic
Item
no contraindications for chemotherapy, with enough liver function and renal function and normal ecg recording peripheral hemogram: neutrophil≥1.5×109/l, plt≥100×109/l, hgb≥90g/l renal function: serum creatinine≤1.5 folds the upper limit of normal (uln) for patients with non-metastatic liver dysfunction:alanine aminotransferase and aspartate aminotransferase≤2.5 uln, for patients with metastatic liver dysfunction: alanine aminotransferase and aspartate aminotransferase≤5 uln
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
C0221130 (UMLS CUI [4])
C0200633 (UMLS CUI [5])
C0032181 (UMLS CUI [6])
C0518015 (UMLS CUI [7])
C0201976 (UMLS CUI [8])
C0086565 (UMLS CUI [9,1])
C0332288 (UMLS CUI [9,2])
C0027627 (UMLS CUI [9,3])
C0201836 (UMLS CUI [10])
C0201899 (UMLS CUI [11])
C0086565 (UMLS CUI [12,1])
C1522484 (UMLS CUI [12,2])
Informed Consent
Item
the patients participate voluntarily and have signed the informed consent form
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent
Item
pregnant and lactating women, or female patients of child-bearing age without taking contraceptive measures
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Communicable Disease Severe Poorly controlled | Infection pyogenic | Chronic infectious disease | Non-healed wound Persistent
Item
patients with severe acute infection without being controlled effectively or having pyogenic and chronic infections with persistently unhealed wounds
boolean
C0009450 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3853134 (UMLS CUI [1,3])
C0858906 (UMLS CUI [2])
C0151317 (UMLS CUI [3])
C0750433 (UMLS CUI [4,1])
C0205322 (UMLS CUI [4,2])
Heart Disease Serious | Cardiac function New York Heart Association Classification | Angina, Unstable | Myocardial Infarction | Cardiac Arrhythmia Requirement Anti-Arrhythmia Agents | Exception Adrenergic beta-1 Receptor Antagonists | Exception Digoxin | Uncontrolled hypertension
Item
past history of serious heart diseases, including: cardiac function classification ≥nyha class ii, unstable angina pectoris, myocardial infarction, arrhythmia requiring anti-arrhythmic drug therapy (excluding β-blockers or digoxin), and uncontrolled hypertension
boolean
C0018799 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0232164 (UMLS CUI [2,1])
C1275491 (UMLS CUI [2,2])
C0002965 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C0003811 (UMLS CUI [5,1])
C1514873 (UMLS CUI [5,2])
C0003195 (UMLS CUI [5,3])
C1705847 (UMLS CUI [6,1])
C0304516 (UMLS CUI [6,2])
C1705847 (UMLS CUI [7,1])
C0012265 (UMLS CUI [7,2])
C1868885 (UMLS CUI [8])
HIV Infection | Hepatitis B, Chronic | Hepatitis C, Chronic
Item
patients with a history of hiv infection or active phase of chronic hepatitis b/c
boolean
C0019693 (UMLS CUI [1])
C0524909 (UMLS CUI [2])
C0524910 (UMLS CUI [3])
Imaging Negative
Item
negative imaging examination result 4 weeks prior to enrollment)
boolean
C0011923 (UMLS CUI [1,1])
C1513916 (UMLS CUI [1,2])
Epilepsy Requirement Pharmacotherapy | Steroids | Antiepileptic Agents
Item
epilepsy patients requiring drug therapy (e.g. steroids or antiepileptic drugs)
boolean
C0014544 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0013216 (UMLS CUI [1,3])
C0038317 (UMLS CUI [2])
C0003299 (UMLS CUI [3])
Organ Transplantation Allogeneic
Item
a history of allogeneic organ transplantation
boolean
C0029216 (UMLS CUI [1,1])
C1515895 (UMLS CUI [1,2])
Patient constitution Hemorrhagic | Hemorrhage In the past
Item
patients with evidence of hemorrhagic constitution or a past history of hemorrhage
boolean
C0683521 (UMLS CUI [1,1])
C0333275 (UMLS CUI [1,2])
C0019080 (UMLS CUI [2,1])
C1444637 (UMLS CUI [2,2])
Dialysis renal
Item
patients currently receiving renal dialysis
boolean
C0011946 (UMLS CUI [1,1])
C0022646 (UMLS CUI [1,2])
Cancer Other | Exception Neoplasm Cured
Item
past or present concomitant tumors with the primary lesions or histological characteristics different from the tumors evaluated in this study, excluding other tumor cured longer than 3 years before enrollment
boolean
C1707251 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0027651 (UMLS CUI [2,2])
C1880198 (UMLS CUI [2,3])
Study Subject Participation Status
Item
patients participating in other clinical trials simultaneously
boolean
C2348568 (UMLS CUI [1])
Condition Inconsistent Inclusion criteria
Item
other conditions unsatisfying the inclusion criteria in the investigator's opinions
boolean
C0348080 (UMLS CUI [1,1])
C0442809 (UMLS CUI [1,2])
C1512693 (UMLS CUI [1,3])
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