Criteria Fulfill Quantity
Item
patients must meet one (or more) of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Ovarian Carcinoma Pre-op diagnosis TNM clinical staging Grade | Fallopian Tube Carcinoma Pre-op diagnosis TNM clinical staging Grade | Primary peritoneal carcinoma Pre-op diagnosisTNM clinical staging Grade
Item
preoperative diagnosis of ovarian, fallopian tube, or primary peritoneal carcinoma (all stage, grade and histology)
boolean
C0029925 (UMLS CUI [1,1])
C1318968 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,4])
C0238122 (UMLS CUI [2,1])
C1318968 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C0441800 (UMLS CUI [2,4])
C1514428 (UMLS CUI [3,1])
C1318968 (UMLS CUI [3,2])
C3258246 (UMLS CUI [3,3])
C0441800 (UMLS CUI [3,4])
Endometrial Carcinoma Pre-op diagnosis Grade TNM clinical staging
Item
preoperative diagnosis of grade iii endometrial carcinoma (all stage, all histology)
boolean
C0476089 (UMLS CUI [1,1])
C1318968 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
C3258246 (UMLS CUI [1,4])
Uterine carcinoma Serous Pre-op diagnosis | Uterine carcinoma Serous TNM clinical staging Grade
Item
preoperative diagnosis of uterine serous carcinoma (all stage, all grade)
boolean
C0848454 (UMLS CUI [1,1])
C0440743 (UMLS CUI [1,2])
C1318968 (UMLS CUI [1,3])
C0848454 (UMLS CUI [2,1])
C0440743 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C0441800 (UMLS CUI [2,4])
Clear cell endometrial carcinoma Pre-op diagnosis TNM clinical staging Grade
Item
preoperative diagnosis of clear cell endometrial carcinoma (all stage, all grade)
boolean
C0279765 (UMLS CUI [1,1])
C1318968 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,4])
Endometrial carcinosarcoma Pre-op diagnosis TNM clinical staging Grade
Item
preoperative diagnosis of endometrial carcinosarcoma (all stage, all grade)
boolean
C4517098 (UMLS CUI [1,1])
C1318968 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,4])
Gastrointestinal carcinoma TNM clinical staging Grade
Item
gastrointestinal carcinoma (all histology, stage and grade)
boolean
C0151544 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
Pancreatic carcinoma TNM clinical staging Grade
Item
pancreatic carcinoma (all histology, stage and grade)
boolean
C0235974 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
Carcinoma of lung TNM clinical staging Grade
Item
lung cancer (all histology, stage and grade)
boolean
C0684249 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
Esophageal carcinoma TNM clinical staging Grade
Item
esophageal carcinoma (all histology, stage and grade)
boolean
C0152018 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
Secondary malignant neoplasm of lung Primary Suspected | Secondary malignant neoplasm of lung Primary
Item
suspected or pathologically confirmed metastatic disease to the lung (all disease primaries)
boolean
C0153676 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0750491 (UMLS CUI [1,3])
C0153676 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
Malignant Pleural Effusion Primary Suspected | Malignant Pleural Effusion Primary
Item
suspected or pathologically confirmed malignant pleural effusion (all disease primaries)
boolean
C0080032 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0750491 (UMLS CUI [1,3])
C0080032 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
Criteria Fulfill All
Item
patients must meet all of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C0444868 (UMLS CUI [1,3])
Thoracoscopic robotic assisted procedure Planned | Laparoscopic Surgical Procedure Planned
Item
planned thorascopic robotic or laparoscopic surgical approach
boolean
C2349252 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0751429 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Age
Item
>18 years old
boolean
C0001779 (UMLS CUI [1])
Pregnancy Absent
Item
not pregnant
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Informed Consent | Study Subject Participation Status | Research Protocol Other allowed
Item
able to give consent participation in other research protocols does not exclude a patient from participation in this study.
boolean
C0021430 (UMLS CUI [1])
C2348568 (UMLS CUI [2])
C0205717 (UMLS CUI [3,1])
C0205394 (UMLS CUI [3,2])
C0683607 (UMLS CUI [3,3])