Metastatic Carcinoma Biopsy | Histology Light microscopy | Adenocarcinoma | Poorly differentiated carcinoma Immunoperoxidase stain | Lymphoma Excluded | Neuroendocrine Carcinoma Excluded | Squamous cell carcinoma Poorly differentiated
Item
biopsy proven metastatic carcinoma with the following light microscopic histologies: adenocarcinoma, poorly differentiated carcinoma(must have immunoperoxidase stains to rule out lymphoma, neuroendocrine carcinoma),or poorly differentiated squamous carcinoma.
boolean
C1384494 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C0344441 (UMLS CUI [2,1])
C0430389 (UMLS CUI [2,2])
C0001418 (UMLS CUI [3])
C0741899 (UMLS CUI [4,1])
C1441617 (UMLS CUI [4,2])
C0024299 (UMLS CUI [5,1])
C2828389 (UMLS CUI [5,2])
C0206695 (UMLS CUI [6,1])
C2828389 (UMLS CUI [6,2])
C0007137 (UMLS CUI [7,1])
C0205617 (UMLS CUI [7,2])
ECOG performance status
Item
ecog performance status 0-1
boolean
C1520224 (UMLS CUI [1])
systemic therapy
Item
no previous treatment with any systemic therapy
boolean
C1515119 (UMLS CUI [1])
Renal function | Liver function | Bone Marrow function
Item
adequate kidney, liver and bone marrow function
boolean
C0232804 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0005953 (UMLS CUI [3,1])
C0031843 (UMLS CUI [3,2])
Informed Consent
Item
be able to understand the nature of the study and give written informed consent
boolean
C0021430 (UMLS CUI [1])
Syndrome Specific
Item
the following specific syndromes:
boolean
C0039082 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
Carcinoma, Neuroendocrine
Item
neuroendocrine carcinoma
boolean
C0206695 (UMLS CUI [1])
Gender | Adenocarcinoma Isolated Axillary lymph nodes
Item
women with adenocarcinoma isolated to axillary lymph nodes
boolean
C0079399 (UMLS CUI [1])
C0001418 (UMLS CUI [2,1])
C0205409 (UMLS CUI [2,2])
C0729594 (UMLS CUI [2,3])
Gender | Adenocarcinoma Isolated Involvement peritoneal
Item
women with adenocarcinoma isolated to peritoneal involvement
boolean
C0079399 (UMLS CUI [1])
C0001418 (UMLS CUI [2,1])
C0205409 (UMLS CUI [2,2])
C1314939 (UMLS CUI [2,3])
C0442034 (UMLS CUI [2,4])
Carcinoma Involving Site Single | Neoplasms Resectable Site
Item
carcinoma involving only one site with resectable tumors at that site
boolean
C0007097 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0205171 (UMLS CUI [1,4])
C0027651 (UMLS CUI [2,1])
C1514888 (UMLS CUI [2,2])
C1515974 (UMLS CUI [2,3])
Squamous cell carcinoma Limited Cervical lymph nodes | Squamous cell carcinoma Limited Supraclavicular lymph nodes | Squamous cell carcinoma Limited Inguinal lymph nodes
Item
squamous carcinoma limited to cervical, supraclavicular, or inguinal lymph nodes
boolean
C0007137 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0588054 (UMLS CUI [1,3])
C0007137 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0229730 (UMLS CUI [2,3])
C0007137 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
C0729596 (UMLS CUI [3,3])
Metastatic malignant neoplasm to brain Uncontrolled | Involvement meningeal
Item
uncontrolled brain metastases and all patients with meningeal involvement
boolean
C0220650 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C1314939 (UMLS CUI [2,1])
C0521400 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
women pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Cardiovascular Disease
Item
clinically significant cardiovascular disease
boolean
C0007222 (UMLS CUI [1])
Myocardial Infarction | Cerebrovascular accident
Item
history of myocardial infarction or stroke within 6 months
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Hemoptysis | Hematemesis
Item
clinical history of hemoptysis or hematemesis
boolean
C0019079 (UMLS CUI [1])
C0018926 (UMLS CUI [2])
Percutaneous endoscopic tube | Gastrostomy tube
Item
patients with peg tubes or g-tubes
boolean
C2985542 (UMLS CUI [1])
C0150595 (UMLS CUI [2])
Proteinuria
Item
proteinuria
boolean
C0033687 (UMLS CUI [1])
Bleeding tendency | Blood Coagulation Disorders
Item
history of bleeding diathesis or coagulopathy
boolean
C1458140 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
Clinical Trial Eligibility Criteria Additional | Study Subject Participation Status
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have. you can then decide if you wish to participate.
boolean
C1516637 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2])