# Long‐Term Real‐World Outcomes of Primary CNS Lymphoma Patients Treated With MATRix Regimen Are Similar to IELSG32 Trial Results

## TL;DR

This study shows that treating primary CNS lymphoma with the MATRix regimen and stem cell transplant in real-world settings has outcomes similar to a clinical trial.

## Contribution

The study provides long-term real-world evidence supporting the effectiveness of the MATRix regimen and auto-SCT in PCNSL patients.

## Key findings

- 4-year progression-free survival and overall survival rates were 53% and 55% after MATRix treatment.
- Treatment-related mortality was 8%, with no significant survival difference between WBRT and auto-SCT consolidation.
- Outcomes in real-world settings were comparable to the IELSG32 trial results.

## Abstract

Primary central nervous system lymphomas (PCNSL) are rare malignancies with poor survival outcomes. The IELSG32 trial demonstrated efficacy of MATRix chemoimmunotherapy followed by autologous stem cell transplantation (auto‐SCT) in PCNSL patients aged ≤ 70 years with a performance status (PS) ECOG ≤ 3. However, long‐term real‐world results of MATRix/auto‐SCT therapy remain limited. This analysis, with a median follow‐up of 52 months, aimed to evaluate the outcomes of MATRix‐treated PCNSL patients in clinical practice. From 2015 to 2022, 280 PCNSL patients who received systemic therapy were identified in the NiHiL project (NCT03199066). Eighty‐eight individuals treated with MATRix entered the analysis. Endpoints included efficacy and safety of induction and consolidation therapy. Seventy‐eight patients who met key IELSG32 inclusion criteria (age ≤ 65 years and PS ECOG ≤ 3, or age 66–70 years and PS ECOG ≤ 2) achieved an overall response rate of 82% (complete remission rate 58%) following MATRix regimen. After median follow‐up of 52 months, 4‐year progression‐free survival and overall survival (OS) rates were 53% and 55%, respectively. Forty‐six (59%) patients completed MATRix treatment, and 32 (41%) discontinued induction therapy (15 toxicity, 11 infections, 5 progressive diseases, 1 refusal). The treatment‐related mortality was 8%. Among 67 patients with responsive/stable disease, 50 underwent consolidation with whole‐brain radiotherapy (WBRT, n = 13) or auto‐SCT (n = 37). No significant survival differences were observed between WBRT and auto‐SCT (4‐year OS 84% vs. 74%, HR 0.61, 95% CI 0.16–2.29, p = 0.467). Long‐term real‐world outcomes of MATRix/auto‐SCT therapy are comparable to IELSG32, supporting its use in younger, fit PCNSL patients.

The data in this analysis were collected in the observational Czech non‐Hodgkin lymphoma registry “NiHiL” (NCT03199066)