ID

13997

Descrição

A Study To Evaluate PF-04449913 With Chemotherapy In Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome; ODM derived from: https://clinicaltrials.gov/show/NCT01546038

Link

https://clinicaltrials.gov/show/NCT01546038

Palavras-chave

  1. 21/03/2016 21/03/2016 -
Transferido a

21 de março de 2016

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Acute Myeloid Leukemia NCT01546038

Eligibility Acute Myeloid Leukemia NCT01546038

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
Patients with aml or raeb 2 high risk mds who are newly diagnosed according to the who 2008 classification and previously untreated.
Descrição

Acute Myelocytic Leukemia

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023467
Patients with aml (arising from an antecedent hematologic disease [ahd]) or mds who may have had one prior regimen with commercially available agents for the treatment of their prior hematologic disease. the patients may not have had a prior therapy for their aml.
Descrição

MDS

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3463824
aml patients include de novo aml, aml evolving from mds or other ahd and aml after previous cytotoxic therapy or radiation (secondary aml)
Descrição

Therapy-related acute myeloid leukemia and myelodysplastic syndrome

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1292776
For a diagnosis of aml, a bone marrow blast count of 20% or more is required.
Descrição

Leukemic Blast Count

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2697913
For a diagnosis of high-risk myelodysplastic syndrome raeb 2 the patient must have 10-19% bone marrow blasts
Descrição

Bone marrow blasts

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1982687
Adequate organ function
Descrição

Organ function

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1254358
ecog performance status 0, 1, or 2
Descrição

ECOG

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
aml m3 acute promyelocytic leukemia (apl) or patients with a t(9:22) cytogenetic translocation.
Descrição

Acute Promyelocytic Leukemia

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023487
patients with known active uncontrolled central nervous system (cns) leukemia.
Descrição

Central nervous system leukaemia

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1332884

Similar models

Eligibility Acute Myeloid Leukemia NCT01546038

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Acute Myelocytic Leukemia
Item
Patients with aml or raeb 2 high risk mds who are newly diagnosed according to the who 2008 classification and previously untreated.
boolean
C0023467 (UMLS CUI [1])
MDS
Item
Patients with aml (arising from an antecedent hematologic disease [ahd]) or mds who may have had one prior regimen with commercially available agents for the treatment of their prior hematologic disease. the patients may not have had a prior therapy for their aml.
boolean
C3463824 (UMLS CUI [1])
Therapy-related acute myeloid leukemia and myelodysplastic syndrome
Item
aml patients include de novo aml, aml evolving from mds or other ahd and aml after previous cytotoxic therapy or radiation (secondary aml)
boolean
C1292776 (UMLS CUI [1])
Leukemic Blast Count
Item
For a diagnosis of aml, a bone marrow blast count of 20% or more is required.
boolean
C2697913 (UMLS CUI [1])
Bone marrow blasts
Item
For a diagnosis of high-risk myelodysplastic syndrome raeb 2 the patient must have 10-19% bone marrow blasts
boolean
C1982687 (UMLS CUI [1])
Organ function
Item
Adequate organ function
boolean
C1254358 (UMLS CUI [1])
ECOG
Item
ecog performance status 0, 1, or 2
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Acute Promyelocytic Leukemia
Item
aml m3 acute promyelocytic leukemia (apl) or patients with a t(9:22) cytogenetic translocation.
boolean
C0023487 (UMLS CUI [1])
Central nervous system leukaemia
Item
patients with known active uncontrolled central nervous system (cns) leukemia.
boolean
C1332884 (UMLS CUI [1])

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