Overview
This study evaluate the efficacy of Tafasitamab and Lenalinomide associated to Rituximab in elderly patients with frontline Diffuse Large B-Cell Lymphoma as assessed by the Overall Response Rate (ORR) after 3 cycles of treatment according to Lugano Response Criteria.
Description
This study is an open-label, multi-centric, phase II study designed to evaluate the efficacy of Tafasitamab and Lenalinomide associated to Rituximab in elderly patients with frontline Diffuse Large B-Cell Lymphoma as assessed by the Overall Response Rate (ORR) after 3 cycles of treatment according to Lugano Response Criteria.
After a screening phase, eligible patients will be enrolled and start the prephase treatment with vincristine and prednisone before day 1 of cycle 1 of the experimental drugs.
Patients with Progressive Disease or Stable Disease after 3 cycles should start a conventional chemotherapy (R-miniCHOP) at Investigator's discretion and will remain in the study.
Eligibility
Inclusion Criteria:
2.Patient with histologically proven CD20+ diffuse large B-cell lymphoma (DLBCL) (WHO
classification 2017) including all clinical subtypes (primary mediastinal, intravascular,
etc…), with all International Prognostic Index (IPI). May also be enrolled the following
malignancies:
- De Novo transformed DLBCL from low grade lymphoma (Follicular, other...) and DLBCL
associated with some small cell infiltration in bone marrow or lymph node.
- High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements
- High-grade B-cell lymphoma, Not Otherwise Specified (NOS)
- Follicular lymphoma grade 3B 3.Positron-Emission Tomography (PET)-positive disease
4.Previously untreated high-grade B-cell lymphoma 5.Aged ≥ 80 years old at the time of
signing the informed consent form (ICF) 6.Ann Arbor stage I, II, III or IV 7.Eastern
Cooperative Oncology Group (ECO)G performance status ≤ 2 8.With a minimum life
expectancy of 3 months 9.Male patients must practice complete abstinence or agree to
use a condom during sexual contact with a pregnant female or a female of childbearing
potential while participating in the study, during dose interruptions, and for 4
months following study drug discontinuation, even if they have undergone a successful
vasectomy 10. Patients should be able to receive R-miniCHOP regimen (left ventricular
ejection fraction > 50% and good general condition, according to investigator's
judgment) 11. Patients should be able to receive adequate prophylaxis and/or therapy
for thromboembolic events (aspirin or low molecular weight heparin) 12. Patient
covered by any social security system (France)
Exclusion Criteria:
1. Any other histological type of lymphoma, Burkitt included
2. Any history of treated or non-treated Small-B cell lymphoma prior Aggressive B Cell
lymphoma diagnosis
3. Central nervous system or meningeal involvement by lymphoma
4. Any serious active disease (according to the investigator's decision)
5. Poor renal function (calculated Cockcroft-Gault creatinine clearance < 30 ml/min)
6. Poor hepatic function (total bilirubin level >30 μmol/l, transaminases >2.5 upper
normal limits) unless these abnormalities are related to lymphoma
7. Poor bone marrow reserve as defined by neutrophils <1.5 G/l or platelets <100 G/l,
unless related to bone marrow infiltration by lymphoma cells (Bone Marrow Aspiration
will be mandatory in case of severe cytopenias prior inclusion)
8. Any history of cancer during the last 5 years with the exception of non-melanoma skin
tumors or stage 0 (in situ) cervical carcinoma. Patients previously diagnosed with
prostate cancer are eligible if (1) their disease was T1-T2a, N0, M0, with a Gleason
score ≤7, and a prostate specific antigen (PSA) ≤10 ng/mL prior to initial therapy,
(2) they had definitive curative therapy (i.e., prostatectomy or radiotherapy) 2 years
before Day 1 of Cycle 1, and (3) at a minimum 2 years following therapy they had no
clinical evidence of prostate cancer, and their PSA was undetectable if they underwent
prostatectomy or <1 ng/mL if they did not undergo prostatectomy
9. Treatment with any investigational drug within 30 days prior to prephase treatment and
during the study
10. Known HIV, active Hepatitis C Virus (HCV) infection or positive Hepatitis B Virus
(HBV) test within 4 weeks before enrollment (except after hepatitis B vaccination or
for patients who are HBs Ag negative, anti-HBs positive and/or anti-HBc positive but
viral DNA negative)
11. Prior treatment with anti-CD20/anti-CD19 monoclonal antibody or alemtuzumab within 3
months prior to prephase treatment
12. Prior ≥ Grade 3 allergic reaction/hypersensitivity to thalidomide
13. Contra-indication to highly dosed glucocorticoid (60 mg/m2/d)
14. Neuropathy ≥ Grade 2 or painful
15. Patient deprived of his/her liberty by a judicial or administrative decision
16. Adult patient under legal protection