age, follicular lymphoma grade, biopsy
Item
adult patients (≥ 18 years old) with histologically documented "follicular lymphoma, grade 1", grade 2", or "follicular lymphoma, grade 3a" diagnosed following an excisional, incisional or generous core biopsy. (i.e. an fna alone is insufficient.)
boolean
C0001779 (UMLS CUI [1])
C0024301 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
C0919553 (UMLS CUI [2,3])
disease stage
Item
disease limited to stages i and ii after adequate staging
boolean
C0699749 (UMLS CUI [1])
life expectancy
Item
anticipated life expectancy > 5 years
boolean
C0023671 (UMLS CUI [1])
informed consent
Item
given written informed consent
boolean
C0021430 (UMLS CUI [1])
assessment
Item
been assessed by a radiation oncologist and a medical oncologist/ haematologist
boolean
C1516048 (UMLS CUI [1])
wbc, platelet count, creatinine
Item
wcc > 3.0 x 10^9/l, platelet count > 100 x 10^9/l, serum creatinine < 0.15 mmol/l
boolean
C0023508 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
radiotherapy
Item
ability to commence radiotherapy within 6 weeks of randomisation
boolean
C1522449 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
contraception, pregnancy
Item
women using effective contraception, are not pregnant and agree not to become pregnant during participating in the trial and during the 12 months thereafter. men agree not to father a child during participation in the trial and during the 12 months thereafter.
boolean
C0700589 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
chemotherapy
Item
received previous systemic cytotoxic chemotherapy.
boolean
C0392920 (UMLS CUI [1])
radiotherapy
Item
received previous radiotherapy, (except superficial radiation therapy for non-melanoma skin cancers).
boolean
C1522449 (UMLS CUI [1])
immunotherapy
Item
received previous immunotherapy.
boolean
C0021083 (UMLS CUI [1])
contraindication
Item
a medical contraindication to radiotherapy, chemotherapy, or rituximab.
boolean
C1301624 (UMLS CUI [1])
malignancy
Item
any previous or concurrent malignancy other than curatively treated non-melanoma skin cancer, level 1 malignant melanoma, or in situ cervical cancer, unless disease and treatment-free for 5 years.
boolean
C0006826 (UMLS CUI [1])
thoracic involvement
Item
such extensive involvement of the thorax that treatment with radiation therapy alone would be hazardous because of excessive lung irradiation, even if a shrinking field technique were employed.
boolean
C0817096 (UMLS CUI [1,1])
C0449290 (UMLS CUI [1,2])
pregnancy, lactation
Item
suspected or confirmed pregnancy. must not be lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
hiv, hbv
Item
patients who have known human immuno-deficiency virus (hiv) infection or active hepatitis b (hbv).
boolean
C0019682 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
study subject participation status
Item
treatment within a clinical study within 30 days prior to study entry.
boolean
C2348568 (UMLS CUI [1])