Multimodal Deep Learning for Predicting Treatment Response to Neoadjuvant Chemoimmunotherapy in Esophageal Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorCentral South University

About this trial

This observational study aims to investigate a clinical cohort of patients with locally advanced esophageal cancer undergoing neoadjuvant chemoimmunotherapy. By integrating multimodal clinical data-including demographic characteristics, medical history, imaging studies, pathological findings, and laboratory tests-and employing deep learning algorithms, the study seeks to develop predictive models for the early and accurate assessment of treatment response prior to surgery. Specifically, this study focuses on addressing the following key scientific questions:

1. Can multimodal clinical data be used to construct an accurate model for predicting pathological complete response (pCR) following neoadjuvant therapy? 2. Can deep learning models enable early identification of patients with suboptimal response to neoadjuvant therapy, defined as stable disease (SD) or progressive disease (PD), before surgery?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with histologically confirmed esophageal cancer based on biopsy results;

Patients recommended for neoadjuvant chemoimmunotherapy following multidisciplinary team (MDT) discussion or evaluation by thoracic surgery specialists;

Patients who received neoadjuvant chemoimmunotherapy;

Patients with complete imaging data before and after neoadjuvant treatment.

Disqualifiers

Patients deemed eligible for surgery by the thoracic surgery team but who refused surgical treatment;

Patients with missing or poor-quality CT images;

Patients with concurrent malignancies other than esophageal cancer;

Patients with incomplete clinical data.

Trial population

Patients with esophageal cancer who received neoadjuvant therapy at the Second Xiangya Hospital of Central South University

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

200 Participants
are grouped into 4 trial groups
Group A: group 1: pCR
Group B: group 2: Non-pCR
Group C: group 3: Non-Favorable Responses
Group D: group 4: Favorable Response

Trial outcomes

Primary outcomes

1

pCR

Pathologic Complete Response

Time frame
From enrollment to the end of surgery

Secondary outcomes

1

Non-Favorable Responses

stable disease/progressive disease

Time frame
From enrollment to the end of surgery

Other outcomes

Sponsors and contacts

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