# Impact of Reirradiation Utilizing Fractionated Stereotactic Radiotherapy for Recurrent Glioblastoma

**Authors:** Lisa B Shields, Patrick O'Dell, Michael W Daniels, Parag R Sevak, Hilary A Highfield, Kaylyn D Sinicrope, David A Sun, Aaron C Spalding

PMC · DOI: 10.7759/cureus.53001 · 2024-01-26

## TL;DR

This study found that reirradiation with fractionated stereotactic radiotherapy improves survival in patients with recurrent glioblastoma.

## Contribution

The study demonstrates that reirradiation with FSRT significantly improves outcomes in recurrent glioblastoma patients.

## Key findings

- Reirradiation with FSRT was associated with longer progression-free and overall survival compared to systemic treatment alone.
- Patients receiving reirradiation had a higher use of bevacizumab and lower TMZ discontinuation due to toxicity.
- The one-year overall survival rate after recurrence was 22% in the reirradiation group.

## Abstract

Background: Patients with recurrent glioblastoma (GBM) have limited treatment options. This study determined whether patients with recurrent GBM treated with initial radiation/temozolomide (TMZ) and reirradiation using fractionated stereotactic radiotherapy (FSRT) had improved outcomes.

Materials and methods: We identified 95 patients with recurrent GBM, 50 of whom underwent FSRT at recurrence and 45 who had systemic treatment only (control). The median total FSRT dose at the time of GBM recurrence was 30 Gy in five fractions of the gadolinium-enhanced tumor only.

Results: With a median follow-up of 18 months, the progression-free survival (PFS) and overall survival (OS) following initial GBM diagnosis were longer in the reirradiation group compared to the control group (13.5 vs. 7.5 months [p=0.001] and 24.6 vs. 12.6 months [p<0.001], respectively). For patients who underwent reirradiation, the median time interval between the end of the initial radiation and reirradiation was 15.2 months. The median OS after GBM recurrence was longer in the reirradiation group versus the control group (9.9 vs. 3.5 months [p<0.001]), with a one-year OS survival rate of 22%. The hazard ratio for death of patients in the reirradiation group was 0.31 [0.19-0.50]. The reirradiation group had a higher percentage of patients who received bevacizumab (BEV, 62.0% vs. 28.9%, p=0.002) and a lower percentage of patients whose TMZ was discontinued due to toxicity (8.0% vs. 28.9%, p=0.017) compared to the control group.

Conclusions: Reirradiation utilizing FSRT was associated with improved PFS and OS after GBM recurrence compared to the control group who did not receive additional irradiation.

## Linked entities

- **Chemicals:** temozolomide (PubChem CID 5394)
- **Diseases:** glioblastoma (MONDO:0018177), GBM (MONDO:0018177)

## Full-text entities

- **Diseases:** tumor (MESH:D009369), death (MESH:D003643), toxicity (MESH:D064420), GBM (MESH:D005909)
- **Chemicals:** TMZ (-), gadolinium (MESH:D005682), temozolomide (MESH:D000077204), BEV (MESH:D000068258)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10894660/full.md

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Source: https://tomesphere.com/paper/PMC10894660