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临床试验/NCT06596954
NCT06596954招募中不适用

Lymphocyte-sparing Thoracic Radiotherapy vs Conventional Radiotherapy for Esophageal Squamous Cell Carcinoma Treated With Neoadjuvant Therapy: an Open Label, Randomized Controlled Trial

Ruijin Hospital2 个研究点 分布在 1 个国家目标入组 212 人开始时间: 2024年6月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
212
试验地点
2
主要终点
acute grade 3/4 lymphopenia

研究概览

简要总结

Esophageal squamous cell carcinoma (ESCC) is one of the most aggressive malignant tumors. Although neoadjuvant chemoradiotherapy combined with surgery has significantly improved the survival rate of patients with locally advanced esophageal cancer, approximately half of the patients will experience local regional recurrence or distant metastasis. Lymphocytes are crucial immune cells in the human body, playing a key role in combating infections and tumor development. In recent years, an increasing body of research has indicated that lymphocyte depletion is a significant factor associated with poor prognosis in various solid tumors, including esophageal cancer. The lymphocyte depletion caused by radiotherapy has garnered considerable attention from oncologists. However, there is still a lack of prospective clinical research data on lymphocyte protection in thoracic tumors. Therefore, this study aims to provide high-level evidence from evidence-based medicine regarding the correlation between lymphocyte depletion and prognosis in esophageal cancer patients, offering more effective strategies and methods to improve the outcomes of neoadjuvant chemoradiotherapy for esophageal cancer.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients are able to understand and are willing to participate in the trial, and a signed consent form can be obtained;
  • •Pathologically confirmed esophageal squamous cell carcinoma;
  • •locally advanced ESCC (cT3-4 or N+);
  • •the age of patients should be more than 18 years, and less than 80 years;
  • •aged between 18 and 80 years;
  • •KPS score of patients should be more than 80

排除标准

  • •diagnosis of metastatic esophageal cancer;
  • •Patient refuses to receive systemic drug treatment;
  • •clinical diagnosis of pleural metastasis or malignant pleural effusion;
  • •Pregnant or breastfeeding women;
  • •Severe non-cancerous medical comorbidities that affect the implementation of radiotherapy.

研究组 & 干预措施

conventional radiotherapy

Active Comparator

ensure coverage of the PTV (Planning Target Volume) and limit the doses to the heart, bilateral lungs, and spinal cord to meet the required dose constraints. do not limits the dose for lymphocyte-related organs

lymphocyte-sparing radiotherapy

Experimental

Firstly, ensure coverage of the PTV (Planning Target Volume). Secondly, limit the doses to the heart, bilateral lungs, and spinal cord to meet the required dose constraints. While maintaining target coverage and traditional OAR (Organs At Risk) dose constraints, also address dose limits for the TVB1-12 thoracic vertebral bodies, ribs, spleen, and major thoracic blood vessels to protect the lymphocyte

结局指标

主要结局

acute grade 3/4 lymphopenia

时间窗: 1 months after surgery

from treatment to 1 months after completion of neoadjuvant chemoradiotherapy

次要结局

  • recurrence-free survival(2 year)
  • Overall survival(3 years)
  • recurrence-free survival(2 year)
  • Lymphocyte-sparing radiotherapy plan pass rate in lymphocyte-sparing group(within 1 week after completion of neoadjuvat radiotherapy plan;)
  • Incidence of grade 3 or higher hematologic toxicity(from neoadjuvant chemoradiotherapy to 1 monther after completion of neoadjuvant chemoradiotherapy)
  • Pathological complete response rate (pCR)(1 months after surgery)
  • R0 resection rate(1 month after surgery)
  • Postoperative complications(1 month after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

QIWEIXIANG

Deputy Chief Physician

Ruijin Hospital

研究点 (2)

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