Child's Nervous System
© The Author(s) 201410.1007/s00381-014-2401-z
The response and survival of children with recurrent diffuse intrinsic pontine glioma based on phase II study of antineoplastons A10 and AS2-1 in patients with brainstem glioma
Burzynski Clinic, 9432 Katy Freeway, Houston, TX 77055, USA
Gregory S. Burzynski
Received: 7 November 2013Accepted: 6 March 2014Published online: 10 April 2014
Brainstem gliomas (BSG) are relatively rare tumors of which recurrent pediatric diffuse intrinsic pontine gliomas (RPDIPG) comprise a distinct group. Numerous trials have been conducted on RPDIPG, none of which have resulted in identifying any proven pharmacological treatment benefit. This study included 40 patients diagnosed with different types of BSG, but it was decided to describe first the encouraging results in the most challenging group of RPDIPG.
Materials and methods
This single-arm phase II study evaluated the efficacy and safety of the combination of antineoplastons A10 and AS2-1 (ANP) in patients with RPDIPG. Seventeen patients (median age 8.8 years) were enrolled, and all were diagnosed with RPDIPG. ANP was administered intravenously daily. Efficacy analyses were conducted in this group of patients.
In this group, complete responses were observed in 6 % of patients, partial responses in 23.5 %, and stable disease in 11.8 %. Six-month progression-free survival was 35.3 %. One-year overall survival was 29.4 %, 2 years 11.8 %, and 5, 10, and 15 years 5.9 %. One patient with DIPG is alive over 15 years post-treatment. Grade 3 and higher toxicities including hypokalemia and fatigue occurred in 6 %, hypernatremia in 18 %, fatigue and urinary incontinence in 6 %, and somnolence in 12 %. In a single patient, grade 4 hypernatremia occurred when he was on mechanical ventilation. He was disconnected from the ventilator and died from brain tumor according to the attending physician. Responding patients experienced improved quality of life.
The results suggest that ANP shows efficacy and acceptable tolerability profile in patients with RPDIPG.
KeywordsAntineoplastons A10 and AS2-1 Brainstem glioma Diffuse intrinsic pontine glioma Recurrent glioma Phase II clinical trial
A comment to this article is available at http://dx.doi.org/10.1007/s00381-014-2557-6.
A comment to this article is available at http://dx.doi.org/10.1007/s00381-014-2515-3.
A comment to this article is available at http://dx.doi.org/10.1007/s00381-014-2514-4.
A comment to this article is available at http://dx.doi.org/10.1007/s00381-014-2513-5.
A comment to this article is available at http://dx.doi.org/10.1007/s00381-014-2511-7.
Brain tumors in children account for 20 % of all neoplasms . Brainstem gliomas are relatively rare tumors which constitute 1.6 % of primary brain and CNS tumors by site . In children, high-grade gliomas—anaplastic astrocytomas (AA), glioblastoma multiforme (GBM), and diffuse intrinsic pontine gliomas (DIPG)—are the most aggressive neoplasms and the leading causes of cancer-related mortality [1, 3, 4]. Based on the most recent studies, pediatric DIPG forms a distinct group which is characterized by recently identified mutations in the histone H3.3 (H3F3A gene) . Numerous clinical trials have been carried out in patients with DIPG, but no pharmacological agents have to date proven efficacious—leaving standard radiation therapy (RT) as the mainstay of treatment [1, 3]. The overall outlook is poor and nearly all children eventually die. In most studies, the median survival time is shorter than 1 year and less than 10 % of patients survive over 2 years .
Antineoplastons A10 and AS2-1 (ANP) are synthetic amino acid derivatives. A10 is a formulation consisting of a 4:1 ratio of phenylacetylglutaminate sodium (PG) and phenylacetylisoglutaminate sodium (isoPG). AS2-1 is a formulation with a 4:1 ratio of phenylacetate sodium (PN) and PG . The proposed antineoplastic activity of ANP in gliomas is shown in Fig. 1 and consists of specific effects on the AKT2 and RAS pathways and tumor suppressor genes TP53 and p21 and on apoptosis [6–16].
Proposed mechanism of action of antineoplastons A10 and AS2-1. The ingredients of antineoplastons A10 and AS2-1, PN and PG, affect signal transmission through AKT and RAS pathways, promote apoptosis, and interrupt cell cycle progression at G1/S and G2/M checkpoints
Genome-wide analyses have been conducted to identify recurrent amplifications of receptor tyrosine kinases (RTKs) and cell cycle regulatory genes in DIPGs and indicated substantial tumor heterogeneity and involvement of RAS and AKT signaling pathways [17, 18]. Successful treatment of a heterogeneous tumor may require inhibitors that affect not only multiple targets, but also multiple pathways, such as ANP.
Phase I studies of injections of antineoplastons A10 and AS2-1 (ANP) as well as prior phase II studies included pediatric patients [5, 19–22]. In two of these studies, complete responses (CR) were observed in pediatric DIPG [5, 23]. In our phase II study (BT-03) of ANP of 20 subjects with astrocytomas, conducted in 1988, CR were documented in two cases of DIPG in young adults [20, 21]. One of these patients is currently surviving tumor free for over 25 years after being treated with ANP for DIPG, which recurred after radiation therapy. These positive preliminary data prompted us to design and conduct a single-arm phase II study of ANP to assess the efficacy and safety of this treatment in pediatric patients diagnosed with recurrent DIPG (RPDIPG).
Patients and methods
The protocol permitted admission of patients with brainstem glioma for whom standard curative treatments are not available. A total of 40 patients were enrolled, but the scope of this paper has been limited to the 17 RPDIPG patients.
Recruited patients were all over 4 years of age and had radiologic evidence of brainstem glioma by gadolinium-enhanced MRI performed 14 days prior to being enrolled in the study. Based on MRI only, DIPG can be diagnosed if the tumor has an epicenter in the pons and involves more than 50 % of the pons. Patients with neurofibromatosis are not covered by this definition and were not included. The tumors involving less than 50 % of the pons or exophytic were classified as DIPG if they had anaplastic or GBM histology [24–26].
Eligibility criteria included a Karnofsky Performance Status (KPS) of 60–100. The subjects were required to have relatively normal hematopoietic and hepatic function with white blood cell count (WBC) over 1,500/mm3 and platelet count over 50,000 mm3, no evidence of hepatic or renal insufficiency, and a total bilirubin and serum creatinine of no higher than 2.5 mg/dL. SGOT and SGPT were to be no higher than 5× the upper limits. At least 8 weeks must have elapsed since the last dose of RT, and at least 4 weeks since the last dose of chemotherapy (6 weeks for nitrosoureas), or immunotherapy. The use of corticosteroids was permitted to reduce symptoms and signs attributed to cerebral edema, but it was recommended that the smallest doses compatible with the preservation of optimal neurologic function be used. Confirmation of the pathologic diagnosis by an outside pathologist was also required.
The exclusion criteria included serious active infection, fever, or other serious concomitant disease that would interfere with the evaluation of the treatment (e.g., severe heart or lung disease). There were no exclusion criteria based on tumor size, multifocality, or leptomeningeal involvement.
All study subjects and/or guardians read, understood, and signed written informed consent prior to enrollment. This study was conducted in accordance with the US Code of Federal Regulations, Title 21, Parts 11, 50, 56, and 312; the Declaration of Helsinki (1964) including all amendments and revisions; the Good Clinical Practices: Consolidated Guideline (E6); International Conference on Harmonization; and the FDA’s Guidance for Industry. The study was sponsored by the Burzynski Research Institute (BRI) and conducted by the Burzynski Clinic (BC) in Houston, TX. The patients did not pay for the investigational agents.
The study was designed as a single-arm, two-stage, phase II trial of ANP as monotherapy. The study was listed by the National Cancer Institute (NCT00003459). It was supervised by an independent Institutional Review Board (BRI-IRB, BC-BT-11).
The study was performed according to Protocol BT-11 which was submitted to the FDA under the IND 43,742. Subsequently, the protocol was amended by BRI several times; however, none of the amendments altered the aim or design of the original study objectives/outcomes.
The sample size was calculated based upon the previously used method described by Chang et al. . A response rate to ANP of ≥10 % was considered “of interest,” and the primary endpoint was to determine the overall response rate which was confirmed CR or partial response (PR) to ANP therapy. Objective response (OR) and progression-free survival (PFS) were measured from the first day of ANP administration. The distributions of survival and treatment failure were estimated by Kaplan-Meier analysis. As mentioned before, this paper described 17 RPDIPG patients out of the total of 40 brainstem glioma patients.
The median maximum dose of ANP A10 was 8.14 g/kg/day (5.69–15.87) and for AS2-1 0.42 g/kg/day (0.21–0.58). The duration of IV ANP therapy ranged from 5 to 178 weeks with a median of 61 weeks.
ANP A10 and AS2-1 were delivered via a dual-channel infusion pump and single-lumen subclavian catheter (Broviac or Groshong) every 4 h. On the first day of administration of ANP, the flow rate of the pump was maintained at 25 mL/h. Beginning from the second day, individual injections were given at 100 to 250 mL/h depending on the patient’s age and tolerance.
Approximate guidelines for flow rates are provided.
Four to 7 years old—flow rate 100 mL/h
Seven to 10 years old—flow rate 150 mL/h
Ten to 16 years old—flow rate 200 mL/h
Sixteen to 18 years old—flow rate 250 mL/h
On the first day of treatment, the pump was loaded with 60 mL of A10 (0.3 g/mL) and 60 mL of AS2-1 (0.08 g/mL). The volume of each injection was 10 mL administered every 4 h, six times a day. Beginning from the second day of treatment in children younger than 12 years of age, the dose of each injection was increased on a daily basis in increments of 10 mL until the highest tolerable dose or effective dose was reached. For children 12 years of age or older, the dose of A10 was escalated in increments of 20 mL daily, and over 16 years of age, in increments of 40 mL. When the study subject reached the highest tolerated dose, the “escalation phase” of the treatment stopped.
In summary, there were three different volumes of daily dosage increments of ANP depending on the patient’s age: 10 mL daily dose increase per injection for children younger than 12 years of age, 20 mL for children between 12 and 15 years of age, and 40 mL for patients over 16 years of age. The complicated part of the regimen, which is escalation of dosage, was finished during the patient’s treatment at BC under careful supervision of the sub-investigator assigned to the case. Upon returning home, the patient is given a regimen that consisted of administration of the fixed dose (volume) of ANP through an automatic pump six times a day. The pump was typically loaded with ANP once a day and the rest of the administration was done automatically. It was possible to disconnect the pump in between IV boluses given every 4 h to permit patient’s physical activities. The single dosing could be completed within 1 h which would leave 3 h until the next dose, and during this time, the pump could be disconnected. Long-term observation of the patients confirmed that the regimen created a limited burden on the quality of life. After symptomatic improvement, the children were able to attend school and graduate from it. The subject continued the daily administration of six doses of A10 and AS2-1 (every 4 h via an automated pump) until a response to the treatment was determined.
The rationale for using two formulations of ANP was based on prior clinical trials, pharmacokinetic studies, and laboratory research . The escalation of the dosage of ANP was recommended based on the positive results of previous studies carried out to determine whether patients were able to tolerate large volume infusions of intravenous fluids associated with higher doses of ANP . As a safety precaution, it was recommended that the escalation of the dosages would continue through phase II and phase III trial programs.
Medications that were considered necessary for the patients’ welfare and that did not interfere with the evaluation of treatment were given at the discretion of the investigator. The use of corticosteroids was carefully monitored. Treatment with other antineoplastic or immunomodulatory agents was not permitted during the study. Subjects received full supportive care, including transfusions of blood products and antibiotics when appropriate.
The initial 3 weeks of therapy was administered by BC staff on an outpatient basis, in Houston, TX. The treatment did not require hospitalization. Subjects and/or their legal guardians were trained by clinic staff to self-administer ANP therapy during this time. Starting on week 4, ANP therapy was administered at home with 24-h support available via phone. Treatment and monitoring of the subject’s condition, once released to self-administered therapy, continued under the supervision of the subject’s local attending physician (physician who signed the FDA form 1572).
Evaluation and follow-up
Prior to the start of treatment, a gadolinium-enhanced MRI measured all contrast-enhancing lesions. The products of the two greatest perpendicular diameters of all lesions were calculated and totaled, providing a baseline evaluation for each study subject. The tumor measurements were based on contrast-enhanced lesions, but the nonenhancing lesion and overall tumor size were also measured including T2 and FLAIR images [26, 28]. CR required the disappearance of all enhancing lesions sustained for at least 4 weeks, with only physiologic replacement doses of steroids acceptable. Positron emission tomography (PET) shows resolution of hypermetabolic lesions. PR required 25 % or higher decrease of the sum of the products of the two largest perpendicular diameters of enhancing lesions and stable or reduced corticosteroid doses. PD was determined when there was over 25 % increase of enhancing lesions or new lesions, and stable disease (SD) was the status between PR and PD. In the case of SD, the duration was measured from the time therapy commenced. The results of all MRI and PET scans were verified by radiologists not affiliated with BRI or BC, and their determination of response was accepted. Complete and partial responses were verified by central radiology review.
Blood and urine tests (complete blood count with differential, platelet count, reticulocyte count, and serum chemistry), anticonvulsant serum levels, prothrombin time, and partial thromboplastin time were carried out on all subjects prior to the start of treatment to establish baseline values. The additional pretreatment measurements included KPS, vital signs, clinical disease status, demographics, medical history and current medications, physical examination with neurologic emphasis, chest X-rays, and EKG. Toxicity was evaluated in all patients enrolled in the study. Data on adverse drug experiences (ADEs) were collected during the initial 3 weeks of ANP therapy by clinic staff at the BC. MRIs were repeated at least every 8 weeks during the first 2 years unless the patient’s condition or confirmation of response required an MRI within 4 weeks. PET scans were performed as necessary. When study subjects transitioned to home-based therapy administration under the care of a local physician, clinic staff made daily telephone contact for the first 2 months to ensure protocol compliance, to resolve any issues with therapy administration, and to continue assessing ADEs. Weekly contact was made starting in the third month. Continued patient treatment with ANP was determined on at least a weekly basis and based upon the trial protocol, patient health status, and the response to treatment.
The records of daily administration of ANP were maintained and carefully checked for drug accountability. The ADEs were graded according to the Common Terminology Criteria for Adverse Events (CTCAE v.3). Pharmacokinetic studies have been previously carried out and were not included in this study. Based on a prior study, there was no indication of interference with essential supportive medications, in particular, antiseizure drugs.
The enrollment of subjects diagnosed with RPDIPG commenced on March 13, 1996 and continued through December 14, 2006. As of September 12, 2007, all subjects were removed from the therapy, as a consequence of either a CR, subject request, PD, or worsening clinical condition.
Demographics for the subjects are summarized in Table 1. Patient demographics did not change during the study and were comparable to the other studies conducted on brainstem glioma. The tumor measurements on MRI T2-weighted images determined from 61 to 100 % involvement of the pons (median 85 %). There were one GBM and one AA as well as two cases of pilocytic astrocytoma, grade 1 in this group. The data on confirmation of diagnosis and tumor recurrence, confirmation of response, and change in tumor measurements during treatment are provided in Table 2.
Study population demographics
Recurrent pediatric DIPG, n = 17
Age (years): median
C—15, H—1, O—1
Astrocytoma, grade I
Karnofsky Performance Score
BT / AT
70 / 80
6 / 4
5 / 2
5 / 6
0 / 1
1 / 2
Duration of symptoms prior to enrollment
Less than 6 months
Greater than 6 months
CH + RT
SU + CH + RT
Confirmation of diagnosis, recurrence, and response
Confirmation of diagnosis
Confirmation of recurrence
Confirmation of response to ANP
Place and date
Place and date
Place and date
Pons T2 %a
Place and date
Cancer Institute/July 12, 1994
Cancer Institute/July 1994
S, RT, CH
External Radiology, CRR/March 25, 1996
External Radiology, CRR
Decreased >50 %
University Hospital/August 17, 1995
External Radiology/March 13, 1996
External Radiology/October 1, 1995
External Radiology/June 17, 1996
External Radiology/November 20, 1996
University Hospital/March 8, 1996
External Radiology, CRR/August 29, 1996
External radiology, CRR/December 5, 1996
Decreased >50 %
University Hospital/March 28, 1996
External Radiology/October 10, 1996
External Radiology/January 13, 1997
Increased >40 %
External Radiology/January 31, 1996
External Radiology/October 25, 1996
External Radiology/January 13, 1997
Increased >50 %
External Radiology/August 26, 1997
External Radiology/October 6, 1997
External Radiology/January 21, 1998
University/February 1, 1993
University Hospital/January 28, 1993
External Radiology, CRR/March 1, 1998
External Radiology, CRR/January 16, 1999 and May 6, 2003
Decreased >50 %
University Hospital/November 11, 1997
University Hospital/April 2, 1998
External Radiology, CRR/October 6, 1998
Decreased >50 %
External Hospital/October 2, 1998
External Hospital/April 9, 1999
External Hospital/July 15, 1999
Increased >25 %
External Hospital, Neuro-Oncology Tumor Board/September 25, 2001
External Radiology/January 8, 2002
External Radiology, CRR/May 30, 2002
Decreased >50 %
University Hospital/September 4, 2002
University Hospital/March 3, 2002
University Hospital/August 29, 2002
University Hospital/December 30, 2002
External Radiology/August 19, 2003
External Radiology/December 29, 2003
Increased >50 %
University Hospital/January 6, 2004
External Radiology/October 5, 2004
External Radiology/January 5, 2005
Increased >25 %
University Hospital/June 1, 2005
External Radiology/September 20, 2005
External Radiology/January 31, 2006
Increased >50 %
University Hospital/March 20, 2006
External Radiology/August 9, 2006
External Radiology/October 31, 2006
Increased >50 %
Cancer Institute/August 2, 2006
Cancer Institute/August 10, 2006
DIPG with leptomeningeal dissemination
RT, 3CH, HDCH
Cancer Institute/October 30, 2006
External Radiology/April 2, 2007
In the group of 17 RPDIPG patients, there were five cases of OR (29.5 %): one CR (6 %) and 4 PR (23.5 %). An additional group of two patients (11.8 %) had stabilization of their disease, eight patients (47 %) developed progressive disease, and two cases (12 %) were nonevaluable (NE). Figures 2 and 3 illustrate the response to treatment with ANP in two patients.
DIPG in a 10-year-old male (case 8) which recurred two times after partial surgical resection. MRI of the head: 1—T1 nonenhanced, 2—contrast-enhanced, 3—T2W, and 4—FLAIR images. PR was documented by the MRI and CR was established by the normalization of the follow-up PET scans. Arrows indicate tumors
DIPG in a 7-year-old female (case 9) which recurred after radiation therapy and chemotherapy with etoposide. MRI of the head: 1—T1 nonenhanced, 2—contrast-enhanced, and 3—T2W images. MRI documented PR. Arrows indicate tumors
The Kaplan-Meier OS and PFS curves are shown in Fig. 4. Estimated overall survival at 10 and 15 years is 5.9 % up to July 2013. The survival is 29.4 % at 1 year and 11.8 % at 2 years. One patient remains alive over 15 years from the start of treatment.
The Kaplan-Meier survival curves from the start of treatment for recurrent pediatric DIPG
Safety and adverse events
Safety assessments were analyzed based upon the total number of enrolled patients (n = 17). Grade 4 toxicities including hypokalemia and fatigue occurred in 6 % and hypernatremia in 18 % of the group. Grade 3 fatigue and urinary incontinence occurred in 6 % and somnolence in 12 %. In patient 2 (Table 2), grade 4 hypernatremia was detected when he was on mechanical ventilation in the intensive care unit. This patient received terminal care and was disconnected from the ventilator upon request of the members of his family. His attending physician determined brain tumor as the cause of death. No chronic events occurred. Responding patients experienced improved quality of life. Brain tumor patients frequently receive corticosteroids as part of their therapeutic regimen to reduce cerebral edema around tumors. The use of corticosteroids, the infusion of large volumes of sodium-containing solutions during ANP therapy, and the brain tumor itself predispose a patient to an increased incidence of serum sodium and potassium concentration abnormalities. As a result, hypernatremia and hypokalemia were reported in a substantial number of patients.
Between 1984 and 2005, 29 studies in DIPG have been reported and were reviewed by Hargrave et al. . The additional clinical trials were reviewed by us previously [3, 29]. These trials did not demonstrate any improvement in efficacy beyond standard radiation therapy which remains the standard treatment. Less than 10 % of children with a diagnosis of DIPG do not survive more than 2 years from diagnosis, and very few live beyond 5 years. In recent years, only seven trials were conducted for a mixed population of pediatric patients, usually with high-grade glioma, with a small percentage of patients diagnosed with DIPG [30–36]. The results from this trial in comparison to other comparable studies are presented in Table 3. Five trials were conducted for recurrent brainstem glioma, usually at the first relapse. The remaining two trials included children with both recurrent as well as newly diagnosed brainstem glioma. Lashford et al. reported data on treatment with RT and temozolomide (TMZ) in 18 eligible patients diagnosed with progressive diffuse intrinsic brainstem glioma with the tumor centered in the pons in 15 subjects . They reported a PR of 6 %, SD of 17 %, and a median survival of 6.2 months. Dreyer et al. evaluated ten brainstem glioma patients with recurrent or progressive disease after conventional RT and chemotherapy . These patients were treated with an analog of daunomycin, idarubicin. No OR was reported, but there were one case of SD and seven cases of PD among eight evaluable patients. Warren et al. used a combination of lobradimil and carboplatin for brainstem glioma at first relapse (12 patients) . There was no OR and the median time to progression was only 84 days. Tipifarnib was used by Fouladi et al. in a phase II trial for recurrent or progressive high-grade glioma including brainstem glioma and PNET . In 41 patients, there were one PR and four cases of SD (11 %). Gururangan et al. used a combination of bevacizumab and irinotecan in children with recurrent DIPG . In the population of 17 patients, there was no OR, but five cases of SD and 13 PD. Median PFS was 2.3 months and 6-month PFS was 9.7 %. Minturn et al. used metronomic oral topotecan in nine children with recurrent brainstem glioma. They reported SD in two patients, but no OR . Warren et al. conducted a phase II study with 06-benzylguanine and TMZ in 16 children with recurrent or progressive brainstem gliomas . No OR was reported and 6-month PFS was zero. These trials failed to prove efficacy for any of the treatment regimens under evaluation and the treatments themselves were associated with substantial toxicity.
Phase II clinical studies in recurrent or progressive brainstem glioma in children
Total no. of patients
Radiation therapy (%)
At 6 months (%)
1 years (%)
2 years (%)
5 years (%)
10 years (%)
15 years (%)
Lashford et al. /temozolomide
Dreyer et al. /idarubicin
Warren et al. /lobradimil and carboplatin
Fouladi et al. /tipifamib
Recurrent refractory brainstem gliomasa
Gururangan et al. /bevacizumab and irinotecan
Minturn et al. /topotecan
Recurrent refractory brainstem gliomasa
Warren et al. /06-benzylguanine and temozolomide
Burzynski et al. /antineoplastons A10 and AS2-1
The review of the literature indicates that there are substantial differences in the definitions of DIPG and the evaluations of the responses. In this study, we accepted the criteria used for all COG and PBTC studies. DIPG are predominantly nongadolinium enhancing, hyperintense on T2-weighted images and hypodense on T1. Despite this fact, all studies conducted within the last 10 years used the Macdonald evaluation criteria, based on measurements of contrast-enhancing lesions. It is generally assumed that it would be preferable to have an objective measure of nonenhancing, recurrent tumor, but the opinion of the response assessment in the neuro-oncology (RANO) working group is that this is not possible at the present time due to limitations of technology . Unfortunately, the evaluation of the response based on the MRI could be misleading, and for this reason, we included the measurement of the nonenhancing tumor, changes in the patient’s clinical condition, as well as PFS and OS. It is generally accepted, although not ideal, that the use of overall survival is the most reliable variable .
The results of this study compare favorably to the other trials in patients with RPDIPG. The survival data in most of these trials are nonexistent simply because patients do not usually survive more than 6 months. Contrary to the other studies, our PFS at 6 months is 35.3 % and overall survival from the treatment start at 1 year is 29.4 % and approximately 11.8 % at 2 years. Even at 15 years, the overall survival is approximately 5.9 % (patient was diagnosed with pilocytic astrocytoma and had tumor involving 72 % of pons at the baseline). The quality of survival is excellent and median KPS at the conclusion of treatment increased to 80. There are no chronic adverse events, and the moderate percentages of serious acute toxicities reported are manageable.
The treatment of brainstem gliomas poses the greatest challenge for pediatric neuro-oncologists. This small phase II study of ANP A10 and AS2-1 reports encouraging CR and PR in recurrent pediatric DIPG with promising survival data. Additional phase II studies of ANP in pediatric high-grade glioma and brainstem glioma as well as astrocytoma and optic pathway glioma have been completed and are being prepared for publication.
The authors express their appreciation to the additional physicians involved in the care of the patients: Robert A. Weaver, M.D.; Robert I. Lewy, M.D.; Alejandro Marquis, M.D.; Eva Kubove, M.D.; Barbara Szymkowski, M.D.; Sheryll Acelar, M.D.; and Mohammad Khan, M.D. Central radiology review was performed by Dieter Schellinger, M.D.; Joshua C. Pleasure, M.D.; and Randall A. Stenoien, M.D. Preparation of the manuscript was provided by Darlene Hodge and Carolyn Powers. Editorial assistance was provided by Malcolm Kendrick, M.D. The clinical trial was sponsored by the Burzynski Research Institute, Inc.
Conflict of interest
The clinical trial was sponsored by Burzynski Research Institute, Inc. The authors are employed by Burzynski Clinic. Dr. Stanislaw R. Burzynski and Dr. Gregory S. Burzynski are shareholders and directors, and Dr. Tomasz J. Janicki is the vice-president of Burzynski Research Institute, Inc.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2005–2009 (2012). Central Brain Tumor Registry of the United States (CBTRUS), Hinsdale, IL, 14:201. http://neuro-oncology.oxfordjournals.org/content/14/suppl_5/v1.extract
Burzynski SR (2007) Recent clinical trials in diffuse intrinsic brainstem glioma. Cancer Ther 5:379–390
Burzynski SR (2006) Targeted therapy for brain tumors. In: Yang A (ed) Brain cancer: therapy and surgical interventions. Nova Science Publishers, New York
Patil SS, Burzynski SR, Mrowczynski E, Grela K, Chittur S (2012) Phenylacetylglutaminate in combination with phenylacetate causes cell cycle blockade and apoptosis by upregulating VDUP1 in U-87 glioblastoma cells. J Cancer Ther 3:192–200CrossRef
Zhou BB, Anderson HJ, Roberge M (2003) Targeting DNA checkpoint kinases in cancer therapy. Cancer Biol Ther 2:16–22CrossRef
Patil S, Burzynski SR, Mrowczynski E, Grela K (2010) Antineoplastons initiate caspase induced apoptosis by suppressing survivin expression in U87 glioblastoma cells. Neuro-Oncol 12:ii87CrossRef
Patil S, Burzynski SR, Mrowczynski E, Grela K (2010) CB-15. Targeting microRNAs in glioma cells with antineoplastons. Neuro-Oncol 12:iv10
Paugh BS, Broniscer A, Qu C, Miller CP, Zhang J, Tatevossian RG, Olson JM, Geyer JR, Chi SN, Saba da Silva N, Onar-Thomas A, Baker JN, Gajjar A, Ellison DW, Baker SJ (2011) Genome-wide analyses identify recurrent amplifications of receptor tyrosine kinases and cell-cycle regulatory genes in diffuse intrinsic pontine glioma. J Clin Oncol 29:3999–4006PubMedCentralPubMedCrossRef
Gilbertson RJ, Hill DA, Hernan R, Kocak M, Geyer R, Olson J, Gaijar A, Rush L, Hamilton RL, Finkelstein SD, Pollack IF (2003) ERBB1 is amplified and overexpressed in high-grade diffusely infiltrative pediatric brain stem glioma. Clin Cancer Res 9:3620–3624PubMed
Burzynski SR, Kubove E (1986) Toxicology studies on antineoplaston A10 injections in cancer patients. Drugs Exp Clin Res 12:47–55PubMed
Burzynski SR, Kubove E, Burzynski B (1992) Phase II clinical trials of antineoplastons A10 and AS2-1 infusions in astrocytoma. In: Adam D (ed) Recent advances in chemotherapy. Futuramed Publishers, Munich
Burzynski SR, Conde AB, Peters A, Saling B, Ellithorpe R, Daugherty JP, Nacht CH (1999) A retrospective study of antineoplastons A10 and AS2-1 in primary brain tumours. Clin Drug Investig 18:1–10CrossRef
Burzynski SR, Janicki TJ, Burzynski GS, Marszalek A (2014) Long term survival (>13 years) in a child with recurrent diffuse pontine gliosarcoma: a case report. J Pediatr Hematol Oncol. doi:10.1097/MPH.0000000000000020
Chang SM et al (1999) Phase II study of phenylacetate in patients with recurrent malignant glioma: a North American Brain Tumor Consortium report. J Clin Oncol 17:984–990PubMed
Burzynski SR (2006) Treatments for astrocytic tumors in children: current and emerging strategies. Pediatr Drugs 8:167–168CrossRef
Fouladi M, Nicholson HS, Zhou T, Laningham F, Helton KJ et al (2007) A phase II study of the farnesyl transferase inhibitor, tipifarnib, in children with recurrent or progressive high-grade glioma, medulloblastoma/primitive neuroectodermal tumor, or brainstem glioma: a Children’s Oncology Group study. Cancer 110:2535–2541PubMedCrossRef
Gururangan S, Chi SN, Young Poussaint T, Onar-Thomas A, Gilbertson RJ et al (2010) Lack of efficacy of bevacizumab plus irinotecan in children with recurrent malignant glioma and diffuse brainstem glioma: a Pediatric Brain Tumor Consortium study. J Clin Oncol 2010(28):3069–3075CrossRef
Warren KE, Gururangan S, Geyer JR, McLendon RE, Poussaint TY et al (2012) A phase II study of 06-benzylguanine and temozolomide in pediatric patients with recurrent or progressive high-grade gliomas and brainstem gliomas: a Pediatric Brain tumor Consortium study. J Neurooncol 106:643–649PubMedCentralPubMedCrossRef