复发/持续性胶质母细胞瘤:1例45岁女性抗瘤细胞瘤治疗的完全缓解和24年无病生存率(抗瘤细胞瘤治疗成功)

S. Burzynski, Gregory S. Burzynski, T. Janicki, S. Beenken
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引用次数: 2

摘要

理由:胶质母细胞瘤(GBM)的预后非常差,占所有恶性中枢神经系统(CNS)肿瘤的48%,胶质瘤的57%。标准治疗后复发/持续性GBM患者通常在6个月内死亡。本文报告一位患有复发性/持续性GBM的成年女性,详细讨论了ANP治疗(抗瘤素A10 {Atengenal}和抗瘤素AS2-1 {Astugenal})治疗该病的疗效。目的:该患者在博金斯基诊所(BC)接受治疗,根据II期协议BT-20,作为同情豁免(CE),该协议使用ANP治疗GBMs患者。ANP治疗先经锁骨下导管和输液泵给药,再经口腔给药。肿瘤反应是通过使用钆增强的脑序贯磁共振成像(MRI)来测量的。结果:该患者于1997年5月被诊断为右颞顶区GBM,年龄45岁,并接受了两次手术切除、放射治疗(RT)和其他部位的伽玛刀消融。在46岁零8个月时,她以复发/持续性疾病向BC报告。她自诉虚弱、头晕、短期记忆丧失和恶心。由于身体不协调和左侧虚弱,她说话和走路都有困难。基线脑MRI在BC显示一个可测量的增强结节在手术床。ANP治疗于1998年8月开始,患者在5个月内达到完全缓解(CR)。现在,24年过去了,病人恢复得很好,没有肿瘤复发的迹象。结论:应用ANP治疗可获得复发/持续性GBM患者的治愈。我们的结论是,ANP治疗是一个有吸引力的治疗选择成人GBM谁是不符合条件或拒绝标准治疗或显示复发/持续的疾病标准治疗后。我们在此报告了ANP疗法(抗肿瘤素A10 {Atengenal}和抗肿瘤素AS2-1 {Astugenal})在治疗复发/持续性GBM中的成功应用,该患者为46岁零8个月的女性,最初在45岁时被诊断出来,并接受了总切除、放射治疗(RT)、复发肿瘤伽玛刀消融和随后的右肺叶切除术。我们还介绍了靶向治疗在GBM治疗中的应用,包括我们自己的初步结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent/Persistent Glioblastoma: Complete Response and 24 Years Disease-free Survival in a 45-Year-Old Female Treated with Antineoplastons (Successful Treatment of Glioblastoma with Antineoplastons)
Rationale: Glioblastoma (GBM), which accounts for 48% of all malignant central nervous system (CNS) tumors and 57% of gliomas, has a very poor prognosis. Patients with recurrent/persistent GBM after standard therapy usually die within six months. The case of an adult female with a recurrent/ persistent GBM is presented here to detail/discuss the efficacy of ANP therapy (Antineoplaston A10 {Atengenal} and Antineoplaston AS2-1 {Astugenal}) in the treatment of this disease. Objectives: This patient was treated at the Burzynski Clinic (BC), as a Compassionate Exemption (CE) according to the Phase II Protocol, BT-20, which utilized ANP therapy in the treatment of patients with GBMs. ANP therapy was delivered via subclavian catheter and infusion pump and then by mouth. Tumor response was measured by sequential magnetic resonance imaging (MRI) of the brain utilizing gadolinium enhancement. Findings: This patient was diagnosed with GBM of the right temporoparietal region in May 1997, at age 45, and underwent two surgical resections, radiation therapy (RT), and gamma knife ablation elsewhere. At age 46 years and eight months, she presented to the BC with recurrent/ persistent disease. She complained of weakness, dizziness, short-term memory loss, and nausea. She had difficulty speaking and walked with assistance due to discoordination and left-sided weakness. Baseline brain MRI at the BC revealed a measurable enhancing nodule in the surgical bed. ANP therapy was initiated in August 1998 and the patient achieved a complete response (CR) within five months. Now, 24 years later, the patient is doing well and showing no evidence of tumor recurrence. Conclusions: The utilization of ANP therapy to obtain a cure in a patient with recurrent/persistent GBM is presented. We conclude that ANP therapy is an attractive therapeutic option for adults with a GBM who are ineligible for or refuse standard therapy or demonstrate recurrent/persistent disease after standard therapy. We present here the successful use of ANP therapy (Antineoplaston A10 {Atengenal} and Antineoplaston AS2-1 {Astugenal}) in the treatment of recurrent/persistent GBM in a 46 year and eight-month-old female, initially diagnosed at age 45 and treated with gross total resection, radiation therapy (RT), gamma knife ablation of recurrent tumor, and subsequent right lobectomy elsewhere. We also present the use of targeted therapy in the treatment of GBM, including our own preliminary results.
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