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CompletedNCT03216551Updated Jul 20, 2023

Mediastinal Staging Accuracy of a Selective Lymphadenectomy Strategy in Early Stage NSCLC (ECTOP-1003)

An observational study in Lymph Node Metastases and Non-small Cell Lung Cancer Stage I, sponsored by Fudan University. Completed at 1 site in China. Per ClinicalTrials.gov, last updated 2023-07-20.

Sponsored by Fudan University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,076
Sex
All
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Study summary

This is a clinical trial from Eastern Cooperative Thoracic Oncology Project (ECTOP), numbered as ECTOP-1003. Systemic mediastinal lymphadenectomy is deemed indispensable in lung cancer surgery for accurate staging and complete resection. However, extensive lymphadenectomy in patients without nodal metastasis may not improve survival and would increase operative duration and cause damage to mediastinal structures.Therefore the precise selection of patients without mediastinal nodal metastasis is the key to avoid unnecessary lymphadenectomy.The investigator's previous retrospective study shows tumor location, ground glass opacity component and histological subtypes are important predictors of negative nodal status in specific mediastinal regions. The current prospective observational study is to further verify the mediastinal staging accuracy of this selective lymphadenectomy strategy.

Read the detailed description

Background:

Complete lung cancer lymphadenectomy in patients without nodal metastasis may not improve survival and would increase operative duration and cause damage to mediastinal structures.The investigator's previous retrospective study of 2749 invasive NSCLC patients showed none of the 151 tumors with consolidation tumor ratios ≤ 0.5 had N2 disease. Tumors with lepidic predominant adenocarcinoma (LPA) histology had zero mediastinal nodal involvement. Tumors in the apical segment of upper lobes had zero inferior mediastinal nodal (IMLN) involvement. Only seven out of 740 (0.9%) peripheral upper lobe tumors had IMLN metastasis. Interestingly, all these seven tumors showed visceral pleural invasion. Among patients with left lower lobe tumors, if hilar nodes were negative, station 4L lymph node metastasis was not found in superior and basal segment tumors, and station 5/6 lymph node involvement was always absent in basal segment tumors.

The current prospective, multi-center, observational study is to verify the staging accuracy of a selective mediastinal lymphadenectomy strategy based on tumor location, ground glass opacity component and intraoperative histological subtyping by frozen section in patients with peripheral clinical T1N0M0 invasive non-small cell lung cancer.

Objectives:

Primary: To determine the mediastinal staging accuracy of the selective mediastinal lymphadenectomy strategy.

Secondary:

  1. To determine the diagnostic accuracy of intraoperative adenocarcinoma histologic subtyping, N1 nodes metastasis and visceral pleural invasion by frozen section.
  2. To determine the mediastinal lymph node metastasis rate in peripheral clinical T1N0M0 lung cancer with different histologic subtypes.
  3. To evaluate the pattern of mediastinal nodal involvement of tumors in different lung segments.
  4. To determine the mediastinal nodal status of tumors with different radiological features (pure ground glass opacity, mixed ground glass opacity and solid nodules).

Outlines:

  1. All recruited patients will undergo systematic mediastinal lymph node dissection (lung resection can be segmentectomy, lobectomy, bilobectomy or pneumonectomy). For tumors in the left lungs, removal of mediastinal nodal stations 4, 5,6,7 and 8 are required. For tumors in the right lungs, removal of mediastinal nodal stations 2,4,7 and 8 are required. For lower lobe tumors, station 9 should also be removed. Stations 10/11/12 should routinely be dissected.
  2. Stations 10/11 are subclassified as follows: Station 10a (the anterior region of the pulmonary veins), Station 10s (between azygos vein and the right upper lobe bronchus), Station 10p (in the posterior region of the right main bronchus for right-side tumors or between left main pulmonary artery and left main bronchus for left-side tumors), Station 11s (between right upper lobe bronchus and the intermediate bronchus), and Station 11i (between right middle lobe bronchus and right lower lobe bronchus).
  3. Intraoperative frozen section analysis should determine whether the tumor is lepidic predominant adenocarcinoma, whether there are N1 nodes involvement (lymph nodes adjacent to the tumor should be sent to intraoperative frozen section), and whether there is viceral pleural invasion. However, intraoperative frozen section results will not affect the surgical predure. Every patient will receive systematic lymph node dissection.
  4. By the assumed selective lymph node dissection strategy, patients with consolidation tumor ratios ≤ 0.5 tumors will be considered to have negative mediastinal metastasis. Patients with intraoperative LPA diagnosis will be considered to have negative mediastinal metastasis. Patients with an apical tumor will be considered to have negative IMLN metastasis. If both N1 nodes and visceral pleural invasion are negative, patients with peripheral non-apical-segment upper lobe tumors will be considered to have negative IMLN metastasis. If N1 nodes are negative, patients with left superior segment tumors will be considered to have negative 4L lymph node metastasis, and patients with left basal segment tumors will be considered to have negative superior mediastinal lymph node metastasis. The virtual mediastinal staging results of this selective lymph node dissection strategy will then be compared with the final staging results by the complete lymphadenectomy.
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Conditions studied

  • Lymph Node Metastases
  • Non-small Cell Lung Cancer Stage I

Keywords

  • selective mediastinal lymphadenectomy
  • minimally invasive surgery
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In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's enrollment of 1,076 is above the median of 189 across 1,514 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Fudan University is the lead sponsor of 1,270 studies on the registry; 623 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with peripheral clinical stage T1N0M0 who intended to be treated by radical surgery.

Inclusion criteria

  • Informed consent must be signed
  • Peripheral clinical stage T1N0M0
  • Invasive non-small cell lung cancer as determined preoperatively or intraoperatively, excluding AIS/MIA
  • Can be completely resected
  • If there are multiple nodules, except the predominant nodule, other nodules should be pure GGO

Exclusion criteria

Exclusion Criteria:

  • Previous malignancy or lung surgery
  • Previous induction therapy for the disease
  • Intolerable to the surgery
  • Incomplete mediastinal lymph node dissection or lymph node sampling
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,076 participants (actual)
Patient registry
No

Groups and cohorts

  • The assumed selective lymph node dissection group

    Patients with consolidation tumor ratios ≤ 0.5 tumors will be considered to have negative mediastinal metastasis. Patients with intraoperative lepidic predominant adenocarcinoma diagnosis will be considered to have negative mediastinal metastasis. Patients with an apical tumor will be considered to have negative inferior mediastinal lymph node metastasis. If both N1 nodes and visceral pleural invasion are negative, patients with peripheral non-apical-segment upper lobe tumors will be considered to have negative inferior medistinal lymph node metastasis. If N1 nodes are negative, patients with left superior segment tumors will be considered to have negative 4L lymph node metasis, and patients with left basal segment tumors will be considered to have negative superior mediastinal lymph node metastasis.

    Diagnostic Test: Intra-operative frozen section

Interventions

  • Diagnostic testIntra-operative frozen section

    Tumor histologic subtypes (whether it is lepidic predominant adenocarcinoma), N1 nodes metastasis (lymph nodes adjacent to the tumor will be sent to frozen section) and visceral pleural invasion will be determined by the intra-operative frozen section.

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What researchers measure

Primary outcomes

  1. Mediastinal staging accuracy of the assumed selective lymph node dissection strategy

    To compare the mediastinal staging results by the assumed selective lymph node dissection strategy and the final staging results by systematic lymph node dissection.

    Time frame: 2-3 weeks after the surgery until the final pathology results are reported.

Secondary outcomes

  1. The accuracy of determining lepidic predominant adenocarcinoma, N1 nodes metastasis and viceral pleural invasion by frozen section

    The concordance rate of intraoperative histologic subtypes, N1 node metastasis and visceral pleural invasion compared to the final pathology.

    Time frame: 2-3 weeks after the surgery until the final pathology results are reported.

  2. The nodal metastasis pattern of tumors in different lung segments.

    The mediastinal nodal metastasis pattern of tumors in different lung segments.

    Time frame: 2-3 weeks after the surgery until the final pathology results are reported.

  3. The nodal status of tumors with various CT appearance

    The nodal status of tumors with CT appearance of pure ground glass opacity, sub-solid and solid nodules.

    Time frame: 2-3 weeks after the surgery until the final pathology results are reported.

  4. The lymph node metastasis rate of different histologic subytpes.

    The lymph node metastasis rate of different adenocarcinoma subytypes, squmous cell carcinoma, etc.

    Time frame: 2-3 weeks after the surgery until the final pathology results are reported.

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Study locations

1 site
  • Fudan University Shanghai Cancer Center
    Shanghai, China
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 20, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03216551
Lead sponsor
Fudan University
Responsible party
Haiquan Chen (Professor, Fudan University) — Principal investigator
First posted
Jul 13, 2017
Start date
Mar 14, 2019
Primary completion
May 30, 2022
Completion
May 30, 2022
Last update
Jul 20, 2023

Study contacts

Haiquan Chen, MD,PhD
study director · Fudan University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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