首页> 外文期刊>European journal of cancer: official journal for European Organization for Research and Treatment of Cancer (EORTC) [and] European Association for Cancer Research (EACR) >Randomised phase II trial of photodynamic therapy plus oral fluoropyrimidine, S-1, versus photodynamic therapy alone for unresectable hilar cholangiocarcinoma
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Randomised phase II trial of photodynamic therapy plus oral fluoropyrimidine, S-1, versus photodynamic therapy alone for unresectable hilar cholangiocarcinoma

机译:光动力疗法加口服氟嘧啶,S-1与单纯光动力疗法治疗不可切除的肝门胆管癌的II期随机试验

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Background Hilar cholangiocarcinoma is an uncommon cancer and its overall incidence is increasing. Photodynamic therapy (PDT) has been proposed as palliative management for unresectable hilar cholangiocarcinoma (UHC). To date, little is known about the role of the addition of systemic chemotherapy to PDT for UHC. We performed a prospective, randomised, phase II trial to compare PDT plus S-1 and PDT alone for UHC. Methods Patients with UHC were randomly assigned (in a 1:1 ratio) to PDT plus S-1 or PDT alone. The primary end-point was overall survival. The secondary end-points were progression-free survival, complications, re-intervention rate and quality of life. This trial is registered with clinicalTrials.gov, number NCT00869635. Findings Between February 2009 and May 2012, we randomly assigned 21 patients to receive PDT plus S-1 and 22 to receive PDT alone. The UHC patients treated with PDT plus S-1 showed higher 1-year survival rate compared with the patients treated with PDT alone (76.2% versus 32%, P = 0.003) and prolonged overall survival (median 17 months, 95% confidence interval [CI]: 12.6-21.4, versus 8 months, 95% CI: 6-10, P = 0.005, hazard ratio [HR], 0.36; 95% CI: 0.17-0.75). Regarding the secondary end-points, PDT plus S-1 was associated with prolonged progression-free survival compared with PDT alone (median 10 months [95% CI: 4.1-16] versus 2 months [95% CI: 0.4-3.5], P = 0.009 (HR for progression 0.39, 95% CI: 0.19-0.83). There were no differences in the number of PDT sessions, the frequency of cholangitis, overall adverse events or the quality of life in either group. Interpretations PDT plus S-1 was well tolerated and was associated with a significant improvement of overall survival and progression-free survival compared with PDT alone in patients with UHC. These findings warrant further clinical investigation of PDT plus S-1 in patients with UHC.
机译:背景肝门胆管癌是一种罕见的癌症,其总发病率正在增加。光动力疗法(PDT)已被提议作为不可切除的肝门胆管癌(UHC)的姑息治疗方法。迄今为止,关于在UDT中向PDT添加全身化疗的作用了解甚少。我们进行了一项前瞻性,随机,II期试验,以比较UHC的PDT加S-1和PDT单独使用。方法将UHC患者随机(按1:1比例)分配给PDT加S-1或PDT。主要终点是总体生存率。次要终点是无进展生存期,并发症,再干预率和生活质量。该试验已在ClinicalTrials.gov上注册,编号为NCT00869635。研究结果在2009年2月至2012年5月之间,我们随机分配了21名接受PDT加S-1的患者和22名单独接受PDT的患者。与仅使用PDT治疗的患者相比,使用PDT + S-1治疗的UHC患者显示出较高的1年生存率(76.2%对32%,P = 0.003),并且总体生存期延长(中位数为17个月,置信区间为95%[ CI:12.6-21.4,而8个月,95%CI:6-10,P = 0.005,危险比[HR]为0.36; 95%CI:0.17-0.75)。关于次要终点,与单独使用PDT相比,PDT加S-1与无进展生存期延长相关(中位10个月[95%CI:4.1-16]比2个月[95%CI:0.4-3.5], P = 0.009(HR进展0.39,95%CI:0.19-0.83)。两组的PDT分期,胆管炎的发生频率,总体不良事件或生活质量均无差异。与单独使用PDT的UHC患者相比,-1的耐受性良好,并且与总体生存期和无进展生存期的显着改善有关,这些发现值得进一步对UHC患者进行PDT加S-1的临床研究。

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