Photoirradiation therapy of experimental malignant glioma with 5-aminolevulinic acid

Object. Accumulation of protoporphyrin IX (PPIX) in malignant gliomas is induced by 5-aminolevulinic acid (5-ALA). Because PPIX is a potent photosensitizer, the authors sought to discover whether its accumulation might be exploited for use in photoirradiation therapy of experimental brain tumors, without injuring normal or edematous brain. Methods. Thirty rats underwent craniotomy and were randomized to the following groups: I) photoirradiation of cortex (200 J/cm(2), 635-nm argon-dye laser); 2) photoirradiation of cortex (200 J/cm(2)) 6 hours after intravenous administration of 5-ALA (100 rng/kg body weight); 3) cortical cold injury for edema induction; 4) cortical cold injury with simultaneous administration of 5-ALA (100 mg/kg body weight) and photoirradiation of cortex (200 J/cm(2)) 6 hourb later; or 5) irradiation of cortex (200 J/cm(2)) 6 hours after intravenous administration of Photofrin 11 (5 mg/kg body weight). Tumors were induced by cortical inoculation of C6 cells and 9 days later, magnetic resonance (MR) images were obtained. On Day, 10, animals were given 5-ALA (100 mg/kg body weight) and their brains were irradiated (100 J/cm(2)) 3 or 6 hours later. Seventy-two hours after irradiation, the brains were removed for histological examination. Irradiation of brains after administration of 5-ALA resulted in superficial cortical damage, the effects of which were not different from those of the irradiation alone. Induction of cold injury in combination with 5-ALA and irradiation slightly increased the depth of damage. In the group that received irradiation after intravenous administration of Photofrin 11 the depth of damage inflicted was significantly greater. The extent of damage in response to 5-ALA and irradiation in brains harboring C6 tumors corresponded to the extent of tumor determined from pretreatment MR images. Conclusions. Photoirradiation therapy in combination with 5-ALA appears to damage experimental brain tumors selectively, with negligible damage to normal or peri focal edematous tissue.