首页> 外文期刊>Journal of Clinical Oncology >Clinical benefit with docetaxel plus fluorouracil and cisplatin compared with cisplatin and fluorouracil in a phase III trial of advanced gastric or gastroesophageal cancer adenocarcinoma: the V-325 Study Group.
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Clinical benefit with docetaxel plus fluorouracil and cisplatin compared with cisplatin and fluorouracil in a phase III trial of advanced gastric or gastroesophageal cancer adenocarcinoma: the V-325 Study Group.

机译:在晚期胃癌或胃食管癌腺癌的III期临床试验中,多西他赛加氟尿嘧啶和顺铂与顺铂和氟尿嘧啶相比具有临床益处:V-325研究组。

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PURPOSE: For patients with advanced gastric or gastroesophageal cancer (AGGEC) providing clinical benefit with improved palliation is highly desirable. However, a prospective evaluation of clinical benefit in AGGEC patients has never before been reported in a phase III setting. PATIENTS AND METHODS: In a multinational trial (V325), 445 patients were randomly assigned and treated with either docetaxel plus cisplatin and fluorouracil (DCF) or cisplatin and fluorouracil (CF). Clinical benefit was prospectively evaluated in this trial as a secondary end point. The primary measure for clinical benefit analysis was time to definitive worsening by one or more categories of Karnofsky performance status (KPS). Secondary clinical benefit end points included time to 5% definitive weight loss, time to definitive worsening of appetite by one grade, pain-free survival (defined as time to first appearance of pain), and time to first cancer pain-related opioid intake. Clinical benefit assessments were recorded at eachclinic visit. RESULTS: Clinical benefit assessments were performed in more than 75% of patients throughout V325. DCF significantly prolonged time to definitive worsening of KPS compared with CF (median, 6.1 v 4.8 months; hazard ratio, 1.38; 95% CI, 1.08 to 1.76; log-rank P = .009). Although time to definitive weight loss and time to definitive worsening of appetite favored DCF, the results were not statistically significant. Pain-free survival and time to first cancer pain-related opioid intake were comparable. CONCLUSION: To our knowledge, V325 is the first phase III trial to report clinical benefit in AGGEC patients. Clinical benefit was assessed beyond protocol-specific chemotherapy. The addition of D to CF not only significantly improved clinical benefit but also improved quality of life, time to progression, and overall survival compared with CF.
机译:目的:对于患有晚期胃癌或胃食管癌(AGGEC)的患者,提供具有改善的缓解症状的临床益处是非常必要的。然而,从未在III期临床中对AGGEC患者的临床获益进行前瞻性评估。患者和方法:在一项跨国试验(V325)中,将445名患者随机分配并接受多西他赛联合顺铂和氟尿嘧啶(DCF)或顺铂和氟尿嘧啶(CF)的治疗。在该试验中前瞻性评估了临床获益,作为其次要终点。临床获益分析的主要指标是通过一种或多种类别的卡诺夫斯基绩效状态(KPS)进行明确恶化的时间。次要临床获益终点包括:达到5%的确定体重减轻的时间,达到食欲的绝对恶化一个等级的时间,无痛生存时间(定义为首次出现疼痛的时间)以及首次与癌症疼痛相关的阿片类药物摄入的时间。每次门诊就诊时记录临床获益评估。结果:在整个V325中,对超过75%的患者进行了临床获益评估。与CF相比,DCF显着延长了KPS最终恶化的时间(中位数为6.1 vs 4.8个月;危险比为1.38; 95%CI为1.08至1.76;对数秩P = 0.009)。虽然最终减肥的时间和食欲的最终恶化的时间有利于DCF,但结果在统计学上并不显着。无痛生存和首次癌痛相关阿片类药物摄入的时间相当。结论:据我们所知,V325是第一个报告AGGEC患者临床获益的III期试验。评估了超出协议特定化学疗法的临床获益。与CF相比,在CF中添加D不仅可以显着改善临床获益,而且还可以改善生活质量,进展时间和总体生存率。

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