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.
研究概览
详细说明
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.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Philippe Schucht, MD
- 电话号码:+41 31 632 00 14
- 邮箱:philippe.schucht@insel.ch
研究联系人备份
- 姓名:Alexis P. R. Terrapon, MD
- 电话号码:+41 31 66 4 02 39
- 邮箱:alexis.terrapon@insel.ch
学习地点
-
-
-
Bern、瑞士、3010
- 招聘中
- Dep. of Neurosurgery, Bern University Hospital
-
接触:
- Alexis Terrapon, MD
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
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:
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:LITT Group
Patients undergoing MR-guided Laser Interstitial Thermal Therapy (LITT) between pre-RT MRI and RT
|
Patients undergoing MR-guided Laser Interstitial Thermal Therapy (LITT) between pre-RT MRI and RT.
|
|
无干预:Control Group 1 ("No recurrence")
Patients with no recurrence on pre-RT MRI, proceeding directly to RT.
|
|
|
无干预:Control Group 2 ("No LITT")
Patients with recurrence but ineligible for LITT, proceeding to another resection or to RT without laser therapy.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Rate of patients who successfully complete the planned treatment
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
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).
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Complications of LITT
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
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
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
|
Delay of Radiotherapy
大体时间:assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
|
Measurement of the time-lag between planning MRI and beginning of radiation, and comparsion to pre-planned radiation start
|
assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
|
|
Use of steroids
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
Use of steroids: Binary (yes/no) and, if applicable, dose and duration
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
|
Evolution of radiation necrosis
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
Any increase of the size of the contrast enhancing lesion
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
|
Evolution of target lesion
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
Any increase of the size of the contrast enhancing lesion
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
|
Evolution of pseudoprogression
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
Any increase of the size of the contrast enhancing lesion
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
|
Time to local recurrence
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
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)
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
|
Time to distant recurrence
大体时间:from enrollment to the end of radiotherapy, an average of 8 weeks
|
Time from detection of relapse to detection of distant glioblastoma recurrence (outside the borders of the surgical cavity or associated FLAIR/T2 hyperintensity)
|
from enrollment to the end of radiotherapy, an average of 8 weeks
|
|
Median overall survival
大体时间:from enrollment to date of death, assessed up to the end of the study period (end of ratiotherapy for the last included patient)
|
Median overall survival measured from first surgery to death
|
from enrollment to date of death, assessed up to the end of the study period (end of ratiotherapy for the last included patient)
|
|
Site of recurrence
大体时间:assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
|
Spatial position of the recurrence (local adjacent, distant)
|
assessed the day of radiation start, ranging from 3 to 6 weeks after GBM resection
|
|
Recruitment rate
大体时间:at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
|
Proportion of CRET patients who agree to participate
|
at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
|
|
Progression rate
大体时间:pre RT-MRI
|
Proportion of recruited patients who present with progression on pre-RT MRI
|
pre RT-MRI
|
|
Inclusion rate
大体时间:pre RT-MRI
|
Rate of recruited patients who agree to receiving LITT
|
pre RT-MRI
|
|
Treatment rate
大体时间:at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
|
Rate of recruited patients who receive LITT
|
at study completion (date of end of radiotherapy for the last included patient, approximately 2 years after enrollment of the first participant
|
合作者和调查者
调查人员
- 首席研究员:Philippe Schucht, MD、Inselspital Bern, Department of Neurosurgery
出版物和有用的链接
一般刊物
- 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.
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 2025-01709
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.