Colon Carcinoma Primary TNM clinical staging | Rectal Carcinoma Primary TNM clinical staging | Operative Surgical Procedure Cure Histologic | Surgical Procedures, Laparoscopic
Item
patients with ptnm stage iib or iii (uicc sixth version) primary colon cancer/rectal cancer who have undergone surgery of histological curability a (including laparoscopic surgery) (the curability is judged after surgery)
boolean
C0699790 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0007113 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C0543467 (UMLS CUI [3,1])
C1880198 (UMLS CUI [3,2])
C0205462 (UMLS CUI [3,3])
C0751429 (UMLS CUI [4])
Primary tumor Visceral Peritoneum TNM clinical staging | Secondary malignant neoplasm of lymph node Histologic Positive
Item
patients with primary tumor that directly invades other organs or structures and/or perforates into the visceral peritoneum (t4) or with histologically positive lymph node metastasis (n+) (to be judged after surgery)
boolean
C0677930 (UMLS CUI [1,1])
C0230206 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0686619 (UMLS CUI [2,1])
C0205462 (UMLS CUI [2,2])
C1514241 (UMLS CUI [2,3])
Age
Item
patients who is between 20 and 80 years old at the time of obtaining informed consent
boolean
C0001779 (UMLS CUI [1])
performance status
Item
patients with performance status of 0 - 2
boolean
C1518965 (UMLS CUI [1])
cancer treatment Absent | Therapeutic radiology procedure | Chemotherapy | Immunotherapy | Operative Surgical Procedures
Item
patients without receiving any cancer treatment such as radiation, chemotherapy, and immunotherapy before surgical operation
boolean
C0920425 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2])
C0392920 (UMLS CUI [3])
C0021083 (UMLS CUI [4])
C0543467 (UMLS CUI [5])
Renal dysfunction Severe Absent | Liver Dysfunction Severe Absent | Bone Marrow Dysfunction Severe Absent
Item
patients without severe dysfunction of renal, hepatic, or bone marrow function
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0086565 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0005953 (UMLS CUI [3,1])
C3887504 (UMLS CUI [3,2])
C0205082 (UMLS CUI [3,3])
C0332197 (UMLS CUI [3,4])
Complication Serious Absent | Bone Marrow Suppression | Diarrhea | Communicable Diseases
Item
patients without serious complications such as bone marrow suppression, diarrhea, and infections diseases
boolean
C0009566 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0280962 (UMLS CUI [2])
C0011991 (UMLS CUI [3])
C0009450 (UMLS CUI [4])
Informed Consent | Informed Consent Family
Item
patients who have given consent to participate in this clinical study by himself/herself or his/her family
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0015576 (UMLS CUI [2,2])
Malignant Neoplasm Bottom Peritoneum
Item
patients in whom the bottom of tumor reaches the peritoneal reflection
boolean
C0006826 (UMLS CUI [1,1])
C1511276 (UMLS CUI [1,2])
C0031153 (UMLS CUI [1,3])
Rectal Carcinoma Lower | Malignant neoplasm of anal canal | Malignant Neoplasms Perianal skin
Item
patients with lower rectal cancer (rb), anal canal (p), or circumanal skin (e)
boolean
C0007113 (UMLS CUI [1,1])
C0441994 (UMLS CUI [1,2])
C0153445 (UMLS CUI [2])
C0006826 (UMLS CUI [3,1])
C1704244 (UMLS CUI [3,2])
Multiple malignancy | Life Expectancy Disease Free of | Malignant Neoplasms Timepoint Different | Carcinoma in Situ | Skin carcinoma
Item
patients who has active multiple cancers or whose disease-free survival is less than 5 years even though the cancers are metachronous (except carcinoma in situ and skin cancers)
boolean
C0346429 (UMLS CUI [1])
C0023671 (UMLS CUI [2,1])
C0012634 (UMLS CUI [2,2])
C0332296 (UMLS CUI [2,3])
C0006826 (UMLS CUI [3,1])
C2348792 (UMLS CUI [3,2])
C1705242 (UMLS CUI [3,3])
C0007099 (UMLS CUI [4])
C0699893 (UMLS CUI [5])
Pregnancy | Pregnancy, Planned
Item
women who are currently pregnant or wish to be pregnant during this clinical study
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Study Subject Participation Status Inappropriate
Item
patients who are judged to be inappropriate to participate in this clinical study by the investigator or subinvestigator
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])