Brain Stem Gliomas Treated With Adoptive Cellular Therapy During Focal Radiotherapy Recovery Alone or With Dose-intensified Temozolomide (Phase I) (BRAVO)

• ClinicalTrials.gov Identifier: NCT03396575
• Recruitment Status: Recruiting
• First Posted: January 11, 2018
• Last Update Posted: February 3, 2023
• Sponsor: University of Florida
• Collaborators: Accelerate Brain Cancer Cure; Lyla Nsouli Foundation
• Information provided by (Responsible Party): University of Florida

Study Description

Brief Summary:

The standard of care for children with DIPG includes focal radiotherapy (RT) but outcomes have remained dismal despite this treatment. The addition of oral Temozolomide (TMZ) concurrently with RT followed by monthly TMZ was also found to be safe but ineffective. Recent studies in adults have shown that certain types of chemotherapy induce a profound but transient lymphopenia (low blood lymphocytes) and vaccinating and/or the adoptive transfer of tumor-specific lymphocytes into the cancer patient during this lymphopenic state leads to dramatic T cell expansion and potent immunologic and clinical responses. Therefore, patients in this study will either receive concurrent TMZ during RT and immunotherapy during and after maintenance cycles of dose-intensive TMZ (Group A) or focal radiotherapy alone and immunotherapy without maintenance DI TMZ (Group B). Immune responses during cycles of DC vaccination with or without DI TMZ will be evaluated in both treatment groups.

Condition or disease	Intervention/treatment	Phase
Diffuse Intrinsic Pontine Glioma (DIPG); Brain Stem Glioma	Biological: TTRNA-DC vaccines with GM-CSF; Biological: TTRNA-xALT; Drug: Cyclophosphamide + Fludarabine Lymphodepletive Conditioning; Drug: Dose-Intensified TMZ; Drug: Td vaccine; Biological: Autologous Hematopoietic Stem Cells (HSC)	Phase 1

Detailed Description:

The standard of care for children with DIPG includes external beam focal radiotherapy (RT) but outcomes have remained dismal despite this treatment. The addition of oral Temozolomide (TMZ) concurrently with focal irradiation followed by maintenance monthly TMZ was also found to be safe but ineffective. However, in the context of an immunotherapy strategy, it might be beneficial to use TMZ as an adjuvant therapy during and following radiotherapy. Recent pre-clinical and clinical studies in adults with have shown that both myeloablative (MA) and non-myeloablative (NMA) chemotherapy induce a profound but transient lymphopenia and, somewhat counterintuitively, vaccination during recovery from this lymphopenic state and/or the adoptive transfer of tumor-specific lymphocytes into lymphodepleted hosts leads to dramatic in vivo T cell expansion and potent immunologic and clinical responses. Therefore, the study team expects that tumor-specific lymphocytes, expanded ex vivo with the use of TTRNA-pulsed DCs may provide a source of lymphocytes that preferentially expand in this lymphopenic environment following TMZ, and serve as a source of responder cells to subsequent DC vaccination.

TMZ induces profound lymphopenia in children with central nervous system (CNS) tumors. It has not been conclusively shown to help in augmenting vaccine-induced immune responses in this population. Patients in this study will either receive concurrent TMZ during RT and immunotherapy during and after maintenance cycles of dose-intensive TMZ (Group A) or focal radiotherapy alone and immunotherapy without maintenance DI TMZ (Group B). Immune responses during cycles of DC vaccination with or without DI TMZ will be evaluated in both treatment groups. The immunotherapy regimen will consist of TTRNA-DC vaccines alone followed by adoptive cellular therapy consisting of ex vivo expanded tumor-reactive lymphocytes coupled with TTRNA-DC vaccines and autologous HSCs.

Patients in Group B will not receive DI TMZ, however, they will receive lymphodepletion with cyclophosphamide + fludarabine after DC vaccination and prior to the intravenous infusion of ex vivo expanded tumor-reactive lymphocytes. T cell engraftment and persistence has been shown to be augmented by lymphodepletion in numerous studies. TTRNA-pulsed DCs will be given in conjunction with the adjuvants GM-CSF and tetanus-diphtheria toxoid (Td) vaccine which the study team have shown can significantly enhance clinical responses to DC vaccination.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 21 participants
• Allocation: Non-Randomized
• Intervention Model: Sequential Assignment

Intervention Model Description

Patients in this study will either receive concurrent TMZ during RT and dose-intensive TMZ as maintenance treatment (Group A) or radiotherapy only prior to DC vaccination and without maintenance DI TMZ (Group B). Immune responses during cycles of DC vaccination with or without DI TMZ will be evaluated in both treatment groups.

Once Group A accrual is completed and evaluated for toxicity, 6 Group B patients will be enrolled and treated at the Maximally Achievable Dose (MAD) or (Maximum Tolerated Dose) MTD determined in Group A cohort.

• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: BRAVO: Newly-Diagnosed Brain Stem Gliomas Treated With Adoptive Cellular Therapy During Recovery From Focal Radiotherapy Alone or Focal Radiotherapy and Dose-intensified Temozolomide (Phase I)
• Actual Study Start Date: May 17, 2018
• Estimated Primary Completion Date: December 2024
• Estimated Study Completion Date: June 2025

Arms and Interventions

Arm	Intervention/treatment
Experimental: Group A; TTRNA-DC vaccines with GM-CSF and TTRNA-xALT plus Td vaccine with Autologous Hematopoietic Stem cells (HSCs) during cycles of Dose-intensified TMZ	Biological: TTRNA-DC vaccines with GM-CSF; After chemoradiation subjects will receive the first cycle of dose-intensified TMZ followed by three biweekly TTRNA-DC vaccines with GM-CSF. Monthly DC vaccines will be given during TMZ Cycles 2-5 for Groups A and B and 48-96 hours after completion of TMZ Cycle 6 Day 21 for Group A and 12-36 hours after HSCs for Group B. All subjects will receive an additional two bi-weekly vaccines during Cycle 6 for a total of 10 DC vaccines. All DC vaccines will be embedded with GM-CSF (150 µg per injection) and given intradermal.; Biological: TTRNA-xALT; During TMZ Cycle 4 and with DC vaccine #6, an infusion of T-cells will be administered to all subjects.; Drug: Dose-Intensified TMZ; After chemoradiation, subjects in Group A will receive the first cycle of dose-intensified TMZ followed by three biweekly TTRNA-DC vaccines with GM-CSF. All subjects will have an additional five cycles of dose-intensified TMZ (for a total of 6 Cycles) with concurrent monthly DC vaccinations.; Drug: Td vaccine; A full Td booster vaccine will be administered IM at Vaccine #1 to all subjects, and vaccine site pretreatment will be administered to all subjects prior to Vaccine#3, #6, and #8.; Biological: Autologous Hematopoietic Stem Cells (HSC); During Cycle 4, all patients will receive HSCs prior to xALT infusion and DC vaccine #6.
Experimental: Group B; TTRNA-DC vaccines with GM-CSF and TTRNA-xALT plus Td vaccine with Autologous Hematopoietic Stem cells (HSCs) with Cyclophosphamide + Fludarabine Lymphodepletive Conditioning	Biological: TTRNA-DC vaccines with GM-CSF; After chemoradiation subjects will receive the first cycle of dose-intensified TMZ followed by three biweekly TTRNA-DC vaccines with GM-CSF. Monthly DC vaccines will be given during TMZ Cycles 2-5 for Groups A and B and 48-96 hours after completion of TMZ Cycle 6 Day 21 for Group A and 12-36 hours after HSCs for Group B. All subjects will receive an additional two bi-weekly vaccines during Cycle 6 for a total of 10 DC vaccines. All DC vaccines will be embedded with GM-CSF (150 µg per injection) and given intradermal.; Biological: TTRNA-xALT; During TMZ Cycle 4 and with DC vaccine #6, an infusion of T-cells will be administered to all subjects.; Drug: Cyclophosphamide + Fludarabine Lymphodepletive Conditioning; Subjects in Group B, however, will receive lymphodepletion with cyclophosphamide + fludarabine after DC vaccination and prior to the intravenous infusion of ex vivo expanded tumor-reactive lymphocytes.; Drug: Td vaccine; A full Td booster vaccine will be administered IM at Vaccine #1 to all subjects, and vaccine site pretreatment will be administered to all subjects prior to Vaccine#3, #6, and #8.; Biological: Autologous Hematopoietic Stem Cells (HSC); During Cycle 4, all patients will receive HSCs prior to xALT infusion and DC vaccine #6.

Outcome Measures

Primary Outcome Measures :

1. Feasibility and safety of adoptive cellular therapy in pediatric patients with DIPG with or without dose-intensified TMZ during cycles of DC vaccination [ Time Frame: From first DC Vaccine through 30 days after administration of the last dose of trial drug or subject death ]
   Number of subjects with immunotherapy-related dose-limiting toxicities including 1) Grade III or greater non-neurologic toxicity; 2) Grade III neurologic toxicity that does not improve to Grade II or better within 5 days; or 3) Grade IV neurologic toxicity.
2. Determine the maximally achievable dose (MAD) or maximum tolerated dose (MTD) of xALT plus DC and HSC in Group A and Group B subjects [ Time Frame: From first DC vaccine in Group A until 14 days after administration of the last dose of investigational product is given. ]
   The first 6 patients in Group A (receiving DI TMZ) at a dose of 3 x 107 cells /kg xALT and if dose-limiting toxicities are observed in no more than 1 of 6 patients, the study team will enroll another 6 patients at the next dose level of 3 x108 cells /kg. If no more than 1 patient suffers dose limiting toxicity (DLT) at this dose level, it will declared the MAD of T cells. Subjects enrolled in Group B will be treated at the MAD or MTD determined in the Group A Cohort.

Secondary Outcome Measures :

1. Post-immunotherapy functional anti-tumor immune responses [ Time Frame: Up to 10 months ]
   The in vivo expansion, persistence, and function of tumor-specific lymphocytes will be followed serially in these patients using T-cell receptor (TCR) sequencing and functional immunologic analysis.
2. Analysis of progression-free survival (PFS) [ Time Frame: Up to 5 years ]
   Days of PFS
3. Analysis of overall survival (OS) [ Time Frame: Up to 5 years ]
   Days of OS

Eligibility Criteria

• Ages Eligible for Study: 3 Years to 30 Years (Child, Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

Initial Screening

• Radiologically confirmed DIPG or other diffuse intrinsic brain stem glioma (Grade III or IV).
• Patient and/or parents/guardian willing to consent to biopsy for obtaining tumor material for confirmatory diagnosis and/or tumor RNA extraction and amplification.
• Biopsy confirmation of any grade of glioma (for patients with classic DIPG on neuroimaging or at least grade III glioma in case of other diffuse intrinsic brain stem gliomas)
• Karnofsky Performance Status (KPS) of > 50% (KPS for > 16 years of age) or Lansky performance Score (LPS) of ≥ 50 (LPS for ≤ 16 years of age) assessed within 2 weeks prior to registration;
• Bone Marrow;
• ANC (absolute neutrophil count) ≥ 1000/µl (unsupported)
• Platelets ≥ 100,000/µl (unsupported)
• Hemoglobin > 8 g/dL (can be transfused)
• Renal;
• Serum creatinine ≤ upper limit of institutional normal
• Hepatic;
• Bilirubin ≤ 1.5 times upper limit of institutional normal for age
• SGPT (ALT) ≤ 3 times upper limit of institutional normal for age
• SGOT (AST) ≤ 3 times upper limit of institutional normal for age
• Patients of childbearing or child-fathering potential must be willing to use medically acceptable forms of birth control while being treated on this study.
• Signed informed consent according to institutional guidelines.

Post Biopsy

• Patients with post-surgical neurological deficits should have deficits that are stable for a minimum of 1 week prior to registration;
• Pathologic diagnosis of glioma on tumor biopsy.

Exclusion Criteria:

• Patients with severe dysphagia, obtundation, or tetraplegia (poor risks for anesthesia and biopsy procedure);
• Absence of tumor on biopsy specimen;
• Pregnant or need to breast feed during the study period (Negative serum pregnancy test required)
• Known autoimmune or immunosuppressive disease or human immunodeficiency virus infection;
• Patients with significant renal, cardiac, pulmonary, hepatic or other organ dysfunction;
• Severe or unstable concurrent medical conditions;
• Patients who require corticosteroids above physiologic doses (>4 mg/day dexamethasone) after chemoradiotherapy;
• Patients scheduled to receive any other concurrent anticancer or investigational drug therapy;
• Prior allergic reaction to TMZ, GM-CSF, or Td;
• Patients who are unwilling or unable to receive treatment and undergo follow-up evaluations at University of Florida;
• Patient and/or parent/guardian demonstrating an inability to comply with the study and/or follow-up procedures.

Contacts and Locations

Contacts

Contact: Marcia Hodik, RN; 352-273-6971; marcia.hodik@neurosurgery.ufl.edu

Locations

United States, Florida

UF Health Shands Children's Hospital; Recruiting

Gainesville, Florida, United States, 32610

Contact: Marcia Hodik, RN 352-273-6971 marcia.hodik@neurosurgery.ufl.edu

Principal Investigator: Elias Sayour, MD, PhD

Sponsors and Collaborators

University of Florida

Accelerate Brain Cancer Cure

Lyla Nsouli Foundation

Investigators

• Principal Investigator: Elias Sayour, MD, PhD; University of Florida

More Information

• Responsible Party: University of Florida
• ClinicalTrials.gov Identifier: NCT03396575
• Other Study ID Numbers: IRB201701296; OCR16024 ( Other Identifier: University of Florida )
• First Posted: January 11, 2018
• Last Update Posted: February 3, 2023
• Last Verified: February 2023

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by University of Florida:

Tumor mRNA-pulsed autologous Dendritic Cells (TTRNA-DCs); Tumor-specific autologous lymphocyte transfer (TTRNA-xALT); Autologous G-CSF mobilized HSCs; Temozolomide (TMZ); Cyclophosphamide (CTX); Fludarabine (Flu); Immunotherapy; Pediatric; Young Adult; Brain Tumor; CNS; Vaccine Therapy

Additional relevant MeSH terms:

Glioma; Diffuse Intrinsic Pontine Glioma; Neoplasms, Neuroepithelial; Neuroectodermal Tumors; Neoplasms, Germ Cell and Embryonal; Neoplasms by Histologic Type; Neoplasms; Neoplasms, Glandular and Epithelial; Neoplasms, Nerve Tissue; Brain Stem Neoplasms; Infratentorial Neoplasms; Brain Neoplasms; Central Nervous System Neoplasms; Nervous System Neoplasms; Neoplasms by Site; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Cyclophosphamide; Fludarabine; Vaccines; Immunologic Factors; Physiological Effects of Drugs; Immunosuppressive Agents; Antirheumatic Agents; Antineoplastic Agents, Alkylating; Alkylating Agents; Molecular Mechanisms of Pharmacological Action; Antineoplastic Agents; Myeloablative Agonists