Lenalidomide and Radiation Therapy in High Grade Gliomas or Diffuse Intrinsic Pontine Gliomas

Inclusion Criteria

• •ELIGIBILITY CRITERIA:
• •Histological diagnosis:
• •Histological confirmation of a high-grade malignant glioma is required. Histologic diagnoses include, but are not limited to, anaplastic astrocytoma and glioblastoma multiforme. Patients with DIPG are exempt from histologic verification if they have typical MRI findings of DIPG (i.e. hypo- or isointense on T1-weighted imaging, hyperintense on FLAIR or T2-weighted imaging, epicenter in the pons, greater than 50% of pons involved) in the face of a typical clinical presentation.
• •Inoperable tumor or residual disease after resection
• •Prior therapy:
• •No prior chemotherapy or radiation therapy for HGG or DIPG is permitted. Prior chemotherapy or radiation therapy for treatment of other malignancies is permitted.
• •Age:
• •Patients must be less than 22 years of age at the time of diagnosis.
• •Able to swallow capsules whole
• •Performance Score:
• •Patients should have a Karnofsky/Lansky score of greater than or equal to 60. Patients who require special assistance due to tumor-related paralysis, but who are out of bed during the day will be considered ambulatory for the purpose of calculating the performance score. Patients must be able to communicate any symptoms.
• •Laboratory Evaluation:
• •The following laboratory values must be assessed within seven (7) days prior to the start of therapy. Laboratory tests should be repeated within 48 hours of beginning therapy if there has been a significant clinical change.
• •Patients must have adequate organ and marrow function as defined below:
• •* absolute neutrophil count greater than or equal to 1,000/mcL
• •* platelets greater than or equal to 100,000/mcL
• •* total bilirubin less than 1.5 times upper limit of normal
• •* AST(SGOT)/ALT(SGPT) less than or equal to 2.5 times institutional upper limit of normal
• •* creatinine below age-adjusted maximum limits below
• •OR
• •creatinine clearance greater than or equal to 60 mL/min/1.73 m(2)
• •Age (Years) Maximum Serum Creatinine (mg/dl):
• •* Less than or equal to 5 years; 0.8
• •* Age greater than 5, but less than or equal to 10 ; 1.0
• •* Age greater than 1, but less than or equal to 15 ; 1.2
• •* Less than 15 years of age; 1.5
• •Females only:
• •urine or serum pregnancy test negative
• •No overt renal, hepatic, cardiac or pulmonary disease.
• •Steroids:
• •Newly diagnosed patients may need to be on steroids due to surgery or control of neurologic symptoms. Patients on steroids postoperatively or for control of tumor-related edema are eligible, but attempts to keep patients on the lowest dose necessary to control symptoms should be made.
• •Patients of childbearing potential:
• •Female Subjects:
• •Definition of female of childbearing potential (FCBP)
• •This protocol defines a female of childbearing potential as a sexually mature woman who: 1) has not undergone a hysterectomy or bilateral oophorectomy or 2) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).
• •-Criteria for female children of childbearing potential (FCCBP)
• •This protocol defines FCCBP as females who have:
• •Achieved menarche and/or breast development in Tanner stage 2 or greater
• •----Onset of fertility typically occurs within 3-12 months after menarche. Menarche varies considerably from person to person, and thus no age cut off can be attributed. One of the primary tools used to follow a girl s progress through puberty is the Tanner staging system, which describes the pattern of development of the secondary sex characteristics. Tanner stage 2 corresponds to the beginning of breast development, which is the first visible sign of puberty in girls. Breast development is estrogen stimulated, and since ovulation cannot occur without estrogen, Tanner stage 2 will be a reliable marker for the definition of fertility.
• •Has not undergone a hysterectomy or bilateral oophorectomy.
• •Note: Amenorrhea following cancer therapy does not rule out childbearing potential
• •-Criteria for female children not of childbearing potential (FCNCBP)
• •This protocol defines FCNCBP as females:
• •Who have not yet experienced menarche or breast development in Tanner stage 2.
• •Who have undergone a hysterectomy or bilateral oophorectomy.
• •Females of childbearing potential (FCBP) must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 10 14 days and again within 24 hours prior to starting Course 1 of lenalidomide. Further, they must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control: one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before starting lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP, even if they have had a successful vasectomy. A FCBP is a sexually mature woman who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months). All patients must be counseled by a trained counselor every 28 days about pregnancy precautions and risks of fetal exposure.
• •Male Subjects:
• •Appropriate male subjects (i.e. those who have reached puberty and are sexually active) will be counseled regarding birth control methods. They must agree to use a latex condom during sexual contact with females of childbearing potential while participating in the study and for at least 28 days following discontinuation from the study even if he has undergone a successful vasectomy.
• •Appropriate male patients will be given a reproductive risks handout and counseled by a provider. For sexually active patients, the counseling session, consent and counseling checklist will be documented monthly.
• •Informed consent:
• •All patients or their legal guardians (if the patient is less than18 years old) or durable power of attorney (DPA) must sign a document of informed consent indicating their understanding of the investigational nature and the risks of this study. When appropriate, pediatric patients will be included in all discussions in order to obtain verbal assent.
• •In the event that the patient and/or the patient s parents are unable to travel to NIH should re-consenting be necessary, a telephone consent may be performed by the principal investigator according to Clinical Center Policy M77-2. The telephone consent will be
• •witnessed by a member of the research team who is on the telephone with the patient and PI and who can confirm the patient s consent to participate. A copy of the signed consent will be mailed to the participant. The consenting process will be documented in the
• •patient s record which is signed by the PI and co-signed by the witness to the consent.
• •Durable Power of Attorney:
• •Assignment of DPA to a family member or guardian should be offered to all patients 18 years of age.
• •Signed informed consent according to institutional guidelines must be obtained.