# Real-world survival patterns and multimodal therapy utilization in small cell lung cancer: a retrospective cohort study in a Chinese countryside hospital

**Authors:** Taosheng Huang, Linjie Ma, Mingfang Wang, Xumei Pang, Jiying Xu, Xi Chen, Yutao Xia, Min Yan, Wenxiang Zhao, Congcong Cheng, Runqing Wang, Kai Sun, Peng Wang

PMC · DOI: 10.3389/fonc.2025.1636533 · Frontiers in Oncology · 2025-10-23

## TL;DR

This study examines survival and treatment patterns in small cell lung cancer patients in a rural Chinese hospital, highlighting the benefits of certain therapies.

## Contribution

The study provides real-world evidence on multimodal therapy effectiveness and survival outcomes for SCLC in a developing region.

## Key findings

- Concurrent chemoradiotherapy and prophylactic cranial irradiation improved survival in limited-stage SCLC.
- Palliative radiotherapy showed potential benefits in extensive-stage SCLC.
- Platinum sensitivity predicted better outcomes in second-line treatment for SCLC.

## Abstract

Small cell lung cancer (SCLC) accounts for 13–15% of all lung malignancies and remains a highly aggressive disease with limited therapeutic progress, particularly in rural settings. Despite advances such as immune checkpoint inhibitors and multimodal therapy, real-world evidence on treatment utilization and survival outcomes in developing regions is scarce. This retrospective cohort study aimed to evaluate survival patterns and multimodal therapy use in SCLC patients from a Chinese countryside hospital.

A total of 132 patients diagnosed with SCLC at Weifang Yidu Central Hospital between 2014 and 2023 were retrospectively analyzed. Patients were classified as limited-stage (LS) or extensive-stage (ES) using the Veterans Administration Lung Study Group (VALG) system. Clinical data, including demographics, treatment regimens, and outcomes, were collected. Overall survival (OS) and progression-free survival (PFS) were calculated using the Kaplan-Meier method, and subgroup analyses assessed the effects of platinum sensitivity, prophylactic cranial irradiation (PCI), concurrent chemoradiotherapy (CCRT), and palliative radiotherapy.

Of 132 patients (64 LS-SCLC, 68 ES-SCLC), most received first-line platinum–etoposide regimens, with diminishing treatment continuity in later lines due to cumulative toxicities. Median OS was significantly longer in LS-SCLC than ES-SCLC (50.2 vs. 16.8 months, p<0.05). PCI reduced brain metastases (0% vs. 27%) and improved OS (50.2 vs. 36.4 months; HR=0.47), though not statistically significant. CCRT achieved longer OS than sequential chemoradiotherapy (54.9 vs. 50.2 months; HR=0.54). In second-line therapy, platinum-sensitive patients benefited from platinum rechallenge (median OS 17.7 vs. 12.5 months, p<0.05), whereas platinum-resistant patients showed no improvement. Palliative radiotherapy in ES-SCLC prolonged PFS (16.1 vs. 7.8 months) and OS (30.2 vs. 16.1 months) with near-significant trends (HR≈0.5).

This real-world study confirms that concurrent chemoradiotherapy (CCRT) and prophylactic cranial irradiation (PCI) confer survival advantages in LS-SCLC, while palliative radiotherapy yields potential benefits in ES-SCLC. Platinum sensitivity remains a crucial predictor of second-line treatment efficacy, supporting reintroduction of platinum in sensitive relapses per guideline recommendations. Conversely, irinotecan–lobaplatin combinations provided limited benefit. Findings emphasize the need for personalized treatment sequencing and improved access to standardized multimodal care in rural healthcare settings.

## Linked entities

- **Chemicals:** platinum (PubChem CID 23939), etoposide (PubChem CID 36462), irinotecan (PubChem CID 60838), lobaplatin (PubChem CID 10000860)
- **Diseases:** small cell lung cancer (MONDO:0008433)

## Full-text entities

- **Diseases:** metastases (MESH:D009362), ES-SCLC (MESH:D055752), toxicities (MESH:D064420), lung malignancies (MESH:D008175)
- **Chemicals:** irinotecan (MESH:D000077146), Platinum (MESH:D010984), etoposide (MESH:D005047), lobaplatin (MESH:C066228)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12588810/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12588810/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12588810/full.md

---
Source: https://tomesphere.com/paper/PMC12588810