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

NCT ID: NCT06150053

Last Updated: 2023-11-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

79 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-07-01

Study Completion Date

2023-11-01

Brief Summary

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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.

Detailed Description

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Conditions

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DLBCL Old Age; Debility

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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R-CHOP-14

No interventions assigned to this group

R-mini-CHOP

No interventions assigned to this group

Eligibility Criteria

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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
Minimum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Saarland

OTHER

Sponsor Role lead

Responsible Party

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Konstantinos Christofyllakis

Consultant

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Saarland University Medical Center

Homburg, Saarland, Germany

Site Status

Countries

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Germany

Other Identifiers

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DOME-80

Identifier Type: -

Identifier Source: org_study_id