Department of Neurosurgery, University Hospital Munich, Ludwig-Maximilians-University, Marchioninistrasse 15, 81377, Munich, Germany.
Department of Neurosurgery, University Hospital Salzburg, Paracelsus Medical University Salzburg, Salzburg, Austria.
J Neurooncol. 2023 Mar;162(1):217-223. doi: 10.1007/s11060-023-04284-9. Epub 2023 Mar 16.
Innovative, efficient treatments are desperately needed for people with glioblastoma (GBM).
Sixteen patients (median age 65.8 years) with newly diagnosed, small-sized, not safely resectable supratentorial GBM underwent interstitial photodynamic therapy (iPDT) as upfront eradicating local therapy followed by standard chemoradiation. 5-aminolevulinic acid (5-ALA) induced protoporphyrin IX was used as the photosensitizer. The tumors were irradiated with light at 635 nm wavelength via stereotactically implanted cylindrical diffuser fibers. Outcome after iPDT was retrospectively compared with a positively-selected in-house patient cohort (n = 110) who underwent complete tumor resection followed by chemoradiation.
Median progression-free survival (PFS) was 16.4 months, and median overall survival (OS) was 28.0 months. Seven patients (43.8%) experienced long-term PFS > 24 months. Median follow-up was 113.9 months for the survivors. Univariate regression revealed MGMT-promoter methylation but not age as a prognostic factor for both OS (p = 0.04 and p = 0.07) and PFS (p = 0.04 and p = 0.67). Permanent iPDT-associated morbidity was seen in one iPDT patient (6.3%). Patients treated with iPDT experienced superior PFS and OS compared to patients who underwent complete tumor removal (p < 0.01 and p = 0.01, respectively). The rate of long-term PFS was higher in iPDT-treated patients (43.8% vs. 8.9%, p < 0.01).
iPDT is a feasible treatment concept and might be associated with long-term PFS in a subgroup of GBM patients, potentially via induction of so far unknown immunological tumor-controlling processes.
迫切需要为胶质母细胞瘤(GBM)患者提供创新、有效的治疗方法。
16 名新诊断为小尺寸、不能安全切除的幕上 GBM 患者接受间质光动力疗法(iPDT)作为初始局部根治性治疗,随后进行标准放化疗。使用 5-氨基酮戊酸(5-ALA)诱导原卟啉 IX 作为光敏剂。通过立体定向植入的圆柱形扩散光纤,用 635nm 波长的光照射肿瘤。回顾性比较 iPDT 后的结果与经完全肿瘤切除后行放化疗的内部患者队列(n=110)。
中位无进展生存期(PFS)为 16.4 个月,中位总生存期(OS)为 28.0 个月。7 名患者(43.8%)经历了长期 PFS>24 个月。幸存者的中位随访时间为 113.9 个月。单变量回归显示 MGMT 启动子甲基化而非年龄是 OS(p=0.04 和 p=0.07)和 PFS(p=0.04 和 p=0.67)的预后因素。1 名 iPDT 患者(6.3%)出现永久性 iPDT 相关并发症。与接受完全肿瘤切除的患者相比,接受 iPDT 治疗的患者 PFS 和 OS 更优(p<0.01 和 p=0.01)。iPDT 治疗组的长期 PFS 率更高(43.8% vs. 8.9%,p<0.01)。
iPDT 是一种可行的治疗方案,可能与 GBM 患者亚组的长期 PFS 相关,其潜在机制可能是诱导目前未知的免疫性肿瘤控制过程。