Eligibility Lung Cancer NCT00986297

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Non-Small Cell Lung Carcinoma
Item
histologically or cytologically confirmed non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
TNM clinical staging | Recurrent disease
Item
stage ii-iv and/or recurrent disease
boolean
C3258246 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
Exclusion Cell Small Histology
Item
no small cell histology
boolean
C2828389 (UMLS CUI [1,1])
C0007634 (UMLS CUI [1,2])
C0700321 (UMLS CUI [1,3])
C4048239 (UMLS CUI [1,4])
Measurable Disease | Evaluable Disease
Item
measurable or evaluable disease
boolean
C1513041 (UMLS CUI [1])
C1516986 (UMLS CUI [2])
Tumor Excision Unsuccessful
Item
tumor not amenable to surgical resection
boolean
C0027651 (UMLS CUI [1,1])
C0728940 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Tumor Ineligible Stereotactic Body Radiotherapy
Item
tumor not eligible for stereotactic body radiation therapy
boolean
C0027651 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
C1720823 (UMLS CUI [1,3])
Exclusion Criteria | Prior radiation therapy Region Neoplasm Involved | Overlap Radiation Field Current
Item
no prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields
boolean
C0680251 (UMLS CUI [1])
C0279134 (UMLS CUI [2,1])
C0205147 (UMLS CUI [2,2])
C0027651 (UMLS CUI [2,3])
C1314939 (UMLS CUI [2,4])
C1948020 (UMLS CUI [3,1])
C1882536 (UMLS CUI [3,2])
C0521116 (UMLS CUI [3,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Zubrod Performance Status
Item
zubrod performance status 2-4
boolean
C3714786 (UMLS CUI [1])
Pregnancy Absent | Breast Feeding Absent
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Pregnancy test negative
Item
negative pregnancy test
boolean
C0427780 (UMLS CUI [1])
Fertility Contraceptive methods
Item
fertile patients must agree to use effective contraception
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Evaluation pre treatment Completed
Item
must complete all required pretreatment evaluations
boolean
C1261322 (UMLS CUI [1,1])
C2709094 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.15
Item
see disease characteristics
boolean
Prior Chemotherapy | Chemoradiotherapy Previous
Item
more than 1 week since prior chemotherapy or chemoradiation therapy
boolean
C1514457 (UMLS CUI [1])
C0436307 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Exclusion Chemotherapy
Item
no concurrent chemotherapy
boolean
C2828389 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Exclusion Criteria | Antineoplastic Drug/Agent Therapy | Therapeutic radiology procedure Chest | Chemotherapy | Biological treatment | Vaccine Therapy | Operative Surgical Procedures
Item
no other concurrent antineoplastic therapy (including standard-fractionated radiotherapy to the chest, chemotherapy, biological therapy, vaccine therapy, and surgery) 1 week before, during, and for 1 week after completion of study therapy
boolean
C0680251 (UMLS CUI [1])
C2346834 (UMLS CUI [2])
C1522449 (UMLS CUI [3,1])
C0817096 (UMLS CUI [3,2])
C0392920 (UMLS CUI [4])
C1531518 (UMLS CUI [5])
C0042209 (UMLS CUI [6])
C0543467 (UMLS CUI [7])
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