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

DOI

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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)
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