Inclusion Criteria:
Patient must:
Have histologically confirmed WHO Grade II or III meningioma that is residual, progressive
or recurrent following at least minimally safe resection and radiation therapy. Metastatic
meningiomas are allowed.
- - Residual disease is defined as residual measurable disease (without a requirement for
progression).
Residual measurable disease is defined by bidimensionally measurable
lesions with clearly defined margins by MRI scan(s) with a minimum diameter of 10mm in
both dimensions.
- - Progressive disease is defined as an increase in size of the measurable primary lesion
on imaging by 25% or more (bidirectional area).
The change must occur between scans
separated by no more than 24 months.
- - Recurrent disease is defined as new evidence of measurable disease following complete
resection (10mm in both dimensions).
- - Be on a stable or decreasing dose of steroids for at least five days prior to the date
of informed consent.
- - Participants must have failed maximal safe resection and radiation therapy.
There is no limit on the number of prior surgeries, radiation therapy, radiosurgery
treatments or systemically administered therapeutic agents, however, these treatment (s)
must comply with the following:
- - There is no limit on the number of prior therapies.
- - Prior medical therapy is allowed but is not required.
- - No chemotherapy, other investigational agents within 14 days of study treatment.
- - For prior systemic agents, participants must be at least 4 weeks (or 5 half-lives,
whichever is shorter) from other prior cytotoxic chemotherapy (6 weeks from
nitrosoureas/alkylating agents) or biologic therapies.
- - No other concurrent receipt of investigational agents or other meningioma-directed
therapy (chemotherapy, radiation) while on study.
- - Patients may have been treated with standard external beam radiation or radiosurgery
in any combination, however an interval of ≥12 weeks (84 days) must have elapsed from
the completion of the radiation therapy to the initiation of study therapy unless
there is histopathologic confirmation of recurrent tumor or there is new enhancing
tumor outside the radiation field (beyond the high dose region or the 80% isodose
line).
In addition, there must be subsequent evidence of tumor progression after
completion of radiation therapy;
- - An interval of ≥ 28 days and full recovery (no ongoing safety issues) from surgical
resection is required;
- Meningioma that have resulted from prior radiation therapy are allowed.
- - There must be an interval of ≥ 7 days from stereotactic biopsy; and Participants must
have recovered to grade ≤1 or pretreatment baseline from clinically significant
adverse events related to prior therapy (exclusions include but are not limited to
alopecia, laboratory values listed per inclusion criteria and lymphopenia).
Patient must be ≥ 12 years of age. Patient must have an ECOG performance status of 0-2 or
KPS ≥ 60. Patient must have an expected survival of at least three months. Patient must be
willing to provide blood samples for pharmacokinetic study (to assess proper administration
of NEO100).
Patient must have adequate organ and marrow function as defined below:
- - White blood cell (WBC) ≥2000/microliter.
- - Absolute neutrophil count ≥ 1,500/mcL.
- - Platelets ≥ 100,000/mcL.
- - AST (SGOT)/ALT (SPGT) ≤ 2.5 × laboratory upper limit of normal (ULN)
- Serum creatinine ≤ 1.5 x laboratory upper limit of normal (ULN) or.
- - Creatinine clearance (meas or calc) ≥60mL/min for participants with creatinine levels
>1.5x laboratory upper limit of normal (ULN)
- Total serum bilirubin ≤ 1.5 x laboratory upper limit of normal (ULN) except
participants with Gilbert's Syndrome who can have a total serum bilirubin of <5 x
laboratory upper limit of normal (ULN) MRI (or CT if MRI contraindicated) within 14
days prior to start of study drug.
Corticosteroid dose must be stable or decreasing
for at least 5 days prior to the scan. If steroids are added or the steroid dose is
increased between the date of the screening scan and the start of treatment, a new
baseline scan is required.
Female patients of child-bearing potential and male patients must agree to use adequate
contraception (hormonal or barrier method of birth control; abstinence) for 30 days prior
to the first administration of study drug, for the duration of study participation, and for
90 days following completion of therapy. Should a female patient become pregnant, or
suspect she is pregnant, while participating in this study, she should inform her treating
physician immediately.
- - A female of child-bearing potential is any woman (regardless of sexual orientation,
not having undergone a tubal ligation, or remaining celibate by choice) who meets the
following criteria:
- Has not undergone a hysterectomy or bilateral oophorectomy; or.
- - Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has
had menses at any time in the preceding 12 consecutive months).
- - A negative serum pregnancy test will be required of all female patients of
child-bearing potential within seven days prior to initiating study drug.
- - A serum pregnancy test will be repeated immediately if pregnancy is suspected.
Women
must not be breastfeeding. Patient must have the ability to understand, and the
willingness to sign, a written informed consent.
Exclusion Criteria. If the patient meets any of the following criteria, the patient must not be enrolled:
Patients who have had chemotherapy, targeted small molecule therapy or study therapy within
14 days (or 5 half-lives, whichever is shorter) of study treatment.
Patient has completed chemo-radiation within the last 84 days prior to the first
administration of study drug, unless new contrast enhancement is outside of radiation
field, or there is tissue proven recurrence or progression.
Patient has had surgery within seven days prior to the date of informed consent.
Patient has had cytotoxic chemotherapy within 4 weeks (or 5 half-lives, whichever is
shorter), nitrosoureas/alkylating agents within 6 weeks or biologic therapies.
Prior treatment with interstitial brachytherapy within 6 months of start of study therapy.
Current or planned participation in a clinical trial of an investigational agent or using
an investigational medical device.
The patients disease is primarily localized to the brainstem or spinal cord. Patient has
not recovered from adverse events due to chemotherapy, immunotherapy, or radiation therapy.
Patient has had prior treatment with perillyl alcohol, administered either intravenously or
intranasally.
Patient has a history of allergic reactions attributed to perillyl alcohol. Patient has
uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with study
requirements.
Patient has uncontrolled intercurrent illness including, but not limited to, ongoing or
active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with study
requirements.
Patient must not be pregnant or nursing due to the potential for congenital abnormalities
and the potential of this regimen to harm nursing infants.
Patient has a history of new diagnosis or treatment of cancer other than meningioma within
five years prior to the date of informed consent, except for basal cell carcinoma or
squamous cell carcinoma of the skin.
Leptomeningeal involvement of the patient's tumor.
