Clinical trial · Observational
Liquid Biopsy in Advanced Oligometastatic NSCLC Receiving Surgery
NCT05648370CI-TRIAL-00062643unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
A prospective, observational study that assesses the clinical feasibility of ctDNA-based liquid biopsy in patients with oligometastatic NSCLC receiving surgery.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| Oligometastatic Disease | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ctDNA testing and whole exome sequencing | Genetic | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- oligometastatic disease
- description
- Dynamic blood samples before and after surgery and tissue samples from oligometastatic NSCLC undergone surgery will be obtained for exploratory analysis.
- interventionNames
- Genetic: ctDNA testing and whole exome sequencing
Primary outcomes (2)
- measure
- Association between perioperative ctDNA-MRD characteristics and rogression-free survival
- timeFrame
- 2-year PFS
- description
- To explore the potential association among perioperative ctDNA-MRD characteristics and rogression-free survival within 2 years.
- measure
- Construction of a survival-prediction model
- timeFrame
- Through study completion, up to 5 years
- description
- The survival-prediction model based on clinicopathological and genomic characteristics.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Written informed consent must be obtained from patients and ability for patients to comply with the requirements of the study; * Patients must be a man or woman of more than 18 years; * ECOG PS ≦1; * The function of the organs was evaluated by the surgeon to tolerate local surgical treatment; * The classification was evaluated as simultaneous oligometastases at initial treatment or oligoresidual/oligoprogression/oligorecurrence after induction therapy; \[Define: Initial treatment of simultaneous oligometastases: without systemic treatment, at the time of diagnosis, up to 5 metastases and up to 3 organs were involved, excluding pleural metastases or myeloid metastases. Oligoresidual after induction therapy: after systemic therapy, distant metastases were stable or reduced, primary lesions were stable or reduced, PET/CT metabolism was reduced, and no more than 5 residual lesions and no more than 3 organs were involved. Oligoprogression after induction therapy: After systemic therapy, some lesions were stable or reduced, while some original lesions were larger than before. Oligorelapses after induction therapy: after systemic therapy, systemic lesions were stable or reduced, and new local lesions appeared.\] * Lesion evaluation can be surgically removed. \[Definition of operable resection: the lesion is limited and can be completely removed through surgery as assessed by the surgeon, with no significant impact on postoperative quality of life. Pulmonary surgical procedures include lobectomy, segmental resection and wedge resection. Pneumonectomy is not included.\] Exclusion Criteria: * Patients with a confirmed or suspected autoimmune disease; * Patients with a history of human immunodeficiency virus (HIV) positive or acquired immunodeficiency syndrome (AIDS); * Patients with a history of any arterial thrombosis within 6 months and history of deep vein thrombosis, pulmonary embolism, or any other severe thromboembolism within 3 months; * Patients with any unstable systemic disease (eg, active infection, high-risk hypertension, unstable angina, congestive heart failure, etc.); * Patients with a history of other malignancies in the past 5 years; * Patients identified by the investigators patients with contraindications to local treatment; * Patients with serious mental illness; * Patients who cannot sign informed consent; * Patients who cannot be followed up as scheduled;
References
Publications (0)
Data not yet available
No reference posted for this study.