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Clinical Trials/NCT03632317
NCT03632317
Withdrawn
Phase 2

A Phase 2 Study of Panobinostat in Combination With Everolimus for Children and Young Adults With Gliomas Harboring H3.3 or H3.1 K27M Mutation

University of Michigan Rogel Cancer Center1 site in 1 countryOctober 2019

Overview

Phase
Phase 2
Intervention
Panobinostat
Conditions
Glioma
Sponsor
University of Michigan Rogel Cancer Center
Locations
1
Primary Endpoint
Median Progression Free Survival (PFS) at 1 Year
Status
Withdrawn
Last Updated
6 years ago

Overview

Brief Summary

This phase 2 trial will evaluate the activity of Panobinostat in combination with Everolimus for children with gliomas harboring H3.1 or H3.3K27M mutation, including newly diagnosed high-grade glioma or DIPG (diffuse intrinsic pontine glioma) after radiation (stratum A) and recurrent/progressive glioma (grade II-IV, including DIPG) (stratum B).

Registry
clinicaltrials.gov
Start Date
October 2019
End Date
October 2025
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All patients and/or a legal guardian must sign institutionally approved written informed consent and assent documents.
  • Patient must be greater than 2 years and less than 30 years
  • BSA (body surface area) greater than 0.3 m2
  • Functional status: Karnofsky \> 50% for patients \> 16 years of age and Lansky \> 50% for patients \< 16 years of age (Karnofsky and Lansky is a scoring system used to quantify the general well being of cancer patients where 100% represents perfect health and 0% represents death). Neurologic deficits in patients with CNS tumors must have been relatively stable for a minimum of 7 days. Patients who are unable to walk because of paralysis, but who are able to sit in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score.
  • Adequate bone marrow function
  • Adequate liver function
  • Adequate renal and metabolic function
  • Urine protein:creatinine (UPC) ratio of \< 1; or a urinalysis that is negative for protein; or 24-hour urine protein level \< 1000 mg/dL
  • Patients must have Magnesium \> 1.5 mg/dL and potassium \> 3.5 mmol/L
  • Patients with known seizure disorder must have seizures adequately controlled with non- enzyme inducing antiepileptic medications

Exclusion Criteria

  • Patients who are breastfeeding, pregnant or refuse to use an effective form of birth control are excluded. Abstinence is considered an effective form of birth control.
  • Patients with uncontrolled infection are excluded.
  • Inability to swallow oral pill (panobinostat does not have liquid formulation).
  • Other medications: Patients receiving other anti-neoplastic agents are excluded; patients on enzyme-inducing anticonvulsive agents are excluded; patients requiring strong CYP3A4 or PGP inducers or inhibitors are excluded; patients on steroids for symptom management must be on a stable dose for 7 days prior to start of treatment.
  • Allogeneic stem cell transplant: Patients within 1 year of allogeneic stem cell transplant, patients with active GVHD or requiring immunosuppression are excluded.
  • Previous hypersensitivity to rapamycin or rapamycin derivatives.
  • Baseline QTc of \>450 msec on EKG OR electrolyte imbalance predisposing to QTc prolongation (baseline ≥ Grade 1 hypokalemia or hyperkalemia; and baseline ≥ Grade 2 Ca++, Mg++, phosphate abnormalities). Repletion/correction is allowed to achieve eligibility. Use of QTC prolonging medications will be monitored throughout the trial.

Arms & Interventions

Panobinostat and Everolimus

Panobinostat daily M, W, F for 2 weeks every 28 days for the first cycle (28 days). After first cycle Panobinostat daily M, W, F for 2 weeks every 28 days combined with Everolimus daily.

Intervention: Panobinostat

Panobinostat and Everolimus

Panobinostat daily M, W, F for 2 weeks every 28 days for the first cycle (28 days). After first cycle Panobinostat daily M, W, F for 2 weeks every 28 days combined with Everolimus daily.

Intervention: Everolimus

Outcomes

Primary Outcomes

Median Progression Free Survival (PFS) at 1 Year

Time Frame: 1year

Median PFS at 1 year for stratum A will be measured. Progression is defined as \> 25% increase in the size of the tumor or appearance of new lesions.

Median Progression Free Survival (PFS) at 2 Years

Time Frame: 2years

Median PFS at 1 year for stratum A will be measured. Progression is defined as \> 25% increase in the size of the tumor or appearance of new lesions.

Overall Survival at 2Years

Time Frame: 2years

The proportion of patients alive at 2 years for stratum A.

Overall Response Rate (ORR) After Two Cycles of Panobinostat + Everolimus

Time Frame: 84 Days

Overall Response Rate (ORR) After Two Cycles of Panobinostat + Everolimus for stratum B. Overall response is defined as a partial or complete response. Partial response is defined as a ≥50% decrease in size of tumor in comparison to baseline measurements. Complete response is defined as the disappearance of all abnormal signal. This includes return to normal size of the brainstem for brainstem lesions.

Overall Survival at 1Year

Time Frame: 1year

The proportion of patients alive at 1 year for stratum A.

Study Sites (1)

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