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The Impact of Surgical Treatment on Survival in Localized Small Cell Esophageal Cancer

The Impact of Surgical Versus Non-surgical Treatment on Survival in Localized Esophageal Small Cell Carcinoma: a Single-center Retrospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07596654
Enrollment
4
Registered
2026-05-19
Start date
2026-05-15
Completion date
2026-12-31
Last updated
2026-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Carcinoma, Limited-Stage Small Cell Esophageal Carcinoma

Keywords

Small Cell Esophageal Carcinoma, Limited-Stage Esophageal Small Cell Carcinoma, Surgery, Chemoradiotherapy, Survival, Prognosis, Retrospective Cohort Study

Brief summary

Limited-stage small cell esophageal carcinoma (LS-SCEC) is a rare and highly aggressive malignancy with poor prognosis and no established standard treatment strategy. Due to its low incidence, current evidence is mainly derived from small retrospective studies, and the role of surgery in multimodal treatment remains controversial. In particular, the survival benefit of surgical treatment compared with definitive non-surgical therapy has not been fully clarified. This single-center retrospective cohort study aims to evaluate the impact of surgical versus non-surgical treatment strategies on survival outcomes in patients with LS-SCEC. Patients receiving surgical treatment, including surgery alone, neoadjuvant therapy followed by surgery, or surgery followed by adjuvant therapy, will be compared with patients receiving definitive non-surgical treatment, including chemoradiotherapy-based approaches. Clinical characteristics, treatment patterns, and survival outcomes will be retrospectively collected and analyzed. The primary endpoint is overall survival (OS). Secondary endpoints include progression-free survival (PFS) and treatment-related prognostic factors. Propensity score-based methods and multivariable survival analyses will be performed to reduce potential selection bias and evaluate the independent association between treatment strategy and prognosis. The study is expected to provide additional real-world evidence regarding the optimal management of LS-SCEC and help guide individualized treatment decision-making for this rare disease.

Interventions

None listed

Sponsors

yi shen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients pathologically diagnosed with primary small cell esophageal carcinoma (SCEC). * Patients classified as having limited-stage disease at initial diagnosis, defined as tumor confined to the esophagus and/or regional lymph nodes without evidence of distant metastasis. * Patients who received definitive treatment at the study institution, including surgical treatment (with or without neoadjuvant or adjuvant therapy) or definitive non-surgical treatment such as chemoradiotherapy-based therapy. * Patients with complete baseline clinicopathological and treatment information available in the medical records. * Patients with available follow-up and survival outcome data.

Exclusion criteria

* Patients with extensive-stage disease or distant metastasis at diagnosis. * Patients with mixed histological subtypes in which small cell carcinoma was not the predominant component. * Patients who received palliative treatment only. * Patients with a history of other active malignant tumors within the previous 5 years. * Patients with incomplete key clinical, treatment, or follow-up data. * Patients under 18 years old.

Design outcomes

Primary

MeasureTime frame
Overall SurvivalFrom the date of diagnosis until death from any cause or last follow-up, assessed up to 5 years.

Secondary

MeasureTime frame
progression-free survivalFrom the date of diagnosis until disease progression, death from any cause, or last follow-up, assessed up to 5 years.

Countries

China

Contacts

CONTACTYi Shen, MD
dryishen@nju.edu.cn+8613913907880
CONTACTZhuangzhuang Cong, PhD
czz061231007@126.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 7, 2026