Instructions: Please complete after each cycle of treatment. All dates are MONTH, DAY, YEAR. Explain any blank fields or blank dates in the Comments section. Place an X in appropriate boxes. Circle AMENDED items in red.

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Toxicity
C0013221 (UMLS CUI-1)
C0040539 (UMLS CUI-2)
C0023418 (UMLS CUI-3)
C2242529 (UMLS CUI-4)
toxicities
Item
Were toxicities assessed for this treatment cycle?
boolean
C0013221 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C2242529 (UMLS CUI [2])
Date toxicity assessment
Item
Date of most recent toxicity assessment
date
C0013221 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2242529 (UMLS CUI [2])
whyweretoxicitiesnotassessed?
Item
why were toxicities not assessed?
text
C0013221 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C2242529 (UMLS CUI [2])
CTC Code
Item
Code
text
C0805701 (UMLS CUI [1,1])
C1516728 (UMLS CUI [1,2])
Item
Toxicity
integer
C0877248 (UMLS CUI [1,1])
C1516728 (UMLS CUI [1,2])
CL.2
Code List
Toxicity
CL Item
Cardiac left ventricular function (1)
(Comment:en)
CL Item
Cardiac ischemia/infarction (2)
(Comment:en)
CL Item
Hypertension (3)
(Comment:en)
CL Item
Hypotension (4)
(Comment:en)
CL Item
Conjunctivitis (5)
(Comment:en)
CL Item
Photophobia (6)
(Comment:en)
CL Item
Fever (7)
(Comment:en)
CL Item
Chills (8)
(Comment:en)
CL Item
Sweating (9)
(Comment:en)
CL Item
Fatigue/malaise/lethargy (10)
(Comment:en)
CL Item
Weight loss (11)
(Comment:en)
CL Item
Flushing (12)
(Comment:en)
CL Item
Nausea (13)
(Comment:en)
CL Item
Anorexia (14)
(Comment:en)
CL Item
Vomiting (15)
(Comment:en)
CL Item
Diarrhea (16)
(Comment:en)
CL Item
Dehydration (17)
(Comment:en)
CL Item
Constipation (18)
(Comment:en)
CL Item
Gastritis (19)
(Comment:en)
CL Item
Duodenal ulcer (20)
(Comment:en)
CL Item
Gastric ulcer (21)
(Comment:en)
CL Item
Stomatitis/pharyngitis (22)
(Comment:en)
CL Item
Pancreatitis (23)
(Comment:en)
CL Item
Creatinine increase (24)
(Comment:en)
CL Item
Renal failure (25)
(Comment:en)
CL Item
Hemorrhage (26)
(Comment:en)
CL Item
Hematuria (27)
(Comment:en)
CL Item
Melana/GI bleeding (28)
(Comment:en)
CL Item
Allergic reaction (29)
(Comment:en)
CL Item
Infection w/o neutropenia (30)
(Comment:en)
CL Item
Infection w/ neutropenia (31)
(Comment:en)
CL Item
Bilirubin increase (32)
(Comment:en)
CL Item
SGOT increase (33)
(Comment:en)
CL Item
SGPT increase (34)
(Comment:en)
CL Item
Pneumonitis/infiltrates (35)
(Comment:en)
CL Item
Cough (36)
(Comment:en)
CL Item
ARDS (37)
(Comment:en)
CL Item
Hypocalcemia (38)
(Comment:en)
CL Item
Hyperkalemia (39)
(Comment:en)
CL Item
Hyperglycemia (40)
(Comment:en)
CL Item
Hypercalcemia (41)
(Comment:en)
CL Item
Somnolence (42)
(Comment:en)
CL Item
Mood alteration-depression (43)
(Comment:en)
CL Item
Personality/ behavioral change (44)
(Comment:en)
CL Item
Seizures (45)
(Comment:en)
CL Item
Motor neuropathy (46)
(Comment:en)
CL Item
Sensory neuropathy (47)
(Comment:en)
CL Item
Speech impairment (48)
(Comment:en)
CL Item
Dizziness/lightheadedness (49)
(Comment:en)
CL Item
Headache (50)
(Comment:en)
CL Item
Bone pain (51)
(Comment:en)
CL Item
Myalgia (52)
(Comment:en)
CL Item
Arthralgia (53)
(Comment:en)
CL Item
Rash/desquamation (54)
(Comment:en)
CL Item
Urticaria (55)
(Comment:en)
CL Item
Pruritis (56)
(Comment:en)
CL Item
Photosensitivity (57)
(Comment:en)
CL Item
Bruising (58)
(Comment:en)
CL Item
Alopecia (59)
(Comment:en)
CL Item
Libido loss (60)
(Comment:en)
CL Item
Other (61)
(Comment:en)
Item
Grade
integer
C0877248 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C1516728 (UMLS CUI [1,3])
CL.3
Code List
Grade
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
Item
Treatment Relation
integer
C1706735 (UMLS CUI [1,1])
C1516728 (UMLS CUI [1,2])
CL.4
Code List
Treatment Relation
CL Item
Unrelated (1)
CL Item
Unlikely (2)
CL Item
Possible (3)
CL Item
Probable (4)
CL Item
Definite (5)
comment
Item
Notes
text
C0947611 (UMLS CUI [1,1])
C2242529 (UMLS CUI [1,2])
Item Group
Ccrr Module For S0100 Induction And Consolidation Toxicity Form
C0013221 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0023418 (UMLS CUI-3)
C2242529 (UMLS CUI-4)
Patient ID
Item
SWOG Patient ID
text
C2348585 (UMLS CUI [1])
Study Number
Item
SWOG Study No.
text
C0008976 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Registration Step
Item
Registration Step
text
C1514821 (UMLS CUI-1)
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Institution
Item
Institution/Affiliate
text
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Treating Physician
Item
Physician
text
C25364 (NCI Thesaurus Property)
C25741 (NCI Thesaurus ObjectClass)
C25705 (NCI Thesaurus ObjectClass-2)
C1710470 (UMLS CUI [1])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial