oncological and hematological diseases C00-D48
Conditions
Interventions
Group 1: Data from patients with oncological or hematological disease are recorded in a questionnaire structured by history, the course of therapy and final survey . Follow-up data will be documented
Sponsors
rgb Onkologisches Management GmbH
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Patient with confirmed oncological / hematological diagnosis - At least one oncological treatment - Beginning of documented therapy must not be longer than 10 months. - Declaration of consent
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective is the acquisition and representation of real-life treatment in the outpatient sector. Recorded variables are defined in the common single oncological basic data set of ADT /GEKID. Additionally, data of therapy regime and its change over time is collected. The entire therapy course of a Patient will be collected from diagnosis until death or for a five year period in adjuvant therapies each patient history including all therapies of a patient. The following epidemiological surveys should be specified ubiquitously: - Relative survival of cancer patients in Germany - Penetration guideline-based therapies in oncology outpatient practice - Definition of reference- or metadata Furthermore, the possibility of defining reference intervals for measures (quality indicators) that could be used as the basis for quality management systems should be analyzed. | — |
Secondary
| Measure | Time frame |
|---|---|
| not relevant | — |
Countries
Germany
Contacts
Public ContactMarkus Kersting
rgb Onkologisches Management GmbH
Outcome results
None listed