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临床试验/NCT04945928
NCT04945928进行中(未招募)不适用

Safety and Feasibility of Surgery After Conversion Therapy for Locally Advanced and Advanced NSCLC

Ruijin Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2021年8月27日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
30
试验地点
1
主要终点
perioperative morbidity

研究概览

简要总结

Lung cancer is one of the most common malignant tumors worldwide and the mortality ranks first in the world. In recent years, with the development of targeted therapy and immunotherapy, the overall survival of lung cancer patients has improved significantly. However, the inoperable advanced tumor remains the main reason for the poor prognosis of lung cancer. Thus, we aim to carry out this single-arm, prospective study to evaluate the safety and feasibility of surgery after conversion therapy for locally advanced and advanced non-small cell lung cancer.

详细描述

Previous studies have shown that selective surgery after conversion therapy is feasible and safe in locally advanced or stage IV patients, and indicates potential benefits for these patients. However, surgery after conversion therapy is difficult and has high risk of postoperative complications which requires strict operation indications and patient screening. At present, there are only relevant retrospective studies and no prospective evidence. Therefore, our team plans to carry out this single-arm prospective clinical trial to evaluate the safety and feasibility of surgery in patients with locally advanced and advanced non-small cell lung cancer after conversion therapy, so as to lay the foundation for further research and clinical application.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Volunteer to participate in the study with good compliance. Able to complete the observation and follow-up and have signed the informed consent;
  • More than 18 years old with no limit of sex;
  • Pathologically confirmed stage T4N0-3 or T1-3N2-3 NSCLC with residual tumor after first-line treatment (first-line chemotherapy, targeted therapy, immunotherapy, chemotherapy combined with immunotherapy, etc.) evaluated operable for radical resection; pathologically confirmed stage IVA NSCLC evaluated operable after first-line treatment (first-line chemotherapy, targeted therapy, immunotherapy, chemotherapy combined with immunotherapy, etc.);
  • ASA score: I-III;
  • Cardiopulmonary functions meet the requirements of radical operation for lung cancer with normal liver and kidney functions.

排除标准

  • Serious heart, lung, liver and kidney dysfunction and unable to tolerate the operation;
  • Neurologic, mental illness or mental disorder which is hard to control, poor compliance, unable to cooperate or describe the treatment response;
  • Unable to receive radical resection;
  • Need of palliative or emergency operation due to lung abscess or hemoptysis;
  • Having received neoadjuvant chemoradiotherapy.

结局指标

主要结局

perioperative morbidity

时间窗: postoperative in-hospital stay up to 30 days

rate of perioperative complications, mainly include: pneumonia, arrhythmia, incision infection, vocal cord paralysis, trachea cannula

次要结局

  • lymph nodes counts(At operation day)
  • 1-year overall survival (OS)(1 year after surgery)
  • 3-year overall survival (OS)(3 year after surgery)
  • R0 rate(postoperative in-hospital stay up to 30 days)
  • operative complications(At operation day)
  • postoperative hospital stay(postoperative in-hospital stay up to 30 days)
  • 30-day mortality(postoperative in-hospital stay up to 30 days)
  • operation time(At operation day)
  • blood loss(At operation day)
  • 3-year disease-free survival (DFS)(3 year after surgery)
  • 1-year disease-free survival (DFS)(1 year after surgery)

研究者

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

Hecheng Li M.D., Ph.D

Professor

Ruijin Hospital

研究点 (1)

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