A Study to Explore Prognoses of the Patients With N2 Non-small Cell Lung Cancer

NCT ID: NCT03451526

Last Updated: 2018-05-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

2929 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-12-01

Study Completion Date

2018-03-30

Brief Summary

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The trial was designed to compare the effectiveness of radical resections of lung cancer plus adjuvant chemotherapies and perioperative chemotherapies in the patients with N2 non-small cell lung cancer

Detailed Description

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The trial is a multi-centre real-world non-interventional observational study. The Chinese patients with N2 non-small cell lung cancer enrolled from 2014 to 2017 who received radical resections of lung cancer and adjuvant chemotherapies will be included in the study and the study data on patient demographic/tumor biological characteristics and clinical treatment will be collected to evaluate compare effectiveness of radical resection of lung cancer plus adjuvant chemotherapies and perioperative chemotherapies after surgeries.

Conditions

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Non-small Cell Lung Cancer

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Surgeries+adjuvant chemotherapies

Patients who received radical resection of lung cancer + adjuvant chemotherapies

Surgeries

Intervention Type PROCEDURE

Surgeries plus adjuvant chemotherapies or perioperative chemotherapies

Perioperative chemotherapies

Patients who received perioperative chemotherapies

Surgeries

Intervention Type PROCEDURE

Surgeries plus adjuvant chemotherapies or perioperative chemotherapies

Interventions

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Surgeries

Surgeries plus adjuvant chemotherapies or perioperative chemotherapies

Intervention Type PROCEDURE

Other Intervention Names

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Adjuvant chemotherapies or perioperative chemotherapies

Eligibility Criteria

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Inclusion Criteria

* Patients with radical resection of lung cancer enrolled from 2014 to 2019;
* Pathologically diagnosed patients with non-small cell lung cancer;
* Patients with age \> 18 years old;
* Patients who did not receive chest surgeries before hospitalization;
* Patients with N2 lymph nodes (+) after surgeries;
* Patients who received lymphadenectomy for one group or more groups of lymph nodes;

Exclusion Criteria

* Patients with second primary tumors or multiple primary tumors;
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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LinkDoc Technology (Beijing) Co. Ltd.

INDUSTRY

Sponsor Role collaborator

Tang-Du Hospital

OTHER

Sponsor Role lead

Responsible Party

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lixiaofei

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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China-Japan Friendship Hospital

Beijing, Beijing Municipality, China

Site Status

China PLA General Hospital

Beijing, Beijing Municipality, China

Site Status

Henan cancer hospital

Zhengzhou, Henan, China

Site Status

Tongji Hospital Affiliated to Huazhong Technology Hospital

Wuhan, Hubei, China

Site Status

Jiangsu cancer hospital

Nanjing, Jiangsu, China

Site Status

Xi'an Tangdu Hospital

Xi'an, Shaanxi, China

Site Status

Shanghai Chest Hospital

Shanghai, Shanghai Municipality, China

Site Status

Huaxi Hospital Affiliated to Sichuan University

Chengdu, Sichuan, China

Site Status

Tianjin Chest Hospital

Tianjin, Tianjin Municipality, China

Site Status

First Hospital Affiliated to Zhejiang University

Hangzhou, Zhejiang, China

Site Status

Countries

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China

Other Identifiers

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W-TONG04

Identifier Type: -

Identifier Source: org_study_id

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