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NCT Number: NCT07193654

Stupp Treatment With Intrathecal Injection of Thiotepa for Glioblastoma With Advanced Spread

The goal of this clinical trial is to learn if a combined treatment approach can treat glioblastoma (GBM) with ventricular invasion or meningeal metastasis in adults. The main questions it aims to answer are:

Does the combined treatment of radical radiotherapy, the Stupp regimen (oral temozolomide), and intrathecal injection of thiotepa improve progression-free survival compared to standard treatment alone?

Does the combined treatment improve overall survival compared to standard treatment alone?

Participants will:

* Undergo maximal surgical resection of the tumor; * Receive radical radiotherapy; * Take oral temozolomide according to the Stupp regimen; * Receive intrathecal injections of thiotepa。

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

2nd Affiliated Hospital, School of Medicine

Hangzhou, Zhejiang, 310000, China

Location status: Recruiting

Location contact

Ting Zhang phD

CONTACT

[email protected]

+86571-87783521

phD

CONTACT

About this study

Glioblastoma (GBM) is the most common and aggressive primary malignant brain tumor in adults, with a dismal prognosis despite standard treatment. The standard treatment for GBM, which includes surgery, radiotherapy, and chemotherapy with temozolomide (known as the Stupp regimen), has remained largely unchanged for over two decades. Patients with GBM who have tumor invasion of the brain ventricles or meningeal metastasis face an even worse prognosis, with significantly shorter progression-free survival and overall survival compared to patients without these complications. The blood-brain barrier poses a significant challenge to effective chemotherapy delivery, limiting the efficacy of systemic treatments for central nervous system tumors. Intrathecal chemotherapy administration represents a promising strategy to overcome this barrier by directly delivering chemotherapeutic agents into the cerebrospinal fluid, potentially improving tumor control and survival outcomes in patients at high risk for intraventricular dissemination.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18 - 75, any gender.
  • Newly diagnosed WHO grade 4 brain tumor with at least one evaluable lesion, imaging suggesting ventricular or meningeal invasion.
  • History of intraoperative intraventricular or cisternal opening.
  • Malignant cells found in cerebrospinal fluid pre-radiotherapy.
  • ECOG score 0 - 2, expected survival≥3 months.
  • Stable neurological symptoms for over 7 days.
  • Neutrophil count≥1.5×10⁹/L, hemoglobin≥90 g/L, platelet count≥75×10⁹/L.
  • PT/INR and PTT≤1.5×upper limit of normal.
  • Total bilirubin≤1.5×upper limit of normal, AST and ALT≤1.5×upper limit of normal, albumin≥30 g/L, creatinine≤2×upper limit of normal, calculated or 24-hour urine creatinine clearance rate≥50 mL/min.
  • Agree to effective contraception from first to 3 months after last dose.

Exclusion criteria

  • Pregnant or breastfeeding women.
  • Active infection within 7 days before starting study drug requiring IV antibiotics or therapeutic warfarin.
  • Other malignancies in past 5 years.
  • HIV/AIDS history; past immunodeficiency, or active autoimmune disease needing systemic treatment.
  • Severe medical, neurological, or psychiatric conditions preventing full adherence to study treatment or assessments.
  • Ventricular drainage tube rupture or inability to undergo lumbar puncture.
  • Uncontrolled chronic diseases like diabetes, CHF, liver cirrhosis, or CKD.

Treatment and study plan

Intrathecal injection of thiotepa

Drug

Intrathecal injection of thiotepa: Administered via lumbar puncture or OMMAYA reservoir according to the study protocol.

Stupp regimen (oral temozolomide)

Drug

Stupp regimen (oral temozolomide)::75 mg/m² daily during radiotherapy; 150-200 mg/m² daily for 5 days every 28 days for 6 cycles after radiotherapy;

Radical radiotherapy

Radiation

Radical radiotherapy: Delivery of 60 Gy of radiation, typically divided into 30 fractions of 2 Gy each;

Maximal surgical resection

Procedure

Maximal surgical resection: Removal of as much tumor as possible while preserving neurological function;

Primary outcomes

  1. Safety assessment

    Time frame: From first dose of study treatment until 30 days after last dose, assessed up to 52 weeks.

    Incidence and severity of treatment-related adverse events using CTCAE 5.0.

Secondary outcomes

  1. Progression-free survival

    Time frame: 3 months,6 months and 1 year after treatment

    Time from treatment initiation until disease progression( RECIST1.1 )

  2. Overall survival

    Time frame: Until date of death from any cause, assessed up to 24 months.

    Time from treatment initiation until death

Study contacts

Contact information is provided by the study sponsor or research team.

Ting Zhang, phD.

CONTACT

[email protected]

+86-571-87783521

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Other

Registry information

Official study title

Stupp Regimen Combined With Intrathecal Injection of Thiotepa for the Treatment of Glioblastoma With Ventricular Invasion or Meningeal Metastasis:a Prospective, Single-Arm, Exploratory Study

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Sep 26, 2025
Registry last updated
Sep 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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