Yasemin Söyler, Pınar AKIN KABALAK, Suna Kavurgacı, Funda Demi̇rağ, Ülkü Yilmaz
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摘要

背景:鉴别高级别神经内分泌癌(HGNEC)是困难的。我们旨在评估未分类HGNEC (uHGNEC)的临床特征和生存结果,并将其与小细胞肺癌(SCLC)进行比较。材料和方法:这是一项针对HGNEC患者的回顾性观察性研究。Kaplan-Meier法评估无进展生存期(PFS)和总生存期(OS)。采用cox -回归分析确定与PFS和OS独立相关的危险因素。结果:共分析了121例患者[uHGNEC (n = 35), SCLC (n = 86)]。原发肿瘤主要位于右侧,位于肺中心。诊断时IASLC阶段为局部晚期的患者43例(35.5%),晚期的患者78例(64.5%)。uHGNEC组和SCLC组具有相似的临床特征。研究人群的中位PFS和OS分别为8.8 (95%Cl 7.29 - 10.30)和10.9 (95%Cl 9.9 - 11.8)个月。uHGNEC组和SCLC组的PFS (9.4 vs 8.6个月,p = 0.99)和OS (12 vs 10.7个月,p = 0.51)相似。两组患者的6个月、1年和2年PFS和OS也相似。在所有患者中,右侧肿瘤(HR: 1.558, 95%Cl: 1.044 ~ 2.325, p = 0.03)和晚期疾病(HR: 1.928, 95%Cl: 1.292 ~ 2.877, p = 0.001)是不良OS的预后因素。cox -回归分析显示,组织病理学对PFS和OS无影响。结论:病理不能分类的HGNEC患者表现与SCLC相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sınıflandırılamayan akciğer yüksek dereceli nöroendokrin karsinomaların klinik özellikleri ve sağ kalım sonuçları
Background: Differentiating high-grade neuroendocrine carcinomas (HGNEC) is difficult. We aimed to assess the clinical features and survival outcomes of unclassified HGNEC (uHGNEC) and to compare it with small-cell lung cancer (SCLC). Material and Methods: This was a retrospective and observational study of HGNEC patients. Kaplan-Meier method was used to estimate progression-free survival (PFS) and overall survival (OS). Cox-regression analyses were used to determine the risk factors independently associated with PFS and OS. Results: One hundred twenty-one patients [uHGNEC (n = 35), SCLC (n = 86)] were analysed. The primary tumour was mostly right-sided, located in the centre of the lungs. The IASLC stage at diagnosis was locally advanced in 43 (35.5%) patients and advanced in 78 (64.5%) patients. uHGNEC and SCLC groups shared similar clinical features. The study population's median PFS and OS were 8.8 (95%Cl 7.29 – 10.30) and 10.9 (95%Cl 9.9 – 11.8) months, respectively. uHGNEC- and SCLC groups had a similar PFS (9.4 vs 8.6 months, p = 0.99) and OS (12 vs 10.7 months, p = 0.51). The six-month, one- and two-year PFS and OS of two groups were also similar. Among all patients, a right-sided tumour (HR: 1.558, 95%Cl 1.044 – 2.325, p = 0.03) and advanced-stage disease (HR: 1.928, 95%Cl 1.292 – 2.877, p = 0.001) were prognostic factors for poor OS. Cox-regression analysis indicated that histopathology did not have an impact on PFS and OS. Conclusion: HGNEC patients who cannot be classified pathologically behave like SCLC.
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