Age
Item
18 Years and older
boolean
NHL III/IV
Item
Non Hodgkin Lymphoma stage III or IV at timepoint of diagnosis
boolean
remission after first line chemotherapy
Item
Patients who have achieved a remission after first line chemotherapy
boolean
6-12 weeks since last dose of chemotherapy
Item
No less than 6 weeks and no more than 12 weeks since last dose of chemotherapy
boolean
consent
Item
written informed consent
boolean
Any other anticancer treatment for NHL except the preceding first line chemotherapy
Item
Any other anticancer treatment for NHL except the preceding first line chemotherapy
boolean
Prior radiation therapy
Item
Prior radiation therapy
boolean
no recovery from chemotherapy
Item
Patients who have not recovered from the toxic effects of the first line chemotherapy
boolean
other cancer
Item
Any other cancer or history of cancer less than 10 years ago
boolean
HIV
Item
Patients with known HIV positivity
boolean
pleural effusion or ascites
Item
patients with pleural effusion or ascites
boolean
pregnant or breast feeding
Item
female patients who are pregnant or breast feeding (women of childbearing potential must have a negative serum pregnancy test at study entry)
boolean
no contraception
Item
Adults not employing an effective method of birth control during study treatment and 12 months thereafter
boolean
non-compliance
Item
Patients unable or unwilling to comply with protocol
boolean
Age
Item
Age
string
C0001779 (UMLS CUI)
102518004 (SNOMED CT 2010_0731)
Diagnosis
Item
Diagnosis
string
C0011900 (UMLS CUI)
439401001 (SNOMED CT 2010_0731)
MTHU008876 (LOINC Version 232)
NHL
Item
Lymphoma, Non-Hodgkin (Non-Hodgkins lymphoma)
string
C0024305 (UMLS CUI)
118601006 (SNOMED CT 2010_0731)
10029547 (MedDRA 13.1)
C85.9 (ICD-10-CM Version 2010)
Tumor Staging
Item
Diagnostic Neoplasm Staging
string
C0027646 (UMLS CUI)
254292007 (SNOMED CT 2010_0731)
LP78422-0 (LOINC Version 232)
Remission
Item
Disease remission
string
C0544452 (UMLS CUI)
277022003 (SNOMED CT 2010_0731)
Pharmaceutical Preparations
Item
Medication
string
C0013227 (UMLS CUI)
Chemotherapy
Item
Chemotherapy
string
C0392920 (UMLS CUI)
150415003 (SNOMED CT 2010_0731)
Informed Consent
Item
Informed Consent
string
C0021430 (UMLS CUI)
First-Line Therapy (primary therapy)
Item
First-Line Treatment (primary treatment)
string
C1708063 (UMLS CUI)
Radiotherapy
Item
Radiotherapy
string
C1522449 (UMLS CUI)
302505005 (SNOMED CT 2010_0731)
Recovery
Item
Recovery - healing process
string
C2004454 (UMLS CUI)
Cancer
Item
Malignant Neoplasms
string
C0006826 (UMLS CUI)
363346000 (SNOMED CT 2010_0731)
10028997 (MedDRA 13.1)
MTHU010328 (LOINC Version 232)
C00-C96 (ICD-10-CM Version 2010)
HIV negative
Item
HIV negative
string
C0481430 (UMLS CUI)
143223008 (SNOMED CT 2010_0731)
10020179 (MedDRA 13.1)
Pleural effusion
Item
Pleural effusion disorder
string
C0032227 (UMLS CUI)
60046008 (SNOMED CT 2010_0731)
10035598 (MedDRA 13.1)
J90 (ICD-10-CM Version 2010)
511.9 (ICD-9-CM Version 2011)
E13486 (CTCAE Version 4.03)
Ascites
Item
Ascites
string
C0003962 (UMLS CUI)
389026000 (SNOMED CT 2010_0731)
10003445 (MedDRA 13.1)
R18 (ICD-10-CM Version 2010)
789.5 (ICD-9-CM Version 2011)
E10502 (CTCAE Version 4.03)
pregnant
Item
pregnant
string
C0549206 (UMLS CUI)
10036586 (MedDRA 13.1)
Lactation
Item
Breast feeding, Nursing
string
C0006147 (UMLS CUI)
10006247 (MedDRA 13.1)
Serum pregnancy test
Item
Serum pregnancy test (B-HCG)
string
C0430060 (UMLS CUI)
166434005 (SNOMED CT 2010_0731)
Contraception
Item
Contraception
string
C0700589 (UMLS CUI)
146680009 (SNOMED CT 2010_0731)
10010808 (MedDRA 13.1)
Compliance
Item
Compliance
string
C1321605 (UMLS CUI)
405078008 (SNOMED CT 2010_0731)