# Case report: A rare case of a long-term survivor of glioblastoma who underwent two courses of hypofractionated radiotherapy as part of her care

**Authors:** Midhad Mrvoljak, Shubhendu Mishra, Liam Chen, Elizabeth Neil, Eric Ehler, Stephanie Terezakis, Lindsey Sloan

PMC · DOI: 10.3389/fonc.2025.1501466 · Frontiers in Oncology · 2025-02-04

## TL;DR

A 75-year-old woman with glioblastoma survived for years after receiving two courses of hypofractionated radiotherapy, an unusual treatment for long-term survival.

## Contribution

This case report highlights a rare long-term survival in glioblastoma using two hypofractionated radiotherapy courses.

## Key findings

- The patient remained progression-free for 20 months after initial hypofractionated radiotherapy and temozolomide.
- She survived 8 months after a second hypofractionated radiotherapy course following recurrence.
- The case demonstrates the potential for hypofractionated radiotherapy in long-term glioblastoma survival.

## Abstract

Glioblastoma (GB) is a primary brain tumor that is lethal and challenging to treat. The 3-year overall survival (OS) of patients with this diagnosis has stayed the same since 2005. The patient is a 75-year-old woman who presented with progressive aphasia and was diagnosed with GB (WHO grade 4, IDH1/IDH2 wild type, ATRX intact, p53 and PTEN mutant, BRAF non-mutated, O6-methylguanine-DNA methyltransferase promoter methylated) and who underwent surgical resection, hypofractionated radiotherapy (HFRT) using intensity-modulated radiotherapy (IMRT) (4,005 cGy in 15 fractions) alone, and adjuvant temozolomide (TMZ). She was progression-free for approximately 20 months. Although planned, concurrent TMZ was not used during the complete first course of HFRT due to the patient’s performance status. After recurrence, another HFRT (35 Gy in 10 fractions) was employed. She was progression-free on imaging for 8 months until a recent follow-up scan showed potential progression versus radiation-related change. At the time of this case report, her care is still ongoing. This represents a rare case of a long-term survivor of GB who has received two courses of HFRT, a treatment option that is usually used in those with predicted shorter survival times.

## Linked entities

- **Genes:** IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417], IDH2 (isocitrate dehydrogenase (NADP(+)) 2) [NCBI Gene 3418], ATRX (ATRX chromatin remodeler) [NCBI Gene 546], TP53 (tumor protein p53) [NCBI Gene 7157], PTEN (phosphatase and tensin homolog) [NCBI Gene 5728], BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673]
- **Chemicals:** temozolomide (PubChem CID 5394)
- **Diseases:** glioblastoma (MONDO:0018177)

## Full-text entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, IDH2 (isocitrate dehydrogenase (NADP(+)) 2) [NCBI Gene 3418] {aka D2HGA2, ICD-M, IDH, IDH-2, IDHM, IDP}, ATRX (ATRX chromatin remodeler) [NCBI Gene 546] {aka JMS, MRX52, RAD54, RAD54L, XH2, XNP}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, MGMT (O-6-methylguanine-DNA methyltransferase) [NCBI Gene 4255]
- **Diseases:** brain tumor (MESH:D001932), GB (MESH:D005909), aphasia (MESH:D001037)
- **Chemicals:** TMZ (MESH:D000077204)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11832352/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC11832352/full.md

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Source: https://tomesphere.com/paper/PMC11832352