Has the patient received low-dose radiotherapy during the study treatment period?
Item
Has the patient received low-dose radiotherapy during the study treatment period?
boolean
C1522449 (UMLS CUI [1,1])
C1708745 (UMLS CUI [1,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Item
Radiotherapy Site
integer
C1522449 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
Code List
Radiotherapy Site
CL Item
Primary tumor/recurrence (1)
CL Item
Lymphnode regional (2)
CL Item
Lymphnode distant (3)
CL Item
Cutaneous/subcutaneous regional (4)
CL Item
Cutaneous/subcutaneous distant (5)
CL Item
Confluent skin lesions regional (6)
CL Item
Confluent skin lesions distant (7)
Other site, specify
Item
Other site, specify
text
C1515974 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Cumulative dose
Item
Cumulative dose
float
C2986497 (UMLS CUI [1])
Item
Units
text
C1519795 (UMLS CUI [1])
Date of first administration
Item
Date of first administration
date
C3173309 (UMLS CUI [1])
Date of last administration
Item
Date of last administration
date
C1762893 (UMLS CUI [1,1])
C1533734 (UMLS CUI [1,2])
Item
Status of the lesion before radiotherapy
text
C0449438 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
Code List
Status of the lesion before radiotherapy
CL Item
Progressive lesion (PD)
CL Item
Stable lesion (SD)
CL Item
Regressive lesion (Reg)
Item
Type of lesion (Radiotherapy)
text
C0221198 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2])
Code List
Type of lesion (Radiotherapy)
CL Item
Target lesion (TG)
CL Item
Non-Target lesion (NT)
If target lesion, specify number (Radiotherapy)
Item
If target lesion, specify number (Radiotherapy)
integer
C1521840 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C2348235 (UMLS CUI [2])
C0237753 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
Have some lesions been resected during the study treatment period?
Item
Have some lesions been resected during the study treatment period?
boolean
C0221198 (UMLS CUI [1,1])
C0728940 (UMLS CUI [1,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Item
Surgery Site
integer
C1515974 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
CL Item
Primary tumor/recurrence (1)
CL Item
Lymphnode regional (2)
CL Item
Lymphnode distant (3)
CL Item
Cutaneous/subcutaneous regional (4)
CL Item
Cutaneous/subcutaneous distant (5)
CL Item
Confluent skin lesions regional (6)
CL Item
Confluent skin lesions distant (7)
Date of surgery
Item
Date of surgery
date
C3258210 (UMLS CUI [1])
Item
Status of the lesion before surgery
text
C0449438 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
Code List
Status of the lesion before surgery
CL Item
Progressive lesion (PD)
CL Item
Stable lesion (SD)
CL Item
Regressive lesion (Reg)
Item
Type of lesion (Surgery)
text
C0221198 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2])
Code List
Type of lesion (Surgery)
CL Item
Target lesion (TG)
CL Item
Non-Target lesion (NT)
If target lesion, specify number (Surgery)
Item
If target lesion, specify number (Surgery)
integer
C0221198 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C0237753 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
C0543467 (UMLS CUI [3])