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Completed

NCT Number: NCT00639262

Combination of Sorafenib and Radiation for Brain Metastases and Primary Brain Tumors

Sorafenib™ has the potential to inhibit tumor growth, tumor angiogenesis , and enhance radiation response. This study will test the combination of Sorafenib™ and radiation therapy with or without temozolomide to determine tolerance of the combined treatments. Defining safe dosing of Sorafenib™ in this combination therapy will be achieved.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Thomas Jefferson University

Philadelphia, Pennsylvania, 19107, United States

About this study

The current standard of care for patients with brain metastatic malignancies is to receive radiation therapy alone, while the standard of care for patients with high grade primary brain malignancies, astrocytomas, is to receive to receive concurrent temozolomide with radiation therapy. In this phase I study, based on the range of efficacy of kinase inhibitors and its ability to cross the blood-brain barrier we will conduct two parallel studies. The first is to combine sorafenib and radiation therapy for the treatment of patients with brain metastases and the second is to combine sorafenib with temozolomide for primary brain tumors.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients requiring a minimum 2-week course of radiation therapy
  • Age > or = 18
  • All tumors of the central nervous system, or metastasis to the central nervous system.
  • Measurable disease preferred but not required for eligibility
  • Histologically or cytologically documented evidence of malignancy (for infratentorial and supratentorial glioma patients only).
  • Radiographic evidence of brain metastasis
  • ECOG performance status of 0 or 1
  • Life expectancy of > or = 3 months

Exclusion criteria

  • Patients receiving chemotherapy or other investigational drugs must be discontinued 14 days prior to enrollment.
  • Cardiac disease: Congestive heart failure > class II NYHA. Patients must not have unstable angina (anginal symptoms at rest) or new onset angina (began within the last 3 months) or myocardial infarction within the past 6 months.
  • Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.
  • Uncontrolled hypertension defined as systolic blood pressure > 150 mmHg or diastolic pressure > 90 mmHg, despite optimal medical management.
  • Known human immunodeficiency virus (HIV) infection or chronic Hepatitis B or C.
  • Active clinically serious infection > CTCAE Grade 2

Treatment and study plan

Sorafenib

Drug

Sorafenib 200mg twice daily during XRT and 30 days after. (Sorafenib will be escalated for both cohorts to determine maximum tolerated dose)

Other names: Nexavar

Temozolomide

Drug

For Cohort 2 - Gliomas only.

Other names: Temodar, Temodal

Radiotherapy

Radiation

Radiation Therapy (XRT)

Other names: XRT, Radiation therapy, radiation oncology

Primary outcomes

  1. Maximum Tolerated Dose of Sorafenib

    Time frame: 30 days post-treatment

    To determine the maximum tolerated dose (MTD) and a recommended phase II dose (RP2D) of Sorafenib and radiotherapy -/+ temozolomide patients with malignancies of the brain.

Secondary outcomes

  1. Response Rate

    Time frame: 30 days post-treatment

    Response rate (in those patients with measurable disease)

  2. Prediction of 1-year Recurrence

    Time frame: 1 year post-treatment

    Determine if an increase in urinary VEGF and MMP levels, from the end of treatment to a patient's 1-month follow-up examination, is predictive of 1-year recurrence

  3. Safety and Toxicity of Sorafenib

    Time frame: 30 days post-treatment

    To evaluate the safety and toxicity profile of Sorafenib in combination with radiation therapy -/+ temozolomide

Sponsors and collaborators

Lead sponsor

Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University

Other

Collaborators

  • Bayer

Registry information

Official study title

Phase I Study of the Combination of Sorafenib and Radiation Therapy -/+ Temozolomide for the Treatment of Patients With Brain Metastases and Primary Brain Tumors

Important dates

Study start
2008
Primary completion
2012
Study completion
2012
First posted
Mar 20, 2008
Registry last updated
May 2, 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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