Journal of Clinical Oncology  
Search for:
Limit by:
  Browse by Topic or Issue
Home Search/Browse Subscriptions PDA Services My JCO Customer Service

Journal of Clinical Oncology, 2005 ASCO Annual Meeting Proceedings.
Vol 23, No 16S (June 1 Supplement), 2005: 4002
© 2005 American Society of Clinical Oncology
This Article
Right arrow Alert me when this article is cited
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 Download to citation manager
Right arrowRights & Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Moiseyenko, V. M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Moiseyenko, V. M.

Abstract

Final results of a randomized controlled phase III trial (TAX 325) comparing docetaxel (T) combined with cisplatin (C) and 5-fluorouracil (F) to CF in patients (pts) with metastatic gastric adenocarcinoma (MGC)

V. M. Moiseyenko, J. Ajani, S. A. Tjulandin, A. Majlis, M. Constenla, C. Boni, A. Anelli, A. J. Yver, E. van Cutsem on behalf of the TAX 325 Study Group

Sanofi-Aventis, Bridgewater, NJ; Cancer Research Institute; Cancer Research Institute, St.Petersburg, Russian Federation; The Russian Cancer Research Ctr, Moscow, Russian Federation; Fundación Arturo López Pérez; C.H. de Pontevedra; Arcispedale Santa Maria Nuova; Hosp A. C. Camargo, São Paulo, Brazil; Univ Hosp Gasthuisberg, Leuven, Belgium

4002

Background: Locally advanced or MGC has a poor prognosis (2-year survival 11.5%). Different treatments are used with no evidence of survival benefit. Methods: Pts with chemotherapy-naive MGC were randomized to either TCF: T 75 mg/m2 day (d) 1, C 75 mg/m2 d 1, and F 750 mg/m2/d continuous infusion (c.i.) d 1–5 every (q) 3 weeks (w) or CF: C 100 mg/m2 d 1 and F 1000 mg/m2/d c.i. d 1–5 q 4 w. Pts with locally recurrent or metastatic gastric adenocarcinoma (including gastroesophageal junction in 22% pts) and measurable/evaluable disease were eligible. Biased-coin randomization was stratified for center, liver metastases, prior gastrectomy, 5% weight loss, and measurability. Tumor assessments were performed q 8 w and externally reviewed. Time to progression (TTP) was the primary endpoint; the trial was equally powered for overall survival (OS). Results: 457 pts (227/230 TCF/CF) were randomized between Nov 99-Jan 03. Median age was 55 yrs and 97% pts had metastatic cancer. Weight loss in prior 3 months [mo] was >5–10%: 29% pts and >10%: 27% pts. TTP was longer with TCF (5.6 mo) compared to CF (3.7 mo; risk reduction 32%; log-rank p=0.0004). With median follow-up of 23 mo, OS was longer with TCF (risk reduction 23%, log-rank p=0.0201). 2-year survival was 18% with TCF vs 9% with CF. Response rate to TCF (37%) was superior to CF (25%; chi-square p=0.0106); 17%/31% pts had disease progression as best response to TCF/CF. Grade 3–4 treatment-emergent adverse events occurred in 81% and 75% of TCF and CF pts, the most common of which included diarrhea and stomatitis (20%/8% and 21%/27% TCF/CF pts); neutropenia was more frequent with TCF while anemia was less. With TCF/CF, 60-day all-cause mortality was 7%/9%. The TCF benefit/risk ratio tended to be less in pts ≥65 years. Conclusions: Docetaxel is the first drug with a proven survival benefit in MGC. Tolerance of TCF and CF was limited in this sick patient population. Docetaxel combined with CF and appropriate risk management represents a new option for MGC.


Author Disclosure
Employment or Leadership Consultant or Advisory Role Stock Ownership Honoraria Research Funding Expert Testimony Other Remuneration

sanofi-aventis sanofi-aventis sanofi-aventis AstraZeneca, Aventis, Hoffmann-La Roche Bristol-Myers Squibb, Hoffmann-La Roche, Johnson & Johnson, tbc

Abstract presentation from the 2005 ASCO Annual Meeting




About
JCO
 Editorial
Roster
 Advertising
Information
 Librarians &
Institutions
 Rights &
Permissions

Copyright © 2005 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
Terms and Conditions of Use
HighWire Press HighWire Press™ assists in the publication of JCO Online