Exploring neoadjuvant therapy for lung cancer

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to evaluate the effectiveness of various neoadjuvant therapies, including chemotherapy, immunotherapy, and targeted therapy, in patients with lung cancer. It focuses on understanding how different patient characteristics influence treatment outcomes and the long-term survival rates associated with these therapies. By analyzing real-world clinical data, the study seeks to identify the strengths and weaknesses of different neoadjuvant regimens in improving surgical resection rates and overall therapeutic effects.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Age greater than or equal to 18 years;
2. Pathohistologically confirmed diagnosis of non-small cell lung cancer or small cell lung cancer;
3. Received neoadjuvant therapy after diagnosis;
4. Written informed consent.

Exclusion Criteria:

1. Patients enrolled in other clinical trials;
2. Patients refused enrollment in this study;
3. Patients refused follow-up.

Where it's running

• Shanghai Pulmonary Hospital
  Shanghai, Shanghai Municipality, China Recruiting

Study contacts

• Principal investigator: Peng Zhang, Ph.D. — Shanghai Pulmonary Hospital, Shanghai, China
• Study coordinator: Peng Zhang, Ph.D.
• Email: zhangpeng1121@tongji.edu.cn
• Phone: 021-55672180

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.