Bosutinib in Adult Patients With Recurrent Glioblastoma

Brief Summary

Official Title: “An Open Label, Phase 2 Trial of Orally Administered Bosutinib (SKI-606) in Adult Patients With Recurrent Glioblastoma (GBM)”

For many brain tumors, one reason that chemotherapy drugs might not be effective is that the drug may not be able to get into the brain tumor and kill the cancer cells. The brain is protected by a layer called the blood brain barrier. This barrier prevents substances from entering. The purpose of this research study is to determine if bosutinib can get past the blood brain barrier and into the brain tumor, and to see how well bosutinib works in killing cancer cells.

  • Study Type: Interventional
  • Study Design: Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
  • Study Primary Completion Date: March 2014

Detailed Clinical Trial Description

- Arm A: Participants will receive daily doses of bosutinib orally for 7-9 days prior to surgery. On the day of the scheduled surgery (either craniotomy or surgical resection as planned by the treating doctor), participants will take the bosutinib within 6-12 hours of the surgery. During the surgery, tissue samples of the tumor will be collected to test the levels of bosutinib in the brain. A contrast-enhanced MRI or CT scan will be done within days after the surgery. Daily dosing of bosutinib will resume after a recovery period of 10 days. From then on, the study will be divided into 28-day cycles.

The following tests/procedures will be performed regularly during cycles of study treatment: medical history; physical exam; blood tests; contrast-enhanced CT or MRI scans (even numbered cycles only).

- Arm B: Participants will receive daily doses of bosutinib. The study is divided int 28-day cycles. There are no breaks from taking bosutinib between treatment cycles. The following tests/procedures will be performed regularly during cycles of study treatment: medical history; physical exam; blood tests; contrast-enhanced CT or MRI scans (even numbered cycles only).

- Participants may continue to receive daily bosutinib until their disease worsens, they experience unmanageable side-effects, or they decide to stop treatment.

Interventions Used in this Clinical Trial

  • Drug: bosutinib
    • Taken orally

Arms, Groups and Cohorts in this Clinical Trial

  • Experimental: Arm A
    • Patients who are surgical candidates
  • Experimental: Arm B
    • Patients that are not surgical candidates

Outcome Measures for this Clinical Trial

Primary Measures

  • Progression-Free Survival
    • Time Frame: 2 years
      Safety Issue?: No

Secondary Measures

  • Intratumoral Concentration
    • Time Frame: 2 years
      Safety Issue?: No
  • Safety Profile
    • Time Frame: 2 years
      Safety Issue?: Yes
  • Anti-tumor response
    • Time Frame: 2 years
      Safety Issue?: No

Criteria for Participation in this Clinical Trial

Inclusion Criteria

  • 18 years of age or older
  • Histologically confirmed WHO grade IV astrocytoma (glioblastoma). Patients with recurrent disease whose original pathology confirmed glioblastoma will not need re-biopsy. Patients with prior low-grade glioma or anaplastic glioma are eligible if histological assessment demonstrates transformation to GBM.
  • The first-line regimen must have included, at a minimum, temozolomide and radiation.
  • First or second episode of progressive disease.
  • No more than two prior treatment regimens for progressive disease. Concurrent temozolomide and radiation followed by monthly cycles of temozolomide is counted as one regimen.
  • For all study arms, patients must have at least 15 unstained slides or 1 tissue block available from a prior biopsy or surgery.
  • All patients must have progressive disease on contrast-enhanced brain CT or MRI as defined by MacDonald Criteria, or have documented recurrent glioblastoma on diagnostic biopsy. Arm A patients may continue treatment in the post-operative period even if there is no residual contrast-enhancing tumor after surgery.
  • For Arm A, patients must be candidates for surgical partial or gross-total resection.
  • Interval of at least 2 weeks between prior surgical resection and adequate wound healing.
  • Interval of at least 12 weeks from prior radiotherapy unless there is either a) histopathologic confirmation of recurrent tumor; b) new enhancement on MRI outside of the XRT treatment field.
  • Patients must have sufficient time for recovery from prior therapy
  • Karnofsky Performance Status of 60% or greater
  • Laboratory levels as outlined in the protocol
  • Women of child-bearing potential and men must agree to use adequate contraception prior to study entry, for the duration of study participation and for 3 months thereafter.

Exclusion Criteria

  • Participants may not be receiving any other investigational agents
  • Previously treated with an anti-VEGF agent
  • For subjects in Arm A: if the diagnostic pathology of the biopsy specimen is not consistent with recurrent glioblastoma then the subject will be taken off study and be replaced with another subject that meets the inclusion criteria and is eligible for surgical resection
  • Any surgery within 2 weeks of baseline disease assessments, or not fully recovered from any side effects of previous procedures
  • Any clinically significant gastrointestinal abnormalities, which may impair intake, transit or absorption of the study drug, such as the inability to take oral medications in tablet form.
  • Any psychiatric or cognitive disorder that would limit the understanding or rendering of informed consent and/or compromise compliance with the requirements of this protocol
  • Concomitant use of CYP3A4/5 inhibitors during the treatment phase of the study and within 72 hours prior to starting study drug administration
  • Concomitant use of CYP3A4/5 inducers, which include enzyme inducing antiepileptic drugs during treatment phase of the study and within 2 weeks prior to starting treatment.
  • Uncontrolled or significant cardiovascular disease
  • Prior stereotactic radiotherapy, convection enhanced delivery or brachytherapy as gliosis/scarring from these modalities may limit delivery
  • Pregnant or breast feeding women
  • HIV-positive individuals on combination antiretroviral therapy
  • Other severe acute or chronic medical condition or laboratory abnormality

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial: No

Clinical Trial Investigator Information

  • Lead Sponsor
    • Massachusetts General Hospital
  • Collaborator
    • Dana-Farber Cancer Institute
  • Provider of Information About this Clinical Study
    • Principal Investigator: Tracy T. Batchelor, MD, Principal Investigator – Massachusetts General Hospital
  • Overall Official(s)
    • Tracy Batchelor, MD, Principal Investigator, Massachusetts General Hospital
  • Overall Contact(s)
    • Tracy Batchelor, MD, 617-643-1938, tbatchelor@partners.org

Source

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The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT01331291