跳至主要内容
临床试验/NCT07063901
NCT07063901招募中不适用

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

Central South University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2025年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
1
主要终点
pCR

研究概览

简要总结

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?

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

研究组 & 干预措施

group 2: Non-pCR

group 2: Non-Pathological Complete Response

group 1: pCR

group 1: Pathologic Complete Response

group 3: Non-Favorable Responses

group 3: SD/PD

group 4: Favorable Response

group 4: Non-SD/PD

结局指标

主要结局

pCR

时间窗: From enrollment to the end of surgery

Pathologic Complete Response

pCR

时间窗: From enrollment to the end of surgery

Pathologic Complete Response

次要结局

  • Non-Favorable Responses(From enrollment to the end of surgery)
  • Non-Favorable Responses(From enrollment to the end of surgery)

研究者

发起方
Central South University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Chen Chen

Associate Professor

Central South University

研究点 (1)

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