Skip to content

Liquid Biopsy in Advanced Oligometastatic NSCLC Receiving Surgery

Liquid Biopsy in Advanced Oligometastatic NSCLC Receiving Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05648370
Enrollment
60
Registered
2022-12-13
Start date
2022-07-01
Completion date
2025-06-30
Last updated
2022-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small Cell Lung Cancer, Oligometastatic Disease

Brief summary

A prospective, observational study that assesses the clinical feasibility of ctDNA-based liquid biopsy in patients with oligometastatic NSCLC receiving surgery.

Detailed description

60 eligible patients will be enrolled. Dynamic blood samples before and after surgery and tissue samples will be obtained for exploratory analysis.

Interventions

GENETICctDNA testing and whole exome sequencing

Blood samples will be obtained for ctDNA testing and tumor tissue for whole exome sequencing.

Sponsors

Guangdong Provincial People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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;

Design outcomes

Primary

MeasureTime frameDescription
Association between perioperative ctDNA-MRD characteristics and rogression-free survival2-year PFSTo explore the potential association among perioperative ctDNA-MRD characteristics and rogression-free survival within 2 years.
Construction of a survival-prediction modelThrough study completion, up to 5 yearsThe survival-prediction model based on clinicopathological and genomic characteristics.

Secondary

MeasureTime frameDescription
Potential drug-resistance mechanism identified by plasma ctDNAThrough study completion, up to 5 yearsUsing plasma ctDNA-MRD to identify the potential drug-resistance mechanism.
Association among ctDNA status before surgery, systemic treatment times, and survivalThrough study completion, up to 5 yearsTo explore the potential association among plasma ctDNA status surgery, systemic treatment time duration, PFS and OS.
Heterogeneity in Genomic and transcriptome between primary and metastatic tumors60 patients underwent surgeryUsing whole-exome sequencing and whole transcriptome sequencing to identify genomic and transcriptome heterogeneity between primary and metastatic tumors.
Assess whether ctDNA-MRD is associated with radiological and pathological response after systematic therapy before surgery60 patients underwent surgeryAssociation among perioperative ctDNA-MRD characteristics, imaging response, and pathological response.
Genomic characteristics and clonal evolution after systemic treatmentThrough study completion, up to 5 yearsUsing whole-exome sequencing to identify genomic characteristics and clonal evolution after systemic treatment

Countries

China

Contacts

Primary ContactWen-Zhao Zhong, Ph.D
syzhongwenzhao@scut.edu.cn+86 02083827812
Backup ContactRui Fu, M.D.
ruifu66@foxmail.com+86 02083827812

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026