ID

13008

Descrizione

506U78 in Treating Patients With Refractory or Relapsed Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00003545

collegamento

https://clinicaltrials.gov/show/NCT00003545

Keywords

  1. 11/01/16 11/01/16 -
Titolare del copyright

CC BY-NC 3.0

Caricato su

11 gennaio 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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Eligibility Leukemia NCT00003545

Eligibility Leukemia NCT00003545

  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00003545
Criteria
Descrizione

Criteria

histologically confirmed diagnosis of t-cell acute lymphoblastic leukemia (all) or lymphoblastic lymphoma (lbl)
Descrizione

histologically confirmed diagnosis of t-cell acute lymphoblastic leukemia (all) or lymphoblastic lymphoma (lbl)

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023449
UMLS CUI [2]
C0278721
leukemia or lymphoma cells should express at least two of the following cell surface antigens: cd1a, cd2, cd3 (surface or cytoplasmic), cd4, cd5, cd7, and cd8
Descrizione

leukemia or lymphoma cells should express at least two of the following cell surface antigens: cd1a, cd2, cd3 (surface or cytoplasmic), cd4, cd5, cd7, and cd8

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0003339
leukemia cells should be negative for myeloperoxidase or sudan black b if the only t cell markers present are cd4 and cd7, the leukemic cells should be demonstrated to lack the myeloid markers cd33 and/or cd13
Descrizione

leukemia cells should be negative for myeloperoxidase or sudan black b if the only t cell markers present are cd4 and cd7, the leukemic cells should be demonstrated to lack the myeloid markers cd33 and/or cd13

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2698399
UMLS CUI [2]
C0075489
UMLS CUI [3]
C0003339
refractory to at least one induction treatment regimen or in first or later relapse after achieving a complete remission
Descrizione

induction

Tipo di dati

boolean

Alias
UMLS CUI [1]
C3179010
no cns leukemia or lymphoma requiring intrathecal or craniospinal radiotherapy
Descrizione

no cns leukemia or lymphoma requiring intrathecal or craniospinal radiotherapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1269563
age: 16 and over
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
bilirubin no greater than 2 times upper limit of normal (unless due to leukemia)
Descrizione

bilirubin

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1278039
creatinine clearance at least 50 ml/min (unless due to leukemia)
Descrizione

creatinine clearance

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0373595
no neurologic toxicity of grade 3 or greater during prior treatment of all/lbl
Descrizione

neurologic toxicity

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0600688
no preexisting neuropathy of grade 2 or greater regardless of causality
Descrizione

neuropathy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0442874
no history of seizure disorder
Descrizione

seizure disorder

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0036572
not pregnant or nursing
Descrizione

not pregnant or nursing

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
fertile patients must use effective contraception
Descrizione

contraception

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0700589
no concurrent erythropoietin
Descrizione

erythropoietin

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0014822
no other concurrent chemotherapy
Descrizione

chemotherapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0392920
no concurrent dexamethasone or other steroidal antiemetics
Descrizione

no concurrent dexamethasone or other steroidal antiemetics

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0011777
UMLS CUI [2]
C0001617
no concurrent hormone therapy, except for non-disease-related conditions
Descrizione

hormone therapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0279025

Similar models

Eligibility Leukemia NCT00003545

  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00003545
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
histologically confirmed diagnosis of t-cell acute lymphoblastic leukemia (all) or lymphoblastic lymphoma (lbl)
Item
histologically confirmed diagnosis of t-cell acute lymphoblastic leukemia (all) or lymphoblastic lymphoma (lbl)
boolean
C0023449 (UMLS CUI [1])
C0278721 (UMLS CUI [2])
leukemia or lymphoma cells should express at least two of the following cell surface antigens: cd1a, cd2, cd3 (surface or cytoplasmic), cd4, cd5, cd7, and cd8
Item
leukemia or lymphoma cells should express at least two of the following cell surface antigens: cd1a, cd2, cd3 (surface or cytoplasmic), cd4, cd5, cd7, and cd8
boolean
C0003339 (UMLS CUI [1])
leukemia cells should be negative for myeloperoxidase or sudan black b if the only t cell markers present are cd4 and cd7, the leukemic cells should be demonstrated to lack the myeloid markers cd33 and/or cd13
Item
leukemia cells should be negative for myeloperoxidase or sudan black b if the only t cell markers present are cd4 and cd7, the leukemic cells should be demonstrated to lack the myeloid markers cd33 and/or cd13
boolean
C2698399 (UMLS CUI [1])
C0075489 (UMLS CUI [2])
C0003339 (UMLS CUI [3])
induction
Item
refractory to at least one induction treatment regimen or in first or later relapse after achieving a complete remission
boolean
C3179010 (UMLS CUI [1])
no cns leukemia or lymphoma requiring intrathecal or craniospinal radiotherapy
Item
no cns leukemia or lymphoma requiring intrathecal or craniospinal radiotherapy
boolean
C1269563 (UMLS CUI [1])
age
Item
age: 16 and over
boolean
C0001779 (UMLS CUI [1])
bilirubin
Item
bilirubin no greater than 2 times upper limit of normal (unless due to leukemia)
boolean
C1278039 (UMLS CUI [1])
creatinine clearance
Item
creatinine clearance at least 50 ml/min (unless due to leukemia)
boolean
C0373595 (UMLS CUI [1])
neurologic toxicity
Item
no neurologic toxicity of grade 3 or greater during prior treatment of all/lbl
boolean
C0600688 (UMLS CUI [1])
neuropathy
Item
no preexisting neuropathy of grade 2 or greater regardless of causality
boolean
C0442874 (UMLS CUI [1])
seizure disorder
Item
no history of seizure disorder
boolean
C0036572 (UMLS CUI [1])
not pregnant or nursing
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
contraception
Item
fertile patients must use effective contraception
boolean
C0700589 (UMLS CUI [1])
erythropoietin
Item
no concurrent erythropoietin
boolean
C0014822 (UMLS CUI [1])
chemotherapy
Item
no other concurrent chemotherapy
boolean
C0392920 (UMLS CUI [1])
no concurrent dexamethasone or other steroidal antiemetics
Item
no concurrent dexamethasone or other steroidal antiemetics
boolean
C0011777 (UMLS CUI [1])
C0001617 (UMLS CUI [2])
hormone therapy
Item
no concurrent hormone therapy, except for non-disease-related conditions
boolean
C0279025 (UMLS CUI [1])

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