TY - JOUR
T1 - Rituximab is associated with improved survival for aggressive B cell CNS lymphoma
AU - Gregory, Gareth
AU - Arumugaswamy, Ashwini
AU - Leung, Teresa
AU - Chan, KahLok
AU - Abikhair, Melody
AU - Tam, Constantine
AU - Bajel, Ashish
AU - Cher, Lawrence
AU - Grigg, Andrew
AU - Ritchie, David
AU - Opat, Stephen
PY - 2013
Y1 - 2013
N2 - BackgroundThe optimal treatment strategy in patients with aggressive B cell central nervous system lymphoma suitable to receive intensive therapy is unknown. The benefit of incorporating rituximab in systemic therapy remains unclear. We performed a retrospective study examining the impact of rituximab in the context of concomitant therapies, including methotrexate, cytarabine, and radiotherapy, in patients treated with curative intent at 4 university teaching hospitals during 1996-2011.MethodsA retrospective study of CNS lymphoma cases treated at the participating institutions was performed in accordance with institutional ethical guidelines. Patients were included if they received a diagnosis of primary diffuse large B cell lymphoma of the CNS, were HIV negative, and were treated with curative intent.ResultsOne hundred twenty patients aged 21-81 years were identified. Rituximab recipients and nonrecipients were similar, except for rituximab recipients being more likely to have received a diagnosis after 2004. The median follow-up of surviving patients was 30 months. The 5-year overall survival was 46 . Univariate analysis revealed age =60 years, ECOG performance status =1, normal lactate dehydrogenase, diagnosis after 2004, and treatment with cytarabine and rituximab as predictive of favorable overall survival. Multivariate analysis identified age to be an independent predictor of overall survival, with a trend toward improved survival from the other variables that were significant in univariate analyses.ConclusionsIn this retrospective analysis, the addition of rituximab to high-dose methotrexate-based chemotherapy in patients with aggressive B cell CNS lymphoma was associated with improved overall survival. Further studies are underway to prospectively validate these findings. ? The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.
AB - BackgroundThe optimal treatment strategy in patients with aggressive B cell central nervous system lymphoma suitable to receive intensive therapy is unknown. The benefit of incorporating rituximab in systemic therapy remains unclear. We performed a retrospective study examining the impact of rituximab in the context of concomitant therapies, including methotrexate, cytarabine, and radiotherapy, in patients treated with curative intent at 4 university teaching hospitals during 1996-2011.MethodsA retrospective study of CNS lymphoma cases treated at the participating institutions was performed in accordance with institutional ethical guidelines. Patients were included if they received a diagnosis of primary diffuse large B cell lymphoma of the CNS, were HIV negative, and were treated with curative intent.ResultsOne hundred twenty patients aged 21-81 years were identified. Rituximab recipients and nonrecipients were similar, except for rituximab recipients being more likely to have received a diagnosis after 2004. The median follow-up of surviving patients was 30 months. The 5-year overall survival was 46 . Univariate analysis revealed age =60 years, ECOG performance status =1, normal lactate dehydrogenase, diagnosis after 2004, and treatment with cytarabine and rituximab as predictive of favorable overall survival. Multivariate analysis identified age to be an independent predictor of overall survival, with a trend toward improved survival from the other variables that were significant in univariate analyses.ConclusionsIn this retrospective analysis, the addition of rituximab to high-dose methotrexate-based chemotherapy in patients with aggressive B cell CNS lymphoma was associated with improved overall survival. Further studies are underway to prospectively validate these findings. ? The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.
UR - http://neuro-oncology.oxfordjournals.org/content/15/8/1068.full.pdf
U2 - 10.1093/neuonc/not032
DO - 10.1093/neuonc/not032
M3 - Article
SN - 1522-8517
VL - 15
SP - 1068
EP - 1073
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 8
ER -