Forty-eight patients with advanced gastric cancer and measurable areas of malignant disease were treated with etoposide (130 mg/mz/day X 3 days) plus cisplatin (45 mg/mzday on days 2 and 3). Both drugs were given by constant intravenous infusion and repeated every 4 weeks. Common toxic reactions inc
Phase II study of a modified combination of etoposide, doxorubicin, and cisplatin for patients with advanced gastric cancer
✍ Scribed by Içli, Fikri; Karaoguz, Handan; Akbulut, Hakan; Dinçol, Dilek; Demirkazik, Ahmet; Çay, Filiz
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 52 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0022-4790
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✦ Synopsis
Background:
Based on the promising results of eap (etoposide, doxorubicin, and cisplatin) combination, a phase ii study of modified eap combination was performed in patients with advanced gastric cancer to evaluate the response, toxicity, and survival.
Method:
Fifty-two consecutive patients with measurable or evaluable advanced gastric cancer, who had no prior therapy except surgery, were treated every 28 days with etoposide 120 mg/m2/day, doxorubicin 25 mg/m2/day, and cisplatin 40 mg/m2/day on days 1 and 8, intravenously. forty-seven patients were evaluable for response and toxicity.
Results:
Overall response rate was 40.5% (95% ci = 37-54.7%), including 12.8% complete response. responses were higher in patients with locally advanced disease (57.89%) as compared to those with distant metastases (28.57%) (p = 0.044). the median overall survivals of the entire group and the responders were 7 months and 11 months, respectively. complete responders had significantly longer response duration and overall survival (31.5 months and 45.5 months, respectively), as compared to partial responders (6 months and 9 months, respectively). six of the responders (31.6%) were alive at 2 years. disease extension and pretreatment performance status had significant effects on survival. grade 3-4 toxicity was observed in 33% of patients. there were no deaths related to toxicity.
Conclusions:
Eap as used in this trial is an effective treatment in advanced gastric cancer. the effect is more pronounced in patients with locally advanced disease.
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