C00-C97
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients (=18 years) with malignant oncological diseases whose clinical routine data are documented in the CIO Cancer Registry Bonn. All entities of solid tumors and hematological neoplasms are included (ICD-10: C00–C97).
Exclusion criteria
Exclusion criteria: Incomplete or unusable data records; patients without documented follow-up data in the CIO registry; records outside the defined observation period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| WHAT: Overall survival (OS) and progression-free survival (PFS) depending on therapy, biomarkers and clinical parameters – defined per sub-project. WHEN: At the time of retrospective data analysis; observation period from 01/01/1990 to the current data cut. HOW: Analysis of pseudonymized registry data from the CIO Cancer Registry Bonn; Kaplan-Meier analyses, Cox regression. | — |
Secondary
| Measure | Time frame |
|---|---|
| Objective response rates, recurrence-free survival, treatment-related toxicities, time to treatment initiation, biomarker-associated outcomes, healthcare quality indicators; project-specifically supplemented by machine learning-based predictive models (Explainable AI). | — |
Countries
Germany
Contacts
Medizinische Klinik III, Universitätsklinikum Bonn