ID

15629

Description

Concurrent Chemotherapy in Intermediate Risk Patients Treated With Intensity-modulated Radiotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT02289807

Link

https://clinicaltrials.gov/show/NCT02289807

Keywords

Versions (1)
  1. 06.06.16 06.06.16 -
Uploaded on

6. Juni 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Nasopharyngeal Carcinoma NCT02289807

English

Eligibility Nasopharyngeal Carcinoma NCT02289807

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with newly histologically confirmed non-keratinizing (according to who histologically type).
Description

Nasopharyngeal Nonkeratinizing Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C1334926
tumor staged as t1-2n1/t2-3n0(according to the 7th ajcc edition). no evidence of distant metastasis (m0). satisfactory performance status: karnofsky scale (kps) ≥ 70. adequate marrow: leucocyte count ≥ 4000/μl, hemoglobin ≥ 90g/l and platelet count ≥ 100000/μl.
Description

TNM Staging System | M - Distant metastasis stage | Karnofsky Performance Status | Bone Marrow | White Blood Cell Count procedure | Hemoglobin measurement | Platelet Count measurement

Data type

boolean

Alias
UMLS CUI [1]
C1515169
UMLS CUI [2]
C0449916
UMLS CUI [3]
C0206065
UMLS CUI [4]
C0005953
UMLS CUI [5]
C0023508
UMLS CUI [6]
C0518015
UMLS CUI [7]
C0032181
normal liver function test: alanine aminotransferase (alt), aspartate aminotransferase (ast) < 1.5×upper limit of normal (uln) concomitant with alkaline phosphatase (alp) ≤
Description

Liver function tests normal | Alanine aminotransferase measurement | Aspartate aminotransferase measurement | Alkaline phosphatase measurement

Data type

boolean

Alias
UMLS CUI [1]
C0438235
UMLS CUI [2]
C0201836
UMLS CUI [3]
C0201899
UMLS CUI [4]
C0201850
2.5×uln, and bilirubin ≤ uln.
Description

Serum total bilirubin measurement

Data type

boolean

Alias
UMLS CUI [1]
C1278039
adequate renal function: creatinine clearance ≥ 60 ml/min. patients must be informed of the investigational nature of this study and give written informed consent.
Description

Renal function | Creatinine clearance measurement | Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0373595
UMLS CUI [3]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
who type keratinizing squamous cell carcinoma or basaloid squamous cell carcinoma.
Description

WHO tumor classification | Squamous cell carcinoma, keratinizing | Basaloid squamous cell carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C1301142
UMLS CUI [2]
C0334247
UMLS CUI [3]
C1266005
age > 65 or < 18. treatment with palliative intent. prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer.
Description

Age | Palliative Care | Malignant Neoplasms Previous | Basal cell carcinoma | Squamous cell carcinoma of skin | Carcinoma in situ of uterine cervix

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0030231
UMLS CUI [3,1]
C0006826
UMLS CUI [3,2]
C0205156
UMLS CUI [4]
C0007117
UMLS CUI [5]
C0553723
UMLS CUI [6]
C0851140
pregnancy or lactation (consider pregnancy test in women of child-bearing age and emphasize effective contraception during the treatment period).
Description

Pregnancy | Breast Feeding | Pregnancy Tests | Childbearing Potential Age | Contraceptive methods

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032976
UMLS CUI [4,1]
C3831118
UMLS CUI [4,2]
C0001779
UMLS CUI [5]
C0700589
history of previous rt (except for non-melanomatous skin cancers outside intended rt treatment volume).
Description

prior radiation therapy | Malignant neoplasm of skin | Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1]
C0279134
UMLS CUI [2]
C0007114
UMLS CUI [3]
C1522449
prior chemotherapy or surgery (except diagnostic) to primary tumor or nodes. any severe intercurrent disease, which may bring unacceptable risk or affect the compliance of the trial, for example, unstable cardiac disease requiring treatment, renal disease, chronic hepatitis, diabetes with poor control (fasting plasma glucose > 1.5×uln), and emotional disturbance.
Description

Prior Chemotherapy | Operative Surgical Procedures Previous | Operative Surgical Procedures Diagnostic | primary tumor | lymph nodes | Intercurrent disease Risk | Compliance behavior Limited | Heart Diseases Unstable status | Kidney Diseases | Hepatitis, Chronic | Diabetes mellitus poor control | Plasma fasting glucose measurement | Emotional Disturbances

Data type

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2,1]
C0543467
UMLS CUI [2,2]
C0205156
UMLS CUI [3,1]
C0543467
UMLS CUI [3,2]
C0348026
UMLS CUI [4]
C0677930
UMLS CUI [5]
C0024204
UMLS CUI [6,1]
C0277557
UMLS CUI [6,2]
C0035647
UMLS CUI [7,1]
C1321605
UMLS CUI [7,2]
C0439801
UMLS CUI [8,1]
C0018799
UMLS CUI [8,2]
C0443343
UMLS CUI [9]
C0022658
UMLS CUI [10]
C0019189
UMLS CUI [11]
C0860161
UMLS CUI [12]
C0583513
UMLS CUI [13]
C0013985
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Similar models

Eligibility Nasopharyngeal Carcinoma NCT02289807

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Nasopharyngeal Nonkeratinizing Carcinoma
Item
patients with newly histologically confirmed non-keratinizing (according to who histologically type).
boolean
C1334926 (UMLS CUI [1])
TNM Staging System | M - Distant metastasis stage | Karnofsky Performance Status | Bone Marrow | White Blood Cell Count procedure | Hemoglobin measurement | Platelet Count measurement
Item
tumor staged as t1-2n1/t2-3n0(according to the 7th ajcc edition). no evidence of distant metastasis (m0). satisfactory performance status: karnofsky scale (kps) ≥ 70. adequate marrow: leucocyte count ≥ 4000/μl, hemoglobin ≥ 90g/l and platelet count ≥ 100000/μl.
boolean
C1515169 (UMLS CUI [1])
C0449916 (UMLS CUI [2])
C0206065 (UMLS CUI [3])
C0005953 (UMLS CUI [4])
C0023508 (UMLS CUI [5])
C0518015 (UMLS CUI [6])
C0032181 (UMLS CUI [7])
Liver function tests normal | Alanine aminotransferase measurement | Aspartate aminotransferase measurement | Alkaline phosphatase measurement
Item
normal liver function test: alanine aminotransferase (alt), aspartate aminotransferase (ast) < 1.5×upper limit of normal (uln) concomitant with alkaline phosphatase (alp) ≤
boolean
C0438235 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
C0201850 (UMLS CUI [4])
Serum total bilirubin measurement
Item
2.5×uln, and bilirubin ≤ uln.
boolean
C1278039 (UMLS CUI [1])
Renal function | Creatinine clearance measurement | Informed Consent
Item
adequate renal function: creatinine clearance ≥ 60 ml/min. patients must be informed of the investigational nature of this study and give written informed consent.
boolean
C0232804 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
C0021430 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
WHO tumor classification | Squamous cell carcinoma, keratinizing | Basaloid squamous cell carcinoma
Item
who type keratinizing squamous cell carcinoma or basaloid squamous cell carcinoma.
boolean
C1301142 (UMLS CUI [1])
C0334247 (UMLS CUI [2])
C1266005 (UMLS CUI [3])
Age | Palliative Care | Malignant Neoplasms Previous | Basal cell carcinoma | Squamous cell carcinoma of skin | Carcinoma in situ of uterine cervix
Item
age > 65 or < 18. treatment with palliative intent. prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer.
boolean
C0001779 (UMLS CUI [1])
C0030231 (UMLS CUI [2])
C0006826 (UMLS CUI [3,1])
C0205156 (UMLS CUI [3,2])
C0007117 (UMLS CUI [4])
C0553723 (UMLS CUI [5])
C0851140 (UMLS CUI [6])
Pregnancy | Breast Feeding | Pregnancy Tests | Childbearing Potential Age | Contraceptive methods
Item
pregnancy or lactation (consider pregnancy test in women of child-bearing age and emphasize effective contraception during the treatment period).
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032976 (UMLS CUI [3])
C3831118 (UMLS CUI [4,1])
C0001779 (UMLS CUI [4,2])
C0700589 (UMLS CUI [5])
prior radiation therapy | Malignant neoplasm of skin | Therapeutic radiology procedure
Item
history of previous rt (except for non-melanomatous skin cancers outside intended rt treatment volume).
boolean
C0279134 (UMLS CUI [1])
C0007114 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
Prior Chemotherapy | Operative Surgical Procedures Previous | Operative Surgical Procedures Diagnostic | primary tumor | lymph nodes | Intercurrent disease Risk | Compliance behavior Limited | Heart Diseases Unstable status | Kidney Diseases | Hepatitis, Chronic | Diabetes mellitus poor control | Plasma fasting glucose measurement | Emotional Disturbances
Item
prior chemotherapy or surgery (except diagnostic) to primary tumor or nodes. any severe intercurrent disease, which may bring unacceptable risk or affect the compliance of the trial, for example, unstable cardiac disease requiring treatment, renal disease, chronic hepatitis, diabetes with poor control (fasting plasma glucose > 1.5×uln), and emotional disturbance.
boolean
C1514457 (UMLS CUI [1])
C0543467 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0543467 (UMLS CUI [3,1])
C0348026 (UMLS CUI [3,2])
C0677930 (UMLS CUI [4])
C0024204 (UMLS CUI [5])
C0277557 (UMLS CUI [6,1])
C0035647 (UMLS CUI [6,2])
C1321605 (UMLS CUI [7,1])
C0439801 (UMLS CUI [7,2])
C0018799 (UMLS CUI [8,1])
C0443343 (UMLS CUI [8,2])
C0022658 (UMLS CUI [9])
C0019189 (UMLS CUI [10])
C0860161 (UMLS CUI [11])
C0583513 (UMLS CUI [12])
C0013985 (UMLS CUI [13])
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