Zhou X, Kemp B L, Khuri F R, Liu D, Lee J J, Wu W, Hong W K, Mao L
Department of Thoracic/Head and Neck Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Clin Cancer Res. 2000 Feb;6(2):559-65.
Development of non-small cell lung cancer (NSCLC) is a result of multiple accumulated genetic abnormalities. Profiles of genetic abnormalities may determine tumor behavior and impact on patient outcome. We used microsatellite markers at 3p14, 9p21, and 10q24 to analyze tumor samples from 91 patients with pathologically confirmed stage I NSCLC for microsatellite alterations. Loss of heterozygosity at any single locus was not significantly associated with length of survival. However, patients whose tumors had microsatellite instability (MI) at 10q24 had shortened disease-specific survival. Among 31 such patients, 32% (10 of 31 patients) had died of the disease within 5 years after surgery compared with 16% (9 of 58 patients) without MI at 10q24 (P = 0.07). Interestingly, in the adenocarcinoma subtype, 71% (5 of 7 patients) of the patients with MI at 10q24 succumbed to the disease as compared with only 12% (3 of 26) of the adenocarcinoma patients without such MI (P < 0.001), suggesting the presence of distinct mechanisms in tumorigenesis among different subtypes of lung cancer. It has been noticed that certain microsatellite alteration profiles provide additional values for risk assessment. Of 23 patients who had MI at 10q24 and an alteration at 3p14, 39% (9 of 23 patients) died of the disease within 5 years as compared with only 15% (10 of 66 patients) of the patients without such a profile (P = 0.02). Strikingly, among the 22 patients with no alteration at any loci tested or with loss of heterozygosity at 10q24 and retention of at least one of the other two loci, none died of lung cancer within 5 years after surgery, whereas 28% (19 of 67 patients) of the patients outside these profiles did so (P = 0.01). Our results support the hypothesis that microsatellite alterations can be used as biomarkers for the genetic classification of pathological stage I NSCLC, which may in turn influence treatment decisions dependent on an accurate forecast of patient survival time.
非小细胞肺癌(NSCLC)的发生是多种累积性基因异常的结果。基因异常谱可能决定肿瘤行为并影响患者预后。我们使用位于3p14、9p21和10q24的微卫星标记分析了91例经病理确诊为I期NSCLC患者的肿瘤样本,以检测微卫星改变。任何单个位点的杂合性缺失与生存时间均无显著相关性。然而,肿瘤在10q24处存在微卫星不稳定性(MI)的患者疾病特异性生存期缩短。在31例此类患者中,32%(31例中的10例)在手术后5年内死于该疾病,而10q24处无MI的患者中这一比例为16%(58例中的9例)(P = 0.07)。有趣的是,在腺癌亚型中,10q24处有MI的患者中有71%(7例中的5例)死于该疾病,而无此类MI的腺癌患者中只有12%(26例中的3例)死亡(P < 0.001),这表明肺癌不同亚型的肿瘤发生存在不同机制。已经注意到某些微卫星改变谱为风险评估提供了额外价值。在10q24处有MI且3p14处有改变的23例患者中,39%(23例中的9例)在5年内死于该疾病,而无此改变谱的患者中这一比例仅为15%(66例中的10例)(P = 0.02)。引人注目的是,在22例在所检测的任何位点均无改变或在10q24处有杂合性缺失且至少保留其他两个位点之一的患者中,无人在手术后5年内死于肺癌,而不在这些改变谱中的患者中有28%(67例中的19例)死于肺癌(P = 0.01)。我们的结果支持这样的假设,即微卫星改变可作为病理I期NSCLC基因分类的生物标志物,这反过来可能会影响依赖于准确预测患者生存时间的治疗决策。