Cargando…

A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy.

A fluorinated 2-nitroimidazole radiosensitizer KU-2285 was given before intraoperative radiotherapy (IORT) to 30 patients with unresectable, unresected or macroscopic residual tumours. Twenty-three patients had pancreatic cancer and five had osteosarcoma. The IORT dose was 30 Gy for unresectable pan...

Descripción completa

Detalles Bibliográficos
Autores principales: Shibamoto, Y., Ohshio, G., Hosotani, R., Nishimura, Y., Manabe, T., Imamura, M., Abe, M.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228186/
https://www.ncbi.nlm.nih.gov/pubmed/9400944
_version_ 1782149852670459904
author Shibamoto, Y.
Ohshio, G.
Hosotani, R.
Nishimura, Y.
Manabe, T.
Imamura, M.
Abe, M.
author_facet Shibamoto, Y.
Ohshio, G.
Hosotani, R.
Nishimura, Y.
Manabe, T.
Imamura, M.
Abe, M.
author_sort Shibamoto, Y.
collection PubMed
description A fluorinated 2-nitroimidazole radiosensitizer KU-2285 was given before intraoperative radiotherapy (IORT) to 30 patients with unresectable, unresected or macroscopic residual tumours. Twenty-three patients had pancreatic cancer and five had osteosarcoma. The IORT dose was 30 Gy for unresectable pancreatic cancer and 60 Gy for osteosarcoma. The dose of KU-2285 administered ranged from 1 to 9 g m-2. Four patients received a dose of 9 g m-2, and ten received 6.8-7 g m-2. All patients tolerated KU-2285 well, and no drug-related toxicity was observed. The average tumour concentration of KU-2285 immediately after IORT was 166 microg g-1 at dose of 6.8-7 g m-2 and 333 microg g-1 at 9 g m-2. The average tumour-plasma ratio was > or = 0.82. Eleven patients with unresectable but localized pancreatic cancer treated with KU-2285 plus IORT and external beam radiotherapy had a median survival time of 11 months and 1-year local control rate of 50%, which compares favourably with those of 8 months (P = 0.26) and 28% (P = 0.10) for 22 matched historical control patients. The five patients with osteosarcoma attained local control. The results of this first study on KU-2285 and IORT appear encouraging, and further studies of this compound seem to be warranted.
format Text
id pubmed-2228186
institution National Center for Biotechnology Information
language English
publishDate 1997
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-22281862009-09-10 A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy. Shibamoto, Y. Ohshio, G. Hosotani, R. Nishimura, Y. Manabe, T. Imamura, M. Abe, M. Br J Cancer Research Article A fluorinated 2-nitroimidazole radiosensitizer KU-2285 was given before intraoperative radiotherapy (IORT) to 30 patients with unresectable, unresected or macroscopic residual tumours. Twenty-three patients had pancreatic cancer and five had osteosarcoma. The IORT dose was 30 Gy for unresectable pancreatic cancer and 60 Gy for osteosarcoma. The dose of KU-2285 administered ranged from 1 to 9 g m-2. Four patients received a dose of 9 g m-2, and ten received 6.8-7 g m-2. All patients tolerated KU-2285 well, and no drug-related toxicity was observed. The average tumour concentration of KU-2285 immediately after IORT was 166 microg g-1 at dose of 6.8-7 g m-2 and 333 microg g-1 at 9 g m-2. The average tumour-plasma ratio was > or = 0.82. Eleven patients with unresectable but localized pancreatic cancer treated with KU-2285 plus IORT and external beam radiotherapy had a median survival time of 11 months and 1-year local control rate of 50%, which compares favourably with those of 8 months (P = 0.26) and 28% (P = 0.10) for 22 matched historical control patients. The five patients with osteosarcoma attained local control. The results of this first study on KU-2285 and IORT appear encouraging, and further studies of this compound seem to be warranted. Nature Publishing Group 1997 /pmc/articles/PMC2228186/ /pubmed/9400944 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Shibamoto, Y.
Ohshio, G.
Hosotani, R.
Nishimura, Y.
Manabe, T.
Imamura, M.
Abe, M.
A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy.
title A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy.
title_full A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy.
title_fullStr A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy.
title_full_unstemmed A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy.
title_short A phase I/II study of a hypoxic cell radiosensitizer KU-2285 in combination with intraoperative radiotherapy.
title_sort phase i/ii study of a hypoxic cell radiosensitizer ku-2285 in combination with intraoperative radiotherapy.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228186/
https://www.ncbi.nlm.nih.gov/pubmed/9400944
work_keys_str_mv AT shibamotoy aphaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT ohshiog aphaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT hosotanir aphaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT nishimuray aphaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT manabet aphaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT imamuram aphaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT abem aphaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT shibamotoy phaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT ohshiog phaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT hosotanir phaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT nishimuray phaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT manabet phaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT imamuram phaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy
AT abem phaseiiistudyofahypoxiccellradiosensitizerku2285incombinationwithintraoperativeradiotherapy