Renal Clear Cell Carcinoma TNM clinical staging
Item
histologically confirmed stage iv kidney clear cell carcinoma.
boolean
C0279702 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Progressive Disease | Systemic therapy | Standard of Care Quantity
Item
confirmed progressive disease after receiving a previous systemic therapy, including at least one line of standard of care.
boolean
C1335499 (UMLS CUI [1])
C1515119 (UMLS CUI [2])
C2936643 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Measurable Disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Age
Item
age >18 years.
boolean
C0001779 (UMLS CUI [1])
Life Expectancy
Item
life expectancy of greater than 3 months.
boolean
C0023671 (UMLS CUI [1])
Cancer Other Free of | Basal cell carcinoma Acceptable | Infiltrating basal cell carcinoma Absent | Sclerosing basal cell carcinoma Absent | Carcinoma in situ of uterine cervix Acceptable
Item
at least 5 years free of any other cancer(s). basal cell carcinoma, provided that is neither infiltrating nor sclerosing and carcinoma in situ of the cervix, is acceptable.
boolean
C1707251 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
C0007117 (UMLS CUI [2,1])
C1879533 (UMLS CUI [2,2])
C0334257 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0862888 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C0851140 (UMLS CUI [5,1])
C1879533 (UMLS CUI [5,2])
ECOG performance status | Karnofsky Performance Status
Item
ecog performance status 2 or lower (karnofsky 60%).
boolean
C1520224 (UMLS CUI [1])
C0206065 (UMLS CUI [2])
Organ function | Bone Marrow function
Item
normal organ and marrow function
boolean
C0678852 (UMLS CUI [1])
C0005953 (UMLS CUI [2,1])
C0031843 (UMLS CUI [2,2])
Contraceptive methods
Item
adequate contraception prior to study entry and for the duration of study participation.
boolean
C0700589 (UMLS CUI [1])
Informed Consent
Item
ability to understand and have the willingness to sign a written informed consent document.
boolean
C0021430 (UMLS CUI [1])
Central venous catheter Receive Ability | Infusion Pump Managing Ability
Item
ability to receive central vein access catheter and manage an infusion pump.
boolean
C1145640 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C0021436 (UMLS CUI [2,1])
C1273870 (UMLS CUI [2,2])
C0085732 (UMLS CUI [2,3])
Childbearing Potential Pregnancy test negative
Item
women of child bearing potential must have a negative serum pregnancy test.
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
Cancer treatment
Item
anti-cancer therapy within 4 weeks prior to entering the study
boolean
C0920425 (UMLS CUI [1])
Investigational New Drugs
Item
investigational agents less than 30 days prior to enrollment in the study.
boolean
C0013230 (UMLS CUI [1])
Metastatic malignant neoplasm to brain
Item
known brain metastases
boolean
C0220650 (UMLS CUI [1])
Allergic Reaction Compound CAP-232 Similar
Item
history of allergic reactions attributed to compounds of similar composition to cap-232.
boolean
C1527304 (UMLS CUI [1,1])
C1706082 (UMLS CUI [1,2])
C1879913 (UMLS CUI [1,3])
C2348205 (UMLS CUI [1,4])
Cancer Other | Exception Curative treatment Skin carcinoma | Exception Curative treatment Carcinoma in situ of uterine cervix | Exception Curative treatment Cancer Other Disease Absent
Item
past or current cancer other than kidney cancer, except for: curatively treated non-melanoma skin cancer, in situ carcinoma of the cervix, other cancer curatively treated and with no evidence of disease for at least 5 years
boolean
C1707251 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C1273390 (UMLS CUI [2,2])
C0699893 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C1273390 (UMLS CUI [3,2])
C0851140 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C1273390 (UMLS CUI [4,2])
C1707251 (UMLS CUI [4,3])
C0012634 (UMLS CUI [4,4])
C0332197 (UMLS CUI [4,5])
Comorbidity Uncontrolled Protocol Compliance Limited | Social situation Protocol Compliance Limited
Item
uncontrolled intercurrent illness /social situations that would limit compliance with study requirements.
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,4])
C0748872 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
Breast Feeding
Item
breastfeeding
boolean
C0006147 (UMLS CUI [1])
Study Subject Participation Status | Patient withdrawn from trial
Item
patients previously enrolled into this study and subsequently withdrawn
boolean
C2348568 (UMLS CUI [1])
C0422727 (UMLS CUI [2])