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首页> 外文期刊>The Chinese-German Journal of Clinical Oncology >Gemcitabine and oxaliplatin combination chemotherapy in 30 patients with advanced pancreatic carcinoma
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Gemcitabine and oxaliplatin combination chemotherapy in 30 patients with advanced pancreatic carcinoma

机译:吉西他滨联合奥沙利铂联合化疗治疗晚期胰腺癌30例

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摘要

Objective: To evaluate the activity and safety of combination chemotherapy with gemcitabine plus oxaliplatin (GEMOX regimen) in patients of advanced pancreatic carcinoma. Methods: 30 patients with advanced pancreatic cancer were enrolled into this study. All patients received gemcitabine 1000 mg/m~2, given by 30-minute intravenous infusion, on days 1 and 8 of each 21-day cycle. Oxaliplatin 100 mg/m~2 was administered as a 2 h infusion on day 1 of each 21 day. Clinical outcomes for patients treated with two cycles of chemotherapy were evaluated according to WHO criteria. Results: All 30 patients were eligible for effectiveness and safety analysis. Objective response rate was approximately 20.0%. Clinical benefit response (CBR) was a composite of assessment of pain, performance status and body weight. The pain relief rate, improvement rate of performance status and body weight were 53.3%, 46.7% and 36.7%, respectively. The main adverse effects were bone marrow depression, peripheral nerve toxicity and gastrointestinal reaction. There was no treatment-related death during the chemotherapy. Conclusion: The high response rate with low toxicity observed in this study suggests that GEMOX regimen may be an effective alternative curative treatment for patients with advanced pancreatic carcinoma and can be used more extensively in clinical practice.
机译:目的:评价吉西他滨联合奥沙利铂(GEMOX方案)联合化疗对晚期胰腺癌的活性和安全性。方法:30例晚期胰腺癌患者入选本研究。在每个21天周期的第1天和第8天,所有患者均接受30分钟静脉输注吉西他滨1000 mg / m〜2。在每21天的第1天输注2小时,以100毫克/米2的剂量服用奥沙利铂。根据WHO标准评估了接受两个化疗周期的患者的临床结局。结果:30例患者均符合有效性和安全性分析要求。客观回应率约为20.0%。临床受益反应(CBR)是对疼痛,表现状态和体重的评估的综合。疼痛缓解率,性能状况改善率和体重分别为53.3%,46.7%和36.7%。主要不良反应为骨髓抑制,周围神经毒性和胃肠道反应。化疗期间没有与治疗相关的死亡。结论:本研究中观察到的高反应率和低毒性表明GEMOX方案可能是晚期胰腺癌患者的一种有效的替代治疗方法,可在临床实践中得到更广泛的应用。

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