Everolimus and Whole-Brain Radiation Therapy in Treating Patients With Brain Metastasis From Non-Small Cell Lung Cancer

NCT ID: NCT00892801

Last Updated: 2012-03-12

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 5 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-05-31
• Study Completion Date: 2011-02-28

Brief Summary

RATIONALE: Everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving everolimus together with whole-brain radiation therapy may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects and best dose of everolimus and to see how well it works when given together with whole-brain radiation therapy in treating patients with brain metastasis from non-small cell lung cancer.

Detailed Description

Phase I is intended to determine the maximum tolerated dose. Study drug will be administered orally, once a day, for 15 days, one day prior to initiation of WBRT at 5 or 10 mg/day during the phase I component. One of these doses will be selected as the maximum tolerable dose and will be selected for the phase II component.

OBJECTIVES:

Primary

• To determine the maximum-tolerated dose of everolimus when combined concurrently with whole-brain radiotherapy in patients with brain metastasis from stage IV non-small cell lung cancer. (Phase I)
• To evaluate the median survival of these patients treated with this regimen. (Phase II)

Secondary

• To assess the response rates in these patients. (Phase II)
• To assess the safety and tolerability of this regimen in these patients. (Phase II)
• To determine time to CNS (neurological) progression, confirmed by MRI, in these patients. (Phase II)
• To determine time to systemic (non-CNS) progression in these patients. (Phase II)

OUTLINE: This is a multicenter, dose-escalation study of everolimus.

Patients undergo 10 fractions of whole-brain radiotherapy (WBRT) beginning on day 0, 5 days per week, and receive oral everolimus once daily on days -1 to 13. Beginning 2 weeks after completion of WBRT, patients receive oral everolimus once daily for 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 2 months for 2 years.

Conditions

Lung Cancer; Metastatic Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment

RAD001 + radiation therapy

Group Type: EXPERIMENTAL

RAD001

Intervention Type: DRUG

Taken by mouth once a day, for 15 days, one day prior to initiation of whole brain radiation therapy at 5 or 10 mg/day during the phase I component. One of these doses will be selected as the maximum tolerable dose and will be selected for the phase II component

whole-brain radiation therapy

Intervention Type: RADIATION

Standard whole brain radiation therapy (WBRT) 30 Gy will be given in ten fractions.

Interventions

RAD001

Taken by mouth once a day, for 15 days, one day prior to initiation of whole brain radiation therapy at 5 or 10 mg/day during the phase I component. One of these doses will be selected as the maximum tolerable dose and will be selected for the phase II component

Intervention Type: DRUG

whole-brain radiation therapy

Standard whole brain radiation therapy (WBRT) 30 Gy will be given in ten fractions.

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Radiographically confirmed brain metastases with histopathologically confirmed primary non-small cell lung cancer that will benefit from whole-brain radiotherapy
• Must have ≥ 1 measurable intracranial site of disease, according to RECIST criteria, that has not been previously treated with stereotactic radiation
• Must have stable extracranial disease for 4 weeks

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2
• Life expectancy ≥ 12 weeks
• ANC > 1,500/mm³
• Platelets > 100,000/mm³
• Hemoglobin > 11 g
• BUN ≤ 25 mg
• Serum creatinine < 1.5 times upper limit of normal (ULN)
• Serum bilirubin ≤ 1.5 times ULN
• Serum transaminases ≤ 2 times ULN (< 5 times ULN if patient has liver metastases)
• Cholesterol ≤ 300 mg/dL
• Triglycerides ≤ 2.5 times ULN
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception during and for ≥ 3 months after completion of study treatment
• No other malignancies within the past 3 years, except for adequately treated carcinoma in situ of the cervix or basal or squamous cell carcinomas of the skin
• No severe and/or uncontrolled medical conditions or other conditions that could affect participation in the study, including any of the following:

• Unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction within the past 6 months, or serious uncontrolled cardiac arrhythmia
• Severely impaired lung function (i.e., FEV1 < 0.8 cc)
• Uncontrolled diabetes as defined by fasting serum glucose ≥ 1.5 times ULN
• Any active (acute or chronic) or uncontrolled infection/disorders
• Non-malignant medical illnesses that are uncontrolled or whose control may be jeopardized by the treatment with the study therapy
• Liver disease, such as cirrhosis, chronic active hepatitis, or chronic persistent hepatitis
• No known history of HIV seropositivity
• No impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of everolimus (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection)
• No active, bleeding diathesis
• No known hypersensitivity to everolimus or other rapamycin (i.e., sirolimus, temsirolimus) or to its excipients
• No history of noncompliance to medical regimens

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• Recovered from the acute toxicities of any prior therapy
• Prior surgical resection of a brain metastasis allowed

• The extent of surgical resection in patients having prior resection of 1 of multiple metastases shall be documented as a biopsy, subtotal resection, or total resection as described by the operative report and/or post-operative imaging
• At least 3 weeks since prior major surgery or completion of extracranial radiation
• At least 3 weeks since prior and no concurrent systemic anticancer therapy, other than the study medications administered as part of this study protocol
• At least 6 weeks since prior nitrosoureas
• More than 1 week since prior and no concurrent immunization with attenuated live vaccines
• More than 3 weeks since prior chemotherapy
• No prior brain radiotherapy of any form
• No concurrent chronic treatment with systemic steroids or other immunosuppressive agents, except steroids for neurological stability following the diagnosis of brain metastases
• No prior treatment with an mTOR inhibitor
• No concurrent anti-vitamin K medication, except low dose coumarin
• No concurrent drugs or substances known to be inhibitors or inducers of the isoenzyme CYP3A
• No other concurrent investigational therapy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Vanderbilt-Ingram Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Vicki Keedy, MD

Medical Director, Vanderbilt-Ingram Cancer Center, Clinical Trials Shared Resource; Assistant Professor, Medical Oncologist

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Vicki Keedy, MD

Role: PRINCIPAL_INVESTIGATOR

Vanderbilt-Ingram Cancer Center

Locations

Vanderbilt-Ingram Cancer Center - Cool Springs

Nashville, Tennessee, United States

Vanderbilt-Ingram Cancer Center

Nashville, Tennessee, United States

Countries

United States

Other Identifiers

P30CA068485

Identifier Type: NIH

Identifier Source: secondary_id

View Link

VU-VICC-THO-0772

Identifier Type: -

Identifier Source: secondary_id

IRB#090314

Identifier Type: -

Identifier Source: secondary_id

VICC THO 0772

Identifier Type: -

Identifier Source: org_study_id