CCI-779 in Treating Patients With Recurrent Glioblastoma Multiforme

National Cancer Institute (NCI)

Status and phase: Completed; Phase 2

Conditions: Recurrent Adult Brain Tumor; Adult Glioblastoma; Adult Giant Cell Glioblastoma; Adult Gliosarcoma

Treatments: Other: laboratory biomarker analysis; Drug: temsirolimus; Other: pharmacological study

Study type: Interventional

Funder types: NIH

Identifiers

NCT00016328

NCCTG-N997B

NCI-2012-01858

CDR0000068623

N997B

U10CA025224 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Phase II trial to study the effectiveness of CCI-779 in treating patients who have recurrent glioblastoma multiforme. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

Full description

OBJECTIVES:

I. Determine the efficacy of CCI-779, in terms of the percentage of patients who are progression-free at 6 months, time to progression, and time to death, in patients with recurrent glioblastoma multiforme.

II. Determine the toxic effects of this drug in these patients. III. Correlate molecular alterations in the tumors of these patients with response to treatment with this drug.

OUTLINE: This is a multicenter study. Patients are stratified according to concurrent P450 anticonvulsant use (yes vs no).

Patients receive CCI-779 IV over 30 minutes once weekly for 4 weeks. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.

Patients are followed every 6 months for 5 years and then annually for up to 10 years.

PROJECTED ACCRUAL: A total of 63 patients will be accrued for this study within 39 months.

Enrollment: 33 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologically confirmed grade 4 astrocytoma at primary diagnosis or recurrence

  • Gliosarcoma allowed

• Evidence of tumor progression by MRI or CT scan after radiotherapy or first-line chemotherapy

• Measurable or evaluable disease by MRI or CT scan

• Performance status - ECOG 0-2

• Absolute neutrophil count at least 1,500/mm^3

• Platelet count at least 100,000/mm^3

• Hemoglobin at least 9 g/dL

• Bilirubin no greater than 1.5 mg/dL

• SGOT no greater than 3 times upper limit of normal

• Creatinine no greater than 2.0 mg/dL

• No myocardial infarction within the past 6 months

• No congestive heart failure requiring ongoing maintenance therapy for life-threatening ventricular arrhythmias

• Cholesterol no greater than 350 mg/dL

• Triglycerides no greater than 400 mg/dL

• Willing to provide correlative laboratory samples

• No uncontrolled infection

• No known hypersensitivity to any components of CCI-779, diphenhydramine hydrochloride, or other similar antihistamines

• No other medical reason that would preclude diphenhydramine premedication

• No other active malignancy

• No other severe disease that would preclude study participation

• Not immunocompromised unless due to corticosteroids

• HIV negative

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• See Disease Characteristics

• Prior adjuvant chemotherapy allowed

• More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas)

• No more than 1 prior chemotherapy regimen for recurrent/progressive disease

• No prior polifeprosan 20 with carmustine implant (Gliadel)

• Must be on fixed dose of corticosteroids (or no corticosteroids) at least 1 week prior to baseline scan

• See Disease Characteristics

• At least 12 weeks since prior radiotherapy

• No prior stereotactic radiosurgery or interstitial brachytherapy unless there is a separate lesion on MRI that is outside of the previously treated field

• No prior resection since last chemotherapy or radiotherapy unless there is unequivocal tumor growth on neuro-imaging study since surgery or there is a separate lesion not present in the surgical bed

• More than 4 weeks since prior investigational agents

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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33 participants in 1 patient group

Treatment (temsirolimus)

Experimental group

Description:

Patients receive CCI-779 IV over 30 minutes once weekly for 4 weeks. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.

Treatment:

Other: pharmacological study

Drug: temsirolimus

Other: laboratory biomarker analysis