A NOVEL IMPROVEMENT ON RADIOTHERAPY FOR SCCHN
A NOVEL IMPROVEMENT ON RADIOTHERAPY FOR SCCHN
批准号:
6379918
负责人:
Esther H Chang
金额:
$57.57万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-09-01 至 2003-08-31
关键词:
apoptosis athymic mouse clinical research clinical trial phase I combination cancer therapy drug delivery systems drug design /synthesis /production folate head /neck neoplasm histopathology human subject human therapy evaluation liposomes neoplasm /cancer radionuclide therapy neoplasm /cancer transplantation p53 gene /protein radiation resistance radiation sensitivity radiosensitizer squamous cell carcinoma
中文摘要
头颈部鳞状细胞癌(SCCHN),包括口腔鳞状细胞癌,具有显著的死亡率和高复发率。这些临床失败的很大一部分是由于肿瘤细胞的辐射抵抗(RR)。因此,开发一种使头颈部肿瘤对放射治疗增敏的有效方法将对这种疾病的治疗产生深远的影响。野生型(wt) p53在导致肿瘤细胞死亡的凋亡通路中起关键作用。许多SCCHN肿瘤细胞缺乏功能性p53被认为是其RR的原因。wtp53功能的恢复可能会恢复p53介导的凋亡通路,从而更有效地治疗。wtp53基因治疗联合放疗将用于恢复对RR SCCHN的放射敏感性。癌症基因治疗的长期目标是有选择性地靶向肿瘤细胞(包括转移细胞)的全身传递系统。本应用提出优化叶酸连接脂质体wtp53全身递送系统,以提高传统放疗的疗效。初步的体内实验结果原则上证明,恢复wtp53功能可增强辐射诱导的细胞凋亡,导致肿瘤整体长期消退。通过与制药合作伙伴的合作,我们将获得GMP级试剂,进行毒理学和药代动力学研究,以获得IRB, IBC和FDA的批准。一旦获得批准,我们将在I期临床试验中使用这种联合疗法,努力将这种新的、可能更有效的治疗方式转化为头颈癌的临床治疗。
英文摘要
Squamous cell carcinoma of the head and neck (SCCHN), including that of the oral cavity, has a significant level of mortality and a high rate of recurrence. A significant portion of these clinical failures result from tumor cell radiation resistance (RR). Thus, the development of an effective method for sensitizing head and neck tumors to radiotherapy would have a profound effect on the treatment of this disease. Wild-type (wt) p53 plays a crucial role in apoptotic pathways leading to tumor cell death. The lack of functional p53 in many SCCHN tumor cells is thought to be responsible for their RR. The restoration of wtp53 function may restore the p53-mediated apoptotic pathway resulting in more efficient treatment. A combination of wtp53 gene therapy and radiation will be used to restore radiation sensitivity to RR SCCHN. A long-standing goal in gene therapy for cancer is a systemic delivery system that selectively targets tumor cells, including metastases. This application proposes to optimize a folate-linked liposome systemic delivery system for wtp53 to improve the efficacy of conventional radiotherapy. Preliminary in vivo results have proved in principle that restoration of wtp53 function enhances radiation induced apoptosis, leading to long term total tumor regression. In collaboration with a pharmaceutical partner, we will obtain GMP grade reagent, perform toxicology and pharmacokinetic studies to obtain IRB, IBC and FDA approval. Once approvals are obtained we will use this combination therapy in a Phase I clinical trial in an effort to translate this new and potentially more effective treatment modality into the clinic for head and neck cancer.
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