[HTML][HTML] Randomized trial on adjuvant treatment with FOLFIRI followed by docetaxel and cisplatin versus 5-fluorouracil and folinic acid for radically resected gastric …

E Bajetta, I Floriani, M Di Bartolomeo, R Labianca… - Annals of oncology, 2014 - Elsevier
E Bajetta, I Floriani, M Di Bartolomeo, R Labianca, A Falcone, F Di Costanzo, G Comella…
Annals of oncology, 2014Elsevier
Background Some trial have demonstrated a benefit of adjuvant fluoropirimidine with or
without platinum compounds compared with surgery alone. ITACA-S study was designed to
evaluate whether a sequential treatment of FOLFIRI [irinotecan plus 5-fluorouracil/folinic
acid (5-FU/LV)] followed by docetaxel plus cisplatin improves disease-free survival in
comparison with 5-FU/LV in patients with radically resected gastric cancer. Patients and
methods Patients with resectable adenocarcinoma of the stomach or gastroesophageal …
Background
Some trial have demonstrated a benefit of adjuvant fluoropirimidine with or without platinum compounds compared with surgery alone. ITACA-S study was designed to evaluate whether a sequential treatment of FOLFIRI [irinotecan plus 5-fluorouracil/folinic acid (5-FU/LV)] followed by docetaxel plus cisplatin improves disease-free survival in comparison with 5-FU/LV in patients with radically resected gastric cancer.
Patients and methods
Patients with resectable adenocarcinoma of the stomach or gastroesophageal junction were randomly assigned to either FOLFIRI (irinotecan 180 mg/m2 day 1, LV 100 mg/m2 as 2 h infusion and 5-FU 400 mg/m2 as bolus, days 1 and 2 followed by 600 mg/m2/day as 22 h continuous infusion, q14 for four cycles) followed by docetaxel 75 mg/m2 day 1, cisplatin 75 mg/m2 day 1, q21 for three cycles (sequential arm) or De Gramont regimen (5-FU/LV arm).
Results
From February 2005 to August 2009, 1106 patients were enrolled, and 1100 included in the analysis: 562 in the sequential arm and 538 in the 5-FU/LV arm. With a median follow-up of 57.4 months, 581 patients recurred or died (297 sequential arm and 284 5-FU/LV arm), and 483 died (243 and 240, respectively). No statistically significant difference was detected for both disease-free [hazard ratio (HR) 1.00; 95% confidence interval (CI): 0.85–1.17; P = 0.974] and overall survival (OS) (HR 0.98; 95% CI: 0.82–1.18; P = 0.865). Five-year disease-free and OS rates were 44.6% and 44.6%, 51.0% and 50.6% in the sequential and 5-FU/LV arm, respectively.
Conclusions
A more intensive regimen failed to show any benefit in disease-free and OS versus monotherapy.
Clinical trial registration
ClinicalTrials.gov Identifier: NCT01640782.
Elsevier
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