4.6 Article

Nedaplatin concurrent with three-dimensional conformal radiotherapy for treatment of locally advanced esophageal carcinoma

Journal

WORLD JOURNAL OF GASTROENTEROLOGY
Volume 19, Issue 48, Pages 9447-9452

Publisher

BAISHIDENG PUBL GRP CO LTD
DOI: 10.3748/wjg.v19.i48.9447

Keywords

Esophageal carcinoma; Chemoradiotherapy; Nedaplatin; Cisplatin

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AIM: To evaluate the efficacy and toxicity of nedaplatin (NDP) concurrent with radiotherapy in the treatment of locally advanced esophageal carcinoma. METHODS: Sixty-eight patients with locally advanced esophageal carcinoma were randomized into either a NDP group (n = 34) or a cisplatin (DDP) group (n = 34). The NDP group received NDP 80-100 mg/m(2) iv on day 1 + leucovorin (CF) 100 mg/m(2) iv on days 1-5 + 5-fluorouracil (5-FU) 500 mg/m(2) iv on days 1-5. The DDP group received DDP 30 mg/m(2) iv on days 1-3 + CF 100 mg/m(2) on days 1-5 + 5-FU 500 mg/m(2) iv on days 1-5. The treatment was repeated every 4 wk in both groups. Concurrent radiotherapy [60-66 Gy/(30-33 f)/(6-7 wk)] was given during chemotherapy. RESULTS: There was no significant difference in the short-term response rate between the NDP group and DDP group (90.9% vs 81.3%, P = 0.528). Although the 1- and 2-year survival rates were higher in the NDP group than in the DDP group (75.8% vs 68.8%, 57.6% vs 50.0%), the difference in the overall survival rate was not statistically significant between the two groups (P = 0.540). The incidences of nausea, vomiting and nephrotoxicity were significantly lower in the NDP group than in the DDP group (17.6% vs 50.0%, P = 0.031; 11.8% vs 47.1%, P = 0.016; 8.8% vs 38.2%, P = 0.039). There was no significant difference in the incidence of myelosuppression, radiation-induced esophagitis or radiation-induced pneumonia between the two groups. CONCLUSION: NDP-based concurrent chemoradiotherapy is effective and well-tolerated in patients with locally advanced esophageal carcinoma. NDP-based regimen has comparable efficacy to DDP-based regimen but is associated with lower incidences of gastrointestinal and renal toxicity. (C) 2013 Baishideng Publishing Group Co., Limited. All rights reserved.

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