Fujiwara Yoshiro, Kiura Katsuyuki, Toyooka Shinichi, Hotta Katsuyuki, Tabata Masahiro, Takigawa Nagio, Soh Junichi, Tanimoto Yasushi, Kanehiro Arihiko, Kato Katsuya, Date Hiroshi, Tanimoto Mitsune
Department of Hematology, Oncology and Respiratory Medicine, Okayama University Medical Graduate School of Medicine, Dentistry and Pharmaceutical Sciences. 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
Lung Cancer. 2008 Jan;59(1):81-7. doi: 10.1016/j.lungcan.2007.07.018. Epub 2007 Aug 31.
The factors affecting survival after gefitinib treatment in patients with non-small cell lung cancer (NSCLC) remain to be fully elucidated, although epidermal growth factor receptor (EGFR) mutation is a substantial prognostic factor. KL-6 has been studied as a useful indicator for interstitial lung diseases; however, it was first discovered as a lung cancer-related antigen. The aim of this study was to investigate the prognostic value of the serum KL-6 levels in advanced NSCLC patients treated with gefitinib and thus determine its association with the EGFR mutation status.
Between September 2002 and September 2005, 41 patients with NSCLC were treated with gefitinib after having their serum KL-6 levels measured at Okayama University Hospital. EGFR mutations were analyzed by direct sequence methods.
The serum KL-6 levels ranged from 199 to 9080U/ml (median, 550U/ml), and 54% of 41 patients showed a level higher than the cut-off level of 500U/ml. The median progression-free survival (PFS) time and the median overall survival (OS) time were 4.7 months and 13.9 months, respectively. Multivariate analyses revealed that the elevated KL-6 level was an independent adverse prognostic factor for PFS (hazard ratio: 2.278, p=0.040) as well as OS (hazard ratio: 4.858, p=0.002) in NSCLC patients treated with gefitinib. The EGFR mutation status was analyzed in 22 patients (54%). Among those with wild-type EGFR, the patients with high serum KL-6 levels also had a worse survival than those within normal serum KL-6 levels (6.5 months versus 13.3 months, p=0.0194).
Our data suggest that NSCLC patients with high serum KL-6 levels tended to have a poor clinical outcome when treated with gefitinib.
尽管表皮生长因子受体(EGFR)突变是一个重要的预后因素,但影响非小细胞肺癌(NSCLC)患者吉非替尼治疗后生存的因素仍有待充分阐明。KL-6已被作为间质性肺疾病的有用指标进行研究;然而,它最初是作为一种肺癌相关抗原被发现的。本研究的目的是探讨血清KL-6水平在接受吉非替尼治疗的晚期NSCLC患者中的预后价值,并确定其与EGFR突变状态的关联。
2002年9月至2005年9月期间,41例NSCLC患者在冈山大学医院测定血清KL-6水平后接受吉非替尼治疗。通过直接测序法分析EGFR突变。
血清KL-6水平范围为199至9080U/ml(中位数,550U/ml),41例患者中有54%的患者KL-6水平高于500U/ml的临界值。无进展生存期(PFS)的中位数和总生存期(OS)的中位数分别为4.7个月和13.9个月。多因素分析显示,在接受吉非替尼治疗的NSCLC患者中,KL-6水平升高是PFS(风险比:2.278,p = 0.040)以及OS(风险比:4.858,p = 0.002)的独立不良预后因素。对22例患者(54%)进行了EGFR突变状态分析。在EGFR野生型患者中,血清KL-6水平高的患者的生存期也比血清KL-6水平正常的患者差(6.5个月对13.3个月,p = 0.0194)。
我们的数据表明,血清KL-6水平高的NSCLC患者在接受吉非替尼治疗时往往临床结局较差。