Inclusion Criteria:
- - Male or female patients of age > 18 years.
- - Patients with 68Ga-DOTATATE positive recurrent or progressive meningiomas, any World
Health Organization (WHO) grade, who have progressed after first line treatment.
- - For Grade I meningioma, patients must have either:
- Progressive disease after at least surgical resection and radiotherapy, as
defined as an increase in size of the measurable primary lesion
(bidirectional area) on imaging by 25% or more between scans separated by
no more than 12 months; or.
- - Progressive residual tumor after maximal safe resection, located at or
near critical organs at-risk and considered to be high-risk for radiation
injury by the treating investigator.
Prior external beam radiotherapy is
not required for these subjects.
- - For Grade II or III meningioma, subjects must have either:
- Progressive disease after at least surgical resection and radiotherapy, as
defined as an increase in size of the measurable primary lesion
(bi-directional area) on imaging by 25% or more between scans separated by
no more than 12 months or.
- - Residual measurable disease after prior surgery without requirement of
progression, or.
- - Unsuitable for, or decline other standard of care treatment.
- - Positive 68Ga-DOTATATE uptake on PET/CT at baseline, defined as target lesion uptake
higher than the background with SUV ratios adjusted to the liver uptake (Krenning
score ≥ 2)
- Presence of measurable disease defined as at least one lesion measuring ≥ 5 mm in at
least one dimension by contrast-enhanced MRI performed within 30 days prior to study
registration.
- - Multifocal disease allowed but limited to ≤ 3 measurable intracranial lesions on the
most recent post-contrast MRI.
- - There is no limit on the number of prior surgeries, radiation therapy, radiosurgery,
systemically administered therapeutic agents or theranostic agents.
- - For patients treated with external beam radiation, interstitial brachytherapy or
radiosurgery, an interval ≥ 24 weeks must have elapsed from completion from these
therapies to registration 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)
- An interval of ≥ 28 days (or 5 half-lives, whichever is shorter) from prior
cytotoxic chemotherapy (6 weeks from nitrosoureas), biologic agent, investigational
agent or any other systemic agent prescribed for the purpose of treating meningioma.
- - An interval of ≥ 28 days from craniotomy and ≥ 7 days from stereotactic biopsy.
- - Patients must be willing and able to undergo regular MRI scans of the brain.
- - Patients must have recovered to Common Terminology Criteria for Adverse Events
(CTCAE) grade ≤ 1 or pretreatment baseline from clinically significant adverse
events related to prior therapy (exclusions include alopecia, laboratory values
listed per inclusion criteria, lymphopenia, sensory neuropathy ≤ grade 2, or other ≤
grade 2 not constituting a safety risk based on the investigator's judgment)
- Any neurological symptoms must be stable for at least 28 days prior to enrollment
and patients should not require escalating doses of steroids to control neurological
symptoms (stable low dose maintenance steroids at ≤ 8 mg dexamethasone or equivalent
are allowed)
- Sufficient renal function, as evidenced by creatinine clearance (CrCl) ≥ 60 mL/min
calculated using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI)
equation.
- - Hemoglobin concentration ≥ 5.0 mmol/L (≥ 8.0 g/dL)
- Note: Colony-stimulating factors, platelet-production stimulators and/or
transfusions within 4 weeks prior to screening and first dose of study
treatment are not permitted to meet these criteria.
- - Absolute neutrophil count (ANC) ≥ 1000 cells/µL (≥ 1000 cells/mm^3)
- Note: Colony-stimulating factors, platelet-production stimulators and/or
transfusions within 4 weeks prior to screening and first dose of study
treatment are not permitted to meet these criteria.
- - Platelets > 100 × 10^9/L (100 × 10^3/mm^3)
- Note: Colony-stimulating factors, platelet-production stimulators and/or
transfusions within 4 weeks prior to screening and first dose of study
treatment are not permitted to meet these criteria.
- - Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × upper
limit of normal (ULN) (or ≤ 5 × ULN if presence of liver metastases)
- Total bilirubin ≤ 3 × ULN.
- - Serum albumin ≥ 3.0 g/dL.
- - Adequate coagulation function, defined by international normalized ratio (INR) or
prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN,
unless subject is receiving anticoagulant therapy and PT or aPTT is within
therapeutic range of intended use of anticoagulants.
- - For women of childbearing potential (WOCBP):
- Negative pregnancy test within 48 hours prior to the first dose of study
treatment.
- - Agreement to use barrier contraception and a second form of highly effective
contraception while receiving study treatment and for 7 months following their
last dose of study treatment.
Alternatively, total abstinence is also
considered a highly effective contraception method when this is in line with
the preferred and usual lifestyle of the subject. Periodic abstinence (e.g.,
calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are
not acceptable methods of contraception.
A woman is considered to be of childbearing potential if she is postmenarche, has not
reached a postmenopausal state (≥ 12 continuous months of amenorrhea [no menstrual
bleeding of any kind, including menstrual period, irregular bleeding, spotting, etc.]
with no identified cause other than menopause), and has not undergone surgical
sterilization (total hysterectomy, or bilateral tubal ligation or bilateral oophorectomy
at least 6 weeks before first dose of study treatment)
- - Sexually active male subjects must use a condom during intercourse while receiving
RYZ101 and for at least 120 days after the last dose of the study treatment and
should not father a child during this period.
- - Male study subjects whose sexual partners are WOCBP must also agree to use a
second form of highly effective contraception while receiving RYZ101 and for at
least 4 months following their last dose.
Alternatively, total abstinence is
also considered a highly effective contraception method when this is in line
with the preferred and usual lifestyle of the subject.
- - Vasectomized men are also required to use a condom during intercourse,
including with a male partner, to prevent delivery of the drug via seminal
fluid.
Exclusion Criteria:
- - Eastern Cooperative Oncology Group (ECOG) performance status > 2.
- - Received radiation therapy to the brain in last 24 weeks.
- - History of hypersensitivity or allergy to Actinium Ac-225 (225Ac), Gallium Ga 68
(68Ga), Copper Cu 64 (64Cu), octreotate, or any of the excipients of DOTATATE
imaging agents.
- - Prior radiopharmaceutical therapies (RPT), including radioembolization.
- - Prior solid organ or bone marrow transplantation.
- - Any toxicities from prior treatments that have not recovered to CTCAE grade ≤1,
except for alopecia.
- - Significant cardiovascular disease, defined as:
- New York Heart Association (NYHA) Class ≥ II heart failure.
- - Known left ventricular ejection fraction (LVEF) < 50%.
- - History of myocardial infarction, acute coronary syndrome, or coronary
angioplasty/stenting/bypass within the last 6 months.
- - QT interval corrected for heart rate using Fridericia's formula (QTcF) > 470
ms, demonstrated by the average value of 3 consecutive electrocardiograms
(ECGs).
- - Resistant hypertension, defined as persistent uncontrolled blood pressure (BP)
> 140/90 mmHg while on optimal doses of at least 3 antihypertensive medications
with 1 being a diuretic.
Patients with baseline hypertension may be eligible
after initiation of antihypertensive therapy.
- - Uncontrolled diabetes mellitus as defined by hemoglobin A1C (HgB A1c) > 8% in
patients with known diagnosis of diabetes mellitus)
- Liver cirrhosis.
- - Pregnancy or lactation.
- - Unable to understand or unwilling to sign an Institutional review board approved
written informed consent document.
- Current somatic or psychiatric disease/condition that may interfere with the
objectives and assessments of the study
