PRIMARY OBJECTIVE:
I. To determine the efficacy of stereotactic radiation and pembrolizumab for treatment of
recurrent meningioma compared to historical control based on progression free survival at 12
months (PFS12).
SECONDARY OBJECTIVE:
I. To assess overall survival and further assess progression free survival of stereotactic
radiation and pembrolizumab for treatment of recurrent meningioma.
EXPLORATORY OBJECTIVES:
I. To assess immune-related tumor effects pembrolizumab treatment in meningioma using
magnetic resonance (MR) imaging in conjunction with assessment by Response Assessment in
Neuro-Oncology Criteria (RANO) and Immunotherapy (i)RANO criteria.
II. To assess neurocognitive function and quality of life with pembrolizumab and radiation
using the Neurologic Assessment in Neuro-Oncology (NANO) Scale, and European Organisation for
Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire brain tumour module
(QLQ-BN20).
III. To assess safety of the combined treatment modalities in meningioma, through evaluation
of grade III adverse events (AEs) and dose-limiting toxicity (DLT).
OUTLINE:
Within -3 to 0 days from the start of stereotactic radiation therapy, patients receive
pembrolizumab intravenously (IV) over 30 minutes on days 1 and 22. Cycles repeat every 6
weeks in the absence of disease progression or unacceptable toxicity. Patients undergo
stereotactic radiosurgery on day 1 or days 1-5 of cycle 1 in the absence of disease
progression or unacceptable toxicity.
After completion of study treatment, patients are followed up at 30 days, every 12 weeks for
2 years, and then every 6 months thereafter for up to 5 years.
Inclusion Criteria:
- For Stratum A, patients must have histologically confirmed World Health Organization
(WHO) grade II or III meningioma that is progressive or with one or more recurrences
following surgical resection and radiotherapy
- For Stratum B, patients must have histologically WHO grade I meningioma who are
multiply recurrent (>= 2 recurrences) following surgical and radiotherapy intervention
- Patients must be eligible/appropriate for treatment with radiation therapy,
specifically, if radiation is given in a single session, the target volume cannot
exceed 8 ccs or if given in five (consecutive business days) sessions, the target
volume cannot exceed 20 ccs
- Prior therapy:
- There is no limit on the number of prior surgeries or systemically administered
therapeutic agents
- An interval of >= 28 days and full recovery (no ongoing safety issues) from
surgical resection
- An interval of > 7 days from stereotactic biopsy
- 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) or biologic therapies
- For prior radiotherapy, there are no exclusions on number of courses or prior
type of radiotherapy. All modalities including prior fractionated external beam
photon/proton radiotherapy, stereotactic radiosurgery, and/or or brachytherapy
are permissible with a required interval of 6 months from last prior radiotherapy
treatment, unless radiation given outside of the planned field, then within 2
weeks from prior radiotherapy treatment. Patients must have had one prior course
of radiation therapy
- Participants must have recovered to grade =< 1 or pretreatment baseline from
clinically significant adverse events related to prior therapy (excluding alopecia,
laboratory values listed per inclusion criteria and lymphopenia)
- Be >= 18 years of age on day of signing informed consent
- Have a Karnofsky performance status (KPS) >= 70
- Absolute neutrophil count (ANC) >= 1500/microliter (uL) (within 28 days prior to
enrollment)
- Platelets >= 100000/uL (within 28 days prior to enrollment)
- Hemoglobin >= 9.0 g/dL or >= 5.6 mmol/L (within 28 days prior to enrollment)
* Criteria must be met without erythropoietin dependency and without packed red blood
cell (pRBC) transfusion within last 2 weeks
- Creatinine =< 1.5 x upper limit of normal (ULN) OR measured or calculated creatinine
clearance >= 30 mL/min for participant with creatinine levels > 1.5 x institutional
ULN (within 28 days prior to enrollment) (glomerular filtration rate (GFR) can also be
used in place of creatinine or creatinine clearance (CrCl))
* Creatinine clearance (CrCl) should be calculated per institutional standard
- Total bilirubin =< 1.5 x ULN OR direct bilirubin =< ULN for participants with total
bilirubin levels > 1.5 x ULN (within 28 days prior to enrollment)
- Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase (SGOT)) and
alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase (SGPT)) =< 2.5 x
ULN (within 28 days prior to enrollment)
- International normalized ratio (INR) OR prothrombin time (PT) =< 1.5 x ULN unless
participant is receiving anticoagulant therapy as long as PT or activated partial
thromboplastin time (aPTT) is within therapeutic range of intended use of
anticoagulants (within 28 days prior to enrollment)
- Activated partial thromboplastin time (aPTT) =< 1.5 x ULN unless participant is
receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of
intended use of anticoagulants (within 28 days prior to enrollment)
- Magnetic resonance imaging (MRI) within 28 days prior to start of study drug.
Corticosteroid dose must be less than or equal to 2 mg and at a 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 MRI and the start of treatment, a new
baseline MRI is required
- Ability to understand and the willingness to comply with scheduled visits, treatment
schedule, laboratory testing, and other requirements of the study, including disease
assessment by MRI, as confirmed by signing a written informed consent document
- The effects of pembrolizumab on the developing human fetus are unknown. For this
reason:
- Male participants:
** A male participant must agree to use a contraception during the treatment
period and for 120 days after the last dose of study treatment and refrain from
donating sperm during this period
- Female participants:
- A female participant is eligible to participate if she is not pregnant, not
breastfeeding, and at least one of the following conditions applies:
- Not a woman of childbearing potential (WOCBP) OR
- A WOCBP who agrees to follow the contraceptive guidance during the
treatment period and for at least 120 days after the last dose of study
treatment
Exclusion Criteria:
- WOCBP who has a positive urine pregnancy test within 72 hours prior to allocation. If
the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
will be required
- Tumors that are primarily localized to the brainstem or spinal cord, NOTE: patients
with known tumors in these areas that are not progressive are not excluded
- Known metastasis outside if the central nervous system (CNS), however, no baseline
staging is required
- Evidence of intratumoral or peritumoral hemorrhage on baseline MRI scan other than
those that are grade =< 1 and either post-operative or stable on at least 2
consecutive MRI scans
- Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with
an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g.,
cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), OX-40, CD137)
- Has received a live vaccine within 30 days prior to the first dose of study drug.
Examples of live vaccines include, but are not limited to, the following: measles,
mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus
Calmette-Guerin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection
are generally killed virus vaccines and are allowed; however, intranasal influenza
vaccines (e.g., FluMist) are live attenuated vaccines and are not allowed
- Has a known additional malignancy that is progressing or has required active treatment
within the past 3 years. Note: Participants with basal cell carcinoma of the skin,
squamous cell carcinoma of the skin, or carcinoma in situ (e.g. breast carcinoma,
cervical cancer in situ) that have undergone potentially curative therapy are not
excluded
- Prior treatment with systemic immunosuppressive treatments, such as methotrexate,
chloroquine, azathioprine, etc. within 3 months of start of study therapy
- No concurrent treatment on another clinical trial for 4 weeks (or 5 half-lives,
whichever is shorter) for prior systemic agents, other prior cytotoxic chemotherapy (6
weeks from nitrosoureas) or biologic therapies. Supportive care trials or non-
treatment trials, e.g. quality of life, are allowed
- Has severe hypersensitivity (>= grade 3) to pembrolizumab and/or any of its excipients
- Has active autoimmune disease that has required systemic treatment in the past 2 years
(i.e. with use of disease modifying agents, corticosteroids or immunosuppressive
drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid
replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
form of systemic treatment
- Has a history of (non-infectious) pneumonitis that required steroids or has current
pneumonitis
- Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy
(in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of
immunosuppressive therapy within 7 days prior to the first dose of study drug.
Steroids for cerebral edema are allowed if less than or equal to 2 mg of dexamethasone
- Has an active infection requiring systemic therapy
- Has a known history of human immunodeficiency virus (HIV) (testing not required)
- Has a known history of hepatitis B (defined as hepatitis B surface antigen (HBsAg)
reactive) or known active hepatitis C virus (defined as hepatitis C virus (HCV)
ribonucleic acid (RNA) is detected) infection
- Has a known history of active Bacillus tuberculosis (TB)
- Has known psychiatric or substance abuse disorders that would interfere with
cooperation with the requirements of the trial
- Is pregnant or breastfeeding, or expecting to conceive or father children within the
projected duration of the study, starting with the screening visit through 120 days
after the last dose of trial treatment
