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documentation:oncology:meeting_notes_2019_jun-25 [2019/06/26 10:45]
mgurley
documentation:oncology:meeting_notes_2019_jun-25 [2019/06/27 14:10] (current)
mgurley
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 **Topics** **Topics**
  
-    * Rimma Belenkaya went over the ETL instructions for ETLing oncology diagnosis ​modifier ​from NAACCR formatted tumor registry date into the OMOP Oncology CDM extension. ​ See draft document here: https://​github.com/​OHDSI/​OncologyWG/​blob/​master/​documentation/​NAACCR.Ingestion.into.OMOP.Vocabulary.-.Diagnostic.Modifiers.docx+    * Rimma Belenkaya went over the ETL instructions for ETLing oncology diagnosis ​modifiers ​from NAACCR formatted tumor registry date into the OMOP Oncology CDM extension. ​ See draft document here: https://​github.com/​OHDSI/​OncologyWG/​blob/​master/​documentation/​NAACCR.Ingestion.into.OMOP.Vocabulary.-.Diagnostic.Modifiers.docx
     * Maxim Moinat raised the issue of whether he should map European tumor registry data to NAACCR or go directly to SNOMED and/or LOINC.     * Maxim Moinat raised the issue of whether he should map European tumor registry data to NAACCR or go directly to SNOMED and/or LOINC.
     * It was argued that even though it is less than ideal to map to NAACCR, this is the current right choice. We need to conventionalize our representation of oncology diagnosis modifier structure and semantics to make analyses comparable across institutions.     * It was argued that even though it is less than ideal to map to NAACCR, this is the current right choice. We need to conventionalize our representation of oncology diagnosis modifier structure and semantics to make analyses comparable across institutions.
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     * The group was asked for volunteers to write SQL to derive Hemonc.org oncology drug regimens from low-level DRUG_EXPOSURE and EPISODE oncology diagnosis entries. ​ Michael Gurley pointed to the following paper as a starting point: https://​ascopubs.org/​doi/​pdf/​10.1200/​CCI.17.00002     * The group was asked for volunteers to write SQL to derive Hemonc.org oncology drug regimens from low-level DRUG_EXPOSURE and EPISODE oncology diagnosis entries. ​ Michael Gurley pointed to the following paper as a starting point: https://​ascopubs.org/​doi/​pdf/​10.1200/​CCI.17.00002
     * Dmytry Dymshyts expressed doubt about the possibility of derivation of oncology drug regimens from discrete DRUG_EXPOSURE data and EPISODE oncology diagnosis entries.     * Dmytry Dymshyts expressed doubt about the possibility of derivation of oncology drug regimens from discrete DRUG_EXPOSURE data and EPISODE oncology diagnosis entries.
-    * The group agreed that validation of derivation will need to be compered ​to gold standard manually chart abstracted oncology drug regimens. ​ Possibly from clinical trials or registry patients.+    * The group agreed that validation of derivation will need to be compared ​to gold standard manually chart abstracted oncology drug regimens. ​ Possibly from clinical trials or registry patients.
     * Michael Gurley pointed out that some institutions'​ source systems will have pre-derived oncology drug regimens within their oncology drug regimen order template systems. ​ These folks are the "lucky ones".     * Michael Gurley pointed out that some institutions'​ source systems will have pre-derived oncology drug regimens within their oncology drug regimen order template systems. ​ These folks are the "lucky ones".
     * Michael Gurley mentioned that Jeremy Warner (one of the principal architects of Hemonc.org) ​ thinks that the use of NLP against oncologist progress notes will be necessary to derive oncology drug regimens.     * Michael Gurley mentioned that Jeremy Warner (one of the principal architects of Hemonc.org) ​ thinks that the use of NLP against oncologist progress notes will be necessary to derive oncology drug regimens.
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