高级搜索
韩淑华, 黄见玲, 曹丹丹, 苑仁祥, 刘丹丹, 齐保龙. DLL3表达与晚期小细胞肺癌含铂化疗疗效及预后的相关性[J]. 肿瘤防治研究, 2020, 47(11): 846-850. DOI: 10.3971/j.issn.1000-8578.2020.19.1525
引用本文: 韩淑华, 黄见玲, 曹丹丹, 苑仁祥, 刘丹丹, 齐保龙. DLL3表达与晚期小细胞肺癌含铂化疗疗效及预后的相关性[J]. 肿瘤防治研究, 2020, 47(11): 846-850. DOI: 10.3971/j.issn.1000-8578.2020.19.1525
HAN Shuhua, HUANG Jianling, CAO Dandan, YUAN Renxiang, LIU Dandan, QI Baolong. Correlation of DLL3 Expression with Platinum-based Chemotherapy Efficacy and Prognosis of Advanced Small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2020, 47(11): 846-850. DOI: 10.3971/j.issn.1000-8578.2020.19.1525
Citation: HAN Shuhua, HUANG Jianling, CAO Dandan, YUAN Renxiang, LIU Dandan, QI Baolong. Correlation of DLL3 Expression with Platinum-based Chemotherapy Efficacy and Prognosis of Advanced Small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2020, 47(11): 846-850. DOI: 10.3971/j.issn.1000-8578.2020.19.1525

DLL3表达与晚期小细胞肺癌含铂化疗疗效及预后的相关性

Correlation of DLL3 Expression with Platinum-based Chemotherapy Efficacy and Prognosis of Advanced Small Cell Lung Cancer

  • 摘要:
    目的 探讨Delta-like protein 3(DLL3)与晚期小细胞肺癌(SCLC)顺铂/依托泊苷(EP)方案化疗敏感度及预后的关系。
    方法 选取64例明确诊断为Ⅲ/Ⅳ期的SCLC患者,采用免疫组织化学法检测DLL3在SCLC石蜡包埋组织中的表达情况;χ2检验分析DLL3表达与化疗疗效的关系,Kaplan-Meier和Cox多因素分析DLL3表达及其他因素对晚期SCLC患者无进展生存期(PFS)和总生存期(OS)的影响。
    结果 在84.1%(54/64)的SCLC组织中可检测到DLL3表达,其表达与患者性别、年龄、吸烟史、分期无相关性(P > 0.05)。DLL3高表达组的EP方案化疗有效率及疾病控制率均低于DLL3低表达组(P < 0.05);DLL3低表达组的无进展生存期长于DLL3高表达组,差异有统计学意义(P < 0.05)。Cox多因素分析结果显示DLL3表达、肿瘤分期、肿瘤直径是晚期SCLC患者PFS的独立预后因素,肿瘤分期是OS的独立预后因素。
    结论 DLL3表达与晚期SCLC EP方案化疗反应率及PFS相关,可能成为预测化疗敏感度的生物标志物。DLL3表达对于晚期SCLC患者的远期预后无预测价值。

     

    Abstract:
    Objective To explore the association between DLL3 expression and chemosensitivity of advanced SCLC patients to cis-platinum/etoposide therapy, and to evaluate the prognostic value of DLL3.
    Methods We selected 64 patients diagnosed as stage Ⅲ/Ⅳ SCLC. Protein levels of DLL3 were examined by immunohistochemistry. χ2 test was used to analyze the relation between DLL3 expression and chemotherapy efficacy. Kaplan-Meier and Cox multivariate analysis were used to investigate the impacts of DLL3 and other factors on PFS and OS of advanced SCLC patients.
    Results DLL3 was detected in 84.1% (54/64) of the samples and not associated with gender, age, smoking history or stage (P > 0.05). The response rate(RR) and disease control rate in DLL3-high group were lower than those in DLL3-low group (P < 0.05); PFS of patients with low DLL3 expression were better than those with high DLL3 expression (P < 0.05). DLL3 expression, tumor stage and tumor diameter were independent prognostic factors for PFS, and tumor stage was an independent prognostic factor for OS of advanced SCLC patients.
    Conclusion DLL3 is related to the response rate of EP chemotherapy and PFS. It may become a biomarker for predicting chemosensitivity. DLL3 has no predictive value for long-term prognosis of patients with advanced SCLC.

     

/

返回文章
返回