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临床试验/NCT02014324
NCT02014324已完成不适用

Complete Endosonographic Staging of Lung Cancer: a Systematic Single Scope Approach

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)9 个研究点 分布在 2 个国家目标入组 215 人开始时间: 2013年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
215
试验地点
9
主要终点
Sensitivity for locoregional disease (N2, N3, T4 disease).

研究概览

简要总结

Rationale: Lung cancer is the most commonly diagnosed cancer worldwide and is the most frequent cause of cancer death. Accurate staging is important because it directs treatment and prognosis. Mediastinal staging can be done by both EBUS-TBNA and EUS-FNA. These two techniques have a complementary diagnostic range and the combined procedure is suited for assessment of almost the entire mediastinum. In practice, when mediastinal tissue staging is indicated, endoscopists often perform either an EBUS or an EUS investigation (instead of the combined procedure). Second, frequently only one or two, by imaging suspected lymph node stations, are sampled (ie. targeted approach).

Objectives: main and secondary:

  1. Complete endosonographic (combined endobronchial and esophageal) staging using a single EBUS scope improves locoregional staging (N2, N3, T4) versus EBUS staging alone.
  2. Systematic mediastinal staging results in improved locoregional staging compared to PET-CT directed assessment of the mediastinum (ie targeted approach).

Study population: Patients with potentially operable and resectable NSCLC are eligible if there is an indication for mediastinal nodal sampling. Patients have an indication for EBUS-TBNA.

Intervention: Patients will undergo an EBUS investigation followed by EUS-B in the same session. During this single scope procedure, lymph nodes that are suspected on prior CT-PET imaging and on subsequent ultrasound are sampled.

Main study endpoint: The main study parameter is the sensitivity for locoregional disease (N2, N3, T4 disease) of complete endosonographic staging (by EBUS-TBNA and EUS-B-FNA) in comparison with EBUS staging alone.

研究设计

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

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

  • (Suspected) NSCLC;
  • Indication for mediastinal nodal assessment;
  • Suspected mediastinal lymph nodes within reach of EBUS;
  • Age 18 years or older;
  • Clinically fit to undergo surgical resection of the lung tumor;
  • Provision of a written informed consent;

排除标准

  • Mediastinal re-staging after neo-adjuvant treatment;
  • Indication for EUS other than mediastinal staging, eg a for malignancy
  • suspected left adrenal;
  • Active malignancy with a life expectancy of less than two years;
  • Former therapy for lung cancer (chemotherapy, radiotherapy or surgery);
  • Technical contraindication for EBUS or EUS (eg, esophagus stenosis);
  • Pregnancy;
  • Inability to consent;

结局指标

主要结局

Sensitivity for locoregional disease (N2, N3, T4 disease).

时间窗: from inclusion untill either pathological proof of mediastinal metastases by endospnography or 1 week after surgical verification

Sensitivity is defined as number of true positives (pathologic proof of a nodal metastases) divided by the number of true positives and false negatives (thoracotomy with nodal dissection is the reference standard to detect false negatives). The main study parameter is the sensitivity for locoregional disease (N2, N3, T4 disease) of complete endosonographic staging (by EBUS-TBNA and EUS-B-FNA) in comparison with EBUS staging alone. In the event of pathological proof of mediastinal metastases (N2/N3) by endosonography patients are classified as having locally advanced disease (stage III) and the study stops. When no mediastinal metastases are found by endosonography, surgical verification will take place (reference standard).

次要结局

  • Sensitivity for locally advanced disease (N2-3 metastases, T4). Systematic assessment and sampling of mediastinal lymph nodes versus PET-CT directed assessment of the mediastinum.(from inclusion untill either pathological proof of mediastinal metastases by endosonography or 1 week after surgical verification)

研究者

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

Prof J.T. Annema

MD PhD

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (9)

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