Ovarian Carcinoma Primary | Primary peritoneal carcinoma | Fallopian Tube Carcinoma Primary
Item
histologic or cytologic history diagnosis of primary ovarian, primary peritoneal or tubal carcinoma
boolean
C0029925 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C1514428 (UMLS CUI [2])
C0238122 (UMLS CUI [3,1])
C0205225 (UMLS CUI [3,2])
Ovarian Carcinoma Asymptomatic
Item
asymptomatic from ovarian cancer
boolean
C0029925 (UMLS CUI [1,1])
C0231221 (UMLS CUI [1,2])
Ovarian cancer recurrent Evidence of | Carcinoma of peritoneum Recurrent Evidence of | Recurrent Fallopian Tube Carcinoma Evidence of
Item
evidence of recurrent ovarian, peritoneal or tubal carcinoma
boolean
C0278689 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
C0948303 (UMLS CUI [2,1])
C2945760 (UMLS CUI [2,2])
C0332120 (UMLS CUI [2,3])
C3897738 (UMLS CUI [3,1])
C0332120 (UMLS CUI [3,2])
Tumor tissue sample Estrogen receptor positive | Tumor tissue sample Progesterone receptor positive
Item
tumor sample must be positive for er and/or pr
boolean
C0475358 (UMLS CUI [1,1])
C0279754 (UMLS CUI [1,2])
C0475358 (UMLS CUI [2,1])
C0279759 (UMLS CUI [2,2])
Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status of less than or equal to 1
boolean
C1520224 (UMLS CUI [1])
Intake Oral Ability
Item
must be able to tolerate oral intake
boolean
C1512806 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Hypersensitivity Iressa | Hypersensitivity Iressa Excipient
Item
known hypersensitivity to iressa or any of the excipients of this product
boolean
C0020517 (UMLS CUI [1,1])
C0919281 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0919281 (UMLS CUI [2,2])
C0015237 (UMLS CUI [2,3])
Malignant Neoplasms
Item
other coexisting malignancies or malignancies diagnosed within the last 5 years
boolean
C0006826 (UMLS CUI [1])
Phenytoin | Carbamazepine | Barbiturates | Rifampin | Phenobarbital | ST. JOHN'S WORT EXTRACT
Item
concomitant use of phenytoin, carbamazepine, barbiturates, rifampicin, phenobarbital or st. john's wort
boolean
C0031507 (UMLS CUI [1])
C0006949 (UMLS CUI [2])
C0004745 (UMLS CUI [3])
C0035608 (UMLS CUI [4])
C0031412 (UMLS CUI [5])
C0813171 (UMLS CUI [6])
Drugs, Non-Prescription | Investigational New Drugs
Item
treatment with a non-approved or investigational drug within 30 days
boolean
C0013231 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
Toxicity chronic Unresolved Due to cancer treatment | CTCAE Grades | Alopecia
Item
any unresolved chronic toxicity greater than ctc grad 2 from previous anticancer therapy (except alopecia)
boolean
C0600688 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0443342 (UMLS CUI [1,3])
C0678226 (UMLS CUI [1,4])
C0920425 (UMLS CUI [1,5])
C1516728 (UMLS CUI [2])
C0002170 (UMLS CUI [3])
cancer surgery | major surgery | Therapeutic procedure Incomplete
Item
incomplete healing from previous oncologic or other major surgery
boolean
C0920424 (UMLS CUI [1])
C0679637 (UMLS CUI [2])
C0087111 (UMLS CUI [3,1])
C0205257 (UMLS CUI [3,2])
Creatinine measurement, serum | CTCAE Grades
Item
serum creatinine level greater than ctc grade 2
boolean
C0201976 (UMLS CUI [1])
C1516728 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Systemic disease Uncontrolled Severe
Item
severe uncontrolled systemic disease
boolean
C0442893 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
Disease Significant At risk Study Subject Participation Status | Laboratory finding At risk Study Subject Participation Status
Item
significant clinical disorder or laboratory finding that makes it potentially unsafe for the subject to participate
boolean
C0012634 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,4])
C0587081 (UMLS CUI [2,1])
C1444641 (UMLS CUI [2,2])
C2348568 (UMLS CUI [2,3])
Antineoplastic Agents Investigational | Systemic Chemotherapy | Therapeutic radiology procedure
Item
patients currently receiving other investigational antineoplastic agents, on systemic chemotherapy or under radiation therapy treatment
boolean
C0003392 (UMLS CUI [1,1])
C1517586 (UMLS CUI [1,2])
C1883256 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
anastrozole | Aromatase Inhibitors
Item
patients previously treated with anastrozole or other aromatase inhibitor
boolean
C0290883 (UMLS CUI [1])
C0593802 (UMLS CUI [2])
Oral medication Receive Unable
Item
unable to tolerate oral medications
boolean
C0175795 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Intestinal Obstruction Evidence Clinical | Intestinal Obstruction Impending Evidence Clinical | Intestinal Obstruction Evidence roentgenographic | Intestinal Obstruction Impending Evidence roentgenographic
Item
clinical and/or radiographic evidence of current or impending bowel obstruction
boolean
C0021843 (UMLS CUI [1,1])
C3887511 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
C0021843 (UMLS CUI [2,1])
C0332190 (UMLS CUI [2,2])
C3887511 (UMLS CUI [2,3])
C0205210 (UMLS CUI [2,4])
C0021843 (UMLS CUI [3,1])
C3887511 (UMLS CUI [3,2])
C0034571 (UMLS CUI [3,3])
C0021843 (UMLS CUI [4,1])
C0332190 (UMLS CUI [4,2])
C3887511 (UMLS CUI [4,3])
C0034571 (UMLS CUI [4,4])