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Dosimetric evaluation and treatment planning considerations for GammaTile permanent brain implants - a pilot, institutional experience.
Zhang, Shunqing; Patel, Krishnan; Dusenbery, Kathryn; Alshreef, Abdullah; Sterling, David; Sloan, Lindsey; Reynolds, Margaret; Chen, Clark C; Ferreira, Clara.
Afiliação
  • Zhang S; Northwestern Medical Group, Chicago, IL, USA.
  • Patel K; National Institutes of Health, Bethesda, MD, USA.
  • Dusenbery K; University of Minnesota, Minneapolis, MN, USA.
  • Alshreef A; University of Minnesota, Minneapolis, MN, USA.
  • Sterling D; University of Minnesota, Minneapolis, MN, USA.
  • Sloan L; University of Minnesota, Minneapolis, MN, USA.
  • Reynolds M; University of Minnesota, Minneapolis, MN, USA.
  • Chen CC; Brown University, Providence, RI, USA.
  • Ferreira C; University of Minnesota, Minneapolis, MN, USA. cferreir@umn.edu.
J Neurooncol ; 2024 Jun 20.
Article em En | MEDLINE | ID: mdl-38902561
ABSTRACT

PURPOSE:

GammaTile® (GT) is a brachytherapy platform that received Federal Drug Administration (FDA) approval as brain tumor therapy in late 2018. Here, we reviewed our institutional experience with GT as treatment for recurrent glioblastomas and characterized dosimetric parameter and associated clinical outcome. METHODS AND MATERIALS A total of 20 consecutive patients with 21 (n = 21) diagnosis of recurrent glioblastoma underwent resection followed by intraoperative GT implant between 01/2019 and 12/2020. Data on gross tumor volume (GTV), number of GT units implanted, dose coverage for the high-risk clinical target volume (HR-CTV), measured by D90 or dose received by 90% of the HR-CTV, dose to organs at risk, and six months local control were collected.

RESULTS:

The median D90 to HR-CTV was 56.0 Gy (31.7-98.7 Gy). The brainstem, optic chiasm, ipsilateral optic nerve, and ipsilateral hippocampus median Dmax were 11.2, 5.4, 6.4, and 10.0 Gy, respectively. None of the patients in this study cohort suffered from radiation necrosis or adverse events attributable to the GT. Correlation was found between pre-op GTV, the volume of the resection cavity, and the number of GT units implanted. Of the resection cavities, 7/21 (33%) of the cavity experienced shrinkage, 3/21 (14%) remained stable, and 11/21 (52%) of the cavities expanded on the 3-months post-resection/GT implant MRIs. D90 to HR-CTV was found to be associated with local recurrence at 6-month post GT implant, suggesting a dose response relationship (p = 0.026). The median local recurrence-free survival was 366.5 days (64-1,098 days), and a trend towards improved local recurrence-free survival was seen in patients with D90 to HR-CTV ≥ 56 Gy (p = 0.048).

CONCLUSIONS:

Our pilot, institutional experience provides clinical outcome, dosimetric considerations, and offer technical guidance in the clinical implementation of GT brachytherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Neurooncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Neurooncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos