Inclusion Criteria:
1. Signed Informed Consent Form (ICF)
2. Age ≥ 18 years and ≤70 years.
3. Gross total resection equal to or greater than 80% based on post-op MRI, compared to
pre-op MRI (Patients requiring biopsy only is not eligible)
4. Patients newly diagnosed with glioblastoma either radiologically or pathologically
and completed concurrent chemo-radiotherapy (CCRT) with plan to receive adjuvant
temozolomide therapy with curative intent. 5. Adequate hematologic and end organ function, defined by the following laboratory
results obtained within 14 days prior to the randomization.1) Absolute lymphocyte
count (ALC) ≤1×109/L. 2) Absolute neutrophil count (ANC) ≥ 1.5×109/L. 3) Platelet
count ≥ 100×109/L (without transfusion within 14 days prior to Cycle 1, Day 1). 4)
Hemoglobin ≥ 9 g/dL Patients may be transfused or may receive erythropoietic
treatment as per local standard of care. 5) Total bilirubin ≤ 1.5 × the upper limit
of normal (ULN). 6) AST and ALT ≤ 3 × ULN. 7) Alkaline phosphatase ≤ 2.5 × ULN (For
subject with proven liver or bone metastasis, alkaline phosphatase ≤ 5 × ULN is
allowed). 8) Serum albumin ≥ 2.5 g/dL. 9) Serum creatinine ≤ 1.5 mg/dL. 10)
Prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN.
This applies only to patients who are not receiving therapeutic anticoagulation.
Patients receiving therapeutic anticoagulation should be on a stable dose. 6. Karnofsky score ≥ 60. 7. Life expectancy > 12 weeks. 8. For women of childbearing potential*: agreement to remain abstinent (refrain from
heterosexual intercourse) or use contraceptive methods that result in a failure rate
of < 1% per year from the date of informed consent to at least 3 months after the
last dose of study drugs. For men: agreement to remain abstinent (refrain from
heterosexual intercourse) or use contraceptive measures, and agreement to refrain
from donating sperm, as defined below: With female partners of childbearing
potential or pregnant female partners, men must remain abstinent or use a condom
during the treatment period and for at least 3 months after the last dose of study
treatment (TJ107) and 6 months after the last dose of temozolomide to avoid exposing
the embryo. Men must refrain from donating sperm during this same period. The
reliability of sexual abstinence should be evaluated in relation to the duration of
the clinical trial and the preferred and usual lifestyle of the patient. Periodic
abstinence and withdrawal are not acceptable methods of contraception.
- - A woman is of childbearing potential if she is postmenarcheal, has not reached
a postmenopausal state (≥ 12 continuous months of amenorrhea with no identified
cause other than menopause), and has not undergone surgical sterilization
(removal of ovaries and/or uterus).
- - Examples of contraceptive methods with a failure rate of < 1% per year include
bilateral tubal ligation, male sterilization, and established proper use of
hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine
devices, and copper intrauterine devices.
- - Hormonal contraceptive methods must be supplemented by a barrier method plus
spermicide.
- - The reliability of sexual abstinence should be evaluated in relation to the
duration of the clinical trial and the preferred and usual lifestyle of the
patient.
Periodic abstinence (e.g., calendar, ovulation, symptothermal, or
post-ovulation methods) and withdrawal are not acceptable methods of
contraception.
Exclusion Criteria:
1. Subjects receiving 21 days hypofractionated radiotherapy due to clinical condition. 2. Multifocal glioma (≥3 lesions)
3. Patients with primary subtentorial glioblastoma multiforme. 4. Patients who have evidence of leptomeningeal disease. 5. Patients on corticosteroid treatment have not a stable or decreasing dose for 14
days before randomization.
6. Pregnancy, lactation, or breastfeeding (with lactation or breastfeeding required
during the study period)
*Serum pregnancy test for women of childbearing potential (including women who have
had a tubal ligation) must be performed and documented as negative within 14 days
prior to randomization. 7. Significant cardiovascular disease, such as New York Heart Association cardiac
disease (Class II or greater), myocardial infarction within the previous 3 months,
unstable arrhythmias, and/or unstable angina. 8. Known clinically significant liver disease, including active viral, alcoholic, or
other hepatitis, cirrhosis, and inherited liver disease or current alcohol abuse. 9. Poorly controlled Type 2 diabetes mellitus defined as a screening hemoglobin A1C ≥
8% or a fasting plasma glucose ≥ 160 mg/dL (or 8.8 mmol/L)
10. Anticipation of need for a major surgical procedure (requiring general anesthesia)
during the study period. 11. Any evidence of severe or uncontrolled systemic diseases, including uncontrolled
hypertension (defined by blood pressure higher than 150/90mmHg despite effective
anti-hypertensive treatments) and active bleeding diatheses, which in the
investigator's opinion makes it undesirable for the patient to participate in trial
or which would jeopardize compliance with the protocol. 12. Any anti-cancer therapy, whether investigational or approved, including
chemotherapy, immunotherapy, gene therapy, cancer vaccine, cell therapy, cytokines,
hormonal therapy, and/or radiotherapy) received after standard concurrent
chemo-radiotherapy (CCRT)
13. Persisting toxicity related to prior therapy (NCI CTCAE v. 5.0 Grade > 1); however,
alopecia, sensory neuropathy Grade ≤ 2, or other Grade ≤ 2 not constituting a safety
risk based on investigator's judgment are acceptable. 14. Malignancies other than disease under study within 5 years prior to randomization
except for those with a negligible risk of metastasis or death (such as adequately
treated carcinoma in situ of the cervix, basal or squamous cell skin cancer,
localized prostate cancer, or ductal carcinoma in situ)
15. Uncontrolled hypercalcemia (ionized Calcium > 1.5 mmol/L or Calcium > 12 mg/dL or
adjusted serum Calcium ≥ ULN) or symptomatic hypercalcemia requiring bisphosphate or
denosumab. *Patients without history of clinically significant hypercalcemia, receiving either
bisphosphonate or denosumab prophylactically is eligible. ** Denosumab receiving patients should agree to switch to bisphosphate, and not
contraindicated for bisphosphate use are eligible. 16. Patients with active virus infection requiring systemic treatment at screening 1)
Positive test for HIV infection 2) Active HBV hepatitis: positive for HBsAg and
HBV-DNA, if HBsAg positive but HBV-DNA negative during the screening can participate
in the study.3) Active HCV hepatitis: positive for hepatitis C virus (HCV) antibody
and HCV RNA. But the subject can be enrolled with serum anti-HCV positive and HCV
RNA negative.
17. Patients with autoimmune disease requiring treatment at the time of screening
(appendix 3. List of autoimmune disease)1) Patients with adrenal or pituitary
insufficiency requiring physiological dose of corticosteroid such as tyrosine,
insulin. 2) Patients with leukoplakia, resolved pediatric asthma, atopic dermatitis,
type 1 diabetic, hypothyroidism due to autoimmune disease only requiring hormone
replacement therapy, psoriasis not requiring systemic treatment, and other disease
status that recurrence nor exacerbations are not expected unless there is external
contributing factors. 18. Administration of a live, attenuated vaccine within 14 days before randomization or
anticipation that such a live attenuated vaccine will be required during the
study.1) Measles, mumps, rubella, chickenpox, yellow fever, rabies, Bacillus
Calmette-Guérin, BCG, herpes zoster, typhoid vaccines. 2) Seasonal influenza vaccine
in injection formulation are generally not live vaccine, thus are allowed. Yet
intra-nasal influenza vaccine such as Flumist® is attenuated live vaccine, thus is
not allowed. 19. History of severe allergic, anaphylactic, or other hypersensitivity reactions to
chimeric or humanized antibodies or fusion proteins. 20. Severe infections within 2 weeks prior to randomization, including but not limited
to hospitalization for complications of infection, bacteremia, or severe pneumonia. 21. Prior allogeneic bone marrow transplantation or prior solid organ transplantation. 22. Treatment with systemic immunosuppressive medications (including daily prednisone >
30mg, dexamethasone > 5mg, or equivalent dose of corticosteroid, cyclophosphamide,
azathioprine, methotrexate, thalidomide, and TNF-α antagonists but not limited to)
within 2 weeks prior to randomization. 1) Patients who acutely receives low dose
immunosuppressive medication (e.g. daily prednisone ≤ 30 mg or daily dexamethasone ≤
5 mg) can be enrolled upon approval from study medical monitor. 2) The use of
inhaled corticosteroids (e.g., fluticasone for chronic obstructive pulmonary
disease) is allowed. 3) The use of oral mineralocorticoids (e.g., fludrocortisone
for patients with orthostatic hypotension) is allowed.
23. History of idiopathic pulmonary fibrosis, pneumonitis (including drug induced),
organizing pneumonia (i.e., bronchiolitis obliterans, cryptogenic organizing
pneumonia, etc.), or evidence of active pneumonitis * History of radiation
pneumonitis in the radiation field (fibrosis) is allowed."
