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High-dose cytarabine plus high-dose methotrexate versus high-dose methotrexate alone in patients with primary CNS lymphoma: a randomised phase 2 trial

  • Andrés JM Ferreri
  • , Michele Reni
  • , Marco Foppoli
  • , Maurizio Martelli
  • , Gerasimus A. Pangalis
  • , Maurizio Frezzato
  • , Maria Giuseppina Cabras
  • , Alberto Fabbri
  • , Gaetano Corazzelli
  • , Fiorella Ilariucci
  • , Giuseppe Rossi
  • , Riccardo Soffietti
  • , Caterina Stelitano
  • , Daniele Vallisa
  • , Francesco Zaja
  • , Lucía Zoppegno
  • , Gian Marco Aondio
  • , Giuseppe Avvisati
  • , Monica Balzarotti
  • , Alba A. Brandes
  • José Fajardo, Henry Gomez, Attilio Guarini, Graziella Pinotti, Luigi Rigacci, Catrina Uhlmann, Piero Picozzi, Paolo Vezzulli, Maurilio Ponzoni, Emanuele Zucca, Federico Caligaris-Cappio, Franco Cavalli
  • IRCCS San Raffaele Scientific Institute
  • La Sapienza University
  • University of Athens
  • San Bortolo Hospital
  • Hospital Businco
  • Azienda Ospedaliera Universitaria Senese
  • IRCCS Pascale
  • Azienda Ospedaliera di Reggio Emilia
  • Brescia Spedali Civili General Hospital
  • San Giovanni Battista Hospital and University
  • Azienda Ospedaliera di Reggio Calabria
  • Ospedale Civile
  • University of Udine
  • HIGA San Martín
  • Azienda Ospedaliera di Gravedona
  • Division of Haematology
  • IRCCS Humanitas Research Hospital
  • AUSL Bologna
  • Hospital Santa Maria
  • Instituto Nacional de Enfermedades Neoplásicas Eduardo Cáceres Graziani
  • Azienda Ospedaliera di Bari
  • University Hospital of Varese
  • Azienda Ospedaliero-Universitaria Careggi
  • Kantonospital
  • Institute of Oncology of Southern Switzerland
  • Vita-Salute University

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

614 Citas (Scopus)

Resumen

Background: Chemotherapy with high-dose methotrexate is the conventional approach to treat primary CNS lymphomas, but superiority of polychemotherapy compared with high-dose methotrexate alone is unproven. We assessed the effect of adding high-dose cytarabine to methotrexate in patients with newly diagnosed primary CNS lymphoma. Methods: This open, randomised, phase 2 trial was undertaken in 24 centres in six countries. 79 patients with non-Hodgkin lymphoma exclusively localised into the CNS, cranial nerves, or eyes, aged 18-75 years, and with Eastern Cooperative Oncology Group performance status of 3 or lower and measurable disease were centrally randomly assigned by computer to receive four courses of either methotrexate 3·5 g/m2 on day 1 (n=40) or methotrexate 3·5 g/m2 on day 1 plus cytarabine 2 g/m2 twice a day on days 2-3 (n=39). Both regimens were administered every 3 weeks and were followed by whole-brain irradiation. The primary endpoint was complete remission rate after chemotherapy. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00210314. Findings: All randomly assigned participants were analysed. After chemotherapy, seven patients given methotrexate and 18 given methotrexate plus cytarabine achieved a complete remission, with a complete remission rate of 18% (95% CI 6-30) and 46% (31-61), respectively, (p=0·006). Nine patients receiving methotrexate and nine receiving methotrexate plus cytarabine achieved a partial response, with an overall response rate of 40% (25-55) and 69% (55-83), respectively, (p=0·009). Grade 3-4 haematological toxicity was more common in the methotrexate plus cytarabine group than in the methotrexate group (36 [92%] vs six [15%]). Four patients died of toxic effects (three vs one). Interpretation: In patients aged 75 years and younger with primary CNS lymphoma, the addition of high-dose cytarabine to high-dose methotrexate provides improved outcome with acceptable toxicity compared with high-dose methotrexate alone. Funding: Swiss Cancer League.

Idioma originalInglés
Páginas (desde-hasta)1512-1520
Número de páginas9
PublicaciónThe Lancet
Volumen374
N.º9700
DOI
EstadoPublicada - 2009
Publicado de forma externa

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Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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