Individual patient data meta-analysis of docetaxel administered once every 3 weeks compared with once every week second-line treatment of advanced non small-cell lung cancer

被引:90
作者
Di Maio, Massimo
Perrone, Francesco
Chiodini, Paolo
Gallo, Ciro
Camps, Carlos
Schuette, Wolfgang
Quoix, Elisabeth
Tsai, Chun-Ming
Gridelli, Cesare
机构
[1] Univ Naples 2, Clin Trials Unit, Natl Canc Inst, Naples, Italy
[2] Univ Naples 2, Dept Med & Publ Hlth, Naples, Italy
[3] Azienda Osped S Giuseppe Moscati, Div Med Oncol, Avellino, Italy
[4] Consorcio Hosp Gen Univ, Valencia, Spain
[5] Martha Maria City Hosp Halle Doelau, Halle, Germany
[6] Hop Lyautey, Strasbourg, France
[7] Taipei Vet Gen Hosp, Sect Thorac Oncol, Chest Dept, Taipei, Taiwan
关键词
D O I
10.1200/JCO.2006.09.8251
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Although several randomized trials have been performed comparing weekly docetaxel (wD) with standard docetaxel once every 3 weeks (3wD) as second-line treatment of advanced non - small-cell lung cancer (NSCLC), no single trial had sufficient power to detect clinically relevant differences in survival. Methods We performed a meta-analysis based on individual patient data from all identified randomized trials comparing wD with 3wD as second-line treatment of advanced NSCLC. Baseline characteristics, treatment assigned, and outcome data were collected for each patient. The primary end point was overall survival. All statistical analyses were stratified by trial. Results Five eligible trials were identified for a total of 865 patients: 433 patients had been assigned to 3wD, and 432 patients had been assigned to wD. Median age was 62 years ( range, 26 to 80 years). Performance status was 0 in 23%, 1 in 58%, and 2 in 16% of patients; 91% of the patients had received previous platinum, and 14% had received previous paclitaxel. With 733 deaths recorded (85%), median survival was 27.4 weeks for patients treated with 3wD, and 26.1 weeks for patients treated with wD ( P =.24, log-rank test). There was no significant heterogeneity among the five trials. No relevant differential effect was detected in subgroup analyses. Significantly less severe and febrile neutropenia was reported with wD ( P <.00001 for both), whereas no significant differences were observed for anemia, thrombocytopenia, and nonhematologic toxicity. Conclusion wD shows similar efficacy compared with 3wD, and represents an alternative for second-line treatment of advanced NSCLC.
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页码:1377 / 1382
页数:6
相关论文
共 24 条
[1]  
ALBERTI W, 1995, BRIT MED J, V311, P899
[2]   Subgroup analysis and other (mis)uses of baseline data in clinical trials [J].
Assmann, SF ;
Pocock, SJ ;
Enos, LE ;
Kasten, LE .
LANCET, 2000, 355 (9209) :1064-1069
[3]   Second-line treatment for advanced non-small cell lung cancer:: A systematic review [J].
Barlési, F ;
Jacot, W ;
Astoul, P ;
Pujol, JL .
LUNG CANCER, 2006, 51 (02) :159-172
[4]   Randomized phase III study of 3-weekly versus weekly docetaxel in pretreated advanced non-small-cell lung cancer:: a Spanish Lung Cancer Group trial [J].
Camps, C ;
Massuti, B ;
Jiménez, A ;
Maestu, I ;
Gómez, RG ;
Isla, D ;
González, JL ;
Almenar, D ;
Blasco, A ;
Rosell, R ;
Carrato, A ;
Viñolas, N ;
Batista, N ;
Girón, CG ;
Galán, A ;
López, M ;
Blanco, R ;
Provencio, M ;
Diz, P ;
Felip, E .
ANNALS OF ONCOLOGY, 2006, 17 (03) :467-472
[5]   A randomized trial of different docetaxel schedules in non-small cell lung cancer patients who failed previous platinum-based chemotherapy [J].
Chen, YM ;
Shih, JF ;
Perng, RP ;
Tsai, CM ;
Whang-Peng, J .
CHEST, 2006, 129 (04) :1031-1038
[6]   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
[7]   Randomized phase III trial of docetaxel versus vinorelbine or ifosfamide in patients with advanced non-small-cell lung cancer previously treated with platinum-containing chemotherapy regimens [J].
Fossella, FV ;
DeVore, R ;
Kerr, RN ;
Crawford, J ;
Natale, RR ;
Dunphy, F ;
Kalman, L ;
Miller, V ;
Lee, JS ;
Moore, M ;
Gandara, D ;
Karp, D ;
Vokes, E ;
Kris, M ;
Kim, Y ;
Gamza, F ;
Hammershaimb, L .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (12) :2354-2362
[8]   Phase II randomised trial comparing docetaxel given every 3 weeks with weekly schedule as second-line therapy in patients with advanced non-small-cell lung cancer (NSCLC) [J].
Gervais, R ;
Ducolone, A ;
Breton, JL ;
Braun, D ;
Lebeau, B ;
Vaylet, F ;
Debieuvre, D ;
Pujol, JL ;
Tredaniel, J ;
Clouet, P ;
Quoix, E .
ANNALS OF ONCOLOGY, 2005, 16 (01) :90-96
[9]   A randomised clinical trial of two docetaxel regimens (weekly vs 3 week) in the second-line treatment of non-small-cell lung cancer.: The DISTAL 01 study [J].
Gridelli, C ;
Gallo, C ;
Di Maio, M ;
Barletta, E ;
Illiano, A ;
Maione, P ;
Salvagni, S ;
Piantedosi, FV ;
Palazzolo, G ;
Caffo, O ;
Ceribelli, A ;
Falcone, A ;
Mazzanti, P ;
Brancaccio, L ;
Capuano, MA ;
Isa, L ;
Barbera, S ;
Perrone, F .
BRITISH JOURNAL OF CANCER, 2004, 91 (12) :1996-2004
[10]   Phase I trial of docetaxel administered by weekly infusion in patients with advanced refractory cancer [J].
Hainsworth, JD ;
Burris, HA ;
Erland, JB ;
Thomas, M ;
Greco, FA .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (06) :2164-2168