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Assessment of Survival and Autonomy With Rituximab Plus Chemotherapy or Rituximab Plus Lenalidomide for Elderly Patients With Relapsed Diffuse Large B-cell Lymphoma

Assessment of Survival and Autonomy With Rituximab Plus Chemotherapy or Rituximab Plus Lenalidomide for Elderly Patients With Relapsed Diffuse Large B-cell Lymphoma

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04113226
Acronym
Relyage
Enrollment
1
Registered
2019-10-02
Start date
2021-11-09
Completion date
2024-06-04
Last updated
2026-06-12

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

Conditions

Chemotherapy, Diffuse Large B-Cell Lymphoma (DLBCL), Nos, Elderly

Keywords

chemotherapy, Diffuse large B cell lymphoma (DLBCL), Relapse, activities of patients daily living, Elderly, Lenalidomide

Brief summary

Diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma. Annual incidence increases with age and achieves more than 30 per 100 000 patients 65 years old or over. Despite high response rates with conventional regimen as R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, Vincristine and Prednisone), 30% to 40% of patients develop a relapse or a refractory disease, with a poor prognosis. There is no standard chemotherapy in second line for elderly patients, which are not eligible to receive a salvage treatment by high-dose therapy followed by autologous stem cell transplantation. The median progression-free-survival (PFS) is less than one year with the most commonly used regimens including R-Gemcitabine-Oxaliplatin (R-GEMOX) and R-Bendamustine. One the other side, Rituximab plus Lenalidomide, an immunomodulatory agent, is an active new therapeutic approach, with an efficacy proved in a phase II trial with a patients with a prolonged disease-free-survival of 32 months for responders in patients with a median age of 74 years old. This combination is also efficient in the ABC phenotype DLBCL which is more common in elderly patients. For elderly patients, a management of the geriatric impairment together with lymphoma is required. Indeed, a comprehensive geriatric assessment detects frailty and vulnerability in elderly with a lymphoma and predicts severe treatment related toxicity, treatment settings and progression free survival. Moreover, geriatric intervention improved outcome, autonomy and quality of life. Functional status, assessed by Activities of patients Daily Living (ADL) is an independent predictive factor for feasibility of chemotherapy in elderly patients with cancer. The mini Data Set of DIALOG group is a new simplified geriatric assessment for oncologist.

Interventions

DRUGRituximab

patients ≥ 75 years old with relapsed Diffuse large B-cell lymphoma will be treated with classical Rituximab-based chemotherapy or Rituximab plus Lenalidomide.

patients ≥ 75 years old with relapsed Diffuse large B-cell lymphoma will be treated with Rituximab plus Lenalidomide. Four 28-days cycles of oral Lenalidomide (20 mg / d for 21 days) and Rituximab 375mg/m2 on day 1 and day 21. After this induction phase, patients achieving at least stable disease were given lenalidomide maintenance therapy (20 mg for 21 days) until progression

A comprehensive geriatric assessment (CGA) is recommended by the Société Internationale d'Onco Gériatrie (SIOG) in order to assess all geriatric facets (comorbidity, functional impairment, nutritional status, mental and psychological status, environment,…) on which treatment may impact.

OTHERActivities of daily living (ADL) scale

Activities of daily living (ADL) comprise the basic actions that involve caring for one's self and body, including personal care, mobility, and eating. The Index ranks adequacy of performance in the six functions of bathing, dressing, toileting, transferring, continence, and feeding. Clients are scored yes/no for independence in each of the six functions. A score of 6 indicates full function, 4 indicates moderate impairment, and 2 or less indicates severe functional impairment.

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER
cimiez hospital Nice
CollaboratorUNKNOWN
Institut Bergonié
CollaboratorOTHER
groupe hospitalier public sud de l'oise
CollaboratorUNKNOWN
Henri Mondor University Hospital
CollaboratorOTHER
Centre Henri Becquerel
CollaboratorOTHER
Hôpital Charles Foix
CollaboratorOTHER
Saint-Louis Hospital, Paris, France
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Age ≥ 75 years old * Histologically proven CD20+ diffuse large B-cell lymphoma (DLBCL) (WHO classification 2008) including all clinical subtypes (primary mediastinal, intravascular, etc...), with all aaIPI. May also be included : transformed DLBCL from low grade lymphoma (Follicular, other...) and DLBCL associated with some small cell Infiltration in bone marrow or lymph node or CD20+ B-cell lymphoma, with intermediate features between DLBCL and Burkitt or with intermediate features between DLBCL and classical Hodgkin lymphoma or CD20+ Follicular lymphoma grade 3B or CD20+ Aggressive B-cell lymphoma unclassifiable * Relapse ≥ 6 months * ADL ≥ 2 * Negative HIV, HBV (anti-HBc negativity) and HCV serologies test within 4 weeks before inclusion * Patient able to give his consent and having signed a written informed consent * Registration in a national health-care system

Exclusion criteria

* Central nervous system or meningeal involvement by lymphoma * Poor renal function (creatinine clearance \< 30 ml/min, according to MDRD formula) * Poor hepatic function (total bilirubin level\>30mmol/l, transaminases \>2.5 maximum normal level) unless these abnormalities are related to the lymphoma * Neuropathy grade \> 1 * Poor bone marrow reserve as defined by neutrophils\<1.5 G/l or platelets\<100 G/l, unless related to bone marrow infiltration * Other concomitant or previous malignancy, except adequately treated in situ carcinoma of the uterine cervix, basal or squamous cell carcinoma of the skin, or cancer in complete remission for \<5 years * Other serious and uncontrolled non-malignant disease. * Insufficient proficiency of the French language and disability to complete a questionnaire * Patient under guardianship

Design outcomes

Primary

MeasureTime frameDescription
Progression of free survival at 6 months in elderly patients treated with Rituximab plus Lenalidomide or Rituximab plus chemotherapy.at 6 monthsProgression of free survival at 6 months with maintain autonomy without loss of 0.5 point of ADL in elderly patients 75 years old and over with relapsed diffuse large B-cell lymphoma treated with Rituximab plus Lenalidomide or Rituximab plus investigator's choice .

Secondary

MeasureTime frameDescription
Response rate in Rituximab plus Lenalidomide and Rituximab plus chemotherapy groupsat 6 monthsResponse rate in Rituximab plus Lenalidomide and Rituximab plus chemotherapy groups
Overall survival rate in Rituximab plus Lenalidomide and Rituximab plus chemotherapy groupsat 6 monthsResponse rate in Rituximab plus Lenalidomide and Rituximab plus chemotherapy groups

Countries

France

Contacts

PRINCIPAL_INVESTIGATORFrederic Peyrade, MD

Centre Antoine Lacassagne, Nice

PRINCIPAL_INVESTIGATORBoulhassass, MD

Hopital Cimiez NICE

PRINCIPAL_INVESTIGATORSoubeyran, Pr

Institut Bergonié Bordeaux

PRINCIPAL_INVESTIGATORPhilippe Caillet, MD

Hôpital Henri Mondor, APHP CRETEIL

PRINCIPAL_INVESTIGATORFabrice Jardin, MD

Centre Henri Becquerel, ROUEN

PRINCIPAL_INVESTIGATORPascal Chaibi, MD

Hôpital Charles Foix, APHP IVRY/SEINE

PRINCIPAL_INVESTIGATORCatherine Thieblemont, MD

Hôpital Saint-louis, APHP, PARIS

PRINCIPAL_INVESTIGATORDamaj, MD

Centre Hospitalier Universitaire de Caen

PRINCIPAL_INVESTIGATORGaridi, MD

Centre Hospitalier SAINT-QUENTIN

PRINCIPAL_INVESTIGATORLeduc, MD

Centre Hospitalier Abbeville

PRINCIPAL_INVESTIGATORDennetière, MD

Centre Hospitalier COMPIEGNE

PRINCIPAL_INVESTIGATORIvanoff, MD

Hôpital Avicenne, APHP BOBIGNY

PRINCIPAL_INVESTIGATORIsabelle Grulois, MD

CH Saint Malo

PRINCIPAL_INVESTIGATORMargot Robles, MD

CH Périgueux

PRINCIPAL_INVESTIGATORCaroline DELETTE, PhD

CHU Amiens Picardie

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026