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

被引:212
作者
Ajani, Jaffer A.
Moiseyenko, Vladimir M.
Tjulandin, Sergei
Majlis, Alejandro
Constenla, Manuel
Boni, Corrado
Rodrigues, Adriano
Fodor, Miguel
Chao, Yee
Voznyi, Edouard
Marabotti, Cindy
Van Cutsem, Eric
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[2] NN Blokhin Canc Res Ctr, Moscow, Russia
[3] NN Petrov Oncol Res Inst, St Petersburg, Russia
[4] Sci Ctr Radiol Mos, Moscow, Russia
[5] Univ Chile, Hosp Clin, Fdn Arturo Lopez Perez, Santiago, Chile
[6] CH Pontevedra, Pontevedra, Spain
[7] Osped Reggio Emilia, Reggio Emilia, Italy
[8] Hosp Univ Coimbra, Coimbra, Portugal
[9] Taipei Vet Gen Hosp, Taipei, Taiwan
[10] Sanofi Aventis, Antony, France
[11] Univ Leuven Hosp, Louvain, Belgium
关键词
D O I
10.1200/JCO.2006.10.4968
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 each clinic 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% Cl, 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.
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页码:3205 / 3209
页数:5
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