Lenalidomide and Radiation in Glioblastoma and Gliosarcoma and Malignant Gliomas - Clinical Trials Registry

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Patients will receive lenalidomide orally once daily for 21 days followed by a one week rest period (this is equivalent to one cycle).
Four to seven days from the first dose of lenalidomide, the patient will start radiation therapy for approximately 6-7 weeks.
A neurologic exam and routine blood tests will be performed weekly while the patient is receiving radiation therapy.
Following the 11th week of treatment a MRI/CT scan will be performed to assess the status of the tumor. If there is no change, or there is shrinkage in the size of the tumor, the treatment will continue for another 4 week cycle.
The four week cycle will continue as long as the disease remains stable or improved and the patient does not develop intolerable side effects. A MRI/CT scan will be done every 2 cycles (8 weeks).

Study Type

Interventional

Enrollment (Actual)

23

Phase

Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

United States
- Massachusetts
  - Boston, Massachusetts, United States, 02115
    - Dana-Farber Cancer Institute
  - Boston, Massachusetts, United States, 02114
    - Massachusetts General Hospital
  - Boston, Massachusetts, United States, 02115
    - Beth Israel Deaconess Medical Center
- Virginia
  - Charlottesville, Virginia, United States, 22908-0394
    - University of Virginia

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Patients with histologically confirmed newly-diagnosed supratentorial glioblastoma multiforme (GBM) or gliosarcoma will be eligible for this protocol.
The patient must have recovered from the effects of surgery, post-operative infections and other complications before entry into the study.
Diagnosis will have been established by biopsy or resection no more than 28 days prior to registration.
If tumor resection or open biopsy was performed, cranial MRI or contrast CT must have been performed before and after surgery. Imaging within 96 h of surgery is preferred but not required.
If needle biopsy (stereotactic) was performed, gadolinium MRI or contrast CT within 14 days prior to registration is required. A post-operative scan is not required. The use of MRI rather than CT is preferred. The same type of scan, i.e., MRI or CT must be used throughout the period of protocol treatment for tumor measurement. Patients without measurable or assessable disease are eligible.
Patients receiving steroids must be on stable or decreasing doses for at least 5 days prior to entry.
Patients must have a plan to begin partial brain radiotherapy 4-7 days after beginning lenalidomide, and within 35 days of the surgical procedure that established the diagnosis.
Radiotherapy must be at the Radiation Oncology Department of the registered institution.
Patients must be willing to forego cytotoxic and non-cytotoxic drug therapy against the tumor while being treated with lenalidomide.
All patients must sign an informed consent indicating that they are aware of the investigational nature of this study.
Patients must be > 18 years old, and with a life expectancy > 8 weeks.
Patients must have a Karnofsky performance status of > 60.
Patients must have adequate bone marrow, liver, and renal function.
Patients must be willing and able to comply with all study requirements

Exclusion Criteria:

Patient must not have had prior cranial radiation therapy.
Patients must not have received prior cytotoxic drug therapy, non-cytotoxic drug therapy, or experimental drug therapy for brain tumors. Patients who received Gliadel wafers will be excluded.
Patients must not have any significant medical illnesses that in the investigator's opinion cannot be adequately controlled with appropriate therapy or would compromise the patients ability to tolerate this therapy.
Patients with a history of any other cancer (except non-melanoma skin cancer or carcinoma in situ of the cervix), unless in complete remission and off of all therapy for that disease for a minimum of 3 years are ineligible.
Patients must not have active infection.
Patients must not be pregnant/breast feeding and must agree to practice adequate contraception.
Patients must not have any disease that will obscure toxicity or dangerously alter drug metabolism.
Patients must not have serious concurrent medical illness.
Patient with recent thromboembolic disease (deep vein thrombosis and pulmonary embolism) are eligible if they are clinically stable and the thromboembolic event occurred more than 2 weeks prior to enrollment into this protocol.
Patients must not have metastases below the tentorium or beyond the cranial vault.
Patients must not have a known diagnosis of HIV, active infectious hepatitis, or chronic hepatitis.
Patients must have no history of hypersensitivity or development of a desquamating rash while on thalidomide.
Patients must have no prior exposure to lenalidomide.
Previous or planned stereotactic radiosurgery or brachytherapy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Primary Purpose: Treatment
Allocation: Non-Randomized
Interventional Model: Single Group Assignment
Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
To determine the efficacy of lenalidomide with conventional radiation therapy in the treatment of patients with newly-diagnosed supratentorial glioblastoma or gliosarcoma. Time Frame: 3 years	3 years

Secondary Outcome Measures

Outcome Measure	Time Frame
To assess the proportion of patients treated with lenalidomide and radiation therapy surviving at 12 months Time Frame: 3 years	3 years
to evaluate the time to tumor progression Time Frame: 3 years	3 years
the radiologic response Time Frame: 3 years	3 years
to determine the safety and toxicity of the combination of lenalidomide and radiation therapy. Time Frame: 3 years	3 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Dana-Farber Cancer Institute

Collaborators

Massachusetts General Hospital

Beth Israel Deaconess Medical Center

Brigham and Women's Hospital

Celgene Corporation

University of Virginia

Investigators

Principal Investigator: Patrick Y. Wen, MD, Dana-Farber Cancer Institute

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2005

Primary Completion (Actual)

November 1, 2007

Study Completion (Actual)

July 1, 2009

Study Registration Dates

First Submitted

September 9, 2005

First Submitted That Met QC Criteria