Inclusion Criteria:
1. Age ≥18 years. 2. Karnofsky Performance Status (KPS) of 60 or greater. 3. Recurrent supratentorial Glioblastoma that has progressed following standard
therapy; patients must have previously been treated with radiation with or without
temozolomide.
1. Patients will be eligible at first or second recurrence.
2. Patients must be greater than 12 weeks from completion of initial
chemoradiation at the time of progression, with the exception that patients
with biopsy-confirmed recurrent disease prior to this time window can be
enrolled.
4. Diagnosis of Glioblastoma IDH-wildtype, WHO Grade 4 consistent with WHO CNS 2021
criteria. This will include patients with a diagnosis of molecular glioblastoma.
5. Measurable or evaluable disease per RANO criteria. 6. A baseline MRI Brain no more than 14 days prior to study enrollment. 7. Adequate Organ Function, with screening labs performed within 14 days of treatment
initiation:
a. Hematology (no blood transfusions or growth factor therapy used within 7 days of
the screening CBC): i. Absolute neutrophil count (ANC) ≥ 1.5 × 109/L ii. Platelet
count ≥ 100 × 109/L iii. Hemoglobin ≥ 9.0 g/dL b. Kidneys: i. Creatinine clearance*
(CrCL) ≥ 50 mL/min using the Cockcroft-Gault formula or estimated glomerular
filtration rate (eGFR) value ≥50 mL/min using the Chronic Kidney Disease
Epidemiology Collaboration (CKD-EPI) equation (adjustment by BSA is not required for
eGFR)
CrCL or eGFR can be determined using the calculator from the National Kidney
Foundation website (www.kidney.org).
ii. Urine protein < 2+ or 24-hour urine protein quantification < 1.0 g or Urine
protein/Creatinine ratio ≤ 1mg/mg (≤ 113.2mg/mmol) c. Liver: i. Serum total
bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN); For patients with
confirmed/suspected Gilbert syndrome, TBIL ≤3 × ULN ii. Aspartate aminotransferase
(AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN d. Coagulation: prothrombin
time (PT) or international normalized ratio (INR)
- - 1.5 × ULN, and partial prothrombin time (PTT) or activated partial
thromboplastin time (aPTT) ≤ 1.5 × ULN (unless abnormalities are unrelated to
coagulopathy or prophylactic coagulation)
8.
Female patients of childbearing age must have negative serum pregnancy test results
before randomization or per region-specific guidance documented in the informed
consent and a negative urine pregnancy test on the day of first dose prior to
dosing.
9. Female patient of childbearing potential having sex with an unsterilized male
partner must agree to use a highly effective method of contraception from the
beginning of screening until 120 days after the last dose of the ivonescimab.
10. Male patients of childbearing potential having sex with a female partner of
childbearing potential must agree to use an effective method of contraception from
the beginning of screening until Day 120 after the last dose of ivonescimab.
11. Ability to understand and willingness to sign informed consent form prior to the
initiation of study and any study procedures.
1. Participants with cognitive impairment may be enrolled. The formal consent for
such participants will be obtained from their legally authorized
representative. However, participants will be informed about the research to
the maximum extent compatible with their understanding. Assent will be obtained
from such participants who will sign and date the consent form if capable.
2. Non-English speakers are allowed to enroll provided consent and all visits will
be conducted with a medical interpreter.
Exclusion Criteria:
1. Major surgical procedures or serious trauma, or plans for major surgical procedures
within 4 weeks after the first dose (as determined by the investigator).
Minor local procedures (excluding central venous catheterization and port
implantation).
2. Currently pregnant or breastfeeding.
3. History of bleeding tendencies or coagulopathy and/or clinically significant
bleeding symptoms, including but not limited to:
a. Significant intracranial hemorrhage. 1. Note: Patients with clinically asymptomatic presence of hemosiderin, resolving
postoperative changes or punctate intratumoral hemorrhage are permitted. 2. Gastrointestinal bleeding. b. Hemoptysis (defined as coughing up ≥ 0.5 teaspoon of fresh blood or small blood
clots) Note: transient hemoptysis associated with diagnostic bronchoscopy is
allowed. c. Nasal bleeding /epistaxis (bloody nasal discharge is allowed) d. Need
for therapeutic anticoagulant therapy Note: Prophylactic anticoagulation for DVT/PE
or to maintain venous patency is allowed.
4. Current hypertension with systolic blood pressure ≥ 150 mmHg or diastolic blood
pressure ≥ 100 mmHg after oral antihypertensive therapy. 5. Is receiving dexamethasone >2mg daily, or the corticosteroid equivalent thereof.
6. History of major diseases, specifically:
1. Unstable angina, myocardial infarction, congestive heart failure (New York
Heart Association [NYHA] classification ≥ grade 2) or vascular disease (eg,
aortic aneurysm at risk of rupture), or other cardiac impairment that may
affect the safety evaluation of the study drug (eg, poorly controlled
arrhythmias, myocardial ischemia)
2. History of esophageal gastric varices, severe ulcers, wounds that do not heal,
abdominal fistula, intra-abdominal abscesses, or acute gastrointestinal
bleeding. 3. History of arterial thromboembolic event, venous thromboembolic event of Grade
3 and above as specified in National Cancer Institute (NCI) Common Terminology
Criteria for Adverse Events (CTCAE) 5.0, transient ischemic attack,
cerebrovascular accident, hypertensive crisis, or hypertensive encephalopathy. 4. Acute exacerbation of chronic obstructive pulmonary disease within 4 weeks
beforerandomization. 5. History of perforation of the gastrointestinal tract and/or fistula, history of
gastrointestinal obstruction (including incomplete intestinal obstruction
requiring parenteral nutrition), extensive bowel resection (partial colectomy
or extensive small bowel resection)
7. History of other malignancy diagnosed or requiring treatment within the past 3 years
prior to enrolment, with the exception of those with negligible expected risk of
metastasis or death (including adequately treated non- melanoma skin cancer or
cervical carcinoma in situ).
8. History of prior treatment of GB with anti-VEGF and/or anti-PD-1/PDL-1 agents,
including monotherapy with either category or combinations thereof.
9. Has received prior interstitial brachytherapy, interstitial thermal therapy,
implanted chemotherapy, or therapeutics delivered by local injection or convection
enhanced deliver. Prior treatment with Gliadel ® wafers will be excluded. Concurrent
use of devices such as Tumor Treating Fields is not permitted.
10. Has known leptomeningeal disease, gliomatosis cerebri, extracranial disease, or
multicentric disease (regionally multifocal enhancing disease with continguous
T2/FLAIR is permitted to be enrolled)
11. Uncontrolled seizures after best medical therapy or other neurological conditions
including clinically significant autoimmune neurological disorders which can
increase risk for adverse effects or confound assessment of study outcomes as
determined by the treating physician and PI. 12. History of clinically significant autoimmune disease including but not limited to
systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease,
vascular thrombosis associated with antiphospholipid syndrome, granulomatosis with
polyangiitis, Sjogren's syndrome, GuillainBarré syndrome, multiple sclerosis,
vasculitis or glomerulonephritis. 1. Patients with a history of autoimmune hypothyroidism may be eligible if on a
stable dose of thyroid replacement hormone. 2. Patients with controlled Type 1 diabetes mellitus may be eligible if on a
stable insulin regimen. 3. Patients with dermatologic disorders (e.g., eczema) may be eligible if well
controlled at baseline and not requiring systemic treatment or other treatments
beyond low potency topical steroids. 13. Has contraindication for undergoing MRI scans or receiving MRI contrast.
14. History of stroke or TIA within 6 months prior to study enrolment.
15. Imaging during the screening period shows that the patient has:
1. Radiologically documented evidence of major blood vessel invasion or encasement
by cancer. 2. Radiographic evidence of intratumor cavitation
