A phase II study of intra-arterial chemotherapy of 5-fluorouracil, cisplatin, and mitomycin C for advanced nonresectable gastric cancer

The best choice of chemotherapy regimen for patients with advanced gastric cancer (AGC) is still a matter of controversy and requires further investigation. This study was performed to evaluate the efficacy and safety of intra-arterial infusion chemotherapy of 5-fluorouracil 1000 mg/m, cisplatin 50 ...

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Veröffentlicht in:Anti-cancer drugs 2009-11, Vol.20 (10), p.941-945
Hauptverfasser: Li, Maoquan, Zhang, Jiaxing, Wang, Daoyuan, Zhong, Baoliang, Tucker, Steven, Lu, Chenhui, Cheng, Jie, Cao, Chuanwu, Xu, Jiahua, Xu, Jichong, Pan, Hui
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Sprache:eng
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Zusammenfassung:The best choice of chemotherapy regimen for patients with advanced gastric cancer (AGC) is still a matter of controversy and requires further investigation. This study was performed to evaluate the efficacy and safety of intra-arterial infusion chemotherapy of 5-fluorouracil 1000 mg/m, cisplatin 50 mg/m, and mitomycin C 10 mg/m (FCM) repeated every 6 weeks, as first-line treatment for AGC. Forty-seven (95.9%) of the 49 patients were assessable for response. Four cases of complete response and 28 cases of partial response were confirmed, giving an overall response rate of 65.3% [95% confidence interval (CI)52.0–78.6%]. The median time to progression and overall survival for all patients was 8.3 months (95% CI6.8–9.8 months) and 14.5 months (95% CI12.0–17.0 months). The estimate of overall survival at 12 and 24 months was 55.1% (95% CI41.2–69.0%) and 18.4% (95% CI7.5–29.2%), respectively. Most patients experienced neutropenia during their course of therapy with 21.3% of patients (n = 10) for grade 3/4 neutropenia. Grade 3 stomatitis, lethargy, and palmar-plantar erythema were observed in two (4.3%), eight (17.0%), and one (2.1%) patients, respectively. Yet, no grade 4 nonhematological toxicity was observed. Intra-arterial infusion chemotherapy of 5-fluorouracil 1000 mg/m, cisplatin 50 mg/m, and mitomycin C 10 mg/m is a tolerated treatment modality with promising activity in patients with previously untreated AGC.
ISSN:0959-4973
1473-5741
DOI:10.1097/CAD.0b013e328331af3a