跳至主要内容
临床试验/NCT05318612
NCT05318612进行中(未招募)3 期

(Cost)Effectiveness of MR-guided LITT Therapy in Patients With Primary Irresectable Glioblastoma: a Prospective Multicenter Randomized Controlled Trial (EMITT)

Radboud University Medical Center7 个研究点 分布在 1 个国家目标入组 238 人开始时间: 2022年4月8日最近更新:
适应症

试验速览

阶段
3 期
状态
进行中(未招募)
入组人数
238
试验地点
7
主要终点
Health Related Quality of Life (HR-QoL)

研究概览

简要总结

The aim of this study is to investigate the (cost-)effectiveness of LITT (Laser Interstitial Thermal Therapy) in primary irresectable glioblastoma. Glioblastoma are the most common malignant brain tumors and are, due to their devastating nature and the fact that these tumors occur at a relatively young age (median 59 years), responsible for up to 7% of total life years lost from cancer before the age of 70.

The current treatment of glioblastoma consists of maximal safe surgery combined with adjuvant chemoradiation therapy (CRT). However, despite this aggressive treatment, these patients still face a poor prognosis (median overall survival 14.5 - 18.5 months). In addition to that, around 30% of the patients diagnosed with a glioblastoma are not suitable for surgery. These patients miss the benefit of a resection and face an even worse prognosis (median overall survival 5.1 months).

The primary aim of this project is to investigate whether laser therapy combined with CRT improves overall survival, without compromising quality of life, in comparison with CRT alone in patients with primary irresectable glioblastoma.

详细描述

RATIONALE: Glioblastoma (GBM) is the most common primary brain tumor with about 1000 new patients facing this diagnosis each year in the Netherlands alone. It is also one of the most devastating malignancies and due to relatively young age at presentation (median 59 years), GBMs are responsible for up to 7% of total life years lost from cancer before the age of 70. Despite many efforts, patients with glioblastoma face a poor prognosis, with 2-year survival less than 20%. Current standard of care includes maximal safe surgical resection followed by adjuvant chemoradiation therapy (CRT). Subtotal and gross total resection have been associated with significantly longer survival (median OS: 14.5-18.5 months; RR: 0.71-0.84) 6,7, but in 30% of patients surgery is not feasible. These patients miss the benefit of surgical resection and with CRT alone have a profoundly worse survival (median 5.1 months). Laser interstitial thermal therapy (LITT) is recently growing as a minimally invasive alternative to treat brain tumors. Multiple studies have shown the application of LITT in newly diagnosed and recurrent glioblastoma, in radiotherapy and chemotherapy resistant metastases or in tumors in difficult accessible locations, with promising initial results. A recent systematic review of current phase I/II studies in patients with newly diagnosed irresectable glioblastoma who received LITT yields a mean survival of 10.2 months, i.e. twice as long as with CRT alone (5.1 months). However, there is currently no high-quality prospective evidence directly comparing LITT with standard of care, precluding any conclusions on (cost-)effectiveness. After conducting a pilot study at Radboud University Medical Center to locally confirm safety and feasibility of LITT in patients with irresectable glioblastoma, we propose a prospective multicenter randomized controlled study to evaluate (cost-)effectiveness of this technique.

OBJECTIVE: The primary objective is to prove an improvement in survival without substantially compromising quality-of-life (QoL) in patients with primary irresectable glioblastoma (GBM) treated with LITT plus chemoradiation therapy (CRT) vs. CRT alone.

STUDY DESIGN: Prospective multicenter randomized controlled trial. Study population: Adult (>18 years old) patients with a radiologically suspected diagnosis of primary glioblastoma not amenable for surgical resection.

INTERVENTION: Patients will be randomized to receive either (i) biopsy and LITT, followed by standard CRT or (ii) biopsy alone, followed by standard CRT.

MAIN STUDY PARAMETERS/ENDPOINTS: The primary endpoints are overall survival (OS) and quality-of-life (QoL) using QLQ-C30+BN20 questionnaire 5 months after randomization.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Informed consent, age >18 years
  • Suspected glioblastoma
  • Supratentorial localization
  • Patient is not amendable for surgical resection as decided by the tumor board
  • Safe trajectory/trajectories possible for ablation of at least 70% of the tumor, avoiding eloquent structures
  • Karnofsky Performance Status (KPS) >=70

排除标准

  • Contra-indication for general anesthesia or MRI
  • Non-glioblastoma diagnosis on pathology analysis
  • No final pathology available
  • Pregnancy
  • Insufficient command of the Dutch language by the patient or a family member, making it impossible to fill in the questionnaires

结局指标

主要结局

Health Related Quality of Life (HR-QoL)

时间窗: At 5 months after randomization

QoL measured with the QLQ-C30BN20 at 5 months after randomization.

Overall survival

时间窗: Depending on which event occurs first: either when a study participant dies or at the end of the trial (61 months).

Percentage of patients still alive for a given period of time after randomization.

次要结局

  • Ablation rate(Using the MRI made right after LITT procedure)
  • Progression Free Survival (PFS)(During the entire study period, estimated 18 months for each patient)
  • Complication rate(During the entire study period, estimated 18 months for each patient)
  • Disease Specific Survival (DSS)(During the entire study period, estimated 18 months for each patient)
  • Costs(At 1, 2, 3, 4, 5, 6, 12, 18, 30, 42 and 54 months after randomization.)
  • Overall survival since intervention(During the entire study period, estimated 18 months for each patient)
  • Longitudinal effects(During the entire study period, estimated 18 months for each patient.)
  • Tumor volume response(Using the MRI made right after LITT procedure)
  • Effects of LITT on adjuvant treatment(During the entire study period, estimated 18 months for each patient)
  • General Quality of Life(At randomization, 72 hours after surgery, 1, 2, 3, 4, 5, 6, 12, 18, 30, 42 and 54 months after randomization.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (7)

Loading locations...

相似试验