ID

13799

Beschrijving

Trial of a WT-1 Analog Peptide Vaccine in Patients With Acute Myeloid Leukemia (AML) or Acute Lymphoblastic Leukemia (ALL); ODM derived from: https://clinicaltrials.gov/show/NCT01266083

Link

https://clinicaltrials.gov/show/NCT01266083

Trefwoorden

Versies (1)
  1. 07-03-16 07-03-16 -
Houder van rechten

CC BY-NC 3.0

Geüploaded op

7 maart 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Acute Myeloid Leukemia NCT01266083

Engels

Eligibility Acute Myeloid Leukemia NCT01266083

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
morphologic confirmation of a diagnosis of aml or all at mskcc
Beschrijving

AML or ALL

Datatype

boolean

Alias
UMLS CUI [1]
C0023467
UMLS CUI [2]
C0023449
patients will have completed induction therapy, achieved 1st cr and will have completed any planned postremission therapy. patients are not candidates for allogeneic stem cell transplantation. for purposes of this study, patients who are not candidates for allogeneic stem cell transplantation shall be defined as 1) those who do not meet the eligibility criteria of an open allogeneic transplant protocol or 2) those who do not have a suitable available hla matched donor available or 3) those who refuse to undergo stem cell transplantation or 4) those patients whose disease is characterized by "good risk" features (for aml the following cyotogenetic subtypes: t(8;21), inv (16), or t(16;16), t(15;17), normal karyotype with mutated npm1 and negative for tandem duplication of flt-3. for all: t cell phenotype of any b lineage disease exclusive of t(9;22) or t(4;11) in whom allogenic stem cell transplantation in 1st cr would not be offered as standard of care.
Beschrijving

ID.2

Datatype

boolean

alternatively, those patients greater than or equal to 60 years of age who have achieved 1st cr and in whom no further postremission chemotherapy is planned may be enrolled
Beschrijving

Age, remission

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0677874
UMLS CUI [3]
C0392920
patients must have documented wt1 + disease. for purpose of this study, this is defined as detectable presence of any wt1 transcript via rt-pcr on a bone marrow performed at mskcc within 4 weeks prior to the administration of the first dose of vaccine.
Beschrijving

wt1

Datatype

boolean

Alias
UMLS CUI [1]
C0694898
UMLS CUI [2]
C0599161
patients must be within 2 years of achieving cr following chemotherapy
Beschrijving

complete remission following chemotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0677874
UMLS CUI [1,3]
C0332282
UMLS CUI [1,4]
C0392920
at least 4 weeks must have elapsed between the patient's last chemotherapy or radiation treatment and the first vaccination.
Beschrijving

time elapsed between last chemotherapy or radiation therapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C2826303
UMLS CUI [1,2]
C0042196
UMLS CUI [1,3]
C0392920
UMLS CUI [1,4]
C1522449
age > or = to 18 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
karnofsky performance status > or = to 50%
Beschrijving

karnofsky

Datatype

boolean

Alias
UMLS CUI [1]
C0206065
absolute neutrophil count (anc) > or = to 1000/μl
Beschrijving

ANC

Datatype

boolean

Alias
UMLS CUI [1]
C0948762
platelets > 50k/ μl
Beschrijving

platelets

Datatype

boolean

Alias
UMLS CUI [1]
C0005821
total bilirubin < or = to 2.0 mg/dl ast and alt < or = to 2.5 x upper limits of normal
Beschrijving

hepatic function

Datatype

boolean

Alias
UMLS CUI [1,1]
C1278039
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C0201899
creatinine < or = to 2.0 mg/dl
Beschrijving

creatinine

Datatype

boolean

Alias
UMLS CUI [1]
C0201976
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating women
Beschrijving

pregnancy or lactation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
patients with documented evidence of leptomeningeal disease
Beschrijving

leptomeningeal disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C0023418
UMLS CUI [1,2]
C0228126
patients who have undergone autologous or allogeneic stem cell transplantation
Beschrijving

autologous or allogeneic stem cell transplantation

Datatype

boolean

Alias
UMLS CUI [1,1]
C1504389
UMLS CUI [1,2]
C0439859
UMLS CUI [2,1]
C1504389
UMLS CUI [2,2]
C1515895
patients with active infection requiring systemic antimicrobials
Beschrijving

active infection requiring systemic antimicrobials

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C1136254
patients taking systemic corticosteroids
Beschrijving

systemic corticosteroids

Datatype

boolean

Alias
UMLS CUI [1]
C4039704
patients with serious unstable medical illness
Beschrijving

comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
Terug naar het begin van de pagina

Similar models

Eligibility Acute Myeloid Leukemia NCT01266083

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
AML or ALL
Item
morphologic confirmation of a diagnosis of aml or all at mskcc
boolean
C0023467 (UMLS CUI [1])
C0023449 (UMLS CUI [2])
ID.2
Item
patients will have completed induction therapy, achieved 1st cr and will have completed any planned postremission therapy. patients are not candidates for allogeneic stem cell transplantation. for purposes of this study, patients who are not candidates for allogeneic stem cell transplantation shall be defined as 1) those who do not meet the eligibility criteria of an open allogeneic transplant protocol or 2) those who do not have a suitable available hla matched donor available or 3) those who refuse to undergo stem cell transplantation or 4) those patients whose disease is characterized by "good risk" features (for aml the following cyotogenetic subtypes: t(8;21), inv (16), or t(16;16), t(15;17), normal karyotype with mutated npm1 and negative for tandem duplication of flt-3. for all: t cell phenotype of any b lineage disease exclusive of t(9;22) or t(4;11) in whom allogenic stem cell transplantation in 1st cr would not be offered as standard of care.
boolean
Age, remission
Item
alternatively, those patients greater than or equal to 60 years of age who have achieved 1st cr and in whom no further postremission chemotherapy is planned may be enrolled
boolean
C0001779 (UMLS CUI [1])
C0677874 (UMLS CUI [2])
C0392920 (UMLS CUI [3])
wt1
Item
patients must have documented wt1 + disease. for purpose of this study, this is defined as detectable presence of any wt1 transcript via rt-pcr on a bone marrow performed at mskcc within 4 weeks prior to the administration of the first dose of vaccine.
boolean
C0694898 (UMLS CUI [1])
C0599161 (UMLS CUI [2])
complete remission following chemotherapy
Item
patients must be within 2 years of achieving cr following chemotherapy
boolean
C0040223 (UMLS CUI [1,1])
C0677874 (UMLS CUI [1,2])
C0332282 (UMLS CUI [1,3])
C0392920 (UMLS CUI [1,4])
time elapsed between last chemotherapy or radiation therapy
Item
at least 4 weeks must have elapsed between the patient's last chemotherapy or radiation treatment and the first vaccination.
boolean
C2826303 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,4])
age
Item
age > or = to 18 years
boolean
C0001779 (UMLS CUI [1])
karnofsky
Item
karnofsky performance status > or = to 50%
boolean
C0206065 (UMLS CUI [1])
ANC
Item
absolute neutrophil count (anc) > or = to 1000/μl
boolean
C0948762 (UMLS CUI [1])
platelets
Item
platelets > 50k/ μl
boolean
C0005821 (UMLS CUI [1])
hepatic function
Item
total bilirubin < or = to 2.0 mg/dl ast and alt < or = to 2.5 x upper limits of normal
boolean
C1278039 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C0201899 (UMLS CUI [1,3])
creatinine
Item
creatinine < or = to 2.0 mg/dl
boolean
C0201976 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnancy or lactation
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
leptomeningeal disease
Item
patients with documented evidence of leptomeningeal disease
boolean
C0023418 (UMLS CUI [1,1])
C0228126 (UMLS CUI [1,2])
autologous or allogeneic stem cell transplantation
Item
patients who have undergone autologous or allogeneic stem cell transplantation
boolean
C1504389 (UMLS CUI [1,1])
C0439859 (UMLS CUI [1,2])
C1504389 (UMLS CUI [2,1])
C1515895 (UMLS CUI [2,2])
active infection requiring systemic antimicrobials
Item
patients with active infection requiring systemic antimicrobials
boolean
C0009450 (UMLS CUI [1,1])
C1136254 (UMLS CUI [1,2])
systemic corticosteroids
Item
patients taking systemic corticosteroids
boolean
C4039704 (UMLS CUI [1])
comorbidity
Item
patients with serious unstable medical illness
boolean
C0009488 (UMLS CUI [1])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial