Focused Ultrasound Blood-Brain Barrier Opening in Pontine Diffuse Midline Glioma to Enhance Temozolomide Therapy: Pilot Feasibility Study (FIDES) (FIDES)
Focused Ultrasound-mediated Blood-Brain Barrier Opening In Pontine Diffuse Midline Glioma (DMG) to Enhance Systemic Therapy With Temozolomide (FIDES) - an Exploratory Pilot and Feasibility Trial
This study is for people (children and adults) with a rare and aggressive brain tumor called H3K27-altered diffuse midline glioma (DMG) located in the pons, a deep part of the brainstem. These tumors are very difficult to treat because they grow into surrounding brain tissue and cannot be fully removed with surgery. Most patients currently survive less than one year after diagnosis, and treatment options are limited.
Current standard treatment The usual treatment is radiotherapy, sometimes combined with a chemotherapy drug called temozolomide (TMZ). This combination may slightly improve outcomes, but it is often not very effective for tumors in the pons. One possible reason is that the blood-brain barrier (BBB)-a natural protective filter in the brain-may be especially strong in this area, making it harder for medicines to reach the tumor.
What this study is testing This study is exploring a new approach to help chemotherapy reach the tumor more effectively. It uses MRI-guided focused ultrasound (with the Exablate system) to temporarily and safely open the blood-brain barrier in the tumor area. This may allow more temozolomide to enter the tumor.
Study goal
The main goal is to find out:
- Whether this technique is safe
- Whether it may help slow tumor growth or extend survival
Who can join
- Adults and children aged 4 years and older
- Diagnosed with H3K27-altered pontine DMG
- Eligible for temozolomide after completing radiation therapy
The study will include 20 participants (about half children and half adults).
What participants will do
Participants will:
- Receive 6 cycles of temozolomide chemotherapy
- Undergo focused ultrasound blood-brain barrier opening on the first day of each cycle
- Have regular MRI scans and check-ups to monitor safety and tumor response
Each treatment cycle includes 5 days of chemotherapy followed by a rest period of 23 days.
What the study is measuring
Researchers will look at:
- Safety of the procedure and device
- How long patients live without tumor progression (progression-free survival)
- Overall survival
- Tumor response to treatment
- Whether the procedure is practical to use in clinical care
They will also compare results to data from previous patients in international brain tumor registries.
Why this study matters This study is testing whether temporarily opening the brain's natural barrier can help chemotherapy work better in a type of brain tumor that currently has very limited treatment options.
調査の概要
状態
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究場所
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-
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Utrecht、オランダ、3584 CX
- UMC Utrecht
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コンタクト:
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コンタクト:
- Tom J. Snijders, MD, PhD
- 電話番号:+31 88 75 679 95
- メール:fides@umcutrecht.nl
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主任研究者:
- Tom J. Snijders, MD, PhD
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Utrecht、オランダ、3584 CS
- Princess Maxima Center for Pediatric Oncology
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コンタクト:
- Dannis G. van Vuurden, MD, PhD
- 電話番号:+31 88 972 9736
- メール:secretariaatneuro-onco@prinsesmaximacentrum.nl
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コンタクト:
-
主任研究者:
- Dannis G. van Vuurden, MD, PhD
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参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Age ≥ 4 years.
- Histologically/molecularly verified de novo pontine H3K27-altered diffuse midline glioma.
- Main localization ('center of mass') in the brainstem. NB: some degree of extension beyond the brainstem, e.g. cerebellar peduncles, is allowed.
- Karnofsky Performance Score (KPS) or Lansky Performance Score (LPS) of ≥ 70/ KPS or LPS 60 and WHO/ECOG performance status ≤ 2.
- ASA-score of I-III.
- Intention to treat with (TMZ chemo-) radiation and maintenance TMZ as per consensus of the local multidisciplinary tumor board.
- Feasible to schedule the first Exablate BBBO procedure preferably within 4-6 weeks, acceptably within 12 weeks, after successful completion of radiotherapy/ concomitant TMZ-chemoradiation, defined as completed treatment as planned without reported CTCAEv6.0 grade 3-4 toxicities or, in case of reported CTCAEv6.0 grade 3-4 toxicities, the toxicities must be resolved to grade 2 prior to inclusion.
- If on steroids, stable or decreasing dose for at least 7 days prior to inclusion.
- Able to attend all study visits.
- Able and willing to give informed consent or have a legal guardian who is able and willing to do so.
Exclusion Criteria:
- Previous or ongoing participation in other clinical trials with other than standard-of-care tumor-directed treatment(s) for H3K27-altered DMG.
- Multifocal or leptomeningeal metastasized disease. Multifocal disease is defined as multiple FLAIR-hyperintense lesions, separated by normal-appearing brain tissue, with or without gadolinium enhancement. Multiple enhancing regions within one continuous FLAIR lesion can be considered as unifocal disease.
- Signs/symptoms of elevated intracranial pressure (ICP) (e.g. headache, vomiting, impaired vision/papilledema, impaired consciousness), with corresponding radiographic findings on MRI at time of screening.
- Severe dysphagia with feeding tube dependency.
- Evidence of acute clinically significant intracranial hemorrhage. NB: minimal hemorrhagic foci without obvious related clinical symptoms will not serve as grounds for exclusion.
- Tumor not visible on any pre-therapy or post-radiation imaging.
- Presence of extracranial / intracranial structures (e.g. metal prostheses, implants, calcifications) on pre-treatment CT-scan/ MRI-scan, significantly interfering with acoustic impedance as per judgement of the researchers.
- Known co-occurring other malignancy that is progressing or has required active treatment within the past 3 years, with exception of: carcinomas in situ (CIS) and non-melanoma skin cancers.
- Patients with right-to-left, bi-directional or transient right-to-left cardiac shunts.
- Known LVEF < 40 or unstable hemodynamics.
- Severe hypertension, not adequately controlled with study compatible medication (Adults: RR systolic >180 and/ or RR diastolic >100; Children: >p95 + 12mmHg).
- History of bleeding disorder and/or coagulopathy.
- Treatment with anti-coagulant therapy.
- Severely impaired renal function; creatinine clearance <30 mL/ min.
- Subjects with significant liver dysfunction; Child Pugh classification C.
- Known diagnosis of active or untreated hepatitis B, hepatitis C, tuberculosis.
- Any other illness or medical condition that in the investigator's opinion precludes participation in this study.
- Pregnant or lactating women.
- Expected uncontrollable therapy non-compliance/ non-cooperation that is likely to interfere with the study procedure, as per judgement of the investigators.
- Head circumference ≤ 49 cm.
- Weight ≥ 135 kg.
- Patient ≥ 18 years old, who requires general anesthesia to undergo the Exablate BBBO procedure.
- Contra-indication for MRI procedures.
- Known sensitivity to gadolinium-based contrast agents.
- Known sensitivity to the resonator agent (perflutren; Luminity®).
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:FUS-BBBO-mediated delivery of temozolomide
The Exablate Model 4000 Type 2 system is used to induce localized and temporary blood-brain barrier opening in adult and pediatric patients with H3K27-altered pontine DMG undergoing standard of care temozolomide chemotherapy.
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FUS-BBB opening involves the application of acoustic energy at low frequencies from over 1000 individual transducers to induce localized and temporary blood-brain barrier disruption in patients.
FUS-BBBO will be applied during each temozolomide cycle.
他の名前:
Patients will undergo six standard-of-care cycles of temozolomide maintenance therapy.
Each cycle will be combined with FUS-BBBO.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Device and procedure related adverse events
時間枠:Up to 72 hours after each Exablate BBBO procedure
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The number and severity of device and Exablate BBBO procedure related adverse events (CTCAE version 6.0), will be assessed based on radiographical and clinical parameters.
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Up to 72 hours after each Exablate BBBO procedure
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6-month progression-free survival (PFS6)
時間枠:From date of diagnosis until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months.
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Proportion of patients alive and progression-free at 6 months, based on standardized imaging criteria (e.g., RANO or RAPNO for DMG).
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From date of diagnosis until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months.
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協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- UMC_Utrecht
- 2025-520814-78-00 (Ctis)
- NL-009201 (その他の識別子:CCMO)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
IPD 共有時間枠
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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