Objectives
* The primary objective is to evaluate the benefit estimated by the PFS associated with maintenance chemotherapy compared to observation in patients ≥ 60 years having achieved a complete response after a high-dose MTX based induction chemotherapy
* The secondary objectives are to assess:
* Overall survival
* Safety of maintenance chemotherapy
* Neurocognitive outcome
* Quality of life of the patients
Inclusion and exclusion criteria
At registration
* Inclusion criteria
* Newly diagnosed primary cerebral lymphoma
* Age \>60 years
* Pathology proven diagnosis
* Positive cytology of the CSF or vitreous
* Karnofsky Performance Status \>40
* No evidence of systemic NHL (body CT scan, bone marrow biopsy)
* Adequate haematological, renal and hepatic function
* Calculated creatinine clearance \> 40 ml/min
* Non inclusion criteria
* Positive HIV serology
* Preexisting immunodeficiency (organ transplant recipient)
* Prior treatment for PCNSL
* Isolated primary intra-ocular lymphoma
* Low grade lymphoma
* Any other active primary malignancy
At randomization
* Complete response on MRI after induction chemotherapy according to the IPCG criteria
* Karnofsky Performance Status \>40
* Adequate haematological, renal and hepatic function
Study Design
* This study is an open label multicenter randomized phase III trial comparing maintenance chemotherapy versus observation in complete responders to high dose MTX based induction chemotherapy.
* Patients are registered to participate in the study at time of initial diagnosis and study enrolment before the induction chemotherapy.
* Induction chemotherapy (R-MPVA protocol) includes 4 to 5 monthly cycles of high dose MTX (3.5g/m2, D1 and D15), procarbazine, vincristine, rituximab followed by one cycle of high dose cytarabine consolidation.
* Randomization to observation (arm 1) or maintenance (arm 2) will be carried out only for patients in complete response (CR) after induction chemotherapy Arm 1: Observation Arm 2: Seven monthly R-MT cycles including high dose MTX (3.5g/m2, D1), TMZ, rituximab
Sample size, duration of the study, feasibility
* 295 patients need to be enrolled to randomize 192 patients
* Duration of the study: 6 years (accrual period= 4 years; minimal follow-up = 2 years)
26 participating expert centers from the national LOC network
The trial is supported by the neurooncology ANOCEF and the lymphoma LYSA clinical research groups.
Ancillary study LOCALYSE:
Role of \[18F\]-FDG brain PET in newly diagnosed primary cerebral lymphoma, in immunocompetent patient older than 60 years
Rationale Patients older than 60 years account for half of cases of PCNSL and have a poorer outcome. No prognostic or predictive factors exist for survival after initial remission. \[18F\]FDG-PET (Fluoro Deoxy Glucose) plays a key role in grading and therapy monitoring of systemic diffuse large B-cell type.
LOCALYZE is an ancillary PET/MR clinical study from BLOCAGE 01. The aim is to evaluate the usefulness of \[18F\]FDG-PET to monitor treatment response in PCNSL (Primary Central Nervous System Lymphoma) older than 60 years (n=56), in complement to multiparametric MRI.
Hypothesis We assume that the development of new imaging biomarker extracted from PET imaging and multiparametric MRI, could improve the assessment of treatment response in PCNSL.
Primary aim To evaluate the predictive value of \[18F\]FDG-PET assessment performed at the end-of-treatment (high-dose methotrexate based polychemotherapy), on progression free survival in newly diagnosed PCNSL with age ≥60 years (n=56).
Primary Outcome Measures:
Progression free survival calculated from the date of completion of the end of chemotherapy PET
Study design
Three \[18F\]-FDG PET/MR will be performed in the Department of Nuclear Medicine - Pitié-Salpêtrière Hospital:
* prior to initiation of R-MPVA chemotherapy (Rituximab Methotrexate Procarbazine Vincristine Aracytine ) (PET#1),
* after two chemotherapy cycles (PET#2),
* at the end of the first-line chemotherapy regimens (PET#3).
Inclusion criteria (=Blocage-01) Blocage01 eligibility
Exclusion criteria
* Uncontrolled diabetes with fasting glycaemia \> 200 mg/dL
* Sensitivity to active substance in \[18F\]-FDG
* Calculated creatinine clearance \< 40 ml/min
* No contraindication to MRI
