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首页> 外文期刊>Journal of Clinical Oncology >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.
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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.

机译:III期临床试验比较了卡铂,紫杉醇和贝沙罗汀与卡铂和紫杉醇在未接受化疗的初发性晚期或转移性非小细胞肺癌患者中的作用:SPIRIT II。

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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 >or= 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.
机译:目的:本研究的目的是确定在标准的一线卡铂和紫杉醇疗法中是否添加合成类维生素Baxarotene(Targretin; Eisai Inc,Woodcliff Lake,NJ)是否为晚期非小细胞晚期患者提供额外的生存获益肺癌(NSCLC)。患者与方法:将患有胸水的IIIB期疾病,IV期NSCLC和东部合作肿瘤小组的工作状态从0改为1的患者,随机分配贝沙罗汀400 mg / m(2)/ d联合卡铂和紫杉醇,或分配单独使用卡铂和紫杉醇。贝沙罗汀患者在第1天或第1天或之前也接受了降脂药。还进行了次要疗效和支持性分析。结果:总共612例患者(每组306例)被纳入研究。在意向性治疗人群中,两组之间的生存率没有显着差异。但是,经历过国家癌症研究所3/4级高甘油三酯血症的贝沙罗汀治疗患者的亚人群(约40%)的中位生存期明显长于对照患者(12.4 v 9.2个月;对数秩,P = .014)。接受贝沙罗汀治疗的3/4级高甘油三酯血症受益最大的患者包括男性,吸烟者,经历6个月的体重减轻≥5%或患有IV期疾病的患者。尽管贝沙罗汀组的高脂血症,中性粒细胞减少,疲劳,白细胞减少,关节痛和腹泻的发生率更高,但两组之间大多数不良事件的发生率和严重程度相似。结论:尽管在整个研究人群中向化疗中添加贝沙罗汀并不能提高生存率,但贝沙罗汀治疗的患者发生高级别高甘油三酯血症与生存率增加密切相关,这表明贝沙罗汀可能使部分一线NSCLC患者受益。

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