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首页> 外文期刊>Neurosurgery >Combination of intracranial temozolomide with intracranial carmustine improves survival when compared with either treatment alone in a rodent glioma model.
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Combination of intracranial temozolomide with intracranial carmustine improves survival when compared with either treatment alone in a rodent glioma model.

机译:与啮齿类神经胶质瘤模型中的任何一种治疗相比,颅内替莫唑胺与颅内卡莫司汀的组合可提高生存率。

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摘要

BACKGROUND: Local delivery of temozolomide (TMZ) through polymers is superior to oral administration in a rodent glioma model. OBJECTIVE: We hypothesized that the observed clinical synergy of orally administered TMZ and carmustine (BCNU) wafers would translate into even greater effectiveness with the local delivery of BCNU and TMZ and the addition of radiotherapy in animal models of malignant glioma. METHODS: TMZ and BCNU were incorporated into biodegradable polymers that were implanted in F344 rats bearing established intracranial tumors. We used 2 different rodent glioma models: the 9L gliosarcoma and the F98 glioma. RESULTS: In the 9L rodent glioma model, groups treated with the combination of local TMZ, local BCNU, and radiation therapy (XRT) had 75% long-term survivors (defined as animals alive 120 days after tumor implantation), which was superior to the combination of local TMZ and local BCNU (median survival, 95 days; long-term survival, 25%) and the combination of oral TMZ, local BCNU, and XRT (median survival, 62 days; long-term survival, 12.5%). To simulate the effect of this treatment in chemoresistant gliomas, a second rodent model was used with the F98 glioma, a cell line relatively resistant to alkylating agents. F98 glioma cells express high levels of alkyltransferase, an enzyme that deactivates alkylating agents and is the major mechanism of resistance of gliomas. The triple therapy showed a significant improvement in survival when compared with controls (P = .0004), BCNU (P = .0043), oral TMZ (P = .0026), local TMZ (P = .0105), and the combinations of either BCNU and XRT (P = .0378) or oral TMZ and BCNU (P = .0154). CONCLUSION: The survival of tumor-bearing animals in the 9L and F98 glioma models was improved with the local delivery of BCNU and TMZ combined with XRT when compared with either treatment alone or oral TMZ, local BCNU, and XRT.
机译:背景:替莫唑胺(TMZ)通过聚合物的局部递送优于啮齿类神经胶质瘤模型中的口服给药。目的:我们假设观察到的口服TMZ和卡莫司汀(BCNU)薄饼的临床协同作用,将在局部递送BCNU和TMZ以及在恶性神经胶质瘤动物模型中增加放疗后转化为更高的疗效。方法:将TMZ和BCNU掺入可生物降解的聚合物中,然后将其植入患有已确定的颅内肿瘤的F344大鼠中。我们使用了两种不同的啮齿动物胶质瘤模型:9L胶质肉瘤和F98胶质瘤。结果:在9L啮齿动物神经胶质瘤模型中,局部TMZ,局部BCNU和放射疗法(XRT)联合治疗的组具有75%的长期存活者(定义为肿瘤植入后120天还活着的动物),优于局部TMZ和局部BCNU的组合(中位生存期95天;长期生存率25%),以及口服TMZ,局部BCNU和XRT的组合(中位生存期62天;长期生存率12.5%) 。为了模拟这种治疗在化学耐药性神经胶质瘤中的效果,将第二只啮齿动物模型与F98神经胶质瘤(一种对烷化剂相对抗性的细胞系)一起使用。 F98胶质瘤细胞表达高水平的烷基转移酶,该酶可使烷基化剂失活,是胶质瘤抵抗的主要机制。与对照组(P = .0004),BCNU(P = .0043),口服TMZ(P = .0026),局部TMZ(P = .0105)以及以下药物的组合相比,三联疗法显示生存率显着提高BCNU和XRT(P = .0378)或口服TMZ和BCNU(P = .0154)。结论:与单独治疗或口服TMZ,局部BCNU和XRT相比,通过局部递送BCNU和TMZ联合XRT可以改善9L和F98胶质瘤模型中荷瘤动物的存活率。

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