Randomized, multinational, phase III study of docetaxel plus platinum combinations versus vinorelbine plus cisplatin for advanced non-small-cell lung cancer: The TAX 326 study group

被引:752
作者
Fossella, F
Pereira, JR
von Pawel, J
Pluzanska, A
Gorbounova, V
Kaukel, E
Mattson, KV
Ramlau, R
Szczesna, A
Fidias, P
Millward, M
Belani, CP
机构
[1] Univ Pittsburgh, Med Ctr, Inst Canc, Div Med Oncol, Pittsburgh, PA 15232 USA
[2] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Inst Canc Arnaldo Vieira de Carvalho, Sao Paulo, Brazil
[4] Asklepios Fachklin Munchen Gauting, Gauting, Germany
[5] M Kopernik Mem Hosp, Lodz, Poland
[6] RAMS, Canc Res Ctr, Moscow, Russia
[7] AK Hamburg Harbug, Hamburg, Germany
[8] Univ Helsinki, Cent Hosp, Helsinki, Finland
[9] Reg Lung Dis Ctr, Poznan, Poland
[10] Reg Lung Dis Hosp, Otwock, Poland
[11] Massachusetts Gen Hosp, Boston, MA 02114 USA
[12] Sydney Canc Ctr, Camperdown, NSW, Australia
关键词
D O I
10.1200/JCO.2003.12.046
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To investigate whether docetaxel plus platinum regimens improve survival and affect quality of life (QoL) in advanced non-small-cell lung cancer (NSCLC) compared with vinorelbine plus cisplatin as first-line chemotherapy. Patients and Methods: Patients (n = 1,218) with stage IIIB to IV NSCLC were randomly assigned to receive docetaxel 75 mg/m(2) and cisplatin 75 mg/m(2) every 3 weeks (DC); docetaxel 75 mg/m(2) and carboplatin area under the curve of 6 mg/mL . min every 3 weeks (DCb); or vinorelbine 25 mg/ m(2)/wk and cisplatin 100 mg/m(2) every 4 weeks (VC). Results: Patients treated with DC had a median survival of 11.3 v 10.1 months for VC-treated patients (P =.044; hazard ratio, 1.183 [97.2% confidence interval, 0.989 to 1.416]). The 2-year survival rate was 21% for DC-treated patients and 14% for VC-treated patients. Overall response rate was 31.6% for DC-treated patients v 24.5% for VC-treated patients (P =.029). Median survival (9.4 v 9.9 months [for VC]; P =.657; hazard ratio, 1.048 [97.2 confidence interval, 0.877 to 1.253]) and response (23.9%) with DCb were similar to those results for VC. Neutropenia,. thrombocytopenia, infection, and febrile neutropenia were similar with all three regimens. Grade 3 to 4 anemia, nausea, and vomiting were more common (P <.01) with VC than with DC or DCb. Patients treated with either docetaxel regimen had consistently improved Gal. compared with VC-treated patients, who experienced deterioration in QoL. Conclusion: DC resulted in a more favorable overall response and survival rate than VC. Both DC and DCb were better tolerated and provided patients with consistently improved QoL compared with VC. These findings demonstrate that a docetaxel plus platinum combination is an effective treatment option with a favorable therapeutic index for firstline treatment of advanced or metastatic NSCLC.
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收藏
页码:3016 / 3024
页数:9
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