Informace o publikaci

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

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VODICKA Prokop JANÍKOVÁ Andrea BELADA David HANACKOVA Veronika MOCIKOVA Heidi DURAS Juraj STEINEROVA Katerina BENESOVA Katerina KONIROVA Eva PROCHAZKA Tomas POLGAROVA Kamila MASAR Michal DLOUHA Jitka BLAHOVCOVA Petra TRNENY Marek

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj Hematological Oncology
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://onlinelibrary.wiley.com/doi/10.1002/hon.70142
Doi https://doi.org/10.1002/hon.70142
Klíčová slova autologous stem cell transplantation; IELSG32 trial; MATRix regimen; primary central nervous system lymphoma; real-world results
Popis 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.

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