Influence of light fluence rate on the effects of photodynamic therapy in an orthotopic rat glioma model

被引:73
作者
Angell-Petersen, E [1 ]
Spetalen, S
Madsen, SJ
Sun, CH
Peng, Q
Carper, SW
Sioud, M
Hirschberg, H
机构
[1] Norwegian Radium Hosp, Dept Surg Oncol, N-0310 Oslo, Norway
[2] Norwegian Radium Hosp, Dept Radiat Biol, N-0310 Oslo, Norway
[3] Norwegian Radium Hosp, Dept Pathol, N-0310 Oslo, Norway
[4] Norwegian Radium Hosp, Dept Immunol, N-0310 Oslo, Norway
[5] Ullevaal Univ Hosp, Dept Pathol, Oslo, Norway
[6] Univ Nevada, Canc Res Ctr, Dept Hlth Phys, Las Vegas, NV 89154 USA
[7] Univ Nevada, Dept Chem, Las Vegas, NV 89154 USA
[8] Univ Oslo, Rikshosp, Dept Neurosurg, N-0027 Oslo, Norway
[9] Univ Calif Irvine, Beckman Laser Inst & Med Clin, Irvine, CA 92715 USA
关键词
photodynamic therapy; aminolevulinic acid; brain tumor; fluence rate; rat;
D O I
10.3171/jns.2006.104.1.109
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Failure of treatment for high-grade gliomas is usually due to local recurrence at the site of resection, indicating that a more aggressive local therapy could be beneficial. Photodynamic therapy (PDT) is a local treatment involving the administration of a tumor-localizing photosensitizing drug, in this case aminolevulinic acid (ALA). The effect depends on the total light energy delivered to the target tissue, but may also be influenced by the rate Of light delivery. Methods. In vitro experiments showed that the sensitivity to ALA PDT of BT4C multicellular tumor spheroids depended oil the rate of light delivery (fluence rate). The BT4C tumors were established intracranially in BD-IX rats. Microfluorometry of frozen tissue Sections showed that photosensitization is produced with better than 200:1 tumor/normal tissue Selectivity after ALA injection. Four hours after intraperitoneal ALA injection (125 mg/kg), 26 J of 632 nm light was delivered interstitially over 15 (high fluence rate) or 90 (low fluence rate) Minutes. Histological examination of animals treated 14 days after tumor induction demonstrated extensive tumor necrosis after low-fluence-rate PDT, but hardly any necrosis after high-fluence-rate treatment. Neutrophil infiltration in tumor tissue was increased by PDT, but was similar for both treatment regimens. Low-fluence-rate PDT administered 9 days after tumor induction resulted in statistically significant prolongation Of survival for treated rats compared with nontreated control animals. Conclusions. Treatment with ALA PDT induced pronounced necrosis in tumors only if the light was delivered at a low rate. The treatment prolonged the Survival for tumor-bearing animals.
引用
收藏
页码:109 / 117
页数:9
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