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PIRG: The Assessment of Immune Response in Newly Diagnosed Glioblastoma Patients Treated With Pembrolizumab

Sponsor
Medical University of Silesia (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05235737
Collaborator
Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice (Other)
36
Enrollment
3
Arms
51
Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

To evaluate the short-term and longer-term safety, tolerability, and effectiveness of neoadjuvant and adjuvant Pembrolizumab on top of standard therapy (Stupp protocol) in patients with Glioblastoma Multiforme (GBM).

Randomized comparison of safety, tolerability, and clinical efficacy of (1) neoadjuvant and adjuvant Pembrolizumab (on top of Stupp protocol, n=12 patients), (2) neoadjuvant Pembrolizumab (on top of Stupp protocol, n=12 patients), and (3) standard of care (Stupp protocol only, n=12 patients). Immuno-PET examination will be performed before and after surgery in all patients.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

This is an open-label, Phase IV study of Pembrolizumab employed in neoadjuvant and adjuvant setting on top of standard therapy to evaluate the short-term and long-term safety, tolerability and efficacy in disease control in Glioblastoma Multiforme (GBM) patients. The control arm will be a group of patients treated in accordance with Standard of Care (SoC).

The study will include 3 treatment arms (up to n=12 evaluable patients per arm) and will be conducted at single site in Poland.

Patients with GBM will be randomly assigned in 1:1:1 ratio into one of 3 treatment arms:

  • Treatment arm 1 - n=12 evaluable patients - neoadjuvant Pembrolizumab (2 doses, 200mg each) plus adjuvant Pembrolizumab (16 cycles q3w, 200mg each) on top of standard chemo-radiotherapy (Stupp protocol: radiotherapy 60Gy over 6 weeks, 2 Gy per daily fraction Mo-Fri setting plus Temozolomide 75mg/m2 BSA daily during radiotherapy and six cycles post-radiotherapy of 150-200mg/m2 BSA for 5 days in each 28-day cycle)

  • Treatment arm 2 - n=12 evaluable patients - neoadjuvant Pembrolizumab (2 doses, 200mg each) on top of standard chemo-radiotherapy (Stupp protocol: radiotherapy 60Gy over 6 weeks, 2 Gy per daily fraction Mo-Fri setting plus Temozolomide 75mg/m2 BSA daily during radiotherapy and six cycles post-radiotherapy of 150-200mg/m2 BSA for 5 days in each 28-day cycle)

  • Treatment arm 3 - n=12 evaluable patients - standard chemo-radiotherapy (Stupp protocol: radiotherapy 60Gy over 6 weeks, 2 Gy per daily fraction Mo-Fri setting plus Temozolomide 75mg/m2 BSA daily during radiotherapy and six cycles post-radiotherapy of 150-200mg/m2 BSA for 5 days in each 28-day cycle) A pre-screening period will identify potential candidates for enrollment. Once qualified to the study patients will be randomized to one of the treatment arms. Then patients randomized to treatment arm 1 and 2 will receive first dose of neoadjuvant Pembrolizumab on day 4 and day 18 (200mg each). An immuno-PET scan for these arm 1 and 2 patients will be performed on day 29 and 30. Up to 72 hours after last immuno-PET scan all patients will undergo tumor resection. After surgery all patients will be treated in accordance with standard of care (Stupp protocol) with combined radio- and chemotherapy. Radiotherapy will consist of 60Gy over 6 weeks in daily fraction of 2Gy in Mo-Fri setting and parallel chemotherapy with Temozolomide of 75mg/m2 of BSA on a daily basis. After completion of radiotherapy the chemotherapy will continue for six cycles of 28 days with 150-200mg/m2 Temozolomide on days 1-5 of each cycle. In addition, patients randomized to arm 1 will receive 16 cycles of 21 days with Pembrolizumab treatment in adjuvant setting of 200mg/cycle.

During treatment period all patients will be assessed every three months and MRI will be performed in order to evaluate disease status/response.

After EOT patient's follow up period will continue for up to 3 years from initial resection with MRI assessment every 3 months.

If progression/relapse is identified, patients will undergo a tumor resection or biopsy within 48 hours thereafter.

All patients will then stay in follow up until the end of three years follow up period or death from any cause.

The evaluation of safety, tolerability, and quality-of-life (QoL) will be based on adverse event reporting criteria (Common Terminology Criteria for Adverse Events - CTCAE/WHO Classification of Diseases - ICD10), ECOG status assessment, KPS assessment, EORTC - QLQ-C30 and EORTC-QLQ-BN20 scale.

Clinical assessment will be based on Response Assessment in Neuro-Oncology (RANO). For patients treated with immunotherapy beyond onset of objective disease progression, the iRANO scale will be used within first 6 months of immunotherapy.

Due to a significant risk of identifying other pathology than GBM (i.e. metastasic tumor) in post-surgery histopathology it is anticipated that up to additional 6 patients may be recruited in order to achieve planned number of evaluable patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Masking Description:
Open Label
Primary Purpose:
Treatment
Official Title:
A Single Center, Open-Label, Randomized Study to Evaluate the Safety and Efficacy of Neoadjuvant and Adjuvant Pembrolizumab on Top of Standard Chemo-Radiotherapy (Stupp Protocol) in Treatment of Patients With Newly Diagnosed Glioblastoma Multiforme (GBM).
Anticipated Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2025
Anticipated Study Completion Date :
May 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Treatment arm 1

n=12 evaluable patients - neoadjuvant Pembrolizumab (2 doses, 200mg each) plus adjuvant Pembrolizumab (16 cycles q3w, 200mg each) on top of standard chemo-radiotherapy (Stupp protocol: radiotherapy 60Gy over 6 weeks, 2 Gy per daily fraction Mo-Fri setting plus Temozolomide 75mg/m2 of body surface area (BSA) daily during radiotherapy and six cycles post-radiotherapy of 150-200mg/m2 for 5 days in each 28-day cycle)

Drug: Pembrolizumab
Adding Pembrolizumab as a neoadjuvant and adjuvant therapy to the standard of care protocol
Active Comparator: Treatment arm 2

n=12 evaluable patients - neoadjuvant Pembrolizumab (2 doses, 200mg each) on top of standard chemo-radiotherapy (Stupp protocol: radiotherapy 60Gy over 6 weeks, 2 Gy per daily fraction Mo-Fri setting plus Temozolomide 75mg/m2 BSA daily during radiotherapy and six cycles post-radiotherapy of 150-200mg/m2 for 5 days in each 28-day cycle)

Drug: Pembrolizumab
Adding Pembrolizumab as a neoadjuvant therapy to the standard of care protocol
No Intervention: Treatment arm 3

n=12 evaluable patients - standard chemo-radiotherapy (Stupp protocol: radiotherapy 60Gy over 6 weeks, 2 Gy per daily fraction Mo-Fri setting plus Temozolomide 75mg/m2 BSA daily during radiotherapy and six cycles post-radiotherapy of 150-200mg/m2 for 5 days in each 28-day cycle)

Outcome Measures

Primary Outcome Measures

  1. Overall survival [3 years after initial tumor surgery]

    Proportion of patients remaining alive from initial tumor resection

  2. Progression-free survival [3 years after initial tumor surgery]

    Time from initial tumor resection to the first occurrence of progression/relapse or death from any cause, whichever occurs first

Secondary Outcome Measures

  1. Time-to-progression [3 years after initial tumor surgery]

    Time from initiation of study treatment to disease progression/relapse

Other Outcome Measures

  1. Usability assessment of immuno-PET imaging with 89Zr-DFO-Atezolizumab for quantitative analysis of early changes in PD-L1 expression [48 hours after surgery]

    Immuno-PET scans (Standardized Uptake Values) will be correlated with the level and distribution of T cell activation markers.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

  1. Signed Informed Consent Form

  2. Age ≥ 18 years

  3. Age ≤70 years

  4. Able to comply with the study protocol in the investigator's judgment

  5. Clinically and radiologically (contrast CT, full profile MRI - T1-weighted with or without contrast, T2-weighted, FLAIR, DWI, PWI, MR-spectroscopy) confirmed diagnosis of GBM, localized outside eloquent brain areas

  6. Resectable tumor

  7. Fully physically active ≥80 points in Karnofsky performance scale

  8. Life expectancy of at least 3 months

  9. Adequate organ function (confirmed within 1 weeks before enrollment):

  10. Hemoglobin ≥ 9g/dL

  11. Absolute Neutrophils Count (ANC) ≥1.5×109/L

  12. White Blood Cells (WBC) count ≥3×109/L

  13. Platelets (PTL) ≥ 100×109/L

  14. AST/ALT ≤2.5×ULN

  15. Serum creatinine (S-Cr) ≤ ULN

  16. Glomerular Filtration Rate (GFR) ≥50mL/min

  17. Albumin ≥ LLN

  18. Bilirubin ≤ 1.5 ULN (except patients with documented Gilbert's Syndrome, who must present adequate level of direct bilirubin)

  19. International normalized ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5×ULN. (Elevation of INR and aPTT due to administration of anticoagulation drugs is not a contraindication for the enrollment. However, it must return to normal range prior to surgery).

  20. For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use double barrier contraceptive methods that result in a failure rate of < 1% per year during the treatment period and for at least 120 days after the last immuno-PET imaging.

  21. For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use double barrier contraceptive methods that result in a failure rate of < 1% per year during the treatment period and for at least 120 days after the last immuno-PET imaging.

Exclusion criteria:
Patients who meet any of the following criteria will be excluded from study entry:

  1. Any active concomitant malignancy, except:

  2. Locally treated basal or squamous cell carcinoma

  3. Cervical carcinoma in situ

  4. Breast cancer in situ

  5. Bladder cancer in situ

  6. Low grade prostate cancer (under observation with PSA level in normal range)

  7. Any previous systemic cancer treatment, including, but not limited to:

  8. Radiotherapy

  9. Brachytherapy for brain tumor

  10. Chemotherapy

  11. Carmustine wafer treatment (Gliadel®)

  12. Any immune checkpoint inhibitor therapy or any anticancer vaccination

  13. Hypersensitivity or allergy to any substance with similar action mechanism to Pembrolizumab, Atezolizumab, Temozolomide, other monoclonal antibodies or contrast agents

  14. Any active immunosuppressive systemic therapy (except corticosteroids under 12mg)

  15. Any active autoimmune disease or systemic therapy for autoimmune disease within 2 years before enrollment

  16. History of any immunodeficiency

  17. Active infection

  18. Significant cardiovascular disease, such as New York Heart Association cardiac disease ≥ Class III, myocardial infarction within 3 months, coronary artery disease, unstable arrhythmias or unstable angina

  19. Active liver disease, hepatitis, HBV or HCV infection

  20. History of tuberculosis

  21. Any mental disorder that may affect patient's participation

  22. Any drug or psychoactive substance dependence

  23. Evidence of significant uncontrolled concomitant disease that could affect compliance with the protocol

  24. Treatment with any other investigational agent or participation in another clinical trial with therapeutic intent within 28 days prior to study treatment initiation

  25. Major surgical procedure within 4 weeks prior to study enrollment or anticipation of need for a major surgical procedure during the course of the study other than for diagnosis

  26. Any live vaccination within 30 days before enrollment

  27. Any active immunosuppressive systemic infection including history of human immunodeficiency virus (HIV) infection

  28. Body mass index (BMI) ≥ 35 kg/m2

  29. Pregnant or lactating or intending to become pregnant during the study - women who are not postmenopausal (postmenopausal defined as ≥ 12 months of non-drug-induced amenorrhea) or surgically sterile must have a negative serum pregnancy test result within 2 weeks prior to initiation of study treatment

  30. Any condition that the patient's physician determines to be detrimental to the patient participating in this study; including any clinically important deviations from normal clinical laboratory values or concurrent medical events.

  31. Inability to understand the local language for use of the patient QoL instruments.

  32. Tumor other than glioblastoma grade 4 IDH-wildtype, astrocytoma grade 3 or 4 IDH-mutant identified in post-surgery histopathology.

  33. Presence of 1p19q codeletion.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Medical University of Silesia
  • Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Wojciech Kaspera, Principal Investigator, Medical University of Silesia
ClinicalTrials.gov Identifier:
NCT05235737
Other Study ID Numbers:
  • 2019/ABM/01/00062
First Posted:
Feb 11, 2022
Last Update Posted:
Mar 10, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Wojciech Kaspera, Principal Investigator, Medical University of Silesia
Glioblastoma, Pembrolizumab, Immunotherapy, PD-1, PD-L1
Additional relevant MeSH terms:
Glioblastoma
Pembrolizumab

Study Results

No Results Posted as of Mar 10, 2022