Most patients being diagnosed with primary diffuse large B-cell lymphoma of the central nervous system (PCNSL) are 60 years or older. Elderly patients with PCNSL have a poor prognosis and there is a great medical need to improve outcome for this vulnerable population. In Germany and many international centres, there are currently two widely used strategies to treat elderly PCNSL patients who are eligible for high-dose methotrexate (HD-MTX) treatment, which have not yet been compared head-to-head. The R-MP regimen has been established by the Cooperative PCNSL Study Group as a "conventional" immunochemotherapy standard treatment for elderly patients with newly diagnosed disease and consists of Rituximab, HD-MTX and Procarbazine followed by maintenance therapy with Procarbazine. In contrast, another recently established protocol also includes HD-MTX-based induction therapy, but followed by consolidating high-dose chemotherapy and autologous stem cell transplantation (HCT-ASCT). This is an overall more intensive, but substantially shorter treatment approach, feasible for elderly patients being considered eligible for a more intensive treatment. The PRIMA-CNS trial aims to compare these two treatment approaches with respect to survival, response rates and toxicity.
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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
340
Firstline systemic treatment with conventinal immunochemotherapy (3 cycles of Rituximab-MTX-Procarbazine) followed by Procarbazine maintenance
Firstline systemic treatment with age-adjusted MTX based induction (2 cycles of Rituximab-Methotrexate-Cytarabin) followed by consolidating aged-adapted high-dose chemotherapy and autologous stem cell transplantation
University Hospital Freiburg, Department Medicine I, Hematology, oncology and stem cell transplantation
Freiburg im Breisgau, Baden-Wurttemberg, Germany
RECRUITINGKlinikum Stuttgart, Clinic of Hematology, Oncology and Palliative Care, Stuttgart Cancer Center / Tumor Center Eva Mayr-Stihl
Stuttgart, Baden-Wurttemberg, Germany
RECRUITINGUniversity Hospital Aachen
Aachen, Germany
RECRUITINGUniversity Hospital Augsburg
Augsburg, Germany
Progression free survival (PFS) between the 2 arms
PFS is defined as the time from randomization to disease progression or death of any cause, with censoring at the last date the patient was seen alive and free of disease progression
Time frame: up to 6 years
Overall survival (OS) between the 2 arms
OS is defined as time from randomization until death from any cause, with censoring at the last date the patient was seen alive
Time frame: up to 6 years
Event free survival (EFS) between the 2 arms
EFS, defined as time from randomization to premature end of treatment (EOT) due to any reason, lymphoma progression or death, whichever occurs first, with censoring at the last date the patient was seen event-free
Time frame: up to 6 years
Remission status after 2 cycles of rituximab-methotrexate-procarbazine (R-MP) (arm A)/2 cycles of R-MTX/cytarabine (AraC)
Remission status after 2 cycles of RMP (arm A) / 2 cycles of R-MTX/AraC will be determined at response assessment (RA) I in both arms and will be divided in complete remission (CR), unconfirmed complete remission (CRu), partial remission (PR), stable disease (SD), progressive disease(PD) according to international PCNSL collaborative group (IPCG) criteria
Time frame: at RA I: after 8 weeks (Arm A), after 6 weeks (Arm B)
Remission status after 3 cycles of R-MP (arm A)/consolidating HCT-ASCT (arm B)
determined at response assessment (RA) II and will be divided in CR, CRu, PR, SD, PD according to IPCG criteria
Time frame: at RA II: after 12 weeks
Remission status after completion of maintenance treatment (arm A)/6 months follow-up (arm B)
will be determined 6 months after RA II and will be divided in CR, CRu, PR, SD, PD according to IPCG criteria
Time frame: 6 months after RA II
Quality of life (EORTC QLQ-C30)
EORTC quality of life questionnaire (QLQ)-C30 performed at screening, at RA II /premature EOT and thereafter every 12 months during follow-up
Time frame: from date of informed consent form (ICF) signature up to 6 years
Quality of Life (EORTC-QLQ BN 20)
EORTC-QLQ brain neoplasm (BN) 20, performed at screening, at RA II /premature EOT and thereafter every 12 months during follow-up
Time frame: from date of informed consent form (ICF) signature up to 6 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Helios Klinikum Berlin-Buch
Berlin, Germany
NOT_YET_RECRUITINGUniversity Hospital Berlin
Berlin, Germany
RECRUITINGEvangelisches Klinikum Bethel
Bielefeld, Germany
NOT_YET_RECRUITINGUniversitätsklinikum Knappschaftskrankenhaus Bochum GmbH
Bochum, Germany
RECRUITINGStädtisches Klinikum Braunschweig gGmbH
Braunschweig, Germany
RECRUITINGKlinikum Bremen-Mitte gGmbH
Bremen, Germany
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