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用于人类脑内黑色素瘤中子俘获治疗的裸鼠模型。

A nude rat model for neutron capture therapy of human intracerebral melanoma.

作者信息

Barth R F, Matalka K Z, Bailey M Q, Staubus A E, Soloway A H, Moeschberger M L, Coderre J A, Rofstad E K

机构信息

Department of Pathology, Ohio State University, Columbus 43210.

出版信息

Int J Radiat Oncol Biol Phys. 1994 Mar 30;28(5):1079-88. doi: 10.1016/0360-3016(94)90481-2.

Abstract

PURPOSE

The present study was carried out to determine the efficacy of Boron Neutron Capture Therapy (BNCT) for intracerebral melanoma using nude rats, the human melanoma cell line MRA 27, and boronophenylalanine as the capture agent.

METHODS AND MATERIALS

Pharmacokinetic and tissue distribution studies: MRA 27 cells (2 x 10(5)) were implanted intracerebrally, and 30 days later, 120 mg of 10B-L-BPA were injected intraperitoneally into nude rats. Therapy experiments: Thirty days following implantation, tumor bearing rats were irradiated at the Brookhaven Medical Research Reactor.

RESULTS

Pharmacokinetic experiments: Six hours following administration of BPA, tumor, blood, and normal brain boron-10 levels were 23.7, 9.4, and 8.4 micrograms/g respectively. Therapy experiments: Median survival time of untreated rats was 44 days compared to 76 days and 93 days for those receiving physical doses of 2.73 Gy and 3.64 Gy, respectively. Rats that had received both 10B-BPA and physical doses of 1.82, 2.73, or 3.64 Gy had median survival times of 170, 182, and 262 days, respectively. Forty percent of rats that had received the highest tumor dose (10.1 Gy) survived for > 300 days and in a replicate experiment 21% of the rats were longterm survivors (> 220 days). Animals that received 12 Gy in a single dose or 18 Gy fractionated (2 Gy x 9) of gamma photons from a 137Cs source had median survival times of 86 and 79 days, respectively, compared to 47 days for untreated animals. Histopathologic examination of the brains of longterm surviving rats, euthanized at 8 or 16 months following BNCT, showed no residual tumor, but dense accumulations of melanin laden macrophages and minimal gliosis were observed.

CONCLUSION

Significant prolongations in median survival time were noted in nude rats with intracerebral human melanoma that had received BNCT thereby suggesting therapeutic efficacy. Large animal studies should be carried out to further assess BNCT of intracerebral melanoma before any human trials are contemplated.

摘要

目的

本研究旨在使用裸鼠、人黑色素瘤细胞系MRA 27以及硼代苯丙氨酸作为捕获剂,确定硼中子俘获疗法(BNCT)治疗脑内黑色素瘤的疗效。

方法与材料

药代动力学和组织分布研究:将MRA 27细胞(2×10⁵个)植入脑内,30天后,向裸鼠腹腔注射120 mg的¹⁰B-L-BPA。治疗实验:植入后30天,对荷瘤大鼠在布鲁克海文医学研究反应堆进行辐照。

结果

药代动力学实验:给予BPA 6小时后,肿瘤、血液和正常脑的硼-10水平分别为23.7、9.4和8.4微克/克。治疗实验:未治疗大鼠的中位生存时间为44天,而接受2.73 Gy和3.64 Gy物理剂量照射的大鼠分别为76天和93天。接受¹⁰B-BPA和1.82、2.73或3.64 Gy物理剂量照射的大鼠,其中位生存时间分别为170天、182天和262天。接受最高肿瘤剂量(10.1 Gy)的大鼠中有40%存活超过300天,在重复实验中,21%的大鼠为长期存活者(超过220天)。接受来自¹³⁷Cs源的单剂量12 Gy或分次(2 Gy×9)18 Gyγ光子照射的动物,其中位生存时间分别为86天和79天,而未治疗动物为47天。对BNCT后8或16个月实施安乐死的长期存活大鼠的大脑进行组织病理学检查,未发现残留肿瘤,但观察到载有黑色素的巨噬细胞密集积聚和轻度胶质增生。

结论

接受BNCT的脑内人黑色素瘤裸鼠的中位生存时间显著延长,从而提示该疗法具有疗效。在考虑进行任何人体试验之前,应开展大型动物研究以进一步评估脑内黑色素瘤的BNCT。

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