Actively Recruiting

Age: 18Years - 85Years
All Genders
NCT06317558

Real-world Clinical Outcomes of NSCLC Patients Receiving Neoadjuvant Immunotherapy

Led by Cancer Institute and Hospital, Chinese Academy of Medical Sciences · Updated on 2024-07-03

4000

Participants Needed

1

Research Sites

565 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this observational study is to evaluate the efficacy and long-term clinical outcomes of different neoadjuvant immunotherapies in non-small cell lung cancer (NSCLC) patients using the real-world data. The main questions it aims to answer are: * What the best setting for immune checkpoint inhibitors as the neoadjuvant treatment? * How to determine the subgroups of patients benefit from neoadjuvant immunotherapy? Participants will receive neoadjuvant immunotherapy the study will analyze the real-world data.

CONDITIONS

Official Title

Real-world Clinical Outcomes of NSCLC Patients Receiving Neoadjuvant Immunotherapy

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histological diagnosis of non-small cell lung cancer (Stage I-IV, International Association for the Study of Lung Cancer staging eighth edition)
  • Patients who have previously undergone immune checkpoint inhibitors as the neoadjuvant treatment
  • No previous history of malignant tumors and other malignant tumors at the same time, without any anti-tumor treatment
  • Eastern Cooperative Oncology Group (ECOG) score 0-1, heart, lung, liver, brain and kidney function can tolerate surgery
  • At least one measurable lesion (RECIST v1.1)
Not Eligible

You will not qualify if you...

  • Patients included in unblinded clinical trials or anti-tumor drug intervention
  • Radiotherapy or systemic therapy were used for NSCLC patients before the surgery

AI-Screening

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Trial Site Locations

Total: 1 location

1

Shugeng Gao

Beijing, Beijing Municipality, China, 100020

Actively Recruiting

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Research Team

S

Shugeng Gao, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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