metastatic NPC, recent radiotherapy of NPC, recent chemoradiotherapy of NPC
Item
diagnosed metastatic npc patient who have received radiotherapy or chemoradiotherapy with an at least 6 months interval
boolean
C2931822 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
C0332185 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])
C2931822 (UMLS CUI [2,3])
C0332185 (UMLS CUI [3,1])
C0436307 (UMLS CUI [3,2])
C2931822 (UMLS CUI [3,3])
measurable disease
Item
have measurable lesions
boolean
C1513041 (UMLS CUI [1])
absent dysfunction of major organs
Item
no dysfunction of the major organs
boolean
C0332197 (UMLS CUI [1,1])
C0178784 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
C3887504 (UMLS CUI [1,4])
comprehension of study protocol, informed consent
Item
can understand this study and give a signed informed consent certificates
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
medical history, absent allergic reagents to biological agents
Item
without a history of allergic reaction to the biological agents
boolean
C0262926 (UMLS CUI [1,1])
C1527304 (UMLS CUI [1,2])
C0005515 (UMLS CUI [1,3])
C0332197 (UMLS CUI [1,4])
pregnancy, breast-feeding, female of child-bearing age with absent contraception
Item
pregnant or lactating women; women of child-bearing age without contraception
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C1960468 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0700589 (UMLS CUI [3,3])
serious dysfunction of major organs, serious infection of major organs
Item
with a serious infection or dysfunction of the major organs
boolean
C0205404 (UMLS CUI [1,1])
C3887504 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,3])
C0205164 (UMLS CUI [1,4])
C0205404 (UMLS CUI [2,1])
C3714514 (UMLS CUI [2,2])
C0178784 (UMLS CUI [2,3])
C0205164 (UMLS CUI [2,4])
recent other cancer treatment with pharmaceutical preparations
Item
have taken other antitumor drugs during the period of 30 days ahead of this clinical trial
boolean
C0920425 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
hypersensitivity to Escherichia coli pharmaceutical preparations
Item
allergic to the escherichia coli preparations
boolean
C0020517 (UMLS CUI [1,1])
C0014834 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
absent comprehension of study protocol, absent informed consent
Item
cann't understand this study and give a signed informed consent certificates
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])