Literature DB >> 12811531

Local delivery of (131)I-MIBG to treat peritoneal neuroblastoma.

Seigo Kinuya1, Xiao-Feng Li, Kunihiko Yokoyama, Hirofumi Mori, Kazuhiro Shiba, Naoto Watanabe, Noriyuki Shuke, Hisashi Bunko, Takatoshi Michigishi, Norihisa Tonami.   

Abstract

Internal radiotherapy involving systemic administration of iodine-131 metaiodobenzylguanidine ((131)I-MIBG) in neural crest tumours such as neuroblastoma has shown considerable success. Although peritoneal seeding of neuroblastoma occurs less often than metastases to organs such as the liver, no effective treatments exist in this clinical setting. Previous reports have demonstrated the effectiveness of peritoneal application of chemotherapeutic drugs or radiolabelled monoclonal antibodies in several kinds of carcinomas. Local delivery of (131)I-MIBG should produce more favourable dosimetry in comparison with its systemic administration in the treatment of peritoneal neuroblastoma. In the current investigation, a peritoneal model of neuroblastoma was established in Balb/c nu/nu mice by i.p. injection of SK-N-SH neuroblastoma cells. Two weeks after cell inoculation, comparative biodistribution studies were performed following i.v. or i.p. administration of (131)I-MIBG. Mice were treated with 55.5 MBq of (131)I-MIBG administered either i.v. or i.p. at 2 weeks. Intraperitoneal injection of (131)I-MIBG produced significantly higher tumour accumulation than did i.v. injection ( P<0.01). Therapeutic ratios of i.p. injection were 4- to 14-fold higher than those of i.v. injection. Radiotherapy with i.v. administered (131)I-MIBG failed to improve the survival of mice; mean survival of untreated mice and mice treated with i.v. administration of (131)I-MIBG was 59.3+/-3.9 days and 60.6+/-2.8 days, respectively. On the other hand, radiotherapy delivered via i.p. administration of (131)I-MIBG prolonged survival of mice to 94.7+/-17.5 days ( P<0.02 vs untreated controls and mice treated with i.v. (131)I-MIBG therapy). Radiation doses absorbed by tumours at 55.5 MBq of (131)I-MIBG were estimated to be 4,140 cGy with i.p. injection and 450 cGy with i.v. injection. These results indicate the benefits of locoregional delivery of (131)I-MIBG in the treatment of peritoneal neuroblastoma.

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Year:  2003        PMID: 12811531     DOI: 10.1007/s00259-003-1214-1

Source DB:  PubMed          Journal:  Eur J Nucl Med Mol Imaging        ISSN: 1619-7070            Impact factor:   9.236


  24 in total

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Journal:  Int J Cancer       Date:  2000-08-01       Impact factor: 7.396

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Journal:  Cancer Res       Date:  1993-01-15       Impact factor: 12.701

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Journal:  J Nucl Med       Date:  1996-09       Impact factor: 10.057

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  3 in total

1.  Preclinical Development of [211At]meta- astatobenzylguanidine ([211At]MABG) as an Alpha Particle Radiopharmaceutical Therapy for Neuroblastoma.

Authors:  Vandana Batra; Minu Samanta; Mehran Makvandi; David Groff; Paul Martorano; Jimmy Elias; Pietro Ranieri; Matthew Tsang; Catherine Hou; Yimei Li; Bruce Pawel; Daniel Martinez; Ganesan Vaidyanathan; Sean Carlin; Daniel A Pryma; John M Maris
Journal:  Clin Cancer Res       Date:  2022-09-15       Impact factor: 13.801

Review 2.  Hypoxia in microscopic tumors.

Authors:  Xiao-Feng Li; Joseph A O'Donoghue
Journal:  Cancer Lett       Date:  2008-04-01       Impact factor: 8.679

3.  RESEARCH ADVANCES IN NEUROBLASTOMA IMMUNOTHERAPY.

Authors:  Latania Y Booker; Titilope A Ishola; Kanika A Bowen; Dai H Chung
Journal:  Curr Pediatr Rev       Date:  2009-05
  3 in total

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