Journal of Clinical Oncology, Vol 9, 1580-1590, Copyright © 1991 by American Society of Clinical Oncology
Primary CNS lymphoma treated with osmotic blood-brain barrier disruption: prolonged survival and preservation of cognitive function
EA Neuwelt, DL Goldman, SA Dahlborg, J Crossen, F Ramsey, S Roman-Goldstein, R Braziel and B Dana
Department of Neurology, Oregon Health Sciences University, Portland 97201-3098.
Combination chemotherapy with or without radiotherapy has had only modest
efficacy in the treatment of primary CNS lymphoma. Median survival of these
patients, treated primarily with radiotherapy, is 13 months; 5-year
survival is less than 5%. Thirty consecutive non- acquired immune
deficiency syndrome patients with primary CNS lymphoma were treated with
barrier-dependent chemotherapy using intraarterial mannitol to open the
blood-brain barrier (BBB). Follow-up included extensive neuropsychologic
testing of all patients. Thirteen patients received cranial radiation 1 to
9 months before referral (group 1). Seventeen patients received initial BBB
disruption chemotherapy with subsequent radiation only for tumor
progression or recurrence (group 2). The difference in median survivals
from diagnosis--17.8 months for group 1 and 44.5 months for group 2--was
statistically significant (P = .039). Group 1 survival is comparable with
the 20-month median survival of a historical series of patients (n = 208)
treated with radiotherapy with or without chemotherapy. Group 2 patient
survival represents an advance in the survival of CNS lymphoma and was
associated with preservation of cognitive function in six of seven
nonirradiated complete responders observed for 1 to 7 years. Patient
toxicity was manageable in this intensive therapeutic regimen. In this
series, a plateau in survival curves suggests that a major portion of these
patients may be cured without the neuropsychologic sequelae associated with
cranial radiation.

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