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GammaTile® (GT) as a brachytherapy platform for rapidly proliferating glioblastomas: from case series to clinical trials.
Yekula, Anudeep; Gessler, Dominic J; Ferreira, Clara; Shah, Rena; Reynolds, Margaret; Dusenbery, Kathryn; Chen, Clark C.
Afiliación
  • Yekula A; Department of Neurosurgery, University of Minnesota Medical School, D429 Mayo Memorial Building, 420 Delaware St. S. E., MMC96, Minneapolis, MN, 55455, USA.
  • Gessler DJ; Department of Neurosurgery, University of Minnesota Medical School, D429 Mayo Memorial Building, 420 Delaware St. S. E., MMC96, Minneapolis, MN, 55455, USA.
  • Ferreira C; Department of Radiation Oncology, University of Minnesota, Minneapolis, MN, USA.
  • Shah R; Department of Oncology, North Memorial Health, Robbinsdale, MN, USA.
  • Reynolds M; Department of Radiation Oncology, University of Minnesota, Minneapolis, MN, USA.
  • Dusenbery K; Department of Radiation Oncology, University of Minnesota, Minneapolis, MN, USA.
  • Chen CC; Department of Neurosurgery, University of Minnesota Medical School, D429 Mayo Memorial Building, 420 Delaware St. S. E., MMC96, Minneapolis, MN, 55455, USA. clark.chen@lifespan.org.
J Neurooncol ; 166(3): 441-450, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38281303
ABSTRACT

PURPOSE:

Radiation plays a central role in glioblastoma treatment. Logistics related to coordinating clinic visits, radiation planning, and surgical recovery necessitate delay in radiation delivery from the time of diagnosis. Unimpeded tumor growth occurs during this period, and is associated with poor clinical outcome. Here we provide a pilot experience of GammaTile ® (GT), a collagen tile-embedded Cesium-131 (131Cs) brachytherapy platform for such aggressive tumors.

METHODS:

We prospectively followed seven consecutive patients (2019-2023) with newly diagnosed (n = 3) or recurrent (n = 4) isocitrate dehydrogenase wild-type glioblastoma that grew > 100% in volume during the 30 days between the time of initial diagnosis/surgery and the radiation planning MRI. These patients underwent re-resection followed by GT placement.

RESULTS:

There were no surgical complications. One patient developed right hemiparesis prior to re-resection/GT placement and was discharged to rehabilitation, all others were discharged home-with a median hospital stay of 2 days (range 1-5 days). There was no 30-day mortality and one 30-day readmission (hydrocephalus, requiring ventriculoperitoneal shunting (14%)). With a median follow-up of 347 days (11.6 months), median progression free survival of ≥ 320 days (10.6 months) was achieved for both newly and recurrent glioblastoma patients. The median overall survival (mOS) was 304 and 347 days (10 and 11.5 mo) for recurrent and newly diagnosed glioblastoma patients, respectively.

CONCLUSION:

Our pilot experience suggests that GT offers favorable local control and safety profile for patients afflicted with rapidly proliferating glioblastomas and lay the foundation for future clinical trial design.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_brain_nervous_system_cancer Asunto principal: Braquiterapia / Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: J Neurooncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_brain_nervous_system_cancer Asunto principal: Braquiterapia / Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: J Neurooncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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