A randomized trial of induction docetaxel-cisplatin-5FU followed by concomitant cisplatin-RT versus concomitant cisplatin-RT in nasopharyngeal carcinoma (GORTEC 2006-02)

被引:143
作者
Frikha, M. [1 ]
Auperin, A. [2 ]
Tao, Y. [3 ]
Elloumi, F. [4 ]
Toumi, N. [4 ]
Blanchard, P. [3 ]
Lang, P. [5 ]
Sun, S. [6 ]
Racadot, S. [7 ]
Thariat, J. [8 ]
Alfonsi, M. [9 ]
Tuchais, C. [10 ]
Cornely, A. [2 ]
Moussa, A. [2 ]
Guigay, J. [8 ]
Daoud, J. [4 ]
Bourhis, J. [3 ,11 ]
机构
[1] Sfax Univ Hosp, Dept Radiat Oncol, Sfax, Tunisia
[2] Gustave Roussy, Dept Stat, Villejuif, France
[3] Gustave Roussy, Dept Radiat Oncol, Villejuif, France
[4] Sfax Univ Hosp, Dept Radiat Oncol, Sfax, Tunisia
[5] Pitie Salpetriere, Radiat Oncol Dept, Paris, France
[6] Ctr Hosp Montbeliard, Dept Radiat Oncol, Montbeliard, France
[7] Ctr L Berard, Radiat Oncol Dept, Lyon, France
[8] Ctr A Lacassagne, Dept Oncol, Nice, France
[9] Clin St Catherine, Dept Radiat Oncol, Avignon, France
[10] Ctr C Papin, Radiat Oncol Dept, Angers, France
[11] CHU Vaudois, Dept Radiat Oncol, CH-1011 Lausanne, Switzerland
关键词
randomized trials; chemotherapy; nasopharynx carcinoma; PLUS CONCURRENT CHEMORADIOTHERAPY; PATIENT DATA METAANALYSIS; PHASE-II; CHEMOTHERAPY; DOCETAXEL; RADIOTHERAPY; FLUOROURACIL; HEAD;
D O I
10.1093/annonc/mdx770
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Concomitant chemotherapy (CT)-radiotherapy (RT) is a standard of care in locally advanced nasopharyngeal carcinoma (NPC) and a role for induction CT is not established. Patients with locally advanced NPC, WHO type 2 or 3, were randomized to induction TPF plus concomitant cisplatin-RT or concomitant cisplatin-RT alone. The TPF regimen consisted of three cycles of Docetaxel 75 mg/m(2) day 1; cisplatin 75 mg/m(2) day 1; 5FU 750 mg/m(2)/day days 1-5. RT consisted of 70 Gy in 7 weeks plus concomitant cisplatin 40 mg/m(2) weekly. A total of 83 patients were included in the study. Demographics and tumour characteristics were well balanced between both arms. Most of the patients (95%) in the TPF arm received three cycles of induction CT. The rate of grade 3-4 toxicity and the compliance (NCI-CTCAE v3) during cisplatin-RT were not different between both arms. With a median follow-up of 43.1 months, the 3-year PFS rate was 73.9% in the TPF arm versus 57.2% in the reference arm [hazard ratio (HR) = 0.44; 95% confidence interval (CI): 0.20-0.97, P = 0.042]. Similarly the 3 years overall survival rate was 86.3% in the TPF arm versus 68.9% in the reference arm (HR = 0.40; 95% CI: 0.15-1.04, P = 0.05). In conclusion, several important aspects can be emphasized: the compliance to induction TPF was good and TPF did not compromise the tolerance of the concomitant RT-cisplatin phase. The improved PFS and overall survival rates needs to be confirmed by further trials.
引用
收藏
页码:731 / 736
页数:6
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