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颅内替莫唑胺联合卡莫司汀治疗与单一药物治疗相比可提高啮齿动物脑胶质瘤模型的存活率。

Combination of intracranial temozolomide with intracranial carmustine improves survival when compared with either treatment alone in a rodent glioma model.

机构信息

Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Neurosurgery. 2010 Mar;66(3):530-7; discussion 537. doi: 10.1227/01.NEU.0000365263.14725.39.

Abstract

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.

摘要

背景

替莫唑胺(TMZ)通过聚合物局部递送优于在啮齿动物脑胶质瘤模型中的口服给药。

目的

我们假设口服 TMZ 和卡莫司汀(BCNU)片剂的临床协同作用在动物恶性脑胶质瘤模型中通过局部递送 BCNU 和 TMZ 以及添加放射治疗会产生更大的效果。

方法

TMZ 和 BCNU 被掺入可生物降解的聚合物中,这些聚合物被植入携带颅内肿瘤的 F344 大鼠中。我们使用了 2 种不同的啮齿动物脑胶质瘤模型:9L 神经胶质瘤和 F98 神经胶质瘤。

结果

在 9L 啮齿动物脑胶质瘤模型中,接受局部 TMZ、局部 BCNU 和放射治疗(XRT)联合治疗的组有 75%的长期存活者(定义为肿瘤植入后 120 天存活的动物),优于局部 TMZ 和局部 BCNU 的联合治疗(中位生存期,95 天;长期存活率,25%)和口服 TMZ、局部 BCNU 和 XRT 的联合治疗(中位生存期,62 天;长期存活率,12.5%)。为了模拟这种治疗在化疗耐药性脑肿瘤中的效果,使用了第二个啮齿动物模型 F98 神经胶质瘤,这是一种相对对抗癌药物有抗性的细胞系。F98 神经胶质瘤细胞表达高水平的烷化酶,这是一种使烷化剂失活的酶,也是脑肿瘤耐药的主要机制。与对照组相比,三重治疗在存活方面有显著改善(P=0.0004),与 BCNU(P=0.0043)、口服 TMZ(P=0.0026)、局部 TMZ(P=0.0105)以及 BCNU 和 XRT 的联合治疗(P=0.0378)或口服 TMZ 和 BCNU 的联合治疗(P=0.0154)相比。

结论

与单独治疗或口服 TMZ、局部 BCNU 和 XRT 相比,在 9L 和 F98 神经胶质瘤模型中,局部递送 BCNU 和 TMZ 联合 XRT 可提高荷瘤动物的存活。

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