Phase III randomized, double-blind study of maintenance CAI or placebo in patients with advanced non-small cell lung cancer (NSCLC) after completion of initial therapy (NCCTG 97-24-51)

被引:62
作者
Johnson, Elizabeth A. [1 ]
Marks, Randolph S. [2 ]
Mandrekar, Sumithra J. [2 ]
Hillman, Shauna L. [2 ]
Hauge, Mark D. [3 ]
Bauman, Mitchel D. [4 ]
Wos, Edward J. [5 ]
Moore, Dennis F. [6 ]
Kugler, John W. [7 ]
Windschitl, Harold E. [3 ]
Graham, David L. [8 ]
Bernath, Albert M., Jr. [9 ]
Fitch, Tom R. [10 ]
Soori, Gamini S. [11 ]
Jett, James R. [2 ]
Adjei, Alex A. [2 ]
Perez, Edith A. [1 ]
机构
[1] Mayo Clin, Div Hematol Oncol, Jacksonville, FL 32224 USA
[2] Mayo Clin & Mayo Fdn, Rochester, MN 55905 USA
[3] CentraCare Clin, St Cloud, MN 56301 USA
[4] Siouxland Hematol Oncol Associates, Sioux City, IA 51105 USA
[5] Medctr Hlth Syst 1, Bismarck, ND 58506 USA
[6] Wichita Community Clin Oncol Program, Wichita, KS 67214 USA
[7] Illinois Oncol Res Assoc, Community Clin Oncol Program, Peoria, IL 61615 USA
[8] Carle Canc Ctr CCOP, Urbana, IL 61801 USA
[9] Geisinger Clin & Med Ctr CCOP, Danville, PA 17822 USA
[10] Scottsdale CCOP, Scottsdale, AZ 85259 USA
[11] Missouri Valley Canc Consortium, Omaha, NE 68106 USA
关键词
non-small cell lung cancer (NSCLC); maintenance; imidazole; CAI;
D O I
10.1016/j.lungcan.2007.10.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This study assessed whether maintenance therapy with carboxyaminoimidazole (CAI), compared to placebo, prolonged overall survival in stage IIIB/IV NSCLC patients who had tumour regression or stable disease after treatment with one chemotherapy regimen. Methods: After completion of chemotherapy, patients were randomized to receive daily oral CAI at 250mg or placebo. Treatment continued until patient refusal, disease progression or unacceptable adverse event (AE). Quality of life (QOL) was assessed by UNISCALE and Functional Assessment of Cancer Therapy for Lung Cancer (FACT-L). Results: Registration was halted early for slow accrual (targeted 360, randomized 186: 94 CAI, 92 placebo). All patients were off active treatment at time of analyses. Non-haematologic AEs (primarily grade 1, 2) observed significantly more often in the CAI group included fatigue (54.5% versus 29.3%), anorexia (31.1% versus 13.0%), nausea (62.2% versus 30.4%), vomiting (32.2% versus 14.1 %), neurosensory (60.0% versus 44.6%) and ataxia (33.3% versus 16.3%). Patients discontinued treatment for AEs, death on study or refusal more often in the CAI group (36.0% versus 8.7%, p < 0.0001). No significant differences in survival or time to progression were observed (median: CAI versus placebo: 11.4 months versus 10.5 months, log rank p=0.54; 2.8 months versus 2.4 months, log rank p=0.50). More patients receiving CAI reported a clinically significant (10-point) decline in QOL particularly on the functional (58% versus 37%, p=0.05) construct of FACT-L and UNISCALE (72% versus 51 %, p = 0.04). Conclusion: The addition of CAI following chemotherapy does not provide clinical benefit or improvement in QOL over placebo in advanced NSCLC. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:200 / 207
页数:8
相关论文
共 26 条
  • [1] Bauer KS, 2000, J PHARMACOL EXP THER, V292, P31
  • [2] 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
    Belani, CP
    Barstis, J
    Perry, MC
    La Rocca, RV
    Nattam, SR
    Rinaldi, D
    Clark, R
    Mills, GM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (15) : 2933 - 2939
  • [3] Phase I clinical and pharmacokinetic study of oral carboxyamidotriazole, a signal transduction inhibitor
    Berlin, J
    Tutsch, KD
    Hutson, P
    Cleary, J
    Rago, RP
    Arzoomanian, RZ
    Alberti, D
    Feierabend, C
    Wilding, G
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) : 781 - 789
  • [4] BONOMI P, 1996, LUNG CANC PRINCIPLES, P811
  • [5] 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
    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
    [J]. LUNG CANCER, 2006, 52 (02) : 155 - 163
  • [6] RELIABILITY AND VALIDITY OF THE FUNCTIONAL ASSESSMENT OF CANCER-THERAPY - LUNG (FACT-L) QUALITY-OF-LIFE INSTRUMENT
    CELLA, DF
    BONOMI, AE
    LLOYD, SR
    TULSKY, DS
    KAPLAN, E
    BONOMI, P
    [J]. LUNG CANCER, 1995, 12 (03) : 199 - 220
  • [7] COX DR, 1972, J R STAT SOC B, V34, P187
  • [8] Figg WD, 1995, CLIN CANCER RES, V1, P797
  • [9] CAI is a potent inhibitor of neovascularization and imparts neuroprotection in a mouse model of ischemic retinopathy
    Franklin, AJ
    Jetton, TL
    Kuchemann, CL
    Russell, SR
    Kohn, EC
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 (10) : 3756 - 3766
  • [10] Ginsberg RJ, 1997, CANC PRINCIPLES PRAC