Neoadjuvant Chemoimmunotherapy in Stage IIIA- N2IIIB Non-small Cell Lung Cancer

NCT ID: NCT06394427

Last Updated: 2024-05-01

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

NOT_YET_RECRUITING

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-31

Study Completion Date

2025-08-31

Brief Summary

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to explore the impact of preoperative neoadjuvant immunotherapy on perioperative outcomes and long-term prognosis of locally advanced NSCLC in the real world

Detailed Description

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Conditions

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Non-small Cell Lung Cancer Stage ⅢA Non-small Cell Lung Cancer Stage IIIB

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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chemoimmunotherapy group 1

patients received different cycles of neoadjuvant chemoimmunotherapy

cycles of neoadjuvant therapy and duration of waiting for surgery

Intervention Type OTHER

We intended to explore the cycles of neoadjuvant therapy and duration of waiting for surgery on the perioperative outcomes and long-term prognosis of locally advanced NSCLC in the real world

chemoimmunotherapy group 2

the duration of before patients received surgery after neoadjuvant chemoimmunotherapy

cycles of neoadjuvant therapy and duration of waiting for surgery

Intervention Type OTHER

We intended to explore the cycles of neoadjuvant therapy and duration of waiting for surgery on the perioperative outcomes and long-term prognosis of locally advanced NSCLC in the real world

Interventions

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cycles of neoadjuvant therapy and duration of waiting for surgery

We intended to explore the cycles of neoadjuvant therapy and duration of waiting for surgery on the perioperative outcomes and long-term prognosis of locally advanced NSCLC in the real world

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Confirmed as primary lung cancer through cytology or histological examination;

* ECOG score of 0 or 1; ③ 18 years old or above;

* Received imaging examination, with a preliminary clinical staging of stage III;

* Received genetic testing and tested negative for EGFR mutations, ALK or ROS-1 fusion; ⑥ Accepting preoperative neoadjuvant immunotherapy combined with chemotherapy; ⑦ Receive surgical treatment after completion of neoadjuvant therapy; ⑧ The postoperative specimens were sent to the pathology department of our hospital for pathological testing, and a complete pathological report is available.

Exclusion Criteria

* Patients with combined small cell lung cancer; ② Patients with severe liver/kidney dysfunction, cardiovascular disease, or systemic immune disorders;

* Accept other neoadjuvant treatments; ④ Patients participating in any clinical trial.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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West China Hospital

OTHER

Sponsor Role lead

Responsible Party

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Pengfei Li

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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2024-674

Identifier Type: -

Identifier Source: org_study_id

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