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Phase
II study of phenylacetate in patients with recurrent malignant glioma: a North
American Brain Tumor Consortium report
Chang
SM, Kuhn JG, Robins HI, Schold SC, Spence AM, Berger MS, Mehta MP, Bozik ME,
Pollack I, Schiff D, Gilbert M, Rankin C, Prados MD
University
of California Medical Center, San Francisco, USA.
changs@neuro.ucsf.edu
Purpose.
To determine the response rate, time to treatment failure, and toxicity of
phenylacetate in patients with recurrent malignant glioma and to identify plasma
concentrations achieved during repeated continuous infusion of this agent.
Patients
and Methods. Adult patients with recurrent malignant glioma were treated with
phenylacetate.
The schedule consisted of a 2-week continuous, intravenous infusion followed by
a 2-week rest period (14 days on, 14 days off).
A starting dose of 400 mg/kg total body weight per day of phenylacetate was
initially used and subsequently changed to 400 mg/kg/d based on ideal body
weight.
Intrapatient dose escalations were allowed to a maximum of 450 mg/kg ideal body
weight/d.
Tumor response was assessed every 8 weeks.
The National Cancer Institute common toxicity criteria were used to assess
toxicity.
Plasma concentrations achieved during the patients' first two 14-day infusions
were assessed.
Results.
Forty-three patients were enrolled between December 1994 and December 1996.
Of these, 40 patients were assessable for toxicity and response to therapy.
Reversible symptoms of fatigue and somnolence were the primary toxicities, with
only mild hematologic toxicity.
Thirty (75%) of the 40 patients failed treatment within 2 months, seven (17.5%)
had stable disease, and three (7.5%) had a response defined as more than 50%
reduction in the tumor.
Median time to treatment failure was 2 months.
Thirty-five patients have died, with a median survival of 8 months.
Pharmacokinetic data for this dose schedule showed no difference in the mean
plasma concentrations of phenylacetate between weeks 1 and 2 or between weeks 5
and 6.
Conclusion.
Phenylacetate has little activity at this dose schedule in patients with
recurrent malignant glioma.
Further studies with this drug would necessitate an evaluation of a different
dose schedule.
PMID:
10071293 [PubMed - indexed for MEDLINE]
Source:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10071293&dopt=Abstract
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