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Poster Display & Cocktail

55P - Real-world study of serplulimab plus chemotherapy as second or further-line therapy for small cell lung cancer

Date

03 Mar 2025

Session

Poster Display & Cocktail

Presenters

Yanrong Guo

Citation

Annals of Oncology (2025) 10 (suppl_2): 1-8. 10.1016/esmoop/esmoop104198

Authors

Y. Guo1, J. Duan2, S. Han1, Q. Guo1, J. Zhai1, X. Ren1, S. Li1

Author affiliations

  • 1 Pneumology Department, Shanxi province Cancer hospital, Chinese Academy of Medical Sciences, 030013 - Taiyuan/CN
  • 2 Pneumology Department, Chinese Academy of Medical Sciences and Peking Union Medical College - National Cancer Center, Cancer Hospital, 100021 - Beijing/CN

Resources

This content is available to ESMO members and event participants.

Abstract 55P

Background

The landscape of second or further-line treatment on small-cell lung cancer (SCLC) patients is limited, with second-line chemotherapy typically exhibiting diminished efficacy. The ASTRUM-005 study robustly validated the efficacy of first-line serplulimab plus chemotherapy. However, the role of this regimen in subsequent lines of therapy for SCLC remains to be elucidated.

Methods

This study was conducted on adult SCLC patients who underwent second or further-line serplulimab plus chemotherapy from May 2022 to November 2023. The primary outcome was progress-free survival (PFS). Secondary outcomes were objective response rate (ORR), disease control rate (DCR), overall survival (OS), and safety profile. Cox proportional-hazards models were utilized to identify predictors of survival.

Results

A total of 39 patients were eligible for this analysis. As of May 31, 2024, the median follow-up duration since initiating serplulimab was 8.23 months. The mean age was 56.6 ± 10.4 years. The majority were males (87.2%), smokers (79.5%), had ECOG scores of 1 (92.3%), and had stage Ⅳ disease (69.2%). 31 patients (79.5%) achieved ORR events during the first-line phase. Second-line serplulimab was administered to 33 patients (84.6%), and 16 (41.0%) received prior immunotherapy. The median PFS and OS were 4.1 (95%CI 3.1 - 7.2) and 12.0 (95%CI 6.9 - NR) months, respectively. The ORR and DCR were 20.5% (95%CI 9.3 - 36.5) and 64.1% (95%CI 47.2 - 78.8), respectively. Patients who achieved ORR event after initial therapy were more likely to benefit from the subsequent immunochemotherapy, with a median PFS of 10.8 vs. 3.3 months (P = 0.006). While prior immunotherapy didn’t yield a significant effect on survival, patients with such treatment history exhibited a higher ORR (31.3 vs. 13.0%). In multivariate PFS analysis, a significant correlation was found in baseline ProGrp ≥ 300 ng/L (HR 3.0, 95%CI 1.0 - 9.0). Any grade adverse events were reported in 64.1% of patients, and most experienced platelets decreased (23.1%).

Conclusions

Serplulumab-based immunochemotherapy exhibits promising therapeutic efficacy for SCLC patients beyond the initial treatment phase, and further validations are warranted.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Yanrong Guo.

Funding

Shenzhen Xihepu Biomedical Research Institute-Tumour Immunotherapy Project (CCHRPP-ZL-2023-Q-009).

Disclosure

All authors have declared no conflicts of interest.

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