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A Retrospective Clinical Study Exploring Prognostic Factors in Esophageal Cancer Patients

A Retrospective Clinical Study Exploring Prognostic Factors in Esophageal Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06960889
Enrollment
500
Registered
2025-05-07
Start date
2025-04-15
Completion date
2026-06-30
Last updated
2025-05-07

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

Conditions

Esophageal Cancer (EsC)

Keywords

Prognostic factors, Treatment strategies, Efficacy comparison, Esophageal cancer

Brief summary

This single-center, retrospective, 7-year observational study aims to investigate prognostic factors in esophageal cancer patients. Adults (≥18 years) with histologically confirmed esophageal cancer who received antitumor therapy between January 2017 and December 2024 were consecutively enrolled. Patient-level data (clinical characteristics, routine laboratory tests, tumor information, and treatment details) were retrospectively collected from electronic medical records to analyze key factors influencing treatment efficacy.

Interventions

OTHERradiotherapy

Definitive radiotherapy or radiotherapy-based combined modality therapy

DRUGImmunotherapy

Immune checkpoint inhibitors as monotherapy or in combination with other therapies

Sponsors

Nanfang Hospital, Southern Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Waiver of informed consent for deceased or lost-to-follow-up patients (January 2017-March 2024) 2. Voluntary signed informed consent from surviving patients who could be contacted 3. Treatment at Nanfang Hospital, Southern Medical University (January 2017-December 2024) 4. Received antitumor therapy for esophageal cancer 5. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2

Exclusion criteria

1. Concurrent other malignancies 2. Patients deemed ineligible by investigators

Design outcomes

Primary

MeasureTime frameDescription
Overall Survival (OS)From the date of treatment initiation to the date of death from any cause,assessed up to 120 months.The length of time from the start of treatment until death from any cause, evaluating the long-term survival benefit of the combined therapy.

Secondary

MeasureTime frameDescription
Pathologic Complete Response ( pCR )PerioperativeThe absence of residual viable tumor cells in both the primary esophageal tumor and regional lymph nodes after completion of surgery, indicating a complete pathological response.
Major Pathological Response Rate (MPR)PerioperativeThe proportion of patients with ≤10% residual viable tumor cells in resected specimens
Progression-Free Survival (PFS)From treatment initiation to disease progression or death, assessed up to 100 monthsThe duration from treatment start until radiologically confirmed disease progression (per RECIST v1.1) or death from any cause, evaluating therapeutic efficacy in delaying tumor growth.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026