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ID

42808

Description

Combination Chemotherapy Followed By Radiation Therapy in Treating Patients With Aggressive Non-Hodgkin's Lymphoma DISEASE CHARACTERISTICS: - Histologically confirmed aggressive non-Hodgkin's lymphoma - Previously untreated disease - Favorable prognosis - International Prognostic Index score of 0-1 - No more than 25% marrow involvement PATIENT CHARACTERISTICS: Age - 18 to 60 Performance status - ECOG 0-3 OR - Karnofsky 40-100% Life expectancy - Not specified Hematopoietic - Platelet count at least 100,000/mm^3 - WBC at least 2,500/mm^3 Hepatic - No active hepatitis infection Renal - Not specified Other - HIV negative - Not pregnant or nursing - No relevant accompanying disease - No other concurrent malignancy - No contraindications to any study medications - No prior noncompliance by patient PRIOR CONCURRENT THERAPY: Biologic therapy - Not specified Chemotherapy - No prior chemotherapy Endocrine therapy - Not specified Radiotherapy - No prior radiotherapy Surgery - Not specified Other - No other concurrent participation in another treatment study

Keywords

Versions (2)
  1. 12/9/13 12/9/13 - Martin Dugas
  2. 9/17/21 9/17/21 -
Uploaded on

September 17, 2021

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License

Creative Commons BY-NC 3.0 Legacy
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    Eligibility NCT00053768 NHL

    German English

    Eligibility

    1 forms  
    1. StudyEvent: Eligibility
      1. Eligibility
    Disease characteristics
    Description

    Disease characteristics

    Histologically confirmed aggressive non-Hodgkin's lymphoma
    Description

    NHL

    Data type

    boolean

    Previously untreated disease
    Description

    Previously untreated disease

    Data type

    boolean

    Favorable prognosis
    Description

    Prognosis

    Data type

    boolean

    International Prognostic Index score of 0-1
    Description

    International Prognostic Index score

    Data type

    boolean

    No more than 25% marrow involvement
    Description

    Bone marrow involvement

    Data type

    boolean

    Patient characteristics and prior concurrent therapy
    Description

    Patient characteristics and prior concurrent therapy

    Age 18 to 60
    Description

    Age

    Data type

    boolean

    ECOG 0-3 OR Karnofsky 40-100%
    Description

    Performance status

    Data type

    boolean

    Platelet count at least 100,000/mm^3
    Description

    Platelet count

    Data type

    boolean

    WBC at least 2,500/mm^3
    Description

    WBC

    Data type

    boolean

    No active hepatitis infection
    Description

    Hepatitis

    Data type

    boolean

    HIV negative; Not pregnant or nursing; No relevant accompanying disease; No other concurrent malignancy; No contraindications to any study medications; No prior noncompliance by patient
    Description

    Other

    Data type

    boolean

    No prior chemotherapy
    Description

    Chemotherapy

    Data type

    boolean

    No prior radiotherapy
    Description

    Radiotherapy

    Data type

    boolean

    No other concurrent participation in another treatment study
    Description

    Enrollment

    Data type

    boolean

    Medical Concepts
    Description

    Medical Concepts

    Diagnosis
    Description

    Diagnosis

    Data type

    string

    Alias
    UMLS CUI
    C0011900
    SNOMED CT 2010_0731
    439401001
    Therapeutic procedure
    Description

    Therapeutic procedure

    Data type

    string

    Alias
    UMLS CUI
    C0087111
    Medication
    Description

    Pharmaceutical Preparations

    Data type

    string

    Alias
    UMLS CUI
    C0013227
    International Prognostic Index
    Description

    International Prognostic Index

    Data type

    string

    Alias
    UMLS CUI
    C1512894
    Bone Marrow Involvement
    Description

    Bone Marrow Involvement

    Data type

    string

    Alias
    UMLS CUI
    C1517677
    Age
    Description

    Age

    Data type

    string

    Alias
    UMLS CUI
    C0001779
    SNOMED CT 2010_0731
    102518004
    ECOG performance status
    Description

    ECOG performance status

    Data type

    string

    Alias
    SNOMED CT 2010_0731
    423740007
    Karnofsky performance status
    Description

    Karnofsky performance status

    Data type

    string

    Alias
    SNOMED CT 2010_0731
    273546003
    Platelet count - finding
    Description

    Platelet count - finding (Code )

    Data type

    string

    Alias
    SNOMED CT 2010_0731
    365632008
    UMLS CUI
    C1287267
    LOINC
    777-3
    White blood cell count
    Description

    WBC

    Data type

    string

    Alias
    SNOMED CT 2010_0731
    767002
    LOINC
    6690-2
    Hepatitis
    Description

    Hepatitis

    Data type

    string

    Alias
    SNOMED CT 2010_0731
    29001004
    UMLS CUI
    C0019158
    MedDRA 13.1
    10019717
    HIV negative
    Description

    HIV negative

    Data type

    string

    Alias
    UMLS CUI
    C0481430
    SNOMED CT 2010_0731
    143223008
    pregnant
    Description

    pregnant

    Data type

    string

    Alias
    UMLS CUI
    C0549206
    MedDRA 13.1
    10036586
    Breast feeding
    Description

    Breast feeding

    Data type

    string

    Alias
    UMLS CUI
    C0006147
    MedDRA 13.1
    10006247
    Contraindication to medical treatment
    Description

    Contraindication to medical treatment

    Data type

    string

    Alias
    UMLS CUI
    C1301624
    MedDRA 13.1
    10010833
    Treatment noncompliance
    Description

    Treatment noncompliance

    Data type

    string

    Alias
    UMLS CUI
    C0376405
    MedDRA 13.1
    10049414
    Cancer chemotherapy
    Description

    Chemotherapy

    Data type

    string

    Alias
    UMLS CUI
    C0392920
    SNOMED CT 2010_0731
    150415003
    Radiotherapy
    Description

    Radiotherapy

    Data type

    string

    Alias
    UMLS CUI
    C1522449
    SNOMED CT 2010_0731
    302505005
    Enrollment
    Description

    Enrollment

    Data type

    string

    Alias
    UMLS CUI
    C1516879
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    Similar models

    Eligibility

    1 forms
    1. StudyEvent: Eligibility
      1. Eligibility
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Disease characteristics
    NHL
    Item
    Histologically confirmed aggressive non-Hodgkin's lymphoma
    boolean
    Previously untreated disease
    Item
    Previously untreated disease
    boolean
    Prognosis
    Item
    Favorable prognosis
    boolean
    International Prognostic Index score
    Item
    International Prognostic Index score of 0-1
    boolean
    Bone marrow involvement
    Item
    No more than 25% marrow involvement
    boolean
    Item Group
    Patient characteristics and prior concurrent therapy
    Age
    Item
    Age 18 to 60
    boolean
    Performance status
    Item
    ECOG 0-3 OR Karnofsky 40-100%
    boolean
    Platelet count
    Item
    Platelet count at least 100,000/mm^3
    boolean
    WBC
    Item
    WBC at least 2,500/mm^3
    boolean
    Hepatitis
    Item
    No active hepatitis infection
    boolean
    Other
    Item
    HIV negative; Not pregnant or nursing; No relevant accompanying disease; No other concurrent malignancy; No contraindications to any study medications; No prior noncompliance by patient
    boolean
    Chemotherapy
    Item
    No prior chemotherapy
    boolean
    Radiotherapy
    Item
    No prior radiotherapy
    boolean
    Enrollment
    Item
    No other concurrent participation in another treatment study
    boolean
    Item Group
    Medical Concepts
    Diagnosis
    Item
    Diagnosis
    string
    C0011900 (UMLS CUI)
    439401001 (SNOMED CT 2010_0731)
    Therapeutic procedure
    Item
    Therapeutic procedure
    string
    C0087111 (UMLS CUI)
    Pharmaceutical Preparations
    Item
    Medication
    string
    C0013227 (UMLS CUI)
    International Prognostic Index
    Item
    International Prognostic Index
    string
    C1512894 (UMLS CUI)
    Bone Marrow Involvement
    Item
    Bone Marrow Involvement
    string
    C1517677 (UMLS CUI)
    Age
    Item
    Age
    string
    C0001779 (UMLS CUI)
    102518004 (SNOMED CT 2010_0731)
    ECOG performance status
    Item
    ECOG performance status
    string
    423740007 (SNOMED CT 2010_0731)
    Karnofsky performance status
    Item
    Karnofsky performance status
    string
    273546003 (SNOMED CT 2010_0731)
    Platelet count - finding (Code )
    Item
    Platelet count - finding
    string
    365632008 (SNOMED CT 2010_0731)
    C1287267 (UMLS CUI)
    777-3 (LOINC)
    WBC
    Item
    White blood cell count
    string
    767002 (SNOMED CT 2010_0731)
    6690-2 (LOINC)
    Hepatitis
    Item
    Hepatitis
    string
    29001004 (SNOMED CT 2010_0731)
    C0019158 (UMLS CUI)
    10019717 (MedDRA 13.1)
    HIV negative
    Item
    HIV negative
    string
    C0481430 (UMLS CUI)
    143223008 (SNOMED CT 2010_0731)
    pregnant
    Item
    pregnant
    string
    C0549206 (UMLS CUI)
    10036586 (MedDRA 13.1)
    Breast feeding
    Item
    Breast feeding
    string
    C0006147 (UMLS CUI)
    10006247 (MedDRA 13.1)
    Contraindication to medical treatment
    Item
    Contraindication to medical treatment
    string
    C1301624 (UMLS CUI)
    10010833 (MedDRA 13.1)
    Treatment noncompliance
    Item
    Treatment noncompliance
    string
    C0376405 (UMLS CUI)
    10049414 (MedDRA 13.1)
    Chemotherapy
    Item
    Cancer chemotherapy
    string
    C0392920 (UMLS CUI)
    150415003 (SNOMED CT 2010_0731)
    Radiotherapy
    Item
    Radiotherapy
    string
    C1522449 (UMLS CUI)
    302505005 (SNOMED CT 2010_0731)
    Enrollment
    Item
    Enrollment
    string
    C1516879 (UMLS CUI)
    Back to the top of the page 

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