Adjusted High-dose Chemotherapy With Autologous Stem Cell Transplant vs. Conventional Immunochemotherapy in Elderly PCNSL Patients

Primary diffuse large B-cell lymphoma of the central nervous system (PCNSL) is a rare lymphoma affecting only the central nervous system compartment. PCNSL patients are typically 60 years or older and have poor prognoses. However, there are alternative treatment approaches to consider with the potential to improve medical outcomes for this patient population. The current standard of care in Germany and many international centres for patients 65 and older is treatment with R-MP, comprising rituximab, high-dose methotrexate (HD-MTX) and procarbazine followed by maintenance therapy with procarbazine. An alternative approach comprised of a shorter induction treatment with rituximab, HD-MTX and cytarabine (MARTA) followed by age-adjusted high-dose chemotherapy and autologous stem cell transplantation (HCT-ASCT) was recently shown to be feasible and effective in elderly PCNSL patients considered eligible for high-dose chemotherapy requiring autologous stem cell transplantation. Nevertheless, data evaluating this short duration treatment approach remains scarce, and randomized trials have not yet been published. The objective of the PRIMA-CNS trial is to demonstrate that intensified chemotherapy followed by consolidating HCT-ASCT is superior to conventional chemotherapy with R-MP followed by maintenance with procarbazine in elderly patients with newly diagnosed PCNSL; not only regarding survival and remission after treatment but also regarding standards like quality of life (QOL) and treatment related morbidities. Results of this randomized trial will either change the standard of care to an intense and shorter treatment approach or re-define R-MP as a proven treatment standard. In addition, a geriatric assessement is implemented in this trial with the goal to better define transplant eligibility. If this trial shows the superiority of HCT-ASCT, the investigators will establish an improved treatment standard with increased chances for long-term remission and cure and reduced frequency and length of chemotherapy treatment. Considering the poor prognosis of this patient population, this randomized phase III trial is of great clinical importance to provide patients, the patients' families and care takers with optimal treatment.

Inclusion criteria

• Immunocompetent patients with newly-diagnosed primary DLBCL of the central nervous system.
• Age > 70 years or age 65-70 years if not eligible for more intensive treatment (e.g. OptiMATe trial).
• Histologically or cytologically assessed diagnosis of B-cell lymphoma by local pathologist.
• Diagnostic sample obtained by stereotactic or surgical biopsy, cerebrospinal fluid (CSF) cytology examination or vitrectomy.
• Disease exclusively located in the CNS.
• At least 1 measurable lesion.
• Eastern Cooperative Oncology Group (ECOG)-Performance Status (PS) ≤ 2. ECOG PS > 2 accepted if due to PCNSL symptoms.
• Patients possibly eligible for HCT-ASCT as judged by the treating physician.
• Written informed consent obtained according to international guidelines and local laws by patient or authorized legal representative in case patient is temporarily legally not competent due to his or her disease.

Additional randomization criteria:

• Patients eligible for HCT-ASCT defined by the EBL score (at most one of the 3 following conditions may apply: ECOG PS > 1, Barthel Index of activities of daily living (ADL) < 20 and Lachs geriatric screening > 3), improvement of PS after pre-phase treatment or clinical judgement by the treating physician after discussion with the study expert team.
• No evidence of disease progression after pre-phase treatment.

Exclusion criteria

• Congenital or acquired immunodeficiency including HIV infection and previous organ transplantation.
• Systemic lymphoma manifestation (outside the CNS).
• Primary vitreoretinal lymphoma or primary leptomeningeal lymphoma without manifestation in the brain parenchyma or spinal cord.
• Previous or concurrent malignancies with the exception of surgically cured carcinoma in situ or other kinds of cancer without evidence of disease for at least 5 years.
• Previous systemic Non-Hodgkin lymphoma at any time.
• Inadequate renal function (creatinine clearance <60 ml/min).
• Inadequate bone marrow, cardiac, pulmonary or hepatic function according to investigator´s decision.
• Active hepatitis B or C disease.
• Concurrent treatment with other experimental drugs or participation in an interventional clinical trial with administration of study medication within the last thirty days before the start of this study.
• Third space fluid accumulation >500 ml.
• Hypersensitivity to study treatment or any component of the formulation.
• Taking any medications likely to cause interactions with the study medication.
• Known or persistent abuse of medication, drugs or alcohol.
• Active COVID-19-infection or non-compliance with the prevailing hygiene measures regarding the COVID-19 pandemic.
• Patients without legal capacity and who are unable to understand the nature, significance and consequences of the study and without designated legal representative.
• Previous participation in this trial.
• Persons who are in a relationship of dependency/employment to the sponsor and/ or investigator.
• Any familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule.
• Fertile patients refusing to use safe contraceptive methods during the study.