論文

査読有り 国際誌
2017年5月

Convection-enhanced delivery of a hydrophilic nitrosourea ameliorates deficits and suppresses tumor growth in experimental spinal cord glioma models.

Acta neurochirurgica
  • Shogo Ogita
  • ,
  • Toshiki Endo
  • ,
  • Shinichiro Sugiyama
  • ,
  • Ryuta Saito
  • ,
  • Tomoo Inoue
  • ,
  • Akira Sumiyoshi
  • ,
  • Hiroi Nonaka
  • ,
  • Ryuta Kawashima
  • ,
  • Yukihiko Sonoda
  • ,
  • Teiji Tominaga

159
5
開始ページ
939
終了ページ
946
記述言語
英語
掲載種別
DOI
10.1007/s00701-017-3123-2

BACKGROUND: Convection-enhanced delivery (CED) is a technique allowing local infusion of therapeutic agents into the central nervous system, circumventing the blood-brain or spinal cord barrier. OBJECTIVE: To evaluate the utility of nimustine hydrochloride (ACNU) CED in controlling tumor progression in an experimental spinal cord glioma model. METHODS: Toxicity studies were performed in 42 rats following the administration of 4 μl of ACNU CED into the mid-thoracic spinal cord at concentrations ranging from 0.1 to 10 mg/ml. Behavioral analyses and histological evaluations were performed to assess ACNU toxicity in the spinal cord. A survival study was performed in 32 rats following the implantation of 9 L cells into the T8 spinal cord. Seven days after the implantation, rats were assigned to four groups: ACNU CED (0.25 mg/ml; n = 8); ACNU intravenous (i.v.) (0.4 mg; n = 8); saline CED (n = 8); saline i.v. (n = 8). Hind limb movements were evaluated daily in all rats for 21 days. Tumor sizes were measured histologically. RESULTS: The maximum tolerated ACNU concentration was 0.25 mg/ml. Preservation of hind limb motor function and tumor growth suppression was observed in the ACNU CED (0.25 mg/ml) and ACNU i.v. groups. Antitumor effects were more prominent in the ACNU CED group especially in behavioral analyses (P < 0.05; log-rank test). CONCLUSIONS: ACNU CED had efficacy in controlling tumor growth and preserving neurological function in an experimental spinal cord tumor model. ACNU CED can be a viable treatment option for spinal cord high-grade glioma.

リンク情報
DOI
https://doi.org/10.1007/s00701-017-3123-2
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28247160
ID情報
  • DOI : 10.1007/s00701-017-3123-2
  • PubMed ID : 28247160

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