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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05979623
Other study ID # B2021-128
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date December 2022

Study information

Verified date July 2023
Source Shanghai Zhongshan Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observation study is to learn about clinicopathological characteristics and prognostic factors of stage IB NSCLC. The main question it aims to answer is wheather there is relationship between newly proposed clinicopathological features and the prognosis of stage IB NSCLC .The postoperative pathological and follow-up information of participants will be used for subsequent analysis.


Description:

A total of 971 NSCLC patients with pathological stage IB resected by surgery (R0) from January 2016 to December 2020 at Zhongshan Hospital of Fudan University were reviewed. The primary endpoint is RFS (recurrence-free survival) and OS (overall survival) is the secondary endpoint. The baseline characteristics of the patients were obtained statistically, and factors affecting the prognosis of patients with stage IB NSCLC were analyzed using survival analysis and Cox proportional hazard models. The characteristics of the patients include pathological type, STAS, GGO, gene mutation, and postoperative adjuvant chemotherapy.


Recruitment information / eligibility

Status Completed
Enrollment 971
Est. completion date December 2022
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - It was confirmed by histopathology as primary non-small cell lung cancer, and the pathological type was LUSC or LUAD; - According to the 8th edition of TNM clinical staging standards, it is determined as IB stage - No treatment was performed for the primary lesion of lung cancer before surgery; - No history of other malignant tumors before surgery; - Detailed clinical and pathological information, complete survival data, and no missing follow-up data. Exclusion Criteria: - The postoperative histopathological types include non-scale and non adenocarcinoma, such as lung adenosquamous cell carcinoma, large cell lung cancer, or lung sarcomatoid carcinoma; - Multiple lesion staging surgery; - History of merging with other malignant tumors - Having preoperative treatment; - Missing follow-up information.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China 180 Fenglin Road Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary RFS recurrence-free survival 5 years
Secondary OS overall survival 5 years
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