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Hematological oncology · 2026

Intensified Rituximab, Methotrexate, Procarbazine, and Cytarabine (R-MPVA) Regimen With Sequential Addition of Etoposide to R-MPV and Ifosfamide to R-AraC for Newly Diagnosed Primary CNS Lymphoma Patients Aged Between 60 and 70 Years: An LOC Network Study.

СтатьяМногоцентровое исследованиеНазвание и аннотация: Перевод в очереди
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Antherieu Gabriel, Julia Edith, Lapierre Léopoldine, Donzel Marie, Houillier Caroline, Soussain Carole, Nicolas-Virelizier Emmanuelle, Rey Philippe, Ducray François, Meyronet David, Picart Thiébaud, Ysebaert Loïc, Hoang Xuan Khê, Obéric Lucie, Ghesquières Hervé

Аннотация

The treatment efficacy, acute toxicity, and neurocognitive sequelae of older patients with primary central nervous system lymphoma (PCNSL) remain therapeutic challenges. The standard first-line therapy consisted of high-dose methotrexate and cytarabine (AraC) and led to a complete response (CR) in half of the patients. To improve the response rate, we proposed intensifying the standard rituximab, methotrexate, procarbazine, vincristine, and cytarabine (R-MPVA) regimen by sequentially adding etoposide (100 mg/m2 D2) to R-MPV (R-MPV-E) and ifosfamide (1.5 g/m2 Days 1-3) to R-AraC (R-AraC-I) for patients aged between 60 and 70 years. The primary objective of this retrospective study was to determine the CR rates after three and two planned cycles of R-MPV-E and R-AraC-I, respectively. Thirty-two consecutive patients received this regimen between 2013 and 2021 in Lyon University Hospitals. After the R-MPV-E and R-AraC-I sequences, 11 (34.4%) and 26 (81.3%) patients achieved CR or unconfirmed CR (CRu), respectively, with favorable safety profiles (19% and 38%, of ≥ Grade 3 hematological toxicity; 19% and 27%, of ≥ Grade 3 infection during the induction and consolidation, respectively). With a median follow-up of 42.4 months, the 3-year event-free survival (EFS) and overall survival (OS) rates were 40.2% and 63.2%, respectively. Historical comparisons with a subset of patients from the LOC network database revealed an improvement in CR rates of 81% after R-MPV-E/R-AraC-I versus 42.9% and 60.5% after MPVA and R-MPVA, respectively, mainly owing to the addition of ifosfamide to the R-AraC sequence. Similar results were observed in an independent retrospective cohort of 20 patients treated at Toulouse University-Hospital, with a 70% CR rate after R-MPV-E/R-AraC-I. In addition, 7/26 (27%) CR/CRu patients in the main cohort could then be referred for autograft consolidation. In conclusion, this study revealed that ifosfamide combined with R-AraC could increase the CR/CRu rate at the end of induction in 60-70-year-old PCNSL patients.

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