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Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer

To examine whether efficacy of postoperative oral administration of UFT, a 5-fluorouracil derivative chemotherapeutic agent, may be influenced by incidence of apoptosis (apoptosis index) or apoptosis-related gene status (p53 and bcl-2) of the tumour, a total of 162 patients with pathologic stage I n...

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Autores principales: Tanaka, F, Otake, Y, Yanagihara, K, Yamada, T, Miyahara, R, Kawano, Y, Li, M, Inui, K, Wada, H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363717/
https://www.ncbi.nlm.nih.gov/pubmed/11161386
http://dx.doi.org/10.1054/bjoc.2000.1579
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author Tanaka, F
Otake, Y
Yanagihara, K
Yamada, T
Miyahara, R
Kawano, Y
Li, M
Inui, K
Wada, H
author_facet Tanaka, F
Otake, Y
Yanagihara, K
Yamada, T
Miyahara, R
Kawano, Y
Li, M
Inui, K
Wada, H
author_sort Tanaka, F
collection PubMed
description To examine whether efficacy of postoperative oral administration of UFT, a 5-fluorouracil derivative chemotherapeutic agent, may be influenced by incidence of apoptosis (apoptosis index) or apoptosis-related gene status (p53 and bcl-2) of the tumour, a total of 162 patients with pathologic stage I non-small cell lung cancer were retrospectively reviewed. UFT was administrated postoperatively to 44 patients (UFT group), and not to the other 118 patients (Control group). For all patients, 5-year survival rate of the UFT group (79.9%) seemed higher than that of the Control group (69.8%), although without significant difference (P = 0.054). For patients with higher apoptotic index, 5-year survival rate of the UFT group (83.3%) was significantly higher than that of the Control group (67.6%, P = 0.039); for patients with lower apoptotic index, however, there was no difference in the prognosis between these two groups. Similarly, UFT was effective for patients without p53 aberrant expression (5-year survival rates: 95.2% for the UFT group and 74.3% for the Control group, P = 0.022), whereas not effective for patients with p53 aberrant expression. Bcl-2 status did not influence the efficacy of UFT. In conclusion, apoptotic index and p53 status are useful factors to predict the efficacy of postoperative adjuvant therapy using UFT. © 2001 Cancer Research Campaign http://www.bjcancer.com
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spelling pubmed-23637172009-09-10 Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer Tanaka, F Otake, Y Yanagihara, K Yamada, T Miyahara, R Kawano, Y Li, M Inui, K Wada, H Br J Cancer Regular Article To examine whether efficacy of postoperative oral administration of UFT, a 5-fluorouracil derivative chemotherapeutic agent, may be influenced by incidence of apoptosis (apoptosis index) or apoptosis-related gene status (p53 and bcl-2) of the tumour, a total of 162 patients with pathologic stage I non-small cell lung cancer were retrospectively reviewed. UFT was administrated postoperatively to 44 patients (UFT group), and not to the other 118 patients (Control group). For all patients, 5-year survival rate of the UFT group (79.9%) seemed higher than that of the Control group (69.8%), although without significant difference (P = 0.054). For patients with higher apoptotic index, 5-year survival rate of the UFT group (83.3%) was significantly higher than that of the Control group (67.6%, P = 0.039); for patients with lower apoptotic index, however, there was no difference in the prognosis between these two groups. Similarly, UFT was effective for patients without p53 aberrant expression (5-year survival rates: 95.2% for the UFT group and 74.3% for the Control group, P = 0.022), whereas not effective for patients with p53 aberrant expression. Bcl-2 status did not influence the efficacy of UFT. In conclusion, apoptotic index and p53 status are useful factors to predict the efficacy of postoperative adjuvant therapy using UFT. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-01 /pmc/articles/PMC2363717/ /pubmed/11161386 http://dx.doi.org/10.1054/bjoc.2000.1579 Text en Copyright © 2001 Cancer Research Campaign 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 Regular Article
Tanaka, F
Otake, Y
Yanagihara, K
Yamada, T
Miyahara, R
Kawano, Y
Li, M
Inui, K
Wada, H
Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer
title Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer
title_full Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer
title_fullStr Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer
title_full_unstemmed Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer
title_short Apoptosis and p53 status predict the efficacy of postoperative administration of UFT in non-small cell lung cancer
title_sort apoptosis and p53 status predict the efficacy of postoperative administration of uft in non-small cell lung cancer
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363717/
https://www.ncbi.nlm.nih.gov/pubmed/11161386
http://dx.doi.org/10.1054/bjoc.2000.1579
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