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ID
41079
Beschrijving
Biomarkers in Samples From Adult Patients With Acute Myeloid Leukemia Who Failed Existing Standard-of-Care Treatment; ODM derived from: https://clinicaltrials.gov/show/NCT01421862
Link
https://clinicaltrials.gov/show/NCT01421862
Trefwoorden
Versies (1)
- 20-06-20 20-06-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
20 juni 2020
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Leukemia NCT01421862
Eligibility Leukemia NCT01421862
- StudyEvent: Eligibility
Similar models
Eligibility Leukemia NCT01421862
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Specimen AML Untreated | Exception Acute Promyelocytic Leukemia
Item
samples from previously untreated non-m3 acute myeloid leukemia (aml)
boolean
C0370003 (UMLS CUI [1,1])
C0023467 (UMLS CUI [1,2])
C0332155 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0023487 (UMLS CUI [2,2])
C0023467 (UMLS CUI [1,2])
C0332155 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0023487 (UMLS CUI [2,2])
Normal karyotype | Disease Intermediate Risk
Item
normal karyotype (nk) intermediate-risk disease
boolean
C0333684 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C3640764 (UMLS CUI [2,2])
C0012634 (UMLS CUI [2,1])
C3640764 (UMLS CUI [2,2])
Bone Marrow Cells Pretreatment Cryopreserved | Blood Cells Pretreatment Cryopreserved
Item
two or more vials of cryopreserved pretreatment bone marrow cells and/or two or more vials of cryopreserved pretreatment blood cells available from the intergroup aml repository
boolean
C0005955 (UMLS CUI [1,1])
C3539075 (UMLS CUI [1,2])
C0010405 (UMLS CUI [1,3])
C0005773 (UMLS CUI [2,1])
C3539075 (UMLS CUI [2,2])
C0010405 (UMLS CUI [2,3])
C3539075 (UMLS CUI [1,2])
C0010405 (UMLS CUI [1,3])
C0005773 (UMLS CUI [2,1])
C3539075 (UMLS CUI [2,2])
C0010405 (UMLS CUI [2,3])
Blast count
Item
blast count ≥ 60%
boolean
C0523113 (UMLS CUI [1])
Eligibility Clinical Trial | Evaluable Patient Clinical Trial | Toxicity Fatal Absent
Item
eligible and evaluable for the patient's clinical trial, and did not have fatal induction toxicity
boolean
C1548635 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C2986511 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0600688 (UMLS CUI [3,1])
C1302234 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C0008976 (UMLS CUI [1,2])
C2986511 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0600688 (UMLS CUI [3,1])
C1302234 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Response Induction Chemotherapy
Item
response to protocol induction chemotherapy:
boolean
C1704632 (UMLS CUI [1,1])
C3179010 (UMLS CUI [1,2])
C3179010 (UMLS CUI [1,2])
Therapy non-responder | Complete remission failed | Status post Induction Chemotherapy | Cytarabine | Daunorubicin Hydrochloride | Idarubicin
Item
non-response: aml with failure to achieve a complete remission (cr) after induction chemotherapy ("7 & 3"-based therapy using cytatabine and/or daunorobicin hydrochloride (dnr) or idarubicin and/or dnr
boolean
C0919875 (UMLS CUI [1])
C0677874 (UMLS CUI [2,1])
C0231175 (UMLS CUI [2,2])
C0231290 (UMLS CUI [3,1])
C3179010 (UMLS CUI [3,2])
C0010711 (UMLS CUI [4])
C0282123 (UMLS CUI [5])
C0020789 (UMLS CUI [6])
C0677874 (UMLS CUI [2,1])
C0231175 (UMLS CUI [2,2])
C0231290 (UMLS CUI [3,1])
C3179010 (UMLS CUI [3,2])
C0010711 (UMLS CUI [4])
C0282123 (UMLS CUI [5])
C0020789 (UMLS CUI [6])
Therapy responder | Continued Complete Response
Item
responders: continued complete remission (ccr) > 2 years
boolean
C0919876 (UMLS CUI [1])
C2347861 (UMLS CUI [2])
C2347861 (UMLS CUI [2])
Patient Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Prior Therapy Concurrent
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1,1])
C0205420 (UMLS CUI [1,2])
C0205420 (UMLS CUI [1,2])
ID.12
Item
see disease characteristics
boolean