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Recruiting NCT07166003

NCT07166003 Efficacy of Neoadjuvant Immunotherapy in Patients With Lung Cancer

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Clinical Trial Summary
NCT ID NCT07166003
Status Recruiting
Phase
Sponsor Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Condition Lung Cancer, Non-Small Cell
Study Type OBSERVATIONAL
Enrollment 500 participants
Start Date 2025-04-20
Primary Completion 2027-02-02

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 79 Years
Study Type OBSERVATIONAL
Interventions
Pneumonectomylobectomyradiotherapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 500 participants in total. It began in 2025-04-20 with a primary completion date of 2027-02-02.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this observational study is to learn about the long-term effects of neoadjuvant immunotherapy in patients with lung cancer. The main questions it aims to answer are: * Does pneumonectomy bring more benefits for pateints than lobectomy? * Does surgery bring more benefits for patients than non-surgery modalities (such as radiotherapy) after neoadjuvnat immunotherapy? Participants will receive neoadjuvant treatment and the study will analyze the data.

Eligibility Criteria

Inclusion Criteria: 1. Aged between 18 and 79 years; 2. Received at least two cycles of neoadjuvant immunotherapy; 3. ECOG performance status score of 0; 4. Complete clinical information including imaging data available. Exclusion Criteria: 1. Diagnosed with or suspected active autoimmune diseases; 2. Presence of EGFR/ALK sensitive mutations; 3. Pregnant or breastfeeding women; 4. Previous anti-tumor therapies including chemotherapy or radiotherapy; 5. History of organ transplantation or hematopoietic stem cell transplantation; 6. Interstitial pneumonia, pulmonary fibrosis, or severe emphysema; 7. Uncontrolled diabetes mellitus; 8. Uncontrolled hypertension.

Contact & Investigator

Central Contact

Shugeng Gao, MD

✉ gaoshugeng@cicams.ac.cn

📞 8610-87788177

Frequently Asked Questions

Who can join the NCT07166003 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 79 Years, studying Lung Cancer, Non-Small Cell. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07166003 currently recruiting?

Yes, NCT07166003 is actively recruiting participants. Contact the research team at gaoshugeng@cicams.ac.cn for enrollment information.

Where is the NCT07166003 trial being conducted?

This trial is being conducted at Beijing, China.

Who is sponsoring the NCT07166003 clinical trial?

NCT07166003 is sponsored by Cancer Institute and Hospital, Chinese Academy of Medical Sciences. The trial plans to enroll 500 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology