ID

12574

Descrição

Liposomal Cytarabine-Daunorubicin CPX-351 in Treating Patients With Untreated Myelodysplastic Syndrome or Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT01804101

Link

https://clinicaltrials.gov/show/NCT01804101

Palavras-chave

  1. 02/12/2015 02/12/2015 -
Transferido a

2 de dezembro de 2015

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Acute Biphenotypic Leukemia NCT01804101

Eligibility Acute Biphenotypic Leukemia NCT01804101

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
Diagnosis of untreated high-risk myelodysplastic syndrome (>= 10% blasts) or aml
Descrição

other than acute promyelocytic leukemia (apl) with t(15;17)(q22;q12) or variants according to the 2008 world health organization (who) classification; patients with biphenotypic aml are eligible; outside diagnostic material is acceptable as long as peripheral blood and/or bone marrow slides are reviewed at the study institution and cytogenetic/molecular information is available

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3463824
UMLS CUI [2]
C0026998
prior hydroxyurea for aml is permitted but should be discontinued prior to start of cpx-351 treatment
Descrição

prior hydroxyurea for aml

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0020402
UMLS CUI [2]
C0521104
UMLS CUI [3]
C1706472
azacitidine, decitabine, lenalidomide, and growth factors are permitted for low-risk mds (< 10% blasts); all treatments for mds should be discontinued prior to start of cpx-351 treatment
Descrição

discontinue treatment for myelodysplastic syndrome

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0584668
treatment-related mortality (trm) score >= 13.1 as calculated with simplified model
Descrição

treatment-related mortality score

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0457450
bilirubin < 2.0 mg/ml x upper limit of normal; this requirement reflects the excretion of cpx-351 by the liver
Descrição

Liver function

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0232741
aspartate aminotransferase (ast)/alanine aminotransferase (alt) < 4.0 x upper limit of normal; this requirement reflects the excretion of cpx-351 by the liver
Descrição

Liver function

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0232741
left ventricular ejection fraction (lvef) >= 40%, assessed within 28 days prior to registration, e.g. by multi gated acquisition (muga) scan or echocardiography, or other appropriate diagnostic modality
Descrição

left ventricular ejection fraction

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0428772
patients with symptoms/signs of hyperleukocytosis or white blood cell count (wbc) > 100,000/ul can be treated with leukapheresis prior to enrollment
Descrição

hyperleukocytosis or white blood cell count (wbc) > 100,000/ul can be treated with leukapheresis prior to enrollment

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3805210
UMLS CUI [2]
C0023416
provide signed written informed consent
Descrição

informed consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
refractory/relapsing blast crisis of chronic myelogenous leukemia (cml)
Descrição

refractory/relapsing blast crisis of chronic myelogenous leukemia (cml)

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2861579
UMLS CUI [2]
C0205269
concomitant illness associated with a likely survival of < 1 year
Descrição

Comorbidity with a likely survival of < 1 year

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C2919552
active systemic fungal, bacterial, viral, or other infection, unless under treatment with anti-microbials and controlled/stable, as defined as being afebrile and hemodynamically stable for 24-48 hours
Descrição

infection, unless under treatment

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0087111

Similar models

Eligibility Acute Biphenotypic Leukemia NCT01804101

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
untreated high-risk myelodysplastic syndrome or aml
Item
Diagnosis of untreated high-risk myelodysplastic syndrome (>= 10% blasts) or aml
boolean
C3463824 (UMLS CUI [1])
C0026998 (UMLS CUI [2])
prior hydroxyurea for aml
Item
prior hydroxyurea for aml is permitted but should be discontinued prior to start of cpx-351 treatment
boolean
C0020402 (UMLS CUI [1])
C0521104 (UMLS CUI [2])
C1706472 (UMLS CUI [3])
discontinue treatment for myelodysplastic syndrome
Item
azacitidine, decitabine, lenalidomide, and growth factors are permitted for low-risk mds (< 10% blasts); all treatments for mds should be discontinued prior to start of cpx-351 treatment
boolean
C0584668 (UMLS CUI [1])
treatment-related mortality score
Item
treatment-related mortality (trm) score >= 13.1 as calculated with simplified model
boolean
C0457450 (UMLS CUI [1])
Liver function
Item
bilirubin < 2.0 mg/ml x upper limit of normal; this requirement reflects the excretion of cpx-351 by the liver
boolean
C0232741 (UMLS CUI [1])
Liver function
Item
aspartate aminotransferase (ast)/alanine aminotransferase (alt) < 4.0 x upper limit of normal; this requirement reflects the excretion of cpx-351 by the liver
boolean
C0232741 (UMLS CUI [1])
left ventricular ejection fraction
Item
left ventricular ejection fraction (lvef) >= 40%, assessed within 28 days prior to registration, e.g. by multi gated acquisition (muga) scan or echocardiography, or other appropriate diagnostic modality
boolean
C0428772 (UMLS CUI [1])
hyperleukocytosis or white blood cell count (wbc) > 100,000/ul can be treated with leukapheresis prior to enrollment
Item
patients with symptoms/signs of hyperleukocytosis or white blood cell count (wbc) > 100,000/ul can be treated with leukapheresis prior to enrollment
boolean
C3805210 (UMLS CUI [1])
C0023416 (UMLS CUI [2])
informed consent
Item
provide signed written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
refractory/relapsing blast crisis of chronic myelogenous leukemia (cml)
Item
refractory/relapsing blast crisis of chronic myelogenous leukemia (cml)
boolean
C2861579 (UMLS CUI [1])
C0205269 (UMLS CUI [2])
Comorbidity with a likely survival of < 1 year
Item
concomitant illness associated with a likely survival of < 1 year
boolean
C0009488 (UMLS CUI [1])
C2919552 (UMLS CUI [2])
infection, unless under treatment
Item
active systemic fungal, bacterial, viral, or other infection, unless under treatment with anti-microbials and controlled/stable, as defined as being afebrile and hemodynamically stable for 24-48 hours
boolean
C0009450 (UMLS CUI [1])
C0087111 (UMLS CUI [2])

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