Camps Carlos, Sirera Rafael, Bremnes Roy M, Ródenas Vanessa, Blasco Ana, Safont María José, Garde Javier, Juarez Asuncion, Caballero Cristina, Sanchez Josie Javier, Taron Miquel, Rosell Rafael
Servicio de Oncología Médica, Fundación Investigación, Hospital General Universitario, Valencia, Spain.
Anticancer Res. 2006 Nov-Dec;26(6C):4905-9.
The purpose of this analysis was to study the association between the quantity of free circulating DNA and clinical variables in 99 advanced non-small cell lung cancer patients (NSCLC). The quantification in the serum of the gene of the catalytic fraction of telomerase (hTERT) by RT-PCR was used as a reference of the total amount of free DNA in blood. Patients were treated with cisplatin and docetaxel. The median hTERT level for patients in stage IIIB was 70.7 ng/ml vs. 53.1 ng/ml in patients in stage IV (p= 0.35). There was no association between hTERT values and therapy response, 53.9 ng/ml in the complete response (CR) + partial response (PR) group vs. 54.1 ng/ml in the stable disease (SD) + progressive disease (PD) group (p=0.23). In the multivariate analysis, hTERT was an independent predictive variable for time to progression (TTP) Hazard ratio (HR) 2.0, CI 95% 1.2-3.4, p=0.009) and overall survival (OS) (HR 2.4 CI 95% 1.3-4.3, p=0.004). The analysis of TTP and OS with a cut-off of hTERT at 40 ng/ml revealed that patients about this level had statistically poorer TTP (4 vs. 7 months, p= 0.009) and OS (5 vs. 15 months, p<0.0001). In conclusion, in advanced NSCLC, high serum hTERT levels may be a poor prognostic indicator for TTP and OS.
本分析的目的是研究99例晚期非小细胞肺癌(NSCLC)患者循环游离DNA数量与临床变量之间的关联。通过逆转录聚合酶链反应(RT-PCR)对端粒酶催化亚基基因(hTERT)的血清进行定量,以此作为血液中游离DNA总量的参考指标。患者接受顺铂和多西他赛治疗。ⅢB期患者的hTERT水平中位数为70.7 ng/ml,而Ⅳ期患者为53.1 ng/ml(p = 0.35)。hTERT值与治疗反应之间无关联,完全缓解(CR)+部分缓解(PR)组为53.9 ng/ml,疾病稳定(SD)+疾病进展(PD)组为54.1 ng/ml(p = 0.23)。在多变量分析中,hTERT是疾病进展时间(TTP)的独立预测变量(风险比[HR] 2.0,95%置信区间[CI] 1.2 - 3.4,p = 0.009)和总生存期(OS)(HR 2.4,CI 95% 1.3 - 4.3,p = 0.004)。以hTERT 40 ng/ml为临界值对TTP和OS进行分析发现,hTERT高于此水平的患者在统计学上TTP较差(4个月对7个月,p = 0.009),OS也较差(5个月对15个月,p < 0.0001)。总之,在晚期NSCLC中,血清hTERT高水平可能是TTP和OS的不良预后指标。