ID

21698

Description

Association of L-asparaginase-Methotrexate-Dexamethasone for Nasal and Nasal-type Natural Killer (NK)-T-cell Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00283985

Link

https://clinicaltrials.gov/show/NCT00283985

Keywords

Versions (1)
  1. 4/27/17 4/27/17 -
Uploaded on

April 27, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Lymphoma, Non-Hodgkin NCT00283985

English

Eligibility Lymphoma, Non-Hodgkin NCT00283985

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with relapsing/refractory t-nk/nk lymphoma:
Description

Mature T/NK-cell lymphoma Relapse | Refractory Mature T-Cell and NK-Cell Lymphoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0079774
UMLS CUI [1,2]
C0277556
UMLS CUI [2]
C1335727
ages 18 years and above
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
eastern cooperative oncology group performance status 0-1
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
ability to swallow capsules
Description

Able to swallow capsules (

Data type

boolean

Alias
UMLS CUI [1,1]
C2712086
UMLS CUI [1,2]
C0006935
at least 3 weeks from prior systemic treatments including investigational anti-cancer therapy, at least 7 days from prior radiation therapy and have recovered from prior toxicities
Description

systemic therapy | Cancer treatment Investigational | prior radiation therapy | Toxicity Patient recovered

Data type

boolean

Alias
UMLS CUI [1]
C1515119
UMLS CUI [2,1]
C0920425
UMLS CUI [2,2]
C1517586
UMLS CUI [3]
C0279134
UMLS CUI [4,1]
C0600688
UMLS CUI [4,2]
C1115804
at least 3 weeks from major surgery
Description

major surgery

Data type

boolean

Alias
UMLS CUI [1]
C0679637
non-small cell cancer histology contains a component of small cell lung cancer
Description

Non-small cell carcinoma Containing Component Small cell carcinoma of lung

Data type

boolean

Alias
UMLS CUI [1,1]
C1266002
UMLS CUI [1,2]
C0332256
UMLS CUI [1,3]
C1705248
UMLS CUI [1,4]
C0149925
previously untreated cns metastasis or progressive cns metastasis
Description

CNS metastases untreated | CNS metastases Progressive

Data type

boolean

Alias
UMLS CUI [1,1]
C0686377
UMLS CUI [1,2]
C0332155
UMLS CUI [2,1]
C0686377
UMLS CUI [2,2]
C0205329
prior treatment with a cdk inhibitor
Description

Cyclin-Dependent Kinase Inhibitors

Data type

boolean

Alias
UMLS CUI [1]
C1511576
currently receiving radiotherapy, biological therapy, or any other investigational therapy
Description

Therapeutic radiology procedure | Biological treatment | Therapy, Investigational

Data type

boolean

Alias
UMLS CUI [1]
C1522449
UMLS CUI [2]
C1531518
UMLS CUI [3]
C0949266
creatinine less than 3 x upper limit of normal (uln)
Description

Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C0201976
able to give informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
no prior chemotherapy or radiotherapy
Description

Chemotherapy | Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are pregnant or nursing
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
any factor which might limit the patient's ability to provide informed consent
Description

Factor Informed Consent Limited

Data type

boolean

Alias
UMLS CUI [1,1]
C1521761
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C0439801
liver insufficiency
Description

Hepatic Insufficiency

Data type

boolean

Alias
UMLS CUI [1]
C1306571
evolutive thrombosis
Description

Thrombosis

Data type

boolean

Alias
UMLS CUI [1]
C0040053
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Similar models

Eligibility Lymphoma, Non-Hodgkin NCT00283985

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Mature T/NK-cell lymphoma Relapse | Refractory Mature T-Cell and NK-Cell Lymphoma
Item
patients with relapsing/refractory t-nk/nk lymphoma:
boolean
C0079774 (UMLS CUI [1,1])
C0277556 (UMLS CUI [1,2])
C1335727 (UMLS CUI [2])
Age
Item
ages 18 years and above
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
eastern cooperative oncology group performance status 0-1
boolean
C1520224 (UMLS CUI [1])
Able to swallow capsules (
Item
ability to swallow capsules
boolean
C2712086 (UMLS CUI [1,1])
C0006935 (UMLS CUI [1,2])
systemic therapy | Cancer treatment Investigational | prior radiation therapy | Toxicity Patient recovered
Item
at least 3 weeks from prior systemic treatments including investigational anti-cancer therapy, at least 7 days from prior radiation therapy and have recovered from prior toxicities
boolean
C1515119 (UMLS CUI [1])
C0920425 (UMLS CUI [2,1])
C1517586 (UMLS CUI [2,2])
C0279134 (UMLS CUI [3])
C0600688 (UMLS CUI [4,1])
C1115804 (UMLS CUI [4,2])
major surgery
Item
at least 3 weeks from major surgery
boolean
C0679637 (UMLS CUI [1])
Non-small cell carcinoma Containing Component Small cell carcinoma of lung
Item
non-small cell cancer histology contains a component of small cell lung cancer
boolean
C1266002 (UMLS CUI [1,1])
C0332256 (UMLS CUI [1,2])
C1705248 (UMLS CUI [1,3])
C0149925 (UMLS CUI [1,4])
CNS metastases untreated | CNS metastases Progressive
Item
previously untreated cns metastasis or progressive cns metastasis
boolean
C0686377 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0686377 (UMLS CUI [2,1])
C0205329 (UMLS CUI [2,2])
Cyclin-Dependent Kinase Inhibitors
Item
prior treatment with a cdk inhibitor
boolean
C1511576 (UMLS CUI [1])
Therapeutic radiology procedure | Biological treatment | Therapy, Investigational
Item
currently receiving radiotherapy, biological therapy, or any other investigational therapy
boolean
C1522449 (UMLS CUI [1])
C1531518 (UMLS CUI [2])
C0949266 (UMLS CUI [3])
Creatinine measurement, serum
Item
creatinine less than 3 x upper limit of normal (uln)
boolean
C0201976 (UMLS CUI [1])
Informed Consent
Item
able to give informed consent
boolean
C0021430 (UMLS CUI [1])
Chemotherapy | Therapeutic radiology procedure
Item
no prior chemotherapy or radiotherapy
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
patients who are pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Factor Informed Consent Limited
Item
any factor which might limit the patient's ability to provide informed consent
boolean
C1521761 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Hepatic Insufficiency
Item
liver insufficiency
boolean
C1306571 (UMLS CUI [1])
Thrombosis
Item
evolutive thrombosis
boolean
C0040053 (UMLS CUI [1])
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