Eligibility Advanced Adult Hepatocellular Carcinoma NCT02409524

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females who are at least 18 years of age at time of enrollment
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
histologically confirmed hepatocellular carcinoma with or without positive hbv and/or hcv
Beskrivning

hepatocellular carcinoma

Datatyp

boolean

Alias
UMLS CUI [1]
C2239176
minimum of 90 days of sorafenib treatment and unresectable
Beskrivning

sorafenib

Datatyp

boolean

Alias
UMLS CUI [1]
C1516119
child-pugh stage a-b (score ≥ 5 and ≤ 9)
Beskrivning

child-pugh stage

Datatyp

boolean

Alias
UMLS CUI [1]
C4050412
performance status: ecog < 2 with no deterioration over the previous 2 weeks
Beskrivning

ecog

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
measurable disease (for recist)
Beskrivning

measurable disease

Datatyp

boolean

Alias
UMLS CUI [1]
C1513041
lesion amenable for percutaneous tumor harvest and follow up biopsy
Beskrivning

percutaneous tumor harvest

Datatyp

boolean

Alias
UMLS CUI [1]
C0522523
hemoglobin > 10.0 g/dl
Beskrivning

hemoglobin

Datatyp

boolean

Alias
UMLS CUI [1]
C0019046
absolute neutrophil count (anc) > 1,500/mm3
Beskrivning

absolute neutrophil count

Datatyp

boolean

Alias
UMLS CUI [1]
C0948762
platelet count > 75,000/μl
Beskrivning

platelet count

Datatyp

boolean

Alias
UMLS CUI [1]
C0032181
alt and ast < 2.5 x uln
Beskrivning

alt and ast

Datatyp

boolean

Alias
UMLS CUI [1]
C0001899
UMLS CUI [2]
C0004002
alkaline phosphatase < 4 x uln
Beskrivning

alkaline phosphatase

Datatyp

boolean

Alias
UMLS CUI [1]
C0201850
serum creatinine < 1.5
Beskrivning

serum creatinine

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
women of child-bearing potential: negative pregnancy test
Beskrivning

negative pregnancy test

Datatyp

boolean

Alias
UMLS CUI [1]
C0427780
patients of child producing potential: usage of contraception or avoidance of pregnancy measures while enrolled on study and receiving the experimental product
Beskrivning

contraception or avoidance of pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0700589
UMLS CUI [2]
C1821946
ability to understand the study, its inherent risks, side effects and potential benefits and ability to give written informed consent to participate
Beskrivning

informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe ascites, massive or uncontrolled (+3 on child-pugh calculator)
Beskrivning

ascites

Datatyp

boolean

Alias
UMLS CUI [1]
C0003962
severe encephalopathy, uncontrolled (+3 on child-pugh calculator)
Beskrivning

encephalopathy

Datatyp

boolean

Alias
UMLS CUI [1]
C0085584
inr > 1.5
Beskrivning

inr

Datatyp

boolean

Alias
UMLS CUI [1]
C0482691
participation in another clinical trial evaluating experimental treatments or procedures or receiving medication/treatment for hcc other than sorafenib
Beskrivning

participation in another clinical trial

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
any autoimmune disorder
Beskrivning

autoimmune disorder

Datatyp

boolean

Alias
UMLS CUI [1]
C0004364
any clinical condition requiring systemic steroids or current immunosuppressive therapy, including: cyclosporine, antithymocyte globulin, or tacrolimus within 1 month of study entry
Beskrivning

systemic steroids or current immunosuppressive therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C2825233
UMLS CUI [2]
C0021079
hiv positive or syphilis
Beskrivning

hiv positive or syphilis

Datatyp

boolean

Alias
UMLS CUI [1]
C0019699
UMLS CUI [2]
C0039128
history of cardiac disease: congestive heart failure > nyha class 2; cardiac arrhythmias requiring anti-arrhythmic therapy (beta blockers or digoxin are permitted) or uncontrolled hypertension
Beskrivning

cardiac disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0018799
active clinically serious infections (> grade 2 nci-ctcae version 4.0)
Beskrivning

infections

Datatyp

boolean

history of organ or tissue allograft
Beskrivning

history of organ or tissue allograft

Datatyp

boolean

Alias
UMLS CUI [1]
C0040739
advanced liver cirrhosis
Beskrivning

liver cirrhosis

Datatyp

boolean

Alias
UMLS CUI [1]
C0023890
interferon or thalidomide within 1 month prior to signing informed consent
Beskrivning

interferon or thalidomide

Datatyp

boolean

Alias
UMLS CUI [1]
C0039736
UMLS CUI [2]
C0021747
uncontrolled concurrent serious medical or psychiatric illness
Beskrivning

uncontrolled concurrent serious medical or psychiatric illness

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0205420
UMLS CUI [1,2]
C0418964
clinically apparent central nervous system metastases or carcinomatous meningitis
Beskrivning

central nervous system metastases, Meningeal Carcinomatosis

Datatyp

boolean

Alias
UMLS CUI [1]
C0279130
UMLS CUI [2]
C0220654
history of blood transfusion reactions
Beskrivning

history of blood transfusion reactions

Datatyp

boolean

Alias
UMLS CUI [1]
C0274435
known allergy to murine monoclonal antibodies or bovine products or cow milk
Beskrivning

allergy to murine monoclonal antibodies

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C2916903
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0349374

Similar models

Eligibility Advanced Adult Hepatocellular Carcinoma NCT02409524

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
males and females who are at least 18 years of age at time of enrollment
boolean
C0001779 (UMLS CUI [1])
hepatocellular carcinoma
Item
histologically confirmed hepatocellular carcinoma with or without positive hbv and/or hcv
boolean
C2239176 (UMLS CUI [1])
sorafenib
Item
minimum of 90 days of sorafenib treatment and unresectable
boolean
C1516119 (UMLS CUI [1])
child-pugh stage
Item
child-pugh stage a-b (score ≥ 5 and ≤ 9)
boolean
C4050412 (UMLS CUI [1])
ecog
Item
performance status: ecog < 2 with no deterioration over the previous 2 weeks
boolean
C1520224 (UMLS CUI [1])
measurable disease
Item
measurable disease (for recist)
boolean
C1513041 (UMLS CUI [1])
percutaneous tumor harvest
Item
lesion amenable for percutaneous tumor harvest and follow up biopsy
boolean
C0522523 (UMLS CUI [1])
hemoglobin
Item
hemoglobin > 10.0 g/dl
boolean
C0019046 (UMLS CUI [1])
absolute neutrophil count
Item
absolute neutrophil count (anc) > 1,500/mm3
boolean
C0948762 (UMLS CUI [1])
platelet count
Item
platelet count > 75,000/μl
boolean
C0032181 (UMLS CUI [1])
alt and ast
Item
alt and ast < 2.5 x uln
boolean
C0001899 (UMLS CUI [1])
C0004002 (UMLS CUI [2])
alkaline phosphatase
Item
alkaline phosphatase < 4 x uln
boolean
C0201850 (UMLS CUI [1])
serum creatinine
Item
serum creatinine < 1.5
boolean
C0201976 (UMLS CUI [1])
negative pregnancy test
Item
women of child-bearing potential: negative pregnancy test
boolean
C0427780 (UMLS CUI [1])
contraception or avoidance of pregnancy
Item
patients of child producing potential: usage of contraception or avoidance of pregnancy measures while enrolled on study and receiving the experimental product
boolean
C0700589 (UMLS CUI [1])
C1821946 (UMLS CUI [2])
informed consent
Item
ability to understand the study, its inherent risks, side effects and potential benefits and ability to give written informed consent to participate
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ascites
Item
severe ascites, massive or uncontrolled (+3 on child-pugh calculator)
boolean
C0003962 (UMLS CUI [1])
encephalopathy
Item
severe encephalopathy, uncontrolled (+3 on child-pugh calculator)
boolean
C0085584 (UMLS CUI [1])
inr
Item
inr > 1.5
boolean
C0482691 (UMLS CUI [1])
participation in another clinical trial
Item
participation in another clinical trial evaluating experimental treatments or procedures or receiving medication/treatment for hcc other than sorafenib
boolean
C2348568 (UMLS CUI [1])
autoimmune disorder
Item
any autoimmune disorder
boolean
C0004364 (UMLS CUI [1])
systemic steroids or current immunosuppressive therapy
Item
any clinical condition requiring systemic steroids or current immunosuppressive therapy, including: cyclosporine, antithymocyte globulin, or tacrolimus within 1 month of study entry
boolean
C2825233 (UMLS CUI [1])
C0021079 (UMLS CUI [2])
hiv positive or syphilis
Item
hiv positive or syphilis
boolean
C0019699 (UMLS CUI [1])
C0039128 (UMLS CUI [2])
cardiac disease
Item
history of cardiac disease: congestive heart failure > nyha class 2; cardiac arrhythmias requiring anti-arrhythmic therapy (beta blockers or digoxin are permitted) or uncontrolled hypertension
boolean
C0018799 (UMLS CUI [1])
infections
Item
active clinically serious infections (> grade 2 nci-ctcae version 4.0)
boolean
history of organ or tissue allograft
Item
history of organ or tissue allograft
boolean
C0040739 (UMLS CUI [1])
liver cirrhosis
Item
advanced liver cirrhosis
boolean
C0023890 (UMLS CUI [1])
interferon or thalidomide
Item
interferon or thalidomide within 1 month prior to signing informed consent
boolean
C0039736 (UMLS CUI [1])
C0021747 (UMLS CUI [2])
uncontrolled concurrent serious medical or psychiatric illness
Item
uncontrolled concurrent serious medical or psychiatric illness
boolean
C0205420 (UMLS CUI [1,1])
C0418964 (UMLS CUI [1,2])
central nervous system metastases, Meningeal Carcinomatosis
Item
clinically apparent central nervous system metastases or carcinomatous meningitis
boolean
C0279130 (UMLS CUI [1])
C0220654 (UMLS CUI [2])
history of blood transfusion reactions
Item
history of blood transfusion reactions
boolean
C0274435 (UMLS CUI [1])
allergy to murine monoclonal antibodies
Item
known allergy to murine monoclonal antibodies or bovine products or cow milk
boolean
C0020517 (UMLS CUI [1,1])
C2916903 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0349374 (UMLS CUI [2,2])