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点源电穿孔和化疗在治疗脑胶质瘤中的应用:一项随机对照大鼠研究。

The application of point source electroporation and chemotherapy for the treatment of glioma: a randomized controlled rat study.

机构信息

The Advanced Technology Center, Sheba Medical Center, Ramat-Gan, 52621, Israel.

The Joseph Sagol Neuroscience Center, Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel.

出版信息

Sci Rep. 2020 Feb 7;10(1):2178. doi: 10.1038/s41598-020-59152-7.

DOI:10.1038/s41598-020-59152-7
PMID:32034261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7005896/
Abstract

The prognosis of Glioblastoma Multiforme patients is poor despite aggressive therapy. Reasons include poor chemotherapy penetration across the blood-brain barrier and tumor infiltration into surrounding tissues. Here we studied the effects of combined point-source electroporation (EP) and systemic chemotherapy in glioma-bearing rats. 128 rats were studied. Treatment groups were administered systemic Cisplatin/Methotrexate before EP (either 90 or 180 pulses). Control groups were treated by EP, chemotherapy, or no treatment. Tumor volumes were determined by MRI. Tumors growth rates of the EP + Methotrexate group (1.02 ± 0.77) were significantly lower (p < 0.01) than the control (5.2 ± 1.0) 1-week post treatment. No significant difference was found compared to Methotrexate (1.7 ± 0.5). Objective response rates (ORR) were 40% and 57% for the Methotrexate and EP + Methotrexate groups respectively. Tumor growth rates and ORR of the EP + Cisplatin groups (90 pulses 0.98 ± 0.2, 57%, 180 pulses 1.2 ± 0.1, 33%) were significantly smaller than the control (6.4 ± 1.0, p < 0.01, p < 0.02, 0%) and Cisplatin (3.9 ± 1.0, p < 0.04, p < 0.05, 13%) groups. No significant differences were found between the control groups. Increased survival was found in the EP + Cisplatin group, Χ = 7.54, p < 0.006 (Log Rank). Point-source EP with systemic chemotherapy is a rapid, minimal-invasive treatment that was found to induce significant antineoplastic effects in a rat glioma model.

摘要

尽管采用了积极的治疗方法,胶质母细胞瘤患者的预后仍然很差。原因包括血脑屏障通透性差和肿瘤浸润周围组织。在这里,我们研究了联合点源电穿孔(EP)和系统化疗对荷瘤大鼠的影响。研究了 128 只大鼠。实验组在 EP 前给予系统顺铂/甲氨蝶呤(90 或 180 个脉冲)。对照组给予 EP、化疗或不治疗。通过 MRI 确定肿瘤体积。EP+甲氨蝶呤组(1.02±0.77)的肿瘤生长率明显低于对照组(5.2±1.0),治疗后 1 周(p<0.01)。与甲氨蝶呤组(1.7±0.5)相比,无显著差异。甲氨蝶呤组和 EP+甲氨蝶呤组的客观缓解率(ORR)分别为 40%和 57%。EP+顺铂组(90 脉冲 0.98±0.2,57%,180 脉冲 1.2±0.1,33%)的肿瘤生长率和 ORR 明显小于对照组(6.4±1.0,p<0.01,p<0.02,0%)和顺铂组(3.9±1.0,p<0.04,p<0.05,13%)。对照组之间无显著差异。EP+顺铂组的生存时间延长,Χ=7.54,p<0.006(对数秩)。点源 EP 联合全身化疗是一种快速、微创的治疗方法,在大鼠脑胶质瘤模型中发现具有显著的抗肿瘤作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/ae3303029d53/41598_2020_59152_Fig8_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/49505ff9e50a/41598_2020_59152_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/ae3303029d53/41598_2020_59152_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/fbf910781e3b/41598_2020_59152_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/75df1106d546/41598_2020_59152_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/06cb0a5c7e60/41598_2020_59152_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/daf6ff1f9112/41598_2020_59152_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/49505ff9e50a/41598_2020_59152_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2db/7005896/ae3303029d53/41598_2020_59152_Fig8_HTML.jpg

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