Development and Clinical Validation of Early-stage Lung Cancer Prognostic Kit
Launched by CHUNG SHAN MEDICAL UNIVERSITY · Sep 23, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is focused on developing and testing a new tool to help predict the risk of recurrence in patients with early-stage lung cancer. Lung cancer is a serious disease, and even patients diagnosed at an early stage can face challenges, as some may experience a return of the cancer. Researchers have discovered specific markers in the tumors of patients that can help identify those who are at a higher risk for recurrence. The goal of this trial is to validate these markers and create two new kits: one for testing tumor samples and another for non-invasive blood tests.
To participate in this trial, individuals must be at least 20 years old and have been diagnosed with lung adenocarcinoma, a type of lung cancer. They should have had surgery to remove their tumors and be in good overall health. Participants will need to provide samples of their tumor tissue and possibly blood or other fluids for testing. Throughout the trial, they can expect to be closely monitored, and their health will be assessed regularly. This research is important as it aims to improve how we predict and manage lung cancer, ultimately helping to provide better care for patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Willing to sign and provide subject consent.
- • Male or female of age 20 or older.
- • Patients diagnosed with lung adenocarcinoma by tumor pathology.
- • Lung cancer with the pathological stage of IA/IB/II/IIIA according to the American Joint Committee on Cancer Staging Manual (8th Edition).
- • Complete tumor resection (R0 resection).
- • The East Coast Cancer Clinical Research Collaborative (ECOG) performance status was 0 or 1 at the time of grouping.
- • Those willing to provide tumor tissue or cytology specimens (including surgical specimens, tissue biopsy specimens, or cytology specimens), blood and body fluid specimens (for follow-up or disease recurrence, such as urine, malignant pleural effusion, ascites, pericardial fluid, etc.).
- Exclusion Criteria:
- • Not primary lung cancer patients.
- • Lung cancer patients whose pathological stage is not IA/IB/II/IIIA according to the American Joint Committee on Cancer Staging Manual (8th Edition) after surgery.
- • Patients with uncontrolled malignant tumors other than lung cancer.
- • Uncontrolled systemic disease (such as diabetes, hypertension, active infection, etc.) (determined by the principal investigator )
- • Pregnant women.
- • Any condition may put the patient at serious risk, may affect the interpretation of the trial results, or may seriously interfere with the patient's participation in the trial.
About Chung Shan Medical University
Chung Shan Medical University is a distinguished academic institution dedicated to advancing medical education, research, and healthcare services. As a clinical trial sponsor, the university leverages its expertise in medical sciences and innovative research methodologies to conduct rigorous and ethically sound clinical studies. With a commitment to enhancing patient care and contributing to the global body of medical knowledge, Chung Shan Medical University collaborates with healthcare professionals and research institutions to explore new therapeutic interventions and improve clinical outcomes. Through its comprehensive approach to research, the university plays a pivotal role in fostering advancements in medical science and public health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Taichung, , Taiwan
Taipei, , Taiwan
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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