Optimal duration of first-line chemotherapy for advanced non-small cell lung cancer: A systematic review with meta-analysis

被引:34
作者
da Silveira Nogueira Lima, Joao Paulo [1 ]
dos Santos, Lucas Vieira [1 ]
Sasse, Emma Chen [2 ]
Sasse, Andre Deeke [1 ,3 ]
机构
[1] Univ Estadual Campinas UNICAMP, Dept Clin Med, Ctr Evidencias Oncol CEVON, Fac Ciencias Med, BR-13083970 Campinas, SP, Brazil
[2] Dendrix Arquitetura Informacao Cient, Sao Paulo, Brazil
[3] Radium Inst Oncol, Campinas, SP, Brazil
关键词
Lung neoplasms; Meta-analysis; Drug therapy; Antineoplastic agents; Non-small cell lung carcinoma; PHASE-III TRIAL; RANDOMIZED-TRIAL; SUPPORTIVE CARE; STATISTICS; SURVIVAL; 2ND-LINE; THERAPY; COURSES; CYCLES;
D O I
10.1016/j.ejca.2008.11.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The optimal duration of first-line chemotherapy for advanced non-small cell lung cancer (NSCLC) has been a matter for debate for nearly 20 years. In order to elucidate this issue, a meta-analysis comparing the different durations of same treatments was performed. Methods: We searched for all published randomised controlled trials (RCTs) comparing different durations of first-line treatment of advanced NSCLC. The MEDLINE, EMBASE, LILACS and CENTRAL databases were searched for RCTs comparing a defined number of cycles of chemotherapy versus continuing treatment until disease progression, or a defined number of cycles versus a higher number of cycles of the same chemotherapy. Trials including biological agents were excluded. Results: Seven trials that included 1559 patients were analysed. Treatment for more than 4 cycles was associated with a non-statistically significant decrease in the hazard of mortality relative to shorter treatment (hazard ratio (HR) = 0.97; 95% confidence interval (CI) = 0.84-1.11; P = .65). In those treated with third-generation chemotherapy through the whole study time, treatment for more than 4 cycles was associated with a non-statistically significant increase in mortality (HR = 1.08; 95% CI = 0.90-1.28; P = .28). Patients receiving more chemotherapy had significant longer progression-free survival (HR = .75; 95% CI = 0.60-0.85; P < 0.0001) than the group with shorter duration of treatment. In an intent-to-treat analysis, there was no difference in the overall response rate between the groups (odds ratio (OR) = 0.78; 95% CI = 0.60-1.01; P = .96). Longer treatment was associated with more severe leucopaenia but with no significant increase in non-haematological toxicities. Conclusions: In patients with advanced NSCLC the use of more than 4 cycles of first-line chemotherapy with third-generation regimens significantly increases progression-free survival but not overall survival and is associated with higher incidence of adverse events. There is no evidence to support continuous chemotherapy until progression in patients with lung cancer. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:601 / 607
页数:7
相关论文
共 29 条
[1]  
ALBERTI W, 1995, BRIT MED J, V311, P899
[2]  
[Anonymous], LUNG CANC
[3]  
[Anonymous], 2001, SYSTEMATIC REV HLTH
[4]  
[Anonymous], SEER CANC STAT REV 1
[5]  
[Anonymous], COCHRANE DATABASE SY
[6]   Third-generation chemotherapy agents in the treatment of advanced non-small cell lung cancer: A meta-analysis [J].
Baggstrom, Maria Q. ;
Stinchcombe, Thomas E. ;
Fried, Daniel B. ;
Poole, Charles ;
Hensing, Thomas A. ;
Socinski, Mark A. .
JOURNAL OF THORACIC ONCOLOGY, 2007, 2 (09) :845-853
[7]   Multicenter, randomized trial for stage IIIB or IV non-small-cell lung cancer using weekly paclitaxel and carboplatin followed by maintenance weekly paclitaxel or observation [J].
Belani, CP ;
Barstis, J ;
Perry, MC ;
La Rocca, RV ;
Nattam, SR ;
Rinaldi, D ;
Clark, R ;
Mills, GM .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (15) :2933-2939
[8]   Cisplatin and gemcitabine first-line chemotherapy followed by maintenance gemcitabine or best supportive care in advanced non-small cell lung cancer: A phase III trial [J].
Brodowicz, T ;
Krzakowski, M ;
Zwitter, M ;
Tzekova, V ;
Ramlau, R ;
Ghilezan, N ;
Ciuleanuf, T ;
Cucevic, B ;
Gyurkovits, K ;
Ulsperger, E ;
Jassem, J ;
Grgic, M ;
Pinar, S ;
Szilasi, M ;
Wiltschke, C ;
Wagnerova, M ;
Oskina, N ;
Soldatenkova, V ;
Zielinski, C ;
Wenczl, M .
LUNG CANCER, 2006, 52 (02) :155-163
[9]  
BUCCHERI GF, 1989, CANCER-AM CANCER SOC, V63, P428, DOI 10.1002/1097-0142(19890201)63:3<428::AID-CNCR2820630305>3.0.CO
[10]  
2-V