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Clinical Trial Summary

Multi-center retrospective analysis of patients with DLBCL aged ≥80 years old treated with R-CHOP-14 compared to other regimens. Patient data including baseline characteristics, histology, dose intensity and treatment outcomes will be extracted from hospital medical electronic records. Relative dose intensity (RDI) will be calculated as the percentage of the dose intensity achieved divided by the intended dose intensity. Primary endpoints are overall (OS), progression-free (PFS) and event-free survival (EFS), defined as time from diagnosis to death, death or progression/relapse, progression/relapse or treatment discontinuation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06150053
Study type Observational
Source Universität des Saarlandes
Contact
Status Completed
Phase
Start date July 1, 2018
Completion date November 1, 2023

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