The CDE Browser can be used to download collections of meta data describing data held in repositories for cancer research and clinical trials. These CDEs can be downloaded in Excel or XML Format. However, it is not always easy to find the desired collection, as CDEs are organized in the Navigation Tree by Context, not topic. Attempting to download all the Released CDEs would result in a file that is too large for an Excel download. The canned collections in the following list are provided for your convenience.
Bulk Downloads of production CDEs:
- All non-retired production CDEs (CDEs with Workflow status NOT = "RETIRED....") as of Sept 23, 2013
- All production CDEs with Registration Status = "STANDARD"as of Jan 27, 2012
REDCap Utilities:
These are XSLT files that transform caDSR CDEs and Forms in XML format to a file suitable for uploading to REDCap:
CDEs associated with Standard Case Report Forms (CRFs):
Current Downloads:
- Adverse Event and Series Adverse Event NCI CRF Standards created on August 15th, 2012
- Concomitant Medication NCI CRF Standards created on May 1st, 2013
- Consent NCI CRF Standards created on October 4th, 2013
- Demography NCI CRF Standards created on March 22nd, 2013
- Diagnosis Administrative NCI CRF Standards created on October 4th, 2013
- Diagnosis Intervention NCI CRF Standards created on October 4th, 2013
- Eligibility NCI CRF Standards created on October 4th, 2013
- End of Form NCI CRF Standards created on June 29th, 2012
- Enrollment NCI CRF Standards created on August 3rd, 2012
- Equipment NCI CRF Standards created on October 18th, 2013
- Footer NCI CRF Standards created on August 3rd, 2012
- Header NCI CRF Standards created on June 29th, 2012
- Image Quality NCI CRF Standards created on October 4th, 2013
- Laboratory Test Results NCI CRF Standards created on October 4th, 2013
- Medical History NCI CRF Standards created on June 29th, 2012
- Off Study NCI CRF Standards created on October 4th, 2013
- Off Treatment NCI CRF Standards created on October 4th, 2013
- Outcome Measures NCI CRF Standards created on January 28th, 2013
- Participant Identification NCI CRF Standards created on August 24th, 2012
- PET Emissions Scan NCI CRF Standards created on August 29th, 2012
- PET Equipment QC Assessment NCI CRF Standards created on October 4th, 2013
- PET Imaging Agent NCI CRF Standards created on August 29th, 2012
- PET Patient Prep NCI CRF Standards created on October 4th, 2013
- Physical Examination NCI CRF Standards created on August 3rd, 2012
- Prior Post (Other) Therapies NCI CRF Standard created on July 1st, 2013
- Protocol Deviations NCI CRF Standards created on August 15th, 2012
- Radiation NCI CRF Standards created on October 4th, 2013
- Registration NCI CRF Standards created on June 29th, 2012
- Screening NCI CRF Standards created on October 4th, 2013
- Staging/Extent of Disease NCI CRF Standards created on March 22nd, 2013
- Staging/Extent of Disease NCI CRF Standards created on June 29th, 2012
- Staging/Extent of Disease NCI CRF Standards created on June 29th, 2012
- Staging/Extent of Disease NCI CRF Standards created on August 15th, 2012
- Study Agent Administration NCI CRF Standards created on October 4th, 2013
- Study Agent Administration NCI CRF Standards in Excel
- Surgery NCI CRF Standards created on October 4th, 2013
- Vital Signs NCI CRF Standards created on October 4th, 2013
Project related CDEs
- TCGA Phase II Data Elements - as of Oct. 19, 2011
- North American Central Cancer Registries (NAACCR) meta data elements (CDEs)
- Surveillance, Epidemiology and End Results (SEER) meta data elements (CDEs) - as of Dec 23, 2010
- BRIDG metadata elements (CDEs) - as of Feb 03, 2011
- National Biomedical Imaging Archive (NBIA)(formerly NCIA)- as of Feb 09, 2011
- Health Information National Trends Survey (HINTS2005)- as of April 04, 2012
- eMerge Project - as of April 09, 2012
For other formats and prior versions of the files see the attachments listed at the end of this page.
If importing caDSR content into another ISO/IEC 11179 registry, i.e. local implementation of cgMDR, please add the caDSR Registration Authority Identifier (RAI) 2.16.840.1.113883.3.26.2 to the metadata to keep the caDSR content distinct from the local repository. Per ISO/IEC 11179, the RAI is part of a globally unique identifier known as the IRID (Item Registry Identifier), and uniquely identifies registry content as being related to particular registrars. The IRID for all caDSR content is the <caDSR OID + Item public Id + item version>. For example, if the caDSR item public id = 2181292, version = 1.1, when importing you would add the RAI, and the result would be an IRID = 2.16.840.1.113883.3.26.2 + 2181292 + 1.1.
Coming soon! A link to cancerGrid UK cgMDR PTCRi (Particle Therapy Cancer Research) instance of cgMDR where you can download metadata elements in caDSR XML format, the native cgMDR format for importing into your own cgMDR instance, as well as an XML Schema annotated with W3C SAWSDL annotation tags.
The following lists the attachments to this page.
