Diffuse Intrinsic Pontine Glioma in an 11-Year- Old Female Treated with Antineoplastons: Complete Response and >25 Years Survival

Authors

  • Burzynski Stanislaw Burzynski Clinic, Houston, TX, USA
  • Burzynski Gregory Burzynski Clinic, Houston, TX, USA
  • Janicki Tomasz Burzynski Clinic, Houston, TX, USA
  • Beenken Samuel Oncology Writings, Calera, AL, USA

Keywords:

Brain tumor; Diffuse Intrinsic Brainstem Glioma; H3-K27M Diffuse Midline Glioma; Antineoplastons; Phase I I and III Studies

Abstract

Rationale: Diffuse intrinsic pontine glioma (DIPG), a lethal brain tumor, is the leading cause of brain
tumor–related death in children. Over the past few decades clinical trials have shown no improvement
in outcome. The purpose of this case study is to detail and discuss the use of Antineoplastons A-10
(Atengenal) and AS2-1 (Astugenal) in the treatment of an eleven-year-old female with a newly
diagnosed DIPG.

Objectives: The patient described here was enrolled into BT-11, a Phase II protocol utilizing
Antineoplastons A-10 and AS2-1 in the treatment of brainstem gliomas. The patient’s tumor response to
therapy was measured by sequential MRIs of the brain, with and without gadolinium contrast.

Findings: At her presentation to the Burzynski Clinic (BC), the patient was alert, and weighed 42.1 Kg.
Physical examination showed dysfunction of the 6th and 7th cranial nerves, with lateral movement of
the left eye being decreased by approximately 30% and with left-sided facial weakness being present.
The patient obtained a baseline MRI, with and without gadolinium. Post-gadolinium T1-weighted axial
images showed a 0.80 cm2 enhancing pontine mass and a 2.70 cm2 non-enhancing left-sided brainstem
mass. Following Antineoplastons (ANP), the patient achieved a complete response (CR) of the
enhancing pontine mass. At that time, physical examination, especially neurologic examination, showed
no abnormalities. The patient was last seen at the BC on October 15, 2004 and she was in excellent
health with no evidence of new/recurrent disease. On August 10, 2021, correspondence with the patient
indicated that she continued in excellent health (>25 years survival).

Conclusions: ANP is an effective treatment for DIPG and for a variety of low- and high-grade brain
tumors. Multiple Phase II protocols utilizing ANP have now been completed and its impact on the
treatment of brain tumors has been widely published.

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Published

2021-10-13

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Articles