ABSTRACT
Reirradiation of recurrent glioblastomas is most commonly managed with hypofractionated external beam radiation with a modest overall effect. GammaTile, which is a Cesium-131 source embedded in collagen mesh, is an approach that allows the surgical bed of resectable intracranial tumors to receive a greater biological dose than is possible with any form of external beam radiation therapy (EBRT). In this case report, a 28-year-old male presents with a WHO grade 4 isocitrate dehydrogenase (IDH)-mutant astrocytoma (formerly secondary glioblastoma) of the left occipital/parietal lobe after receiving 45 Gy and two cycles of adjuvant temozolomide four years prior for a grade 3 IDH-mutant astrocytoma. The patient proceeded to undergo craniotomy with maximal safe resection and application of GammaTile to a dose of 60 Gy at 5mm depth. Shortly afterward, he developed symptomatic progression of disease in the bilateral splenium and left thalamus/basal ganglia. We irradiated the undertreated residual disease with EBRT to a dose of 35 Gy in 10 fractions without introducing excessive dose to the GammaTile irradiated volume. This was achieved by creating one portion of the planning target volume with a homogeneous dose and another part where the delivered dose decreased with the GammaTile dose buildup. Treatment planning utilized the Gradient Optimization feathering technique with non-coplanar volumetric modulated arc therapy. The resulting composite between the hypofractionated EBRT and GammaTile dose distribution created an approximate dose equivalent of 50 Gy in 2 Gy fractions to the residual disease with no hot spots or areas of under coverage. This is the first report showing the feasibility of combining GammaTile with dose-matched EBRT volumes in a reproducible manner to sub-totally resected, recurrent intracranial neoplasms.
