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Poster Display session

238P - Efficacy of immunotherapy for extensive-stage small cell esophageal cancer: A multicenter real-world retrospective study

Date

27 Jun 2024

Session

Poster Display session

Presenters

bingjie Fan

Citation

Annals of Oncology (2024) 35 (suppl_1): S94-S105. 10.1016/annonc/annonc1479

Authors

B. Fan1, X. Qiu2, L. Wang1

Author affiliations

  • 1 Shandong Cancer Hospital and Institute, Jinan/CN
  • 2 School of Clinical Medicine, Shandong Second Medical University, Weifang/CN

Resources

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Abstract 238P

Background

Small Cell Esophageal Carcinoma (SCEC) is an aggressive neuroendocrine carcinoma with early metastatic potential. Under traditional treatment modalities, radiotherapy, chemotherapy, and surgery have been used as the main treatment strategies for SCEC, but they all lead to poor prognosis. With the successful application of immunotherapy in various advanced cancer types, immunotherapy may be a rational choice for Extensive Stage Small Cell Esophageal Carcinoma (ES-SCEC).

Methods

107 consecutive patients with Extensive Stage Small Cell Esophageal Carcinoma (ES-SCEC) were identified from 5 cancer centers. The patients were divided into two groups including patients receiving immunotherapy or not. The clinicopathological characteristics, treatment information and survival time were collected from included patients. Progression-free survival (PFS) was defined as the time from drug initiation until disease progression or death from any cause, and overall survival (OS) was defined as the time from drug initiation until death or censored at last follow up. OS was assessed by the Kaplan-Meier method, with the log-rank test for comparison between groups.

Results

Patients undergoing immunotherapy demonstrate higher one-year (92.03% vs 68.75%, P=0.037) and two-year survival rates (58.67% vs 36.39%, P=0.014) compared to those who have not received immunotherapy. In the survival analysis, the median PFS was 10.13 months for patients receiving immunotherapy, and was 6.37 months for patients without immunotherapy (P=0.2319). And significant statistical difference was observed on OS between patients with or without immunotherapy (NA vs 20.63, P=0.2319). The median OS in the immunotherapy group was not yet available.

Conclusions

The results of this real-world cohort analysis suggest a positive impact of immunotherapy on OS in ES-SCEC. The immunotherapy is a reasonable treatment option for ES-SCEC.

Legal entity responsible for the study

The authors.

Funding

National Natural Science Foundation of China.

Disclosure

All authors have declared no conflicts of interest.

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