Skip Navigation


Annals of Oncology Advance Access originally published online on February 14, 2008
Annals of Oncology 2008 19(6):1045-1052; doi:10.1093/annonc/mdn024
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
19/6/1045    most recent
mdn024v1
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Aykan, N. F.
Right arrow Articles by Idelevich, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Aykan, N. F.
Right arrow Articles by Idelevich, E.
Related Collections
Right arrow 2008 - Review Articles
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

reviews

The role of UFT in advanced gastric cancer

N. F. Aykan1,* and E. Idelevich2

1 Department of Medical Oncology, Institute of Oncology, Istanbul University, Capa 34390 Istanbul, Turkey
2 Institute of Oncology, Kaplan Medical Center, Rehovot, Israel

* Correspondence to: Prof. N. F. Aykan, Department of Medical Oncology, Institute of Oncology, Istanbul University, Istanbul, Turkey. Tel: +90-533-265-8907; Fax: +90-212-661-9028; E-mail: nfaruk{at}superonline.com

Background: Advanced gastric cancer has a poor prognosis, with a relative 5-year survival rate of 7%–27%. Chemotherapy, which improves overall survival (OS) and quality of life, is the main treatment option. Although numerous regimens have been investigated, there is no standard treatment. Combination chemotherapy, however, is associated with a significant survival benefit compared with monotherapy and i.v. 5-fluorouracil (5-FU) is one of the most widely used agents. UFT (tegafur–uracil) has similar efficacy to continuous infusion 5-FU with improved tolerability and is more convenient for patients.

Design: The efficacy and safety of UFT in the treatment of advanced gastric cancer have been demonstrated in a number of phase II studies.

Results: UFT with leucovorin (folinic acid) monotherapy shows overall response rates (ORRs) of 16%–29% and median OS of 5.8 months. Combination of UFT with cisplatin, etoposide, or paclitaxel shows ORRs of 35%–51% and median OS of 8.3–10.1 months. UFT-based three-drug combinations show ORRs of 41%–57% and median OS of 8.6–15 months. UFT-based combinations have a good tolerability profile, particularly a low incidence of myelosuppression, mucositis, and hand–foot syndrome.

Conclusion: UFT represents a logical replacement for 5-FU in chemotherapy regimens for the treatment of advanced gastric cancer.

Key words: advanced gastric cancer, combination therapy, phase II study, tegafur, UFT, uracil

Received for publication September 30, 2007. Revision received January 9, 2008. Accepted for publication January 10, 2008.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.