Masuda Ken, Yoshida Tatsuya, Motoi Noriko, Shinno Yuki, Matsumoto Yuji, Okuma Yusuke, Goto Yasushi, Horinouchi Hidehito, Yamamoto Noboru, Watanabe Shun-Ichi, Hoshino Tomoaki, Yatabe Yasushi, Ohe Yuichiro
Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Experimental Therapeutics, National Cancer Center Hospital, Tokyo, Japan.
Thorac Cancer. 2025 Jan;16(1):e15529. doi: 10.1111/1759-7714.15529.
Schlafen 11 (SLFN-11) has been identified as a sensitizer of tumor cells to DNA-damaging agents. However, the relationship between SLFN-11 expression and clinical outcomes in patients with small cell lung cancer (SCLC) remains unexplored. Thus, we aimed to evaluate the impact of SLFN-11 expression on survival in patients with limited-stage (LS) SCLC.
We conducted a retrospective review of data from patients pathologically diagnosed with LS-SCLC post-surgery between January 2008 and December 2018. SLFN-11 expression was assessed using immunohistochemistry in tissue microarrays and scored using a histology (H)-score (range: 0-300).
Overall, 86 patients were included in the analysis with a median H-score of 43 for SLFN-11 expression. Among the patients, 44 had high SLFN-11 expression (provisionally defined as H-score ≥ 43). No significant differences in clinical profiles were observed between the two groups (high and low SLFN expression). The median survival durations were not reached (NR; 95% confidence interval [CI]: 65.1 months to NR) and 33.5 months (95% CI: 24.2 months to NR) for patients with high and low SLFN-11 expression, respectively (hazard ratio [HR]: 0.40, 95% CI: 0.19-0.81; p = 0.012). Among patients who relapsed post-surgery (n = 21), the median survival durations were 22.0 (95% CI: 7.6-44.9 months) and 8.1 (95% CI: 1.8-24.6 months) months in patients with high and low SLFN-11 expression, respectively (HR: 0.22, 95% CI: 0.06-0.84; p = 0.026).
High SLFN-11 expression is associated with relatively longer survival in patients with LS-SCLC in both those undergoing surgery and those who have relapsed.
Schlafen 11(SLFN-11)已被确定为肿瘤细胞对DNA损伤剂的敏化剂。然而,小细胞肺癌(SCLC)患者中SLFN-11表达与临床结局之间的关系仍未得到探索。因此,我们旨在评估SLFN-11表达对局限期(LS)SCLC患者生存的影响。
我们对2008年1月至2018年12月间术后经病理诊断为LS-SCLC的患者的数据进行了回顾性分析。使用免疫组织化学在组织微阵列中评估SLFN-11表达,并使用组织学(H)评分(范围:0-300)进行评分。
总体而言,86例患者纳入分析,SLFN-11表达的中位H评分为43。其中,44例患者SLFN-11表达高(临时定义为H评分≥43)。两组(SLFN高表达和低表达)的临床特征未观察到显著差异。SLFN-11表达高和低的患者中位生存期分别未达到(NR;95%置信区间[CI]:65.1个月至NR)和33.5个月(95%CI:24.2个月至NR)(风险比[HR]:0.40,95%CI:0.19-0.81;p=0.012)。在术后复发的患者(n=21)中,SLFN-11表达高和低的患者中位生存期分别为22.0(95%CI:7.6-44.9个月)和8.1(95%CI:1.8-24.6个月)(HR:0.22,95%CI:0.06-0.84;p=0.026)。
SLFN-11高表达与LS-SCLC手术患者和复发患者的生存期相对较长有关。