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Journal of Clinical Oncology, 2005 ASCO Annual Meeting Proceedings.
Vol 23, No 16S (June 1 Supplement), 2005: 4002
© 2005 American Society of Clinical Oncology
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 15 every (q) 3 weeks (w) or CF: C 100 mg/m2 d 1 and F 1000 mg/m2/d c.i. d 15 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 >510%: 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 34 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 |
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| sanofi-aventis |
sanofi-aventis |
sanofi-aventis |
AstraZeneca, Aventis, Hoffmann-La Roche |
Bristol-Myers Squibb, Hoffmann-La Roche, Johnson & Johnson, tbc |
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Abstract presentation from the 2005 ASCO Annual Meeting
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