Overview

This is to study if neoadjuvant atezolizumab therapy is beneficial for patients with recurrent glioblastoma and a low mutational burden.

Eligibility

Inclusion Criteria:

1. Age ≥ 18 years old
2. Pathologically confirmed GBM, IDHwt
3. Clinical or radiologic evidence of first or second recurrence following radiation and TMZ. Note: A diagnostic biopsy is required prior to the commencement of the study drug if there is uncertainty about the MRI findings being true progression versus pseudoprogression.
4. Tissue available from initial diagnosis of primary GBM
5. Adequate organ function:
   1. Hemoglobin ≥ 9 g/dl
   2. Platelet count ≥ 75,000/µl
   3. Neutrophil count ≥ 1000 cells/mm3
   4. Creatinine ≤ 1.5 x ULN (calculated using the Cockcroft-Gault formula)
   5. Total bilirubin ≤ 1.5 x ULN (Exception: Participant has known or suspected Gilbert's Syndrome for which additional lab testing of direct and/or indirect bilirubin supports this diagnosis. In these instances, a total bilirubin of ≤ 3.0 x ULN is acceptable.)
   6. Alkaline phosphatase (ALP) ≤ 2.5 x upper limit of normal (ULN)
   7. AST and ALT ≤ 2.5 x ULN
   8. Serum albumin ≥ 25 g/L (2.5 g/dL)
   9. Prothrombin and Partial Thromboplastin Times ≤ 1.2 x ULN
6. Karnofsky Performance Status (KPS) ≥ 70%
7. Patient or partner(s) meets one of the following criteria:
   1. Non-childbearing potential (i.e., not sexually active, physiologically incapable of becoming pregnant, including any female who is post-menopausal or surgically sterile, or any male who has had a vasectomy). Surgically sterile females are defined as those with a documented hysterectomy and/or bilateral oophorectomy or tubal ligation. Postmenopausal for purposes of this study is defined as 1 year without menses.; or
   2. Childbearing potential and agrees to use one of the following methods of birth control: approved hormonal contraceptives (e.g., birth control pills, patches, implants, or infusions), an intrauterine device, or a barrier method of contraception (e.g., a condom or diaphragm) used with spermicide.
8. A signed informed consent form approved by the Institutional Review Board (IRB) will

   be required for patient enrollment into the study. Patients must be able to read and understand the informed consent document and must sign the informed consent indicating that they are aware of the investigational nature of this study.

9. Negative HIV test at screening, with the following exception: patients with a positive HIV test at screening are eligible provided they are stable on anti-retroviral therapy, have a CD4 count > 200/µL, and have an undetectable viral load
10. Negative hepatitis B surface antigen (HBsAg) test at screening. Negative total hepatitis B core antibody (HBcAb) test at screening, or positive total HBcAb test followed by a negative hepatitis B virus (HBV) DNA test at screening Note: The HBV DNA test will be performed only for patients who have a negative HBsAg test and a positive total HBcAb test.
11. Negative hepatitis C virus (HCV) antibody test at screening, or positive HCV antibody test followed by a negative HCV RNA test at screening Note: The HCV RNA test must be performed for patients who have a positive HCV antibody test.

Exclusion Criteria:

1. Pregnancy or breastfeeding or intention of becoming pregnant during study treatment or within 5 months of final dose of atezolizumab therapy
   1. For women of childbearing potential: Agree to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods as defined below: i) Women must remain abstinent or use contraceptive methods with a failure rate of < 1% per year during the treatment period and for 5 months after the final dose of atezolizumab. Examples of contraceptive methods with a failure rate of < 1% per year include bilateral tubal ligation, male sterilization, hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices. 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 adequate methods of contraception. If required per local guidelines or regulations, locally recognized adequate methods of contraception and information about the reliability of abstinence will be described in the local Informed Consent Form.

     ii) A woman is of childbearing potential if she is post-menarchal, 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, fallopian tubes and/or uterus) or another cause as determined by the
     investigator (e.g., Müllerian agenesis). Per this definition, a woman with a tubal
     ligation is of childbearing potential. The definition of childbearing potential may
     be adapted for alignment with local guidelines or requirements.
     b) For men with pregnant female partners and/or with female partners of childbearing
     potential: Agree to remain abstinent (refrain from heterosexual intercourse) or use
     a condom and refrain from donating sperm.
     i) With a female partner of childbearing potential or pregnant female partner, men
     must remain abstinent or use a condom during the treatment period for 5 months after
     the final dose of atezolizumab 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 (e.g., calendar, ovulation,
     symptothermal, or postovulation methods) and withdrawal are not adequate methods of
     preventing drug exposure. If required per local guidelines or regulations,
     information about the reliability of abstinence will be described in the local
     Informed Consent Form.

2. Prior treatment with immunotherapy

3. Prior treatment with bevacizumab within 4 weeks before biopsy. Note: Bevacizumab

     will be permitted if necessary to control inflammatory side effects 5-7mg/kg Q 3/52
     for up to 3 cycles

4. Treatment with systemic immunosuppressive medication (including, but not limited to,

     more than 2 mg of dexamethasone or equivalent corticosteroids, cyclophosphamide,
     azathioprine, methotrexate, thalidomide, and anti-TNF-a agents) within 2 weeks prior
     to initiation of study treatment, or anticipation of need for systemic
     immunosuppressive medication during study treatment, with the following exceptions:
       1. Patients who received acute, low-dose systemic immunosuppressant medication or
          a one-time pulse dose of systemic immunosuppressant medication (e.g., 48 hours
          of corticosteroids for a contrast allergy) are eligible for the study.
       2. Patients who received mineralocorticoids (e.g., fludrocortisone),
          corticosteroids for chronic obstructive pulmonary disease (COPD) or asthma, or
          low-dose corticosteroids for orthostatic hypotension or adrenal insufficiency
          are eligible for the study.

5. History of severe allergic anaphylactic reactions to chimeric or humanized

antibodies or fusion proteins

6. Known hypersensitivity to Chinese hamster ovary cell products or to any component of

the atezolizumab formulation

7. Active autoimmune disease or immune deficiency, including, but not limited to,

     myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus,
     rheumatoid arthritis, inflammatory bowel disease, antiphospholipid antibody
     syndrome, Wegener granulomatosis, Sjögren syndrome, Guillain-Barré syndrome, or
     multiple sclerosis (see Appendix E in Section 16.5 for a more comprehensive list of
     autoimmune diseases and immune deficiencies), with the following exceptions:
       1. Patients with a history of autoimmune-related hypothyroidism who are on
          thyroid-replacement hormone are eligible for the study.
       2. Patients with controlled Type 1 diabetes mellitus who are on an insulin regimen
          are eligible for the study.
       3. Patients with eczema, psoriasis, lichen simplex chronicus, or vitiligo with
          dermatologic manifestations only (e.g., patients with psoriatic arthritis are
          excluded) are eligible for the study provided all of following conditions are
          met:
     i) Rash must cover < 10% of body surface area ii) Disease is well controlled at
     baseline and requires only low-potency topical corticosteroids iii) There has been
     no occurrence of acute exacerbations of the underlying condition requiring psoralen
     plus ultraviolet A radiation, methotrexate, retinoids, biologic agents, oral
     calcineurin inhibitors, or high-potency or oral corticosteroids within the previous
     12 months.

8. < 12 weeks from radiation therapy, unless progressive disease outside of previous

     radiation field or 2 progressive MRIs, 4 weeks apart; (to avoid enrolling patients
     with pseudoprogression)

9. Contraindication to surgery

10. Significant cardiovascular disease (such as New York Heart Association Class II or

     greater cardiac disease, myocardial infarction, or cerebrovascular accident) within
     3 months prior to initiation of study treatment, unstable arrhythmia, or unstable
     angina

11. Major surgical procedure, other than for diagnosis, within 4 weeks prior to

     initiation of study treatment, or anticipation of need for a major surgical
     procedure during the study

12. History of malignancy within 12 months prior to screening, with the exception of

     malignancies with a negligible risk of metastasis or death (e.g., 5-year OS rate >
     90%), such as adequately treated carcinoma in situ of the cervix, non-melanoma skin
     carcinoma, localized prostate cancer, ductal carcinoma in situ, or Stage 1 uterine
     cancer.

13. Severe infection within 4 weeks prior to initiation of study treatment, including,

     but not limited to, hospitalization for complications of infection, bacteremia, or
     severe pneumonia, or any active infection that could impact patient safety

14. Treatment with a live, attenuated vaccine within 4 weeks prior to initiation of

     study treatment, or anticipation of need for such a vaccine during atezolizumab
     treatment or within 5 months after the final dose of atezolizumab

15. Treatment with investigational therapy within 28 days prior to initiation of study

treatment

16. Prior treatment with CD137 agonists or immune checkpoint blockade therapies,

including anti-CTLA-4, anti-PD-1, and anti-PD-L1 therapeutic antibodies

17. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent

     drainage procedures (once monthly or more frequently). Patients with indwelling
     catheters (e.g., PleurX) are allowed.

18. Uncontrolled or symptomatic hypercalcemia (ionized calcium > 1.5 mmol/L, calcium >

12 mg/dL or corrected serum calcium > ULN)

19. Active tuberculosis

20. History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis

     obliterans), drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of
     active pneumonitis. History of radiation pneumonitis in the radiation field
     (fibrosis) is permitted.

21. Treatment with therapeutic oral or IV antibiotics within 2 weeks prior to initiation

     of study treatment. Patients receiving prophylactic antibiotics (e.g., to prevent a
     urinary tract infection or chronic obstructive pulmonary disease exacerbation) are
     eligible for the study.

22. Prior allogeneic stem cell or solid organ transplantation