Optimizing chemotherapy for advanced non-small cell lung cancer: focus on docetaxel

被引:16
作者
Belani, CP
机构
[1] Univ Pittsburgh, Sch Med, Pittsburgh, PA USA
[2] Univ Pittsburgh, Lung & Thorac Malignancies Program, Inst Canc, Pittsburgh, PA USA
关键词
non-small cell lung cancer; docetaxel; cisplatin; carboplatin;
D O I
10.1016/S0169-5002(05)81567-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Systemic chemotherapy with platinum-based combinations provides modest improvements in both survival and quality of life for patients with advanced non-small cell lung cancer (NSCLC). For first-tine treatment of advanced NSCLC patients with a good performance status, the accepted standard of care is a platinum agent combined with docetaxel, paclitaxel, gemcitabine, vinorelbine or irinotecan. Several studies have attempted to identify an optimal platin-based regimen, however, all regimens offer some combination of clinical benefit with characteristic toxicities and no regimen appears clearly superior. Non-platinum regimens have also shown equivalent efficacy compared to platinum combinations, but again, none are clearly superior. Most recently, the existing standard of care is being amended to reflect the survival advantage gained from adding a new targeted agent, bevacizumab, to traditional platinum-doublet therapy for patients with nonsquamous NSCLC. Docetaxel is the only agent currently approved for both first- and second-tine treatment of advanced NSCLC. Multiple randomized clinical trials have established the efficacy of platin-docetaxel regimens for first-line treatment of advanced NSCLC. Improvements in various lung cancer related symptoms and global quality of life indices have also been noted with docetaxel-based regimens. Based on the efficacy of platin-docetaxel regimens in advanced disease, they are now being incorporated into the adjuvant and neoadjuvant treatment of early-stage disease. (c) 2005 Elsevier Science Ltd.
引用
收藏
页码:S3 / S8
页数:6
相关论文
共 28 条
[1]
Cisplatin plus gemcitabine versus a cisplatin-based triplet versus nonplatinum sequential doublets in advanced non-small-cell lung cancer:: A Spanish lung cancer group phase III randomized trial [J].
Alberola, V ;
Camps, C ;
Provencio, M ;
Isla, D ;
Rosell, R ;
Vadell, C ;
Bover, I ;
Ruiz-Casado, A ;
Azagra, P ;
Jiménez, U ;
González-Larriba, JL ;
Diz, P ;
Cardenal, F ;
Artal, A ;
Carrato, A ;
Morales, S ;
Sánchez, JJ ;
de las Peñas, R ;
Felip, E ;
López-Vivanco, G .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (17) :3207-3213
[2]
[Anonymous], P AM SOC CLIN ONCOL
[3]
[Anonymous], P AM SOC CLIN ONCOL
[4]
[Anonymous], P AM SOC CLIN ONCOL
[5]
[Anonymous], P AM SOC CLIN ONCOL
[6]
[Anonymous], [No title captured]
[7]
Phase III randomized trial comparing weekly vs. standard schedules of paclitaxel (P) plus carboplatin (C) for advanced non-small cell lung cancer (NSCLC): Analyses of elderly patients [J].
Belani, C ;
Ramalingam, S ;
Perry, M ;
LaRocca, R ;
Rinaldi, D ;
Gable, P ;
Tester, W .
LUNG CANCER, 2005, 49 :S32-S32
[8]
Platinum-based versus non-platinum-based chemotherapy in advanced non-small-cell lung cancer: A meta-analysis of the published literature [J].
D'Addario, G ;
Pintilie, M ;
Leighl, NB ;
Feld, R ;
Cerny, T ;
Shepherd, FA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (13) :2926-2936
[9]
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 [J].
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 .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (16) :3016-3024
[10]
Docetaxel versus docetaxel plus cisplatin as front-line treatment of patients with advanced non-small-cell lung cancer: A randomized, multicenter phase III trial [J].
Georgoulias, V ;
Ardavanis, A ;
Agelidou, A ;
Agelidou, M ;
Chandrinos, V ;
Tsaroucha, E ;
Toumbis, M ;
Kouroussis, C ;
Syrigos, K ;
Polyzos, A ;
Samaras, N ;
Papakotoulas, P ;
Christofilakis, C ;
Ziras, N ;
Alegakis, A .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (13) :2602-2609