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ID

12351

Beschrijving

Randomized study with a run-in dose-selection phase to assess the added value of Lenalidomide in combination with standard remission-induction chemotherapy and post-remission treatment in patients aged 18-65 years with previously untreated acute myeloid leukemia (AML) or high risk myelodysplasia (MDS) (IPSS-R risk score> 4.5) Description of Form: Hematological Evaluation Form

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Versies (3)
  1. 10-11-15 10-11-15 -
  2. 23-12-15 23-12-15 -
  3. 11-02-16 11-02-16 -
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10 november 2015

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Creative Commons BY-NC 3.0
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    Hematological Evaluation Form HOVON 132 AML/SAKK 30/13 EudraCT 2013-002843-26

    Engels

    Hematological Evaluation Form

    1 Formulieren  
    Form Relation
    Beschrijving

    Form Relation

    Form related to
    Beschrijving

    Form related to

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C1302181 (Chemotherapy cycle)
    SNOMED
    399042005
    Supportive Care
    Beschrijving

    Supportive Care

    Alias
    UMLS CUI-1
    C0344211 (Supportive care)
    SNOMED
    38678006
    Number of platelet transfusions
    Beschrijving

    Number of platelet transfusions

    Datatype

    float

    Alias
    UMLS CUI [1,1]
    C0086818 (Platelet Transfusion)
    SNOMED
    12719002
    UMLS CUI [1,2]
    C0750480 (Count)
    Date last platelet transfusion
    Beschrijving

    Date last platelet transfusion

    Datatype

    date

    Maateenheden
    • dd/mm/yyyy
    Alias
    UMLS CUI [1,1]
    C0086818 (Platelet Transfusion)
    SNOMED
    12719002
    UMLS CUI [1,2]
    C0011008 (Date in time)
    SNOMED
    410671006
    dd/mm/yyyy
    Number of RBC transfusions
    Beschrijving

    Red Blood Cell Transfusion

    Datatype

    float

    Alias
    UMLS CUI [1,1]
    C0086252 (Red Blood Cell Transfusion)
    SNOMED
    116863004
    UMLS CUI [1,2]
    C0750480 (Count)
    Date of last RBC transfusion
    Beschrijving

    Date of last RBC transfusion

    Datatype

    date

    Maateenheden
    • dd/mm/yyyy
    Alias
    UMLS CUI [1,1]
    C0014772 (Red Blood Cell Count measurement)
    SNOMED
    14089001
    UMLS CUI [1,2]
    C0011008 (Date in time)
    SNOMED
    410671006
    dd/mm/yyyy
    Hematological Evaluations
    Beschrijving

    Hematological Evaluations

    Alias
    UMLS CUI-1
    C0018941 (Hematologic Tests)
    SNOMED
    252275004
    UMLS CUI-2
    C0220825 (Evaluation)
    LOINC
    LP36377-7
    Hematological Evaluation at 1=Start of treatment 2=First evaluation ANC < 0.5 x 109/L 3=First evaluation ANC ≥ 0,5 x 109/L 4=First evaluation ANC ≥ 1,0 x 109/L 5=If not ≥ 1,0 x 109/L, last ANC before next treatment 6=If not ≥ 1,0 x 109/L, last ANC before end of protocol 7=First evaluation platelets < 50 x 109/L 8=First evaluation platelets ≥ 50 x 109/L 9=First evaluation platelets ≥ 100 x 109/L 10=If not ≥ 100 x 109/L, last platelets before next treatment 11=If not ≥ 100 x 109/L, last platelets before end of protocol
    Beschrijving

    Evaluation to be performed at

    Datatype

    float

    Date
    Beschrijving

    Date

    Datatype

    date

    Maateenheden
    • dd/mm/yyyy
    Alias
    UMLS CUI [1]
    C0011008 (Date in time)
    SNOMED
    410671006
    dd/mm/yyyy
    Blasts
    Beschrijving

    Blasts

    Datatype

    float

    Maateenheden
    • %
    Alias
    UMLS CUI [1]
    C1982687 (undefined)
    %
    ANC
    Beschrijving

    Neutrophil count

    Datatype

    float

    Maateenheden
    • 10^9/L
    Alias
    UMLS CUI [1]
    C0200633 (Neutrophil count (procedure))
    SNOMED
    30630007
    10^9/L
    Platelets
    Beschrijving

    Platelets

    Datatype

    float

    Maateenheden
    • x10^9/l
    Alias
    UMLS CUI [1]
    C0005821 (Blood Platelets)
    SNOMED
    16378004
    LOINC
    LP70360-0
    x10^9/l
    Terug naar het begin van de pagina

    Similar models

    Hematological Evaluation Form

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Item
    integer
    C1302181 (UMLS CUI [1])
    Form related to
    Code List
    Form related to
    CL Item
    induction cycle I  (1)
    C3179010 (UMLS CUI-1)
    CL Item
    induction cycle II (2)
    C3179010 (UMLS CUI-1)
    CL Item
    post induction cycle III  (3)
    C0687676 (UMLS CUI-1)
    C3179010 (UMLS CUI-2)
    CL Item
    autoHSCT (4)
    C0194037 (UMLS CUI-1)
    CL Item
    alloHSCT (5)
    C1705576 (UMLS CUI-1)
    CL Item
    observation/maintenance (1-6) (11-16)
    C0481504 (UMLS CUI-1)
    C0700325 (UMLS CUI-3)
    Item Group
    C0344211 (UMLS CUI-1)
    Number of platelet transfusions
    Item
    float
    C0086818 (UMLS CUI [1,1])
    C0750480 (UMLS CUI [1,2])
    Date last platelet transfusion
    Item
    date
    C0086818 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Red Blood Cell Transfusion
    Item
    Number of RBC transfusions
    float
    C0086252 (UMLS CUI [1,1])
    C0750480 (UMLS CUI [1,2])
    Date of last RBC transfusion
    Item
    date
    C0014772 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item Group
    C0018941 (UMLS CUI-1)
    C0220825 (UMLS CUI-2)
    Evaluation to be performed at
    Item
    Hematological Evaluation at 1=Start of treatment 2=First evaluation ANC < 0.5 x 109/L 3=First evaluation ANC ≥ 0,5 x 109/L 4=First evaluation ANC ≥ 1,0 x 109/L 5=If not ≥ 1,0 x 109/L, last ANC before next treatment 6=If not ≥ 1,0 x 109/L, last ANC before end of protocol 7=First evaluation platelets < 50 x 109/L 8=First evaluation platelets ≥ 50 x 109/L 9=First evaluation platelets ≥ 100 x 109/L 10=If not ≥ 100 x 109/L, last platelets before next treatment 11=If not ≥ 100 x 109/L, last platelets before end of protocol
    float
    Date
    Item
    date
    C0011008 (UMLS CUI [1])
    Blasts
    Item
    Blasts
    float
    C1982687 (UMLS CUI [1])
    Neutrophil count
    Item
    ANC
    float
    C0200633 (UMLS CUI [1])
    Platelets
    Item
    Platelets
    float
    C0005821 (UMLS CUI [1])
    Terug naar het begin van de pagina 

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