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LITT for Ultra-early GBM Recurrence
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.
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
Background:
GBM is frequent and still has a poor prognosis. Standard therapy consists of complete resection of enhancing tumor (CRET) followed by RT and CT. At the institution, patients planned for RT undergo a pre-radiotherapy planning MRI. As recently published, >40% of patients exhibit contrast-enhancing tumor recurrence in the short interval between early postoperative MRI and pre-RT MRI, despite CRET in the initial surgery. This ultra-early recurrence is strongly associated with shorter OS: in the cohort, median overall survival (OS) was 13.3m and 24.4m for patients with and without recurrence in pre-RT MRI, respectively. Hence, pre-radiation GBM recurrence is a frequent event with detrimental consequences for patients.
Reoperation in this setting is rarely performed as it delays adjuvant treatment, which worsen prognosis further. LITT is an established, minimally invasive treatment form for brain lesions such as glioblastoma recurrences and metastases. LITT may offer a solution to this dilemma as its minimal invasiveness enables to ablate the recurrent tumor without delaying treatment. As an additional benefit, LITT may work as a potent sensitizer to subsequent RT and CT.
A key challenge in the implementation of LITT in this setting is the tight scheduling window (maximum 1 week) between pre-radiotherapy planning MRI and start of radiotherapy. In order not to delay adjuvant treatment, LITT should optimally be performed within this time window. To be feasible, both planning and execution of LITT, including coordination of intraoperative MRI and engineering support, must occur within this short timeframe. This feasibility study aims to prospectively investigate whether LITT can be integrated into the existing care pathway without postponing of adjuvant treatment. This may lay the groundwork for future clinical trials.
Objective:
The aim is to test feasibility of integrating scheduling, planning and execution of LITT into the standard treatment course of patients with CRET-resected glioblastoma scheduled to receive concomitant radio-chemotherapy. The primary objective of this feasibility study is to evaluate the feasibility of performing LITT for ultra-early recurrence following GBM resection without delaying adjuvant radio-chemotherapy.
Secondary objectives are collected to estimate the effect size of pre-RT LITT on median overall survival compared to patients with ultra-early recurrence who do not receive LITT, and to historic controls; the purpose of these endpoints is to guide power calculations of a subsequent phase II trial.
Methods:
This is a prospective, single-arm, monocentric feasibility study conducted at the University Department of Neurosurgery, Inselspital, Bern. The study is exploratory in nature and aims to generate foundational data for a larger, multi-centric phase II trial. At the University Hospital of Bern, all patients are presented to the tumor board after surgery for brain tumors. All patients with histologically confirmed glioblastoma and without residual contrast enhancement (CRET) meeting the inclusion criteria for study participation will be asked for consent and, where applicable, included in the trial. All patients showing ultra-early recurrence on planning MRI and meeting the inclusion criteria for LITT will be considered to undergo LITT before the beginning of radiotherapy. Patients without recurrence ("no recurrence" group) and patients with recurrence who do not undergo LITT ("recurrence/no LITT" group) will serve as internal control groups.
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Philippe Schucht, MD
- Telefoonnummer: +41 31 632 00 14
- E-mail: philippe.schucht@insel.ch
Studie Contact Back-up
- Naam: Alexis P. R. Terrapon, MD
- Telefoonnummer: +41 31 66 4 02 39
- E-mail: alexis.terrapon@insel.ch
Studie Locaties
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Bern, Zwitserland, 3010
- Werving
- Dep. of Neurosurgery, Bern University Hospital
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Contact:
- Alexis Terrapon, MD
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- 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.
Exclusion Criteria:
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: LITT Group
Patients undergoing MR-guided Laser Interstitial Thermal Therapy (LITT) between pre-RT MRI and RT
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Patients undergoing MR-guided Laser Interstitial Thermal Therapy (LITT) between pre-RT MRI and RT.
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Geen tussenkomst: Control Group 1 ("No recurrence")
Patients with no recurrence on pre-RT MRI, proceeding directly to RT.
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Geen tussenkomst: Control Group 2 ("No LITT")
Patients with recurrence but ineligible for LITT, proceeding to another resection or to RT without laser therapy.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Rate of patients who successfully complete the planned treatment
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Proportion of CRET patients who successfully complete the planned treatment protocol without protocol violation, until the end of radiation therapy.
A protocol violation is defined as any of the following: a delay of more than 7 days in the scheduled pre-RT MRI, LITT procedure, or RT initiation, or an interruption of RT due to a LITT-related event.
The study teams aims to describe logistical and organizational difficulties (coordination of intraoperative MRI-availability, engineering support).
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Complications of LITT
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Any deviation from the normal postoperative course, including any new appearance of blood during LITT MRI, any seeding along the trajectory of the probe, any pathological wound condition such as dehiscence or infection
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Delay of Radiotherapy
Tijdsspanne: assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
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Measurement of the time-lag between planning MRI and beginning of radiation, and comparsion to pre-planned radiation start
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assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
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Use of steroids
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Use of steroids: Binary (yes/no) and, if applicable, dose and duration
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Evolution of radiation necrosis
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Any increase of the size of the contrast enhancing lesion
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Evolution of target lesion
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Any increase of the size of the contrast enhancing lesion
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Evolution of pseudoprogression
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Any increase of the size of the contrast enhancing lesion
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Time to local recurrence
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Time from detection of relapse to detection of local glioblastoma recurrence (lesion within/at the borders of the surgical cavity or associated FLAIR/T2 hyperintensity)
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Time to distant recurrence
Tijdsspanne: from enrollment to the end of radiotherapy, an average of 8 weeks
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Time from detection of relapse to detection of distant glioblastoma recurrence (outside the borders of the surgical cavity or associated FLAIR/T2 hyperintensity)
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from enrollment to the end of radiotherapy, an average of 8 weeks
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Median overall survival
Tijdsspanne: from enrollment to date of death, assessed up to the end of the study period (end of ratiotherapy for the last included patient)
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Median overall survival measured from first surgery to death
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from enrollment to date of death, assessed up to the end of the study period (end of ratiotherapy for the last included patient)
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Site of recurrence
Tijdsspanne: assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
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Spatial position of the recurrence (local adjacent, distant)
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assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
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Recruitment rate
Tijdsspanne: at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
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Proportion of CRET patients who agree to participate
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at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
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Progression rate
Tijdsspanne: pre RT-MRI
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Proportion of recruited patients who present with progression on pre-RT MRI
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pre RT-MRI
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Inclusion rate
Tijdsspanne: pre RT-MRI
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Rate of recruited patients who agree to receiving LITT
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pre RT-MRI
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Treatment rate
Tijdsspanne: at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
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Rate of recruited patients who receive LITT
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at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
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Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Philippe Schucht, MD, Inselspital Bern, Department of Neurosurgery
Publicaties en nuttige links
Algemene publicaties
- Stupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, Taphoorn MJ, Belanger K, Brandes AA, Marosi C, Bogdahn U, Curschmann J, Janzer RC, Ludwin SK, Gorlia T, Allgeier A, Lacombe D, Cairncross JG, Eisenhauer E, Mirimanoff RO; European Organisation for Research and Treatment of Cancer Brain Tumor and Radiotherapy Groups; National Cancer Institute of Canada Clinical Trials Group. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med. 2005 Mar 10;352(10):987-96. doi: 10.1056/NEJMoa043330.
- Terrapon APR, Zattra CM, Voglis S, Velz J, Vasella F, Akeret K, Held U, Schiavolin S, Bozinov O, Ferroli P, Broggi M, Sarnthein J, Regli L, Neidert MC. Adverse Events in Neurosurgery: The Novel Therapy-Disability-Neurology Grade. Neurosurgery. 2021 Jul 15;89(2):236-245. doi: 10.1093/neuros/nyab121.
- Schaff LR, Mellinghoff IK. Glioblastoma and Other Primary Brain Malignancies in Adults: A Review. JAMA. 2023 Feb 21;329(7):574-587. doi: 10.1001/jama.2023.0023.
- Waqar M, Roncaroli F, Lehrer EJ, Palmer JD, Villanueva-Meyer J, Braunstein S, Hall E, Aznar M, De Witt Hamer PC, D'Urso PI, Trifiletti D, Quinones-Hinojosa A, Wesseling P, Borst GR. Rapid early progression (REP) of glioblastoma is an independent negative prognostic factor: Results from a systematic review and meta-analysis. Neurooncol Adv. 2022 Jun 4;4(1):vdac075. doi: 10.1093/noajnl/vdac075. eCollection 2022 Jan-Dec.
- McGrath K, Frain M, Hey G, Rahman M. Complications following laser interstitial thermal therapy: a review. Neurochirurgie. 2025 Jan;71(1):101604. doi: 10.1016/j.neuchi.2024.101604. Epub 2024 Oct 23.
- Rangwala HS, Shafique MA, Mustafa MS, Kumar R, Devi J, Rangwala BS, Ali SMS, Raja A, Iqbal J, Ali M, Haseeb A. Evaluating efficacy and safety of laser interstitial thermal therapy in patients with newly diagnosed and recurrent glioblastoma: a systematic review and meta-analysis. Neurosurg Rev. 2024 Nov 12;47(1):846. doi: 10.1007/s10143-024-03077-6.
- Yu JS, Meade SM, Zhao R, Wei W, Dashora H, Prayson R, Grabowski MM, Stevens G, Lobbous M, Murphy ES, Suh JH, Chao ST, Barnett GH, Peereboom D, Ahluwalia MS, Mohammadi AM. Expedited chemoradiation after laser interstitial thermal therapy (LITT) is feasible and safe in patients with newly diagnosed glioblastoma. Neurooncol Adv. 2025 Feb 14;7(1):vdaf038. doi: 10.1093/noajnl/vdaf038. eCollection 2025 Jan-Dec.
- Hani L, Hakim A, Gehrig L, Staruch M, Goldberg J, Russli S, Soll N, Raabe A, Ermis E, Schucht P. Identification and relevance of ultra-early progression after resection of glioblastoma. J Neurosurg. 2025 Jul 25;143(5):1315-1324. doi: 10.3171/2025.3.JNS242212. Print 2025 Nov 1.
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Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 2025-01709
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