Journal of Clinical Oncology, Vol 5, 1221-1231, Copyright © 1987 by American Society of Clinical Oncology
Eight drugs in one day chemotherapy for brain tumors: experience in 107 children and rationale for preradiation chemotherapy
TW Pendergrass, JM Milstein, JR Geyer, AF Mulne, EJ Kosnik, JD Morris, RL Heideman, FB Ruymann, JT Stuntz and WA Bleyer
The development of a new multidrug chemotherapy regimen for primary brain
tumors was based upon the cellular heterogeneity within individual tumors,
the Goldie-Coldman and Price-Goldie-Hill hypotheses, and known agonistic
effects of certain drug combinations and sequences. Eight drugs
(vincristine [VCR], hydroxyurea, procarbazine, CCNU, cisplatin, cytosine
arabinoside [Ara-C] high-dose methylprednisolone, and either
cyclophosphamide or dacarbazine) were administered within 12 hours in an
attempt to minimize myelosuppression. Courses were repeated at 2- to 4-week
intervals. The regimen was devised to include lipid and water soluble
drugs, polar and nonpolar agents, phase-specific and cell- cycle
independent agents, and antineoplastics with different mechanisms of
action. More than 330 courses of the regimen were administered to 107
children with brain tumors whose tumor had recurred or had been
incompletely resected at diagnosis. Tumor response according to
protocol-specified criteria and independent review was evaluable in 78% of
the patients. After just two cycles of chemotherapy and within a 4- to
6-week interval, 50% had an objective tumor response including 15.5% who
had a complete response (CR). Nephrotoxicity and high-frequency hearing
losses were noted after three to five courses of therapy in approximately
half of the patients. Transfusions with red cells or platelets and use of
antibiotics for fever and neutropenia were required in 10% to 25% of
patients. The regimen appears satisfactory for preradiation chemotherapy in
newly diagnosed patients with residual tumor after surgery, but it must be
compared with standard therapeutic approaches in prospective controlled
trials before its relative value can be established.

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