The clinical evaluation of EOF5 regimen, the combination of epirubicin, oxaliplatin and 5-day continuous infusion of 5-FU, for patients with advanced/metastatic gastric cancer
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The clinical evaluation of EOF5 regimen, the combination of epirubicin, oxaliplatin and 5-day continuous infusion of 5-FU, for patients with advanced/metastatic gastric cancer
China OncologyVol. 24, Issue 8, Pages: 615-621(2014)
朱晓东, 赵晓莹, 彭伟, et al. The clinical evaluation of EOF5 regimen, the combination of epirubicin, oxaliplatin and 5-day continuous infusion of 5-FU, for patients with advanced/metastatic gastric cancer[J]. China Oncology, 2014, 24(8): 615-621.
朱晓东, 赵晓莹, 彭伟, et al. The clinical evaluation of EOF5 regimen, the combination of epirubicin, oxaliplatin and 5-day continuous infusion of 5-FU, for patients with advanced/metastatic gastric cancer[J]. China Oncology, 2014, 24(8): 615-621. DOI: 10.3969/j.issn.1007-3969.2014.08.010.
The clinical evaluation of EOF5 regimen, the combination of epirubicin, oxaliplatin and 5-day continuous infusion of 5-FU, for patients with advanced/metastatic gastric cancer
Background and purpose: Although there is still no standard first line chemotherapy regimen for metastatic gastric cancer (MGC)
the doublet and triplet regimens containing platinum and fluorouracil were most popular worldwidely. The ECF regimen is the classical and one of the most popular treatment choices in this setting
while the marrow suppression
the renal toxicity and poor compliance inhibits its usage. In order to improve its efficacy and tolerability
this study conducted 2 phase Ⅱ trials by modified ECF regimen
the EOF5 regimen (substituting cisplatin with oxaliplatin
shortening the continuous infusion period to 120 h)
to treat patients with MGC since 2004.This paper reported the comprehensive results of the 2 studies. Methods: All the patients who enrolled in our previous 2 phase Ⅱ trials and received EOF5 as first line treatment entered this study. Each patient received the treatment of epirubicin 50 mg/m2 iv d1
oxaliplatin 130 mg/m2 iv gtt d1 and 5-FU 375-425 mg/m2·d-1 civ 120 h
and repeated every 3 weeks. Efficacy was analyzed every 6 weeks. Results: A total number of 178 patients (all were metastatic patients but 2 advanced patients with unresectable lesions) were included into this study. One hundred and seventy patients were evaluable
and 7 patients (3.9%) achieved complete response (CR)
and the cases of stable disease (SD) and progressive disease (PD) were 69 (38.8%) and 18 (10.1%)
respectively. The median progress free survival (PFS) and overall survival (OS) were 6.0 months (95%CI: 5.2-6.8) and 12.6 months (95%CI: 8.9-16.3)
1-year and 2-year survival rate were 50.9% and 28.0%
respectively. Grade 3
4 toxicity including: leucopenia (23.0)
neutropenia (38.8%)
anemia (6.5%)
thrombocytopenia (23.5%)
nausea/vomiting (14.1%)
and peripheral neuropathy toxicity (1.2%). Among 75 patients who received second line treatment
the median survival from second line treatment was 8.0 months (95%CI: 4.8-11.2). Conclusion: EOF5 regimen is a highly effective regimen with moderate and manageable toxicity
and it providesa suitable alternative for the first-line treatment of MGC.