Surgical resection followed by local field radiotherapy is currently our mo
st effective approach to treatment for most patients with malignant glioma.
Carboplatin chemotherapy has direct cytotoxic effects on glioma cells and
acts as a radiation sensitizer to enhance cell killing. Its demonstrated ef
ficacy as a sensitizer in other solid tumors led to this clinical trial of
carboplatin as a radiation sensitizer in the treatment of newly diagnosed g
lioblastoma multiforme (GBM) and anaplastic astrocytoma (AA). Fourteen pati
ents (nine GBM and five AA) were treated with daily low-dose carboplatin 25
mg/m(2) intravenously within 2 h of their fractionated radiotherapy to a t
otal dose of 600 mg/m(2). No significant toxicities attributable to this co
mbined therapy were observed. All patients have progressed, with median tim
e to progression of 16 weeks. Eleven patients have died, with median surviv
al of 38 weeks for the entire cohort. Although this regimen appeared safe,
there was no benefit in survival time compared to historical patients treat
ed with radiotherapy. The limitations and future potential for the strategy
of radiation sensitization are discussed.