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Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
Prognostic significance of the 9th TNM lung cancer staging system in SCLC
Yansu Wang1, Yang Liu1, Yao Fu2
1Clinical Research Big data Center, Jilin Cancer Hospital, Changchun, China.
Background:
Clinical research and decision-making for small cell lung cancer (SCLC) are still based on the dichotomous classification of limited-stage disease or extensive-stage disease. This study aimed to evaluate the prognosis of the 9th edition of the tumor-node-metastasis (TNM) classification for SCLC in a real-world setting.
Methods:
This retrospective study included SCLC patients diagnosed between January 2014 and December 2021 in our center. Patients who had undergone complete staging evaluation were re-staged according to the 8th and 9th editions of the TNM classification for lung cancer. Kaplan-Meier analysis was conducted to determine overall survival (OS). Univariate and multivariate analyses were performed using the Cox proportional hazards model to assess the prognostic impact of the relevant factors.
Results:
A total of 1,329 patients were included in the study. All patients underwent clinical staging, while pathological staging was available on 51 patients. After a median follow-up of 39.67 months [95% confidence interval (CI): 36.28-43.06], the median OS was 15.40 months (95% CI: 14.45-16.35). According to the 8th and 9th TNM classification, the median OS, 1-, 2-, and 3-year OS rates showed a progressive decline with advancing stage. The median OS of the N2a and N2b subclasses that were newly added to the 9th edition was 20.00 months (95% CI: 16.14-23.86) and 14.53 months (95% CI: 12.88-16.18), respectively. The 3-year survival rates were 22.9% and 14.6%, respectively. Patients with N2b exhibited poorer outcomes (P=0.002). However, compared to M1c2, the median OS was numerically longer in patients with M1c1 (11.67 vs. 10.63 months), but it did not achieve a statistically significant difference (P=0.13). Multivariate analysis revealed that both the 8th and 9th editions of the TNM were independent prognostic factors.
Conclusions:
This retrospective analysis confirmed a significant difference in prognosis between the N2a and N2b subgroups in the 9th edition. No statistically significant difference was observed between the M1c1 and M1c2 subgroups. The present study suggests that the 9th edition of TNM requires further validation using external datasets, and factors such as the number of metastatic lesions in a single organ may also be included in future TNM classification systems.
