Department of Oncology and Pathology, Karolinska Institute, Stockholm, Sweden.
Department of Radiology, Karolinska University Hospital, Stockholm, Sweden.
Lung Cancer. 2018 Jun;120:75-81. doi: 10.1016/j.lungcan.2018.03.026. Epub 2018 Mar 30.
The purpose of this study was to evaluate on a Swedish cohort of small cell lung cancer (SCLC) patients whether the 8th TNM staging system can provide additional prognostic information in comparison with the previous 6th and 7th TNM versions and the older 2-stage LD vs ED system.
We reviewed the medical records of patients (pts) with SCLC diagnosed between January 2008 and February 2016 in the Stockholm and Gotland region. Each patient file was revised and reclassified from the VASGL system to the 6, 7 and 8 TNM system respectively. We assessed overall survival (OS) according to the T, N, M-descriptor and compared LD/ED with the 6 -7, -8 editions of TNM. Four separate multivariate models adjusted for basic patient characteristics were performed.
In total, 706 pts were eligible for the study. Median OS was 7.7 months. Differences in survival between less advanced stages (IA-IIB) were difficult to assess since there were few patients (n = 32). The majority of patients (78%) migrated to new stage categories in the 8th TNM edition; IIIC, IVA and IVB. In the 8th TNM edition subjects with M1a disease had a similar prognosis to patients with multiple metastatic diseases, M1c. Conversely, subjects with a single metastasis had a similar prognosis to M0-disease. On multivariate analysis, stage was an independent prognostic factor independently of the classification system used.
In this cohort, the 8th TNM classification system seems to provide more accurate prognostic information in patients with SCLC when compared to the previous TNM versions. There were few cases with Stages I and II and therefore no robust conclusions can be drawn in this category. The reason single metastatic lesions (M1b) had a better prognosis when compared to M1c could be due to a more aggressive treatment approach in these patients.
本研究旨在评估瑞典小细胞肺癌(SCLC)患者队列中,第 8 版 TNM 分期系统与前 6 版和 7 版 TNM 版本以及较旧的 2 期 LD 与 ED 系统相比是否能提供额外的预后信息。
我们回顾了 2008 年 1 月至 2016 年 2 月在斯德哥尔摩和哥特兰地区诊断为 SCLC 的患者的病历。每个患者的病历都根据 VASGL 系统进行修订和重新分类,分别归入第 6、7 和 8 版 TNM 系统。我们根据 T、N、M 描述符评估总生存期(OS),并将 LD/ED 与 6-7、-8 版 TNM 进行比较。进行了四个独立的多变量模型,调整了基本患者特征。
共有 706 名患者符合研究条件。中位 OS 为 7.7 个月。由于患者数量较少(n=32),进展期(IA-IIB)患者之间的生存差异难以评估。大多数患者(78%)在第 8 版 TNM 中转移到新的分期类别;IIIC、IVA 和 IVB。在第 8 版 TNM 中,M1a 疾病患者的预后与多发性转移疾病(M1c)患者相似。相反,单一转移患者的预后与 M0 疾病患者相似。多变量分析显示,分期是独立的预后因素,与使用的分类系统无关。
在本队列中,与之前的 TNM 版本相比,第 8 版 TNM 分类系统似乎为 SCLC 患者提供了更准确的预后信息。I 期和 II 期的病例较少,因此无法对此类病例做出稳健的结论。单转移病灶(M1b)的预后优于 M1c 的原因可能是这些患者的治疗方法更为激进。