Rivera Fernando, Vega-Villegas M Eugenia, López-Brea Marta, Isla Dolores, Mayorga Marta, Galdós Piedad, Rubio Antonio, Del Valle Adolfo, García-Reija Fe, García-Montesinos Belen, Rodríguez-Iglesias Julio, Mayordomo Jose, Rama Julio, Saiz-Bustillo Ramón, Sanz-Ortiz Jaime
Department of Medical Oncology, Hospital Universitario Marqués de Valdecilla, 39008, Santander, Spain.
Cancer Chemother Pharmacol. 2008 Jul;62(2):253-61. doi: 10.1007/s00280-007-0599-0. Epub 2007 Sep 28.
We conducted a multicentric randomized phase II trial comparing 5-FU continuous infusion (PF) and cisplatin, UFT and vinorelbine (UFTVP) as induction chemotherapy (IC) in locally advanced squamous cell head and neck cancer (LA-SCHNC). Primary objective was complete response (CR) to IC and overall survival (OS) was a secondary objective.
PF: cisplatin 100 mg/m(2) i.v. Day 1 (D1) and 5-FU 1,000 mg/m(2) per day i.v. continous infusion D1-D5, every 21 days. UFTVP: cisplatin 100 mg/m(2) i.v. D1; UFT 200 mg/m(2) per day p.o. D1-D21 and vinorelbine 25 mg/m(2) i.v. D1 and D8, every 21 days. Four IC courses were planned in both arms.
A total of 206 patients (pts) were included (PF/UFTVP: 99/107): oral cavity: 8%/10%, oropharynx: 20%/25%, hypopharynx: 17%/14%, larynx: 54%/50%. Stage (TNM, 2002): III: 41%/35%, IVA: 23%/27%, IVB: 35%/38%. Complete response to IC: PF:36%/UFTVP:31% (P: no significative (NS)). G 3-4 toxicity (PF/UFTVP): neutropenia: 52%/72%; febrile neutropenia: 3%/20% (P < 0.001); anaemia:1%/14% (P < 0.001); trombocytopenia: 5%/0% (P = 0.02); mucositis: 15%/7% (P < 0.001). Deaths during IC: 2(2%)/3(3%). IC with UFTVP was associated with a favourable OS in the Cox analysis (actuarial 5 year OS: 49% vs. 34%; HR: 0.67, 95% CI: 0.47-0.95, P: 0.03).
Although clinical response is equal in both arms, overall survival (Cox) is better in the UFTVP arm. Febrile neutropenia and anaemia were more frequent with UFTVP while mucositis and trombocytopenia were more severe with PF.
我们开展了一项多中心随机II期试验,比较5-氟尿嘧啶持续输注(PF)和顺铂、优福定及长春瑞滨(UFTVP)作为局部晚期头颈部鳞状细胞癌(LA-SCHNC)诱导化疗(IC)的疗效。主要目标是IC后的完全缓解(CR),次要目标是总生存期(OS)。
PF方案:顺铂100mg/m²静脉滴注,第1天(D1);5-氟尿嘧啶1000mg/m²每日静脉持续输注,D1 - D5,每21天重复。UFTVP方案:顺铂100mg/m²静脉滴注,D1;优福定200mg/m²每日口服,D1 - D21;长春瑞滨25mg/m²静脉滴注,D1和D8,每21天重复。两组均计划进行4个IC疗程。
共纳入206例患者(PF/UFTVP组分别为99/107例):口腔:8%/10%,口咽:20%/25%,下咽:17%/14%,喉:54%/50%。分期(TNM,2002):III期:41%/35%,IVA期:23%/27%,IVB期:35%/38%。IC后的完全缓解率:PF组为36%/UFTVP组为31%(P:无显著差异(NS))。3 - 4级毒性反应(PF/UFTVP组):中性粒细胞减少:52%/72%;发热性中性粒细胞减少:3%/20%(P < 0.001);贫血:1%/14%(P < 0.001);血小板减少:5%/0%(P = 0.02);黏膜炎:15%/7%(P < 0.001)。IC期间死亡:2例(2%)/3例(3%)。Cox分析显示,UFTVP作为IC与较好的OS相关(5年总生存率:49%对34%;风险比:0.67,95%可信区间:0.47 - 0.95,P:0.03)。
尽管两组临床反应相当,但UFTVP组的总生存期(Cox分析)更好。UFTVP组发热性中性粒细胞减少和贫血更常见,而PF组黏膜炎和血小板减少更严重。