CED of MTX110 Newly Diagnosed Diffuse Midline Gliomas

A Phase I Study Examining the Feasibility of Intermittent Convection-Enhanced Delivery (CED) of MTX110 for the Treatment of Children With Newly Diagnosed Diffuse Midline Gliomas

The blood brain barrier (BBB) prevents some drugs from successfully reaching the target source. Convection-Enhanced Delivery (CED) is a method of direct infusion of drugs under controlled pressure to the tumor that may reduce systemic side effects of drugs in the patient.

The purpose of this Phase I study is to find the maximum tolerated dose of MTX110 (a water-soluble Panobinostat nanoparticle formulation) and Gadolinium that can be given safely in children with newly diagnosed diffuse midline gliomas. All patients enrolled in the study will receive infusion of MTX110 and Gadolinium delivered with a pump directly into the tumor over 9-11 days.

Study Overview

• Status: Completed
• Conditions: Diffuse Intrinsic Pontine Glioma; Diffuse Midline Glioma; Diffuse Pontine and Thalamic Gliomas
• Intervention / Treatment: Drug: Infusate with MTX110 and gadolinium; Device: Convection-Enhanced Delivery (CED)

Detailed Description

Diffuse midline gliomas (DMGs), constitute 10% of all pediatric central nervous system (CNS) tumors. Subjects with Diffuse Intrinsic Pontine Gliomas (DIPG) have a poor prognosis with a median survival that is usually reported to be 9 months, and nearly 90% of children die within 18 months from diagnosis. The mainstay of treatment is radiation to the primary tumor site. Surgical resection does not influence outcome and is often not feasible in this part of the central nervous system.

Many promising drugs for central nervous system (CNS) disorders have failed to attain clinical success due to an intact blood brain barrier (BBB), limiting their access form the systemic circulation into the brain. Systemic administration of high doses may increase delivery to the brain, but this approach risks significant side effects and systemic toxicities. Direct delivery of the drugs to the brain by injection into the parenchyma bypasses the BBB, however, drug distribution form the site of injection tends to be limited. The convection-enhanced delivery (CED) of drugs describes the infusion of drugs under controlled pressure to the brain parenchyma via targeted microcatheter. This technique facilitates and deliver higher drug concentrations in brain tissue or tumor. The BBB can now operate to retain drug and to significantly reduce systemic side effects. In addition, the fact that panobinostat seems to be most efficacious clinically available drug against DIPG cells.

• Study Type: Interventional
• Enrollment (Actual): 9
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Luca Szalontay, MD; Phone Number: (212) 305-9770; Email: ls3399@cumc.columbia.edu
• Study Contact Backup: Name: Jessica Morcone, RNP; Phone Number: 212-305-9770; Email: jm4393@cumc.columbia.edu

Study Locations

• United States
  • New York
    • New York, New York, United States, 10032
      • Columbia University Irving Medical Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 3 years to 18 years (Child, Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Aged more than 3 years up to the 18th birthday
• Radiological diagnosis of DIPG with tumor confined to the region of the pons or
• thalami without cystic changes or hematoma obstructing the planned catheter trajectories
• Radiological diagnosis of thalamic gliomas confined to bilateral thalami without cystic changes or hematoma obstructing the planned catheter trajectories
• Radiological features of DIPG: intrinsic, pontine based infiltrative lesion; hypointense in T1 weighted images (T1WIs) and hyperintense in T2 sequences, with mass effect on the adjacent structures and occupying at least 50% of the pons
• No prior therapy is allowed other than involved field radiotherapy (54Gy) and cerebrospinal fluid (CSF) diversion for hydrocephalus, including endoscopic third ventriculostomy (ETV) or a ventriculo-peritoneal shunt. No concomitant medicine or therapies for treatment are permitted while the patient is enrolled in this study.
• Karnofsky performance status or Lansky play score of ≥70 assessed at diagnosis
• Total bilirubin: within normal institutional limits
• Aspartate Aminotransferase (AST)(SGOT)/Alanine Aminotransferase (ALT)(SGPT): ≤ 2.5 × institutional upper limit of normal (ULN)
• Creatinine: within normal institutional limits
• Creatinine clearance: ≥ 60 mL/min/1.73m2 for patients with creatinine levels above institutional normal
• Absolute neutrophil count: ≥ 1,500/μL
• Platelet count: ≥ 100,000/μL - no transfusion within 7 days
• Hemoglobin level: ≥ 10g/dL - no transfusion within 7 days
• Partial Thromboplastin Time (PT) and activated partial thromboplastin time (APTT): within normal institutional limits
• No documented current bleeding disorder
• No medical condition that would preclude general anesthesia
• No severe acute infection or unexplained febrile illness
• Not pregnant or nursing - negative serum pregnancy test if appropriate within 7 days of study entry (adequate contraceptive methods for females and males required)
• No documented allergy to compounds of similar chemical or biologic composition to MTX110 or gadolinium compounds
• Subjects with a history of seizures/epilepsy should be on anticonvulsant medication prior to the first operative procedure on study, with serum levels within a therapeutic range
• Subjects must be able to undergo MR-imaging with gadolinium-based contrast administration (e.g. no ferrous-containing implants, no pacemakers, etc.)
• All subjects or their legal guardians must sign a document of informed consent indicating their understanding of the investigational nature and the potential risks associated with this study. When appropriate, pediatric subjects will be included in all discussions in order to obtain verbal and written assent

Exclusion Criteria:

• Radiological evidence of distant disease outside the pons or thalami
• Radiological evidence of metastatic disease within the central nervous system (CNS) at diagnosis
• Subjects with an uncorrectable bleeding disorder
• Subjects with multifocal or leptomeningeal disease beyond the pons or the thalami
• Subjects with signs of impending herniation or an acute intratumoral hemorrhage
• Subjects that have received or are on concurrent chemotherapy or biologic therapy for the treatment of their tumor
• Subjects who are pregnant or breastfeeding
• Previous experimental or trial-based therapy
• Patients who are known human immunodeficiency virus (HIV), Hepatitis B or Hepatitis C positive. HIV-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with MTX110.
• Patients with systemic diseases which may be associated with unacceptable anesthetic/operative risk

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: MTX110 and CED; All patients enrolled in the study will receive infusion of MTX110 and Gadolinium delivered by the CED delivery system directly into the tumor over 9-11 days.	Drug: Infusate with MTX110 and gadolinium; Pulses 1 and 2 will be prepared with 30, 60 or 90 uM concentration of MTX110. The infusate consists of gadolinium and MTX110 (30, 60, or 90 uM) at approximately 1:100 ratio.; Device: Convection-Enhanced Delivery (CED); CED is the method by which the drug are delivered to the brain under controlled pressure to the brain by targeted micro-catheters.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incidence of Adverse Events	Safety of repeated convection-enhanced delivery (CED) of MTX110 will be reported by summarizing the incidence rate of adverse events observed or reported. Adverse events will be graded according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.	Up to six weeks after second infusion
Maximum Tolerated Dose (MTD) of MTX110	The MTD will be determined based on the number of dose limiting toxicities (DLT) observed in each of the titrated doses.	14 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Steady state volume of drug distribution	Measured by volumetric contrast enhancement intensity on MRI and magnetic resonance (MR) spectroscopy	14 days
Time to tumor progression/recurrence (PFS)	PFS is defined as the duration of time from start of MTX110 treatment to time of progression or death from any cause, whichever occurs first.	2 years
Overall survival (OS) or time to death	Overall survival is defined as the duration of time from the start of MTX110 treatment to death from any cause. OS will be measured by follow-up with a study participant every 3-6 months until death for any reason.	2 years
Score on PedsQL 4.0 Brain Tumor Module	The 24-item PedsQL 4.0 Brain Tumor Module encompasses six scales: (1) cognitive problems (seven items), (2) pain and hurt (three items), (3) movement and balance (three items), (4) procedural anxiety (three items), (5) nausea (five items), and (6) worry (three items). Each item is measured with a 5-point Likert scale from 0 (never a problem) to 4 (almost always a problem), which is then transformed on a scale from 0-100. Higher scores indicate lower problems and therefore a better outcome.	2 years

Collaborators and Investigators

• Sponsor: Luca Szalontay
• Collaborators: Midatech Pharma US Inc.
• Investigators: Principal Investigator: Luca Szalontay, MD, Columbia University

Study record dates

Study Major Dates

• Study Start (Actual): March 10, 2020
• Primary Completion (Actual): April 25, 2022
• Study Completion (Actual): November 22, 2023

Study Registration Dates

• First Submitted: February 7, 2020
• First Submitted That Met QC Criteria: February 7, 2020
• First Posted (Actual): February 11, 2020

Study Record Updates

• Last Update Posted (Estimated): December 18, 2023
• Last Update Submitted That Met QC Criteria: December 15, 2023
• Last Verified: December 1, 2023

More Information

Terms related to this study

• Keywords: Diffuse Intrinsic Pontine Glioma; Blood brain barrier; Diffuse Midline Gliomas; Thalamic Gliomas; Convection-Enhanced Delivery (CED)
• Additional Relevant MeSH Terms: Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Neoplasms by Histologic Type; Neoplasms; Neoplasms by Site; Neoplasms, Glandular and Epithelial; Neoplasms, Neuroepithelial; Neuroectodermal Tumors; Neoplasms, Germ Cell and Embryonal; Neoplasms, Nerve Tissue; Brain Neoplasms; Central Nervous System Neoplasms; Nervous System Neoplasms; Brain Stem Neoplasms; Infratentorial Neoplasms; Glioma; Diffuse Intrinsic Pontine Glioma
• Other Study ID Numbers: AAAS2936

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: Yes