Informationen:
Fehler:
ID
14469
Beschreibung
ACVBP Followed by ASCT in Patients With BCL-2 Positive Diffuse Large B-Cell Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00169130
Link
https://clinicaltrials.gov/show/NCT00169130
Stichworte
Versionen (1)
- 17.04.16 17.04.16 -
Hochgeladen am
17. April 2016
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Lymphoma, Large-Cell, Diffuse NCT00169130
Eligibility Lymphoma, Large-Cell, Diffuse NCT00169130
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Lymphoma, Large-Cell, Diffuse NCT00169130
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Diffuse large b-cell lymphoma
Item
patient with diffuse large b-cell lymphoma according to the who classification (anti cd20 labeling)
boolean
C0079744 (UMLS CUI [1])
Age
Item
aged 18 to 60 years
boolean
C0001779 (UMLS CUI [1])
Previous treatment
Item
non previously treated
boolean
C0087111 (UMLS CUI [1])
ECOG performance status, ann arbor stage and ldh level
Item
with one and only one of the following adverse characteristics: ecog performance status 2 or more, or ann arbor stage iii or iv, or elevated ldh level
boolean
C1520224 (UMLS CUI [1])
C0432516 (UMLS CUI [2])
C0202113 (UMLS CUI [3])
C0432516 (UMLS CUI [2])
C0202113 (UMLS CUI [3])
HIV, HBV, HVC Serologoy
Item
negative hiv, hbv and hcv serologies (except vaccination)
boolean
C0019698 (UMLS CUI [1])
C0853319 (UMLS CUI [2])
C0201485 (UMLS CUI [3])
C0853319 (UMLS CUI [2])
C0201485 (UMLS CUI [3])
Life expectancy
Item
with a minimum life expectancy of 3 months
boolean
C0023671 (UMLS CUI [1])
Informed consent
Item
having previously signed a written informed consent
boolean
C0021430 (UMLS CUI [1])
Indolent lymphoma
Item
any history of treated or non-treated indolent lymphoma.
boolean
C1334170 (UMLS CUI [1])
T-cell lymphoma
Item
t-cell lymphoma.
boolean
C0079772 (UMLS CUI [1])
CNS or meningeal lymphoma
Item
central nervous system or meningeal involvement by lymphoma.
boolean
C0280803 (UMLS CUI [1])
C2213017 (UMLS CUI [2])
C2213017 (UMLS CUI [2])
Contraindication to chemotherapy
Item
any contra-indication to any drug contained in the chemotherapy regimens.
boolean
C1301624 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,2])
Renal and hepatic functio
Item
poor renal function (creatinin level>150µmol/l), poor hepatic function (total bilirubin level>30mmol/l, transaminases>2.5 maximum normal level) unless these abnormalities are related to the lymphoma.
boolean
C0201976 (UMLS CUI [1])
C0201913 (UMLS CUI [2])
C0919834 (UMLS CUI [3])
C0201913 (UMLS CUI [2])
C0919834 (UMLS CUI [3])
Comorbidity
Item
serious active disease (according to the investigator’s decision).
boolean
C0009488 (UMLS CUI [1])
Bone marrow function
Item
poor bone marrow reserve as defined by neutrophils <1.5g/l or platelets<100g/l, unless related to bone marrow infiltration.
boolean
C0200633 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0032181 (UMLS CUI [2])
Further malignancies
Item
any history of cancer during the last 5 years with the exception of non-melanoma skin tumors or stage 0 (in situ) cervical carcinoma.
boolean
C0006826 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0007114 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C2216722 (UMLS CUI [2,3])
C0332196 (UMLS CUI [1,2])
C0007114 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C2216722 (UMLS CUI [2,3])
Experimental drug
Item
treatment with any investigational drug within 30 days before planned first cycle of chemotherapy and during the study.
boolean
C0304229 (UMLS CUI [1])
Pregnancy
Item
childbearing woman.
boolean
C0032961 (UMLS CUI [1])
Organ transplantation
Item
patients previously treated with an organ transplantation.
boolean
C0029216 (UMLS CUI [1])