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Laser heat treatment for glioblastoma that returns before radiotherapy begins

Tests laser heat therapy in adults whose glioblastoma returns before radiotherapy starts.

Plain-language title generated from the registry record
Registry title: LITT for Ultra-early GBM Recurrence

Key facts

Where
Bern, SwitzerlandSee the site

Where in Switzerland

  • Dep. of Neurosurgery, Bern University HospitalBern, SwitzerlandTaking people

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Trial details

Who runs it
Insel Gruppe AG, University Hospital Bern
Trial code
NCT07616986
Record updated
1 June 2026
Original description
Glioblastoma (GBM) remains aggressive despite standard therapy (surgery (CRET) + RT/CT). Over 40% of patients develop recurrence between surgery and pre-RT MRI, with median overall survival (OS) of 13.3m and 24.4m for patients with and without recurrence in pre-RT MRI, respectively. Reoperation is avoided as it delays adjuvant therapy.Read full original descriptionShow less

Laser Interstitial Thermal Therapy for Ultra-Early, Pre-Radiotherapy Glioblastoma Recurrence

Glioblastoma (GBM) remains aggressive despite standard therapy (surgery (CRET) + RT/CT). Over 40% of patients develop recurrence between surgery and pre-RT MRI, with median overall survival (OS) of 13.3m and 24.4m for patients with and without recurrence in pre-RT MRI, respectively. Reoperation is avoided as it delays adjuvant therapy.

LITT offers a minimally invasive alternative that may:

* Treat recurrence without delaying RT/CT * Potentially sensitize tumors to subsequent therapy This study tests if LITT can be practically integrated within the critical 1-week window between pre-RT MRI and radiotherapy initiation, maintaining the adjuvant schedule.

Inclusion: Histologically confirmed glioblastoma, IDH-wildtype, regardless of MGMT status; ≥18 years of age; CRET; Karnofsky Performance Status (KPS) ≥70; No contra-indication for radio-chemotherapy; Scheduled for adjuvant radio-chemotherapy at University Hospital of Bern; Able to provide informed consent; No contra-indication for LITT; No pregnancy or active breast-feeding; No known coagulopathy independent of medication; No dissemination or multifocal disease; Patients lacking capacity to consent or considered vulnerable (e.g., minors, those under legal protection) are not included.

ClinicalTrials.gov NCT07616986