Predicting early relapse in lung cancer patients after surgery

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 clinical trial aims to develop a combined relapse prediction model for patients with resectable non-small cell lung cancer who have undergone tumor resection. The study focuses on identifying patients at risk of early relapse by analyzing circulating tumor cells (CTCs) and their behavior post-surgery. By monitoring changes in CTC levels within the first three days after surgery, the trial seeks to improve early detection of potential relapses, which could lead to better patient management and outcomes. The intervention involves administering cisplatin-based chemotherapy to eligible participants.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Patients who presented with resectable disease ( Clinical stage 1a to 3a)
2. Patients who received tumor resection

Exclusion Criteria:

1. Pathologic stage greater than stage 3b or 4
2. Pathologic stage less than stage 1a1
3. Could not complete treatment course
4. Could not receive blood sampling for CTC (circulating tumor cell) or regular surveillance

Where it's running

• Ching-Yang Wu
  Taoyuan City, Taiwan Recruiting

Study contacts

• Principal investigator: Ching-Yang Wu — Chang Gung Memorial Hospital
• Study coordinator: Ching-Yang Wu
• Email: wu.chingyang@gmail.com
• Phone: +886975368204

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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.