Clinical Trials Directory

Trials / Terminated

TerminatedNCT01182350

Molecularly Determined Treatment of Diffuse Intrinsic Pontine Gliomas (DIPG)

Phase II Trial of Molecularly Determined Treatment of Children and Young Adults With Newly Diagnosed Diffuse Intrinsic Pontine Gliomas

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
53 (actual)
Sponsor
Karen D. Wright MD · Academic / Other
Sex
All
Age
3 Years – 18 Years
Healthy volunteers
Not accepted

Summary

Diagnosis of diffuse intrinsic pontine glioma (DIPG) for decades has relied on imaging studies and clinical findings. Histologic confirmation has been absent with surgical biopsy of brainstem tumors not believed to have acceptable safety. The prognosis of DIPG has remained quite poor and novel therapeutic strategies are needed. This DIPG Biology and Treatment Study (DIPG-BATS) study incorporates a surgical biopsy at presentation using strict preoperative neurosurgical planning and stratifies participants to receive FDA-approved agents chosen on the basis of specific biologic targets. This is the first prospective national clinical trial to examine the feasibility and safety of incorporating surgical biopsy into potential treatment strategies for children with DIPG.

Detailed description

The primary objective of this study is to estimate the overall survival of children and young adults with DIPG in the context of a molecularly based treatment strategy, compared to historical controls (COG ACNS0126). Secondary objectives were to determine the safety and potential morbidity associated with biopsy of classic DIPGs based on imaging and clinical history as well as ability to perform biologic analyses on the biopsy material obtained to guide therapy. At study entry, a MRI-guided frameless or frame-based stereotactic biopsy will be performed approaching the pontine termentum through a trans-cerebellar or trans-frontal route. The exact biopsy location will be determined by the treating neurosurgeon at the designated participating site with the goal of minimizing procedural risk. Treatment directed based on tumor biopsy results requires classification of patients into 1 of 4 potential cohorts: O\^6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status (negative versus positive) and epidermal growth factor receptor (EGFR) overexpression status (negative versus positive).

Conditions

Interventions

TypeNameDescription
DRUGBevacizumab
DRUGErlotinib
DRUGTemozolomide
RADIATIONRadiation

Timeline

Start date
2011-09-01
Primary completion
2016-06-01
Completion
2016-06-01
First posted
2010-08-16
Last updated
2019-09-04
Results posted
2019-09-04

Locations

23 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01182350. Inclusion in this directory is not an endorsement.