Phase III trial comparing carboplatin, paclitaxel, and bexarotene with carboplatin and paclitaxel in chemotherapy-naive patients with advanced or metastatic non-small-cell lung cancer: SPIRIT II

被引:77
作者
Blumenschein, George R., Jr. [1 ]
Khuri, Fadlo R.
von Pawel, Joachim
Gatzemeier, Ulrich
Miller, Wilson H., Jr.
Jotte, Robert M.
Le Treut, Jacques
Sun, Show-Li
Zhang, Jinkun K.
Dziewanowska, Zofia E.
Negro-Vilar, Andres
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
关键词
D O I
10.1200/JCO.2007.12.2689
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The purpose of this study was to determine whether addition of the synthetic rexinoid bexarotene (Targretin; Eisai Inc, Woodcliff Lake, NJ) to standard first-line carboplatin and paclitaxel therapy provides additional survival benefit in patients with advanced non-small-cell lung cancer (NSCLC). Patients and Methods Patients with stage IIIB disease with pleural effusion, or stage IV NSCLC and Eastern Cooperative Oncology Group performance status 0 to 1, were randomly assigned to bexarotene 400 mg/m(2)/d combined with carboplatin and paclitaxel, or assigned to carboplatin and paclitaxel alone. Bexarotene patients also received lipid-lowering agents on or before day 1. The primary efficacy end point was overall survival; secondary efficacy and supportive analyses were also conducted. Results A total of 612 patients (306 per arm) were enrolled onto the study. In the intent-to-treat population, no significant difference in survival occurred between the two arms. However, a subpopulation (approximately 40%) of bexarotene-treated patients who experienced National Cancer Institute grade 3/4 hypertriglyceridemia had significantly longer median survival than control patients (12.4 v 9.2 months; log-rank, P = .014). Bexarotene-treated patients with grade 3/4 hypertriglyceridemia who received the most benefit included those who were male, were smokers, experienced 6-month prior weight loss >= 5%, and had stage IV disease. The incidence and severity of most adverse events were similar between arms, although hyperlipidemia, neutropenia, fatigue, leukopenia, arthralgia, and diarrhea were more frequent in the bexarotene arm. Conclusion Although the addition of bexarotene to chemotherapy did not improve survival in the overall study population, occurrence of high-grade hypertriglyceridemia in bexarotene-treated patients strongly correlated with increased survival, suggesting that bexarotene may benefit a segment of first-line NSCLC patients.
引用
收藏
页码:1879 / 1885
页数:7
相关论文
共 16 条
[11]  
Rizvi N, 2001, Clin Lung Cancer, V2, P210, DOI 10.3816/CLC.2001.n.005
[12]  
RIZVI N, 2002, P ASCO 2002 MOL THER
[13]  
Rizvi NA, 1999, CLIN CANCER RES, V5, P1658
[14]  
Sandler AB, 2005, J CLIN ONCOL, V23, p2S
[15]   A selective retinoid X receptor agonist bexarotene (Targretin) prevents and overcomes acquired paclitaxel (Taxol) resistance in human non-small cell lung cancer [J].
Yen, WC ;
Corpuz, MR ;
Prudente, RY ;
Cooke, TA ;
Bissonnette, RP ;
Negro-Vilar, A ;
Lamph, WW .
CLINICAL CANCER RESEARCH, 2004, 10 (24) :8656-8664
[16]  
YOCUM RC, 2001, P AM SOC CLIN ONC, V20