Adenovirus Mediated Suicide Gene Therapy With Radiotherapy in Progressive Astrocytoma.

Glioblastoma Clinical Trial

Official title:

Phase I Study of Replication-Competent Adenovirus-Mediated Double Suicide Gene Therapy With Stereotactic Radiosurgery in Patients With Recurrent or Progressive High Grade Astrocytomas

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05686798
• Other study ID #: HFHS-21-02
• Status: Recruiting
• Phase: Phase 1
• Start date: November 29, 2022
• Est. completion date: October 2024

Study information

• Verified date: December 2023
• Source: Henry Ford Health System
• Contact: Tobias Walbert, MD, PhD
• Phone: 3139162723
• Email: twalber1[@]hfhs.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary goal of this Phase I study is to determine the maximum tolerated dose of oncolytic adenovirus mediated double suicide-gene therapy in combination with fractionated stereotactic radiosurgery in patients with recurrent high-grade astrocytoma undergoing resection.

Description:

Detailed study description: Patients with recurrent glioblastoma (GBM) or progressive high grade astrocytoma who are scheduled to undergo repeat surgery are eligible. After the removal of as much tumor tissue as possible, a modified oncolytic adenovirus is injected into the wall of the resection cavity and any residual tumor tissue. The goal of this study is to determine the maximum tolerated dose (MTD) of the injected adenovirus. This treatment is combined with a combination of oral 5-fluorocytosine (5-FC) and valganciclovir (vGCV) prodrug therapy. Following the surgery, patients will be treated with fractionated radiosurgery (fSRS). Patients will be monitored for 30 days before they start on next line anti-cancer therapy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 18
• Est. completion date: October 2024
• Est. primary completion date: October 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subjects with radiologic evidence of intracranial recurrence or progression of a previously diagnosed high-grade astrocytoma.

To be eligible for this trial, the subjects must have:

• Histologically documented glioblastomas or anaplastic astrocytoma prior to the debulking surgery that is suspicious to have progressed on imaging. An interval of at least 3 months must have elapsed since the completion of the most recent course of radiation while at least 4 weeks must have elapsed since the completion of a non-nitrosourea containing chemotherapy regimen and at least 6 weeks since the completion of a nitrosourea containing chemotherapy regimen.
• Patients must be = 18 years of age, able to provide informed consent and express a willingness to meet all the expected requirements of the protocol for the duration of the study.
• Must have recovered from toxicity (grade 2 or less) of prior therapy.
• Eligible for partial or total resection of the recurrent tumor
• No anticipated physical connection between post-resection tumor cavity and cerebral ventricle
• Karnofsky performance status (KPS) = 60 at time of surgery
• No prior treatment of the tumor with gene or virus therapy, immunotherapy, brachytherapy, or implants of polymers containing chemotherapeutic agents (e.g. Gliadel Wafer)
• No immunosuppressive or immune disorder
• Baseline organ function testing intact
• Patients who are candidates for surgical debulking (re-resection) following recurrence of diseases based on multidisciplinary evaluation by neurosurgeons, radiation oncologists, neuro-radiologists, and neuro-oncologists.

2. Subjects must have adequate baseline organ function, as assessed by the following

laboratory values, within 30 days before initiating the study therapy:

• Adequate renal function with creatinine clearance = 50 mL/min/m2
• Platelet count = 100,000/µL
• Absolute neutrophil count = 1,000/µL
• Hemoglobin > 10.0 g/dL
• Bilirubin < 1.5 mg/dL; SGOT and SGPT < 2.5 times upper limit of normal (ULN).

3. Women of child-bearing potential will be required to practice birth control for the duration of the treatment and for at least 90 days after surgery with intratumor virus inoculation. Men must use barrier protection for the duration of treatment and for at least 90 days after surgery with intratumor virus inoculation treatment.

Exclusion Criteria:

• Acute infection. Acute infection is defined by any viral, bacterial, or fungal infection that has required active treatment and caused oral temperature >38.5oC and/or clinically significant leukocytosis
• Serum antibodies to human immunodeficiency virus (HIV)
• Previous history of liver disease including autoimmune or viral hepatitis
• Positive serologic test for Hepatitis B or C at baseline
• Immunosuppressive therapy except for corticosteroid use
• Serious medical or psychiatric illness or concomitant medication, which, in the judgment of the investigator, might interfere with the subject's ability to respond to or tolerate the treatment or complete the trial
• Impaired immunity or susceptibility to serious viral infections
• Pregnant or lactating females
• Allergy to any product used on the protocol
• Patient is not able to undergo a brain MRI.
• Patients who are not eligible for debulking surgery or resection of recurrent disease will be considered ineligible.

Related Conditions & MeSH terms

• Astrocytoma
• Brain Cancer
• Brain Neoplasms
• Brain Tumor
• GBM
• Glioblastoma
• Glioblastoma Multiforme
• Glioma
• Malignant Astrocytoma
• Malignant Glioma of Brain
• Suicide

Intervention

Biological:
• Ad5-yCD/mutTKSR39rep-ADP adenovirus and fractionated stereotactic radiosurgery (fSRS)
Ad5-yCD/mutTKSR39rep-ADP adenovirus will be injected intratumoral

Locations

Country	Name	City	State
United States	Henry Ford Health System	Detroit	Michigan

Sponsors (1)

Lead Sponsor	Collaborator
Henry Ford Health System

Country where clinical trial is conducted

United States, 

References & Publications (6)

Chen SH, Shine HD, Goodman JC, Grossman RG, Woo SL. Gene therapy for brain tumors: regression of experimental gliomas by adenovirus-mediated gene transfer in vivo. Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):3054-7. doi: 10.1073/pnas.91.8.3054. — View Citation

Ene CI, Fueyo J, Lang FF. Delta-24 adenoviral therapy for glioblastoma: evolution from the bench to bedside and future considerations. Neurosurg Focus. 2021 Feb;50(2):E6. doi: 10.3171/2020.11.FOCUS20853. — View Citation

Freytag SO, Rogulski KR, Paielli DL, Gilbert JD, Kim JH. A novel three-pronged approach to kill cancer cells selectively: concomitant viral, double suicide gene, and radiotherapy. Hum Gene Ther. 1998 Jun 10;9(9):1323-33. doi: 10.1089/hum.1998.9.9-1323. — View Citation

Kiyokawa J, Wakimoto H. Preclinical And Clinical Development Of Oncolytic Adenovirus For The Treatment Of Malignant Glioma. Oncolytic Virother. 2019 Oct 24;8:27-37. doi: 10.2147/OV.S196403. eCollection 2019. — View Citation

Mitchell LA, Lopez Espinoza F, Mendoza D, Kato Y, Inagaki A, Hiraoka K, Kasahara N, Gruber HE, Jolly DJ, Robbins JM. Toca 511 gene transfer and treatment with the prodrug, 5-fluorocytosine, promotes durable antitumor immunity in a mouse glioma model. Neuro Oncol. 2017 Jul 1;19(7):930-939. doi: 10.1093/neuonc/nox037. — View Citation

Oldfield EH, Ram Z, Culver KW, Blaese RM, DeVroom HL, Anderson WF. Gene therapy for the treatment of brain tumors using intra-tumoral transduction with the thymidine kinase gene and intravenous ganciclovir. Hum Gene Ther. 1993 Feb;4(1):39-69. doi: 10.1089/hum.1993.4.1-39. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Quality of life as assessed using the European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30	Assessment of quality of life (QOL) by using the European Organization for Research and Treatment of Cancer (EORTC) tools consisting of the EORTC QLQ-C30	Pre-surgery (day 0), 30 days, 90 days
Other	Quality of life as assessed using the European Organization for Research and Treatment of Cancer (EORTC) QLQ-BN20	Assessment of quality of life (QOL) by using the European Organization for Research and Treatment of Cancer (EORTC) QLQ-BN20	Pre-surgery (day 0), 30 days, 90 days
Primary	Maximum Tolerated Dose	The primary objective is to determine the maximum tolerated dose of injected of Ad5-yCD/mutTKSR39rep-ADP adenovirus into the resection cavity at the time of surgery.	30 days
Secondary	1. Assessment of antitumor immune response	Assessment of antitumor immune response by serum levels of interferon-gamma (IFN-?) measured by ELISA and will be described by pico-gram per milliliter (pg/mL).	Pre-surgery (day 0), 3, 7, 14, 21, 30, 90 days.
Secondary	2. Assessment of change in antitumor immune response by peripheral blood monoclonal cell (PBMC) counts	Assessment of change in antitumor immune response by peripheral blood monoclonal cell (PBMC) counts measured by flow cytometry	Pre-surgery (day 0), 3, 7, 14, 21, 30, 90 days.
Secondary	Assessment of antitumor immune response by using antibodies against surface markers	Assessment of antitumor immune response by using antibodies against surface markers (CD3, CD56, CD4, CD8, CD45, CD69).	Pre-surgery (day 0), 3, 7, 14, 21, 30, 90 days.