Burzynski: PRIMITIVE NEUROECTODERMAL TUMORS (PNET)

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# and % of Patients Resolving or Stabilizing Disease = Complete Response + Partial Response + Stable Disease
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10 / 66.7% – 10/2004 – Protocol – Antineoplastons PRIMITIVE NEUROECTODERMAL TUMORS (PNET)
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# and % of Patients Showing Objective Response = Complete Response + Partial Response
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5 / 33.4% – 10/2004 – Protocol – Antineoplastons PRIMITIVE NEUROECTODERMAL TUMORS (PNET)

5 – Objective Response (OR) not treated earlier with radiation therapy and chemotherapy
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# and % of Patients Showing Complete Response
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3 / 20% – 10/2004 – Protocol – Antineoplastons PRIMITIVE NEUROECTODERMAL TUMORS (PNET)
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# and % of Patients Showing Partial Response
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2 / 13.4% – 10/2004 – Protocol – Antineoplastons PRIMITIVE NEUROECTODERMAL TUMORS (PNET)
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# and % of Patients Showing Stable Disease
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5 / 33.3% – 10/2004 – Protocol – Antineoplastons PRIMITIVE NEUROECTODERMAL TUMORS (PNET)
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# and % of Patients Showing Progressive Disease
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5 / 33.3% – 10/2004 – Protocol – Antineoplastons PRIMITIVE NEUROECTODERMAL TUMORS (PNET)
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alive from 7+ – 10+ years from beginning of treatment:
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6 – 6/2005 Antineoplastons: BT-12 – children with PRIMITIVE NEUROECTODERMAL TUMORS (PNET) (5 weren’t treated earlier with radiation therapy or chemotherapy): (Pgs. 168, 170 and 173)
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Alive and Well 6+ – 10 years Post Diagnosis:
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6 – 10/2004 Antineoplastons: Protocol – PRIMITIVE NEUROECTODERMAL TUMORS (PNET)
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6 Alive and Well Post Diagnosis:
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6+ – 10 years
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Survived more than 5 years from Antineoplastons (ANP) Treatment:
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6 / 46% – 6/2005 Antineoplastons: BT-12 – children with PRIMITIVE NEUROECTODERMAL TUMORS (PNET) (5 weren’t treated earlier with radiation therapy or chemotherapy): (Pgs. 168, 170 and 173)
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Overall Survival from Diagnosis (OSD):
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41.8 months (3 years 5.8 months) – 6/2005 Antineoplastons: (4/13/1994–12/4/2001 as of 8/1/2004) Protocol – poor-risk recurrent disease or high risk – BT-12 study (Pgs. 168-170 and 176)
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from Diagnosis:
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41.8 months (3 years 5.8 months) – 10/2004 Antineoplastons: Protocol – BT-12 – Children with PRIMITIVE NEUROECTODERMAL TUMORS (PNET) (7/27/2004)
(Pgs. 171- 173)
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from Diagnosis:
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41.8 months (3 years 5.8 months)
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Overall Survival from start (OSS) of Treatment:
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37.8 months (3 years 1.8 months) 6/2005 Antineoplastons: (4/13/1994–12/4/2001 as of 8/1/2004) Protocol – poor-risk recurrent disease or high risk – BT-12 study (Pgs. 168-170 and 176)
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Median Survival from start of Antineoplastons Treatment:
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20.6 months (1 year 8.6 months) – 10/2004 Antineoplastons: Protocol – BT-12 – Children with PRIMITIVE NEUROECTODERMAL TUMORS (PNET) (7/27/2004)
(Pgs. 171- 173)
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Median Survival from start of Antineoplaston Treatment:
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20.6 months (1 year 8.6 months)
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Burzynski: Complete Response, Partial Response, Stable Disease, Progressive Disease, Objective Response, and Response:
https://stanislawrajmundburzynski.wordpress.com/2013/07/04/burzynski-complete-response-partial-response-stable-disease-progressive-disease-objective-response-and-response/
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Burzynski: Progression-Free Survival:
https://stanislawrajmundburzynski.wordpress.com/2013/07/04/burzynski-progression-free-survival/
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