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[用缓释抗癌药物-聚合物复合材料治疗恶性脑肿瘤]

[Treatment of malignant brain tumors with slowly releasing anticancer drug-polymer composites].

作者信息

Kubo O, Himuro H, Inoue N, Tajika Y, Tajika T, Tohyama T, Sakairi M, Yoshida M, Kaetsu I, Kitamura K

出版信息

No Shinkei Geka. 1986 Sep;14(10):1189-95.

PMID:3024049
Abstract

The purpose of this study is to present the methodology and results of a clinical trial of local chemotherapy of malignant brain tumors based on slowly-releasing anticancer drug-polymer composites. The slowly releasing drugs were prepared by combining and mutually dispersing anticancer agents with glassified monomers containing 10% polymetacrylic methyl acid and then this compound was frozen at -78 degrees C and exposed to 1 X 10(6) rad of gamma rays from cobalt 60. Thus we prepared a compound of polymers and anticancer agents. We used needle-shaped capsules of this compound. These capsules release the drug very slowly over 40 days. We administered locally to the malignant brain tumors with either slowly releasing mitomycin, slowly releasing adriamycin, slowly releasing ACNU or slowly releasing 5 Fu drugs. The following techniques were employed in implantation these capsules. Implantation into the remaining tumor wall at the time of excision. Implantation into the tumor by CT-guided stereotactic method. We implanted these drugs into tumor of 55 cases, thereafter we conducted both radiation and chemotherapy with ACNU in most patients. This method has the following advantages: It is possible to be employed to different types of anticancer agents. Both dosage and releasing time can be adjusted. It is possible to administer these capsules postoperatively by the stereotactic method. The clinical study consists of 55 patients, 20 cases of anaplastic astrocytoma, 23 cases of glioblastoma multiforme, 5 cases of oligodendroglioma, 3 cases of medulloblastoma and 4 cases of others. Survival rate estimated by Kaplan-Meier method was 47% in glioblastoma at 12 months and 91% in anaplastic astrocytoma at 18 months.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是介绍基于缓释抗癌药物 - 聚合物复合材料的恶性脑肿瘤局部化疗的方法和结果。通过将抗癌剂与含10%聚甲基丙烯酸的玻璃化单体混合并相互分散来制备缓释药物,然后将该化合物在-78℃下冷冻,并暴露于来自钴60的1×10(6)拉德的γ射线下。由此我们制备了聚合物与抗癌剂的化合物。我们使用了这种化合物的针状胶囊。这些胶囊在40天内非常缓慢地释放药物。我们将缓释丝裂霉素、缓释阿霉素、缓释ACNU或缓释5 - 氟尿嘧啶药物局部施用于恶性脑肿瘤。在植入这些胶囊时采用了以下技术。在切除时植入剩余的肿瘤壁。通过CT引导立体定向方法植入肿瘤。我们将这些药物植入55例患者的肿瘤中,此后大多数患者同时进行了ACNU放疗和化疗。该方法具有以下优点:可用于不同类型的抗癌剂。剂量和释放时间均可调节。可以通过立体定向方法在术后施用这些胶囊。临床研究包括55例患者,20例间变性星形细胞瘤,23例多形性胶质母细胞瘤,5例少突胶质细胞瘤,3例髓母细胞瘤和4例其他类型。用Kaplan - Meier方法估计的生存率在多形性胶质母细胞瘤12个月时为47%,在间变性星形细胞瘤18个月时为91%。(摘要截断于250字)

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Neuro Oncol. 2015 Dec;17(12):1620-7. doi: 10.1093/neuonc/nov181. Epub 2015 Nov 4.
2
Distribution of drugs following controlled delivery to the brain interstitium.
J Neurooncol. 1995 Nov;26(2):91-102. doi: 10.1007/BF01060215.
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Interstitial chemotherapy with mitoxantrone in recurrent malignant glioma: preliminary data.米托蒽醌间质化疗复发性恶性胶质瘤:初步数据。
J Neurooncol. 1996 Feb;27(2):157-62. doi: 10.1007/BF00177479.
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Interstitial chemotherapy for brain tumors: review.脑肿瘤的间质化疗:综述
J Neurooncol. 1991 Feb;10(1):57-74. doi: 10.1007/BF00151247.
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Affinity of antineoplastic amino acid drugs for the large neutral amino acid transporter of the blood-brain barrier.抗肿瘤氨基酸药物对血脑屏障中大中性氨基酸转运体的亲和力。
Cancer Chemother Pharmacol. 1991;29(2):89-94. doi: 10.1007/BF00687316.