Age
Item
both male and female aged range from 18 years to 65 years.
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
eastern cooperative oncology group(ecog) performance status of 0 or 1.
boolean
C1520224 (UMLS CUI [1])
Diffuse Large B-Cell Lymphoma
Item
all patients had histologically confirmed diffuse large b-cell lymphoma.
boolean
C0079744 (UMLS CUI [1])
Diffuse Large B-Cell Lymphoma Stage Advanced | Diffuse large B-cell lymphoma recurrent | Therapeutic radiology procedure Absent
Item
advanced-stage dlbcl patients at newly diagnosed or recurrent without rt in initial management.
boolean
C0079744 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0205179 (UMLS CUI [1,3])
C0855111 (UMLS CUI [2])
C1522449 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Organ function
Item
adequate organ function.
boolean
C0678852 (UMLS CUI [1])
Pregnancy test negative
Item
negative pregnancy test.
boolean
C0427780 (UMLS CUI [1])
Informed Consent
Item
signed informed consent document on file.
boolean
C0021430 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
woman who were pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Local infection Severe | Communicable Disease General
Item
with severe local infection or general infective disease.
boolean
C1400591 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2,1])
C0205246 (UMLS CUI [2,2])
Lymphoma Primary Organ Special | Cuticle | Central Nervous System | Gastrointestinal tract | Testis | Lung
Item
primary lymphoma in special organ including cuticula, center never system, gastrointestinal tract, testicle, and lung.
boolean
C0024299 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,3])
C0205555 (UMLS CUI [1,4])
C2699479 (UMLS CUI [2])
C3714787 (UMLS CUI [3])
C0017189 (UMLS CUI [4])
C0039597 (UMLS CUI [5])
C0024109 (UMLS CUI [6])
Second Primary Cancer | Exception Skin carcinoma
Item
with other second primary malignancy except cutaneum carcinoma.
boolean
C0751623 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
Study Subject Participation Status | Study Subject Participation Status Planned
Item
being or planning to participate in other study.
boolean
C2348568 (UMLS CUI [1])
C2348568 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Study Subject Participation Status Ineligible
Item
any patient who in the opinion of the investigator should not participate in the study.
boolean
C2348568 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
Withdrawal criteria
Item
withdrawal criteria:
boolean
C1710677 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
Withdrawal Patient Decision
Item
patient are free to withdrawal completely from the study at any time upon request.
boolean
C1710677 (UMLS CUI [1,1])
C4527299 (UMLS CUI [1,2])
Study Subject Participation Status Stopped
Item
patient in the study may be stopped with the patient agreement at any time at the discretion of investigator.
boolean
C2348568 (UMLS CUI [1,1])
C1272691 (UMLS CUI [1,2])
Radiation Field Disease Progression | Therapeutic radiology procedure
Item
in-field progression on irradiation ongoing.
boolean
C1882536 (UMLS CUI [1,1])
C0242656 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2])
Adverse event Chemotherapy | Adverse event Therapeutic radiology procedure
Item
poor tolerability adverse events in the period of chemotherapy or irradiation after enrolled in the study.
boolean
C0877248 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])