Aug 2026· Journal of Thoracic Disease· Vol 18, pp. 860-860· 0 citations· 30 references
Medicine
TL;DR
Patients diagnosed during the immunotherapy era showed improved survival compared with those diagnosed during the pre-immunotherapy era, suggesting that personalized treatment strategies are essential for optimal patient outcomes.
Abstract
Background Extensive-stage small cell lung cancer (ES-SCLC) is a highly aggressive malignancy with limited treatment options. Immune checkpoint inhibitors (ICIs) have marked the beginning of the immunotherapy era for SCLC. However, population-level survival trends following the introduction of immunotherapy remain unclear. Methods We conducted a retrospective study using Surveillance, Epidemiology, and End Results (SEER) data from 2015 to 2021 to analyze survival outcomes in ES-SCLC patients before (2015–2017) and after (2019–2021) the introduction of ICIs. We employed propensity score matching (PSM) to adjust for confounding factors and used Cox regression models to identify prognostic factors. Kaplan-Meier analysis and log-rank tests were used to assess overall survival (OS) and cancer-specific survival (CSS). Results A total of 7,214 patients were included. After PSM, patients diagnosed in the 2019–2021 cohort demonstrated significantly improved survival compared with those diagnosed in the 2015–2017 cohort. The median overall survival (mOS) improved from 4.0 months [95% confidence interval (CI): 4.0–4.0] in the pre-immunotherapy era to 5.0 months (95% CI: 4.0–5.0) in the post-immunotherapy era [hazard ratio (HR) =0.849, 95% CI: 0.800–0.902; P<0.001], indicating that patients diagnosed during the immunotherapy era experienced better survival than those diagnosed during the pre-immunotherapy era. Marital status, geographical area, and metastasis sites were identified as significant prognostic factors. Notably, brain metastasis did not significantly affect survival, likely due to advancements in treatment. Conclusions Patients diagnosed during the immunotherapy era showed improved survival compared with those diagnosed during the pre-immunotherapy era. Socio-economic and geographical factors also play a critical role in prognosis, suggesting that personalized treatment strategies are essential for optimal patient outcomes.
Real-world evidence is provided supporting the use of ICI-based therapy in SCLC, particularly in advanced-stage disease, but should be interpreted cautiously given the retrospective design and subgroup sample sizes.
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Background Metastatic cervical cancer (mCC) remains a highly lethal disease. While clinical trials support the addition of targeted therapy and immunotherapy to chemotherapy, real-world survival trends are less well characterized. This study aimed to evaluate real-world overall survival trends and prognostic factors in...
Cheng Wang, Cai-Hou Xu, Xing-Chen He et al.· Gynecology and Pelvic Medici...· 0 citations
BACKGROUND
For advanced lung cancer patients, an increasing number of long responders to Immune Checkpoint Inhibitors (ICI) is observed. Thus, the optimal treatment duration remains unclear whereas indefinite treatment is associated to immune-related adverse events (irAEs) and financial burden.
OBJECTIVE
To describe...
Arnaud De Gunten, A. Mogenet, A. Bronstein et al.· Lung Cancer· 0 citations
BACKGROUND
Composite scores such as Lung Immune Prognostic Index (LIPI), modified Glasgow Prognostic Score (mGPS), EPSILoN, Pan Immune-Inflammation Value (PIV) and Systemic Immune-Inflammation Index (SII) have shown prognostic value in solid tumors, but evidence in extensive-stage small-cell lung cancer (ES-SCLC) are l...
Teresa Beninato, Giulia Stasi, G. Montelatici et al.· Tumori· 0 citations
Background Immune checkpoint inhibitors (ICIs) are a cornerstone of therapy for advanced non–small cell lung cancer (NSCLC). Elderly patients remain underrepresented in clinical trials, and the prognostic significance of immune-related adverse events (irAEs)—including their cumulative burden—across age groups is not fu...
A. Agbarya, N. S. Shrem, Asmah Miari et al.· Frontiers in Immunology· 0 citations
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