Onconova Implementation Guide
0.2.0 - ci-build
Onconova Implementation Guide - Local Development build (v0.2.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
Extensions The following extensions have been defined for this implementation guide:
The grade of the adverse event as defined by the Common Terminology Criteria for Adverse Events (CTCAE).
Details about an action taken to mitigate or manage the adverse event.
The date when the adverse event was resolved (if applicable).
The approximate age of the patient at the time of diagnosis of the disease.
The approximate age of the patient.
The cause of death for the patient.
The center or hospital where the patient case original records were recorded.
The status of whether the patient has given or revoked consent for research use.
The percentage of data elements categories that have been completed for a patient.
The individuals or organizations that contributed to the patient's case data collection.
Indicates the last known record date of a patient.
The duration of time from either the date of diagnosis or the start of treatment for a disease, such as cancer, that patients diagnosed with the disease are still alive. In a clinical trial, measuring the overall survival is one way to see how well a new treatment works.
The status of whether the patient is alive or deceased or unknown.
The actual measured Breslow depth as a quantity
The morphology of a historical cancer associated to a family member of a patient, represented by an ICD-O-3 code.
The topography of a historical cancer associated to a family member of a patient, represented by an ICD-O-3 code.
Whether the condition contributed to the patient's family member's death
Date at which the genomic variant was assessed and/or reported.
The histological differentiation of the tumor.
The categorical classification of the HRD status interpreted from its value.
Indicates the role of this medication administration in the context of the overall treatment plan.
Indicates which medication administrations were given in combination with the current medication administration.
Indicates the total number of cycles for this medication administration.
Indicates whether this medication administration is the primary therapy within a therapy line.
A characterization of the tumor board review focused on cancer of unknown primary (CUP) origin.
A comparison of molecular findings discussed during the molecular tumor board review.
A therapeutic recommendation or follow-up action resulting from a molecular tumor board review.
Indicates that the condition is a recurrence of a previous condition, and provides a reference to that previous condition.
Indicates the type of recurrence for the condition (local or regional).
The numerical score of the risk assessment.
The intent of the therapy line, such as curative or palliative.
The number representing the sequence of the therapy line in the overall treatment regimen.
The date when disease progression was observed during or after the therapy line.
The progression-free survival duration for the therapy line.
A reference to the therapy line associated with this treatment.
Indicates that whether the RECIST was interpreted from a radiology report rather than extracted.
The specialization or focus area of the tumor board conducting the review, such as hematologic malignancies or solid tumors.
The specific analyte or substance being measured as a tumor marker, such as PSA, CA-125, or CEA.
The categorical classification of the TMB status interpreted from its value.