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Chemotherapy with gemcitabine plus cisplatin in patients with advanced biliary tract carcinoma at Chang gung memorial hospital: A retrospective analysis

机译:长庚纪念医院晚期吉西他滨联合吉西他滨联合顺铂化疗的回顾性分析

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Background: A gemcitabine-cisplatin combination is a standard treatment option for patients with advanced biliary tract carcinoma (BTC). We assessed the efficacy and safety of this regimen at Chang Gung Memorial Hospital. Methods: Between April 2009 and December 2010, 30 chemotherapy-na?ve patients (13 men and 17 women; median age: 61.5 years) with advanced BTC were retrospectively analyzed. Treatment consisted of gemcitabine (Gemmis?; TTY, Taipei, Taiwan) 1000 mg/m2, followed by cisplatin 30 mg/m2 on days 1 and 8 every 3 weeks. Tumor response was evaluated using the Response Evaluation Criteria in Solid Tumors (RECIST) criteria every 2-3 cycles. The toxicity was assessed by the National Cancer Institute Common Terminology Criteria for Adverse Events, Version 3. Results: At the end of July, 2011, 27 patients were evaluated using the RECIST criteria. According to the intent to treat analysis of response, 5 patients (16.7%) had a partial response, 10 patients (33.3%) had stable disease and 12 patients (40.0%) had progressive disease. The median time to progression (TTP) and median overall survival (OS) of the 30 patients were 4.8 months and 13.4 months, respectively. The patients with biliary obstruction requiring drainage before treatment had a significantly shorter OS than those without biliary obstruction (p = 0.02) even though the TTP showed no statistically significant difference (p = 0.69) between groups. The major grade III/IV adverse events in the 30 patients included infection (n = 8, 26.7%), anemia (n = 5, 16.7%), neutropenia (n = 4, 13.3%), and elevated alanine aminotransferase (n = 2, 6.7%). There were no treatment-related deaths. Conclusions: Gemcitabine plus cisplatin is a feasible chemotherapy regimen with manageable toxicity in patients with advanced BTC. Maintaining good biliary drainage is essential for these patients.
机译:背景:吉西他滨-顺铂联合治疗是晚期胆道癌(BTC)患者的标准治疗选择。我们在长庚纪念医院评估了该方案的疗效和安全性。方法:回顾性分析2009年4月至2010年12月间30例初次化疗的初治BTC患者(男13例,中位年龄61.5岁)。治疗包括吉西他滨(Gemmis?; TTY,台湾台北)1000 mg / m2,随后每3周第1天和第8天顺铂30 mg / m2。每2-3个周期使用实体肿瘤反应评估标准(RECIST)标准评估肿瘤反应。通过国家癌症研究所不良事件通用术语标准(版本3)评估了毒性。结果:在2011年7月,使用RECIST标准评估了27名患者。根据对缓解的治疗意图分析,部分缓解5例(16.7%),疾病稳定10例(33.3%),进行性疾病12例(40.0%)。 30名患者的中位进展时间(TTP)和中位总生存期(OS)分别为4.8个月和13.4个月。尽管两组之间的TTP差异无统计学意义(p = 0.69),但在治疗前需要引流的胆道梗阻患者的OS明显短于无胆道梗阻的患者(p = 0.02)。 30例患者的主要III / IV级不良事件包括感染(n = 8、26.7%),贫血(n = 5、16.7%),中性粒细胞减少症(n = 4、13.3%)和丙氨酸转氨酶升高(n = 2、6.7%)。没有与治疗有关的死亡。结论:吉西他滨联合顺铂是晚期BTC患者可行的化疗方案,毒性可控。对于这些患者,保持良好的胆道引流至关重要。

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