Martins Sandro J, Takagaki Teresa Y, Silva Alecsander G P, Gallo Célia P, Silva Fernando B A, Capelozzi Vera L
Pulmonary Division, School of Medicine, University of São Paulo, Av. Dr. Enéas de Carvalho Aguiar 255, 05403-000 São Paulo, Brazil.
Lung Cancer. 2009 Apr;64(1):105-9. doi: 10.1016/j.lungcan.2008.07.017. Epub 2008 Sep 17.
The thyroid transcription factor-1 (TTF-1) is a tissue-specific transcription factor that could play an important role in cell differentiation and morphogenesis of lung tumors. Matrix metalloproteinase-9 (MMP-9) is a protease commonly expressed in non-small cell lung cancer, conferring angiogenic and metastatic potential.
We assessed TTF-1 and MMP-9 tumor expression by immunohistochemistry in 51 patients with lung adenocarcinoma, stage IIIB or IV, treated with platinum regimens. A bicategorical prognostic model was obtained using the Kaplan-Meier method, Cox regression, and conjunctive consolidation.
The median expression of TTF-1 was 30.0% (range: 0-85.9%). All tumors expressed MMP-9 (median: 78.7%; range: 15.2-96.1%). Median survival was 41.6 weeks, with estimated 1- and 2-year survival rates of 45.0% and 22.0%, respectively. Poor performance status (Karnofsky scale) - hazards ratio (HR): 1.03, 95% confidence interval (CI): 1.01-1.06; low TTF-1 expression (<40%) - HR: 4.00, 95% CI: 1.75-9.09; and high MMP-9 expression (> or =80%) - HR: 2.82, 95% CI: 1.30-6.08 were independent prognostic factors. Patients could be stratified in three death risk groups according to markers expression: low risk (high TTF-1 and low MMP-9; median survival: 127.6 weeks), intermediate risk (low TTF-1 or high MMP-9; median survival: 39.0 weeks); and high risk (low TTF-1 and high MMP-9; median survival: 16.4 weeks).
TTF-1 and MMP-9 tumor expression as detected by immunohistochemistry may allow identification of different, clinically meaningful, prognostic groups of advanced lung adenocarcinoma patients treated with platinum regimens.
甲状腺转录因子-1(TTF-1)是一种组织特异性转录因子,可能在肺肿瘤的细胞分化和形态发生中起重要作用。基质金属蛋白酶-9(MMP-9)是一种在非小细胞肺癌中普遍表达的蛋白酶,具有血管生成和转移潜能。
我们通过免疫组织化学评估了51例接受铂类方案治疗的IIIB期或IV期肺腺癌患者的TTF-1和MMP-9肿瘤表达情况。使用Kaplan-Meier法、Cox回归和联合合并获得了一个双分类预后模型。
TTF-1的中位表达为30.0%(范围:0-85.9%)。所有肿瘤均表达MMP-9(中位值:78.7%;范围:15.2-96.1%)。中位生存期为41.6周,估计1年和2年生存率分别为45.0%和22.0%。较差的体能状态(卡诺夫斯基量表)——风险比(HR):1.03,95%置信区间(CI):1.01-1.06;低TTF-1表达(<40%)——HR:4.00,95%CI:1.75-9.09;高MMP-9表达(≥80%)——HR:2.82,95%CI:1.30-6.08是独立的预后因素。根据标志物表达情况,患者可分为三个死亡风险组:低风险(高TTF-1和低MMP-9;中位生存期:127.6周)、中风险(低TTF-1或高MMP-9;中位生存期:39.0周);高风险(低TTF-1和高MMP-9;中位生存期:16.4周)。
免疫组织化学检测到的TTF-1和MMP-9肿瘤表达可能有助于识别接受铂类方案治疗的晚期肺腺癌患者不同的、具有临床意义的预后组。