SUBJECT_ID
Item
De-identified subject ID
string
C4684638 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
study
Item
Participant study [adj5fu_Spain, C08, CetFol_Spain, FolXel_Spain, N0147, N9741]
string
C4554048 (UMLS CUI [1,1])
Item
Gender of participant [Male, Female]
text
C0079399 (UMLS CUI [1,1])
Code List
Gender of participant [Male, Female]
race
Item
Race of participant [American Indian or Alaska Native, Asian, Black or African American, Native Hawaiin or Other Pacific Islander, Other, White]
string
C0034510 (UMLS CUI [1,1])
C0085756 (UMLS CUI [1,2])
C1513907 (UMLS CUI [1,3])
C0005680 (UMLS CUI [1,4])
C0007457 (UMLS CUI [1,5])
C1515945 (UMLS CUI [1,6])
C0078988 (UMLS CUI [1,7])
C0205394 (UMLS CUI [1,8])
ethnicity
Item
Ethnicity of participant
string
C5441552 (UMLS CUI [1,1])
age_dx
Item
Age at CRC diagnoses
text
C1828181 (UMLS CUI [1,1])
C0009402 (UMLS CUI [1,2])
anydeath
Item
All cause mortality
string
C0026565 (UMLS CUI [1,1])
time_surv
Item
Time to event or censoring
text
C0040223 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
C3889990 (UMLS CUI [1,3])
Item
Whether the patients experienced grade 3+ Rash across all cycles of treatment
text
C4686470 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0596545 (UMLS CUI [1,3])
C1302181 (UMLS CUI [1,4])
Code List
Whether the patients experienced grade 3+ Rash across all cycles of treatment
CL Item
Yes, Grade 3+ (1)
Item
Whether the patients experienced grade 3+ nausea or vomiting across all cycles of treatment
text
C0030705 (UMLS CUI [1,1])
C0596545 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Code List
Whether the patients experienced grade 3+ nausea or vomiting across all cycles of treatment
CL Item
Yes, Grade 3+ (1)
Item
Whether the patients experienced grade 3+ Diarrhea across all cycles of treatment
text
C1559310 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0596545 (UMLS CUI [1,3])
C1302181 (UMLS CUI [1,4])
Code List
Whether the patients experienced grade 3+ Diarrhea across all cycles of treatment
CL Item
Yes, Grade 3+ (1)
Item
Whether the patients experienced grade 3+ neutropenia across all cycles of treatment
text
C1556690 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0596545 (UMLS CUI [1,3])
C1302181 (UMLS CUI [1,4])
Code List
Whether the patients experienced grade 3+ neutropenia across all cycles of treatment
CL Item
Yes, Grade 3+ (1)
Item
Whether the patients experienced grade 3+ neuropathy across all cycles of treatment
text
C0030705 (UMLS CUI [1,1])
C0596545 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
C4686431 (UMLS CUI [1,4])
C4686433 (UMLS CUI [1,5])
Code List
Whether the patients experienced grade 3+ neuropathy across all cycles of treatment
CL Item
Yes, Grade 3+ (1)
HEIGHT
Item
Height (cm) at Baseline
text
C0005890 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
WEIGHT
Item
Weight (kg) at Baseline
text
C0005910 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
stage2
Item
Disease stage
text
C0699749 (UMLS CUI [1,1])
Tstage
Item
T stage
text
C0475455 (UMLS CUI [1,1])
NodesPositive_cat
Item
Positive nodes, i.e., nodal status
text
C0449927 (UMLS CUI [1,1])
cancer_site_sum1
Item
Tumor site summary: colon vs.rectal
text
C0475445 (UMLS CUI [1,1])
C0007102 (UMLS CUI [1,2])
C0034885 (UMLS CUI [1,3])
cancer_site_sum2
Item
Tumor Site summary: proximal/distal/rectal
text
C0475445 (UMLS CUI [1,1])
C0205107 (UMLS CUI [1,2])
C0205108 (UMLS CUI [1,3])
C0205052 (UMLS CUI [1,4])
NodesExamined
Item
Number of Examined lymph nodes
text
C5442076 (UMLS CUI [1,1])
trx
Item
Treatment Arm
text
C1522541 (UMLS CUI [1,1])
HistGrade
Item
Histology Grade
text
C0919553 (UMLS CUI [1,1])