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Dose Dense Chemotherapy in Elderly Patients > 80 Years Old With DLBCL

Dose Dense Chemotherapy in Elderly Patients > 80 Years Old With DLBCL

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06150053
Enrollment
79
Registered
2023-11-29
Start date
2018-07-01
Completion date
2023-11-01
Last updated
2023-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

DLBCL, Old Age; Debility

Brief 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.

Interventions

None listed

Sponsors

University Hospital, Saarland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
80 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* histologically proven, untreated diffus large B-cell lymphoma (DLBCL) * diagnosis between 2005 - 2019 * age ≥80 at diagnosis

Exclusion criteria

\- diagnosis revision at a later timepoint

Design outcomes

Primary

MeasureTime frameDescription
Overall survival (OS) death or progression/relapse, progression/relapse or treatment discontinuation.through study completion, an average of 2 yearstime from diagnosis to death
Progression-free survival (PFS)through study completion, an average of 2 yearstime from diagnosis to death or progression/relapse
Event-free survival (EFS)through study completion, an average of 2 yearsdefined as time from diagnosis to death or progression/relapse or treatment discontinuation.

Secondary

MeasureTime frameDescription
Relative Dose intensitywithin the treatment period, up to 36 weeksPercentage of the dose intensity achieved divided by the intended dose intensity

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026