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Development and Application of AI-Based Therapeutic Strategies for Esophageal Cancer Integrating Multimodal Imaging and Digital Pathology

Development and Application of AI-Based Therapeutic Strategies for Esophageal Cancer Integrating Multimodal Imaging and Digital Pathology

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07203690
Enrollment
7000
Registered
2025-10-02
Start date
2025-12-01
Completion date
2027-12-01
Last updated
2025-10-02

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

Conditions

Esophageal Cancer, Neoadjuvant Therapy

Brief summary

The purpose of this clinical study is to conduct a multi-center, big data study to create a neural network decision model for predicting treatment efficacy and prognosis based on multi-modal, multi-temporal imaging features combined with tumor microenvironment scores. It will also use various model interpretation techniques to clarify the role and mechanism of key biomarkers or strongly associated biomarker groups in treatment efficacy and prognosis. Ultimately, it aims to achieve the research and application of AI treatment strategies combining multi-modal imaging and digital pathology to guide clinicians in the personalized treatment strategies for patients with esophageal squamous cell carcinoma.

Interventions

None listed

Sponsors

Xinyang Central Hospital
CollaboratorOTHER
Guangdong Provincial People's Hospital
CollaboratorOTHER
Henan Cancer Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. Aged 18-70 years; 2. Histologically confirmed esophageal carcinoma by biopsy; 3. No prior antitumor therapy received.

Exclusion criteria

1. Contraindications to MRI examination; 2. Poor compliance with antitumor therapy; 3. Unwillingness to participate in the study; 4. Image quality inadequate for diagnostic requirements.

Design outcomes

Primary

MeasureTime frameDescription
Pathological Complete Response (pCR) RateJanuary 2025 - December 2027The proportion of patients achieving pathological complete response (ypT0 ypN0) after neoadjuvant therapy.
Overall Survival (OS)January 2025 - December 2027The time from treatment initiation to death from any cause.
Event-Free Survival (EFS)January 2025 - December 2027The time from treatment initiation to disease progression, recurrence, new primary cancer, or death.
Disease-Free Survival (DFS)January 2025 - December 2027The time from curative-intent surgery to disease recurrence or death.

Contacts

Primary ContactJinrong Qu
qjryq@126.com(86) 0371-65587595

Outcome results

None listed

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