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Clinical and Prognostic Value of Sarcopenia in Patients Older Than 70 Years With Diffuse Large B-cell Lymphoma

Multicentric Prospective Study to Assess the Clinical and Prognostic Value of Sarcopenia in Patients Older Than 70 Years With Diffuse Large B-cell Lymphoma

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01715961
Acronym
SARCOPENIE
Enrollment
98
Registered
2012-10-29
Start date
2012-01-31
Completion date
2016-08-31
Last updated
2016-10-05

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

Conditions

Diffuse Large B Cell Lymphoma, Grade IIIB Follicular Lymphoma

Keywords

70 years old, DLBCL, Rituximab-CHOP, Sarcopenia

Brief summary

This clinical trial is a multicentric prospective study to assess the clinical and prognostic value of sarcopenia in patients older than 70 years with diffuse large B-cell lymphoma.

Detailed description

Sarcopenia status is assessed by CT scan imaging on the overall survival at 18 months in patients older than 70 years with diffuse large B-cell lymphoma treated by R-CHOP.

Interventions

To attest the muscular strength: hand grip test, balance test, up and go test

Sponsors

Centre Henri Becquerel
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients \>= 70 years * DLBCL, grade IIIB follicular lymphoma or histologically proven transformed low grade lymphoma * Whatever the IPI score and the performance status * Treated by Rituximab-CHOP or Rituximab-mini-CHOP * CT scan imaging performed one month or less before inclusion * Signed informed consent

Exclusion criteria

* No initial CT scan imaging performed more than one month before inclusion * Positivity for HCV, HBV and HIV * Anthracycline contra-indication

Design outcomes

Primary

MeasureTime frame
progression free survivalat 18 months

Secondary

MeasureTime frameDescription
progression free survivalat 24 months
rate of over grade 2 toxicitiesat the first and second courses of chemotherapy (day 21 and day 42)
determination of both molecular subtypes GCB and ABCat 24 monthsaccording DASL technology (c-DNA mediated annealing selection extension and ligation)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026