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Radiosurgery guided by a special scan added to Tumor Treating Fields for recurrent glioblastoma

Compares Tumor Treating Fields with or without targeted radiosurgery in adults with recurrent glioblastoma.

Plain-language title generated from the registry record
Registry title: TTFields Plus FET-PET-Guided Stereotactic Radiosurgery Versus TTFields Alone for Recurrent Glioblastoma (Tarrget 2.0)

Key facts

Where
Bydgoszcz, PolandSee the site

Where in Poland

  • Department of Neurooncology and Radiosurgery, Franciszek Lukaszczyk Oncology CenterBydgoszcz, PolandTaking people

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Trial details

Who runs it
Prof. Franciszek Lukaszczyk Memorial Oncology Center
Trial code
NCT07668869
Record updated
25 June 2026
Original description
This study evaluates whether the addition of FET-PET-guided stereotactic radiosurgery (SRS) to Tumor Treating Fields (TTFields) improves survival outcomes in patients with recurrent IDH-wildtype glioblastoma.Read full original descriptionShow less

Tumor Treating Fields (TTFields) Concomitant With Stereotactic Radiosurgery Based on FET-PET vs TTFields Alone for the Treatment of Recurrent, Glioblastoma (Tarrget 2.0)

This study evaluates whether the addition of FET-PET-guided stereotactic radiosurgery (SRS) to Tumor Treating Fields (TTFields) improves survival outcomes in patients with recurrent IDH-wildtype glioblastoma.

Patients with recurrent glioblastoma have limited treatment options and poor prognosis. TTFields is a non-invasive antimitotic therapy that has demonstrated efficacy in recurrent glioblastoma. Stereotactic radiosurgery is commonly used in selected patients with recurrent disease; however, treatment efficacy may be limited by the infiltrative nature of glioblastoma and challenges in accurate target delineation.

The study hypothesizes that combining TTFields with FET-PET-guided stereotactic radiosurgery will improve one-year overall survival compared with TTFields alone. Participants will be randomized in a 1:1 ratio to receive either TTFields plus stereotactic radiosurgery or TTFields alone.

Inclusion: Age ≥18 years; Karnofsky Performance Status ≥70; Histologically confirmed IDH-wildtype glioblastoma; First, second, or third recurrence; Radiological recurrence according to RANO 2.0 criteria; Prior radiotherapy and temozolomide treatment; At least 6 months since completion of previous radiotherapy; Contrast-enhancing recurrent lesion visible on MRI; Maximum recurrent lesion diameter ≤5 cm; Available molecular profile including IDH and MGMT status; Adequate hematologic, renal, and hepatic function; Written informed consent.

Exclusion: Previous bevacizumab treatment; Planned chemotherapy or targeted therapy after study intervention; Previous stereotactic re-irradiation within the planned treatment field; Significant psychiatric disorders; Significant unrelated neurological disease; Active intracranial hemorrhage; Uncontrolled hypertension; More than three recurrences; Implanted pacemaker, defibrillator, deep brain stimulator, or other incompatible electronic device; Pregnancy or breastfeeding; Severe renal dysfunction; Participation in another interventional study likely to interfere with this study.

ClinicalTrials.gov NCT07668869