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The Value Of Circulating Tumor Cells In Patient With NSCLC In Postoperative Recurrence Monitoring

The Value Of Circulating Tumor Cells In Patient With NSCLC In Postoperative Recurrence Monitoring

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02647164
Enrollment
360
Registered
2016-01-06
Start date
2016-01-31
Completion date
Unknown
Last updated
2016-01-06

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

Conditions

Non-small-cell Lung Carcinoma

Keywords

Non-small-cell lung carcinoma, Circulating tumor cells

Brief summary

The purpose of this study is to assess the value of circulating tumor cells (CTC)for non-small cell lung cancer in the postoperative recurrence monitoring by comparing the CTCs, CT and tumor markers at different time points.The time of CTC and carcinoembryonic antigen(CEA) detection is baseline, 2\ 7 days, 3 months, 6 months, 12 months, 24 months, 36 months after the surgery. And the time of CT detection is 6 months, 12 months, 24 months, 36 months after the surgery.

Interventions

None listed

Sponsors

GenoSaber
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-80 years old * Patients with histologically documented (stage Ⅰ/Ⅱ/ⅢA ) non-small cell lung cancer. * Patients will undergo surgery. * Patients with preoperative CTCs ≥8.5 Units / 3 ml * Informed consent must be obtained from all patients prior to beginning therapy. Patients should have the ability to understand and the willingness to sign a written informed consent document.

Exclusion criteria

* Patients with histologically documented not (stage Ⅰ/Ⅱ/ⅢA ) non-small cell lung cancer. * After the operation review, patients' result of CTC, CT and tumor markers is incomplete at the same point. * The blood sample isn't collected in predetermined time. * The blood samples appear hemolysis. * The blood sample isn't enough.

Design outcomes

Primary

MeasureTime frame
Circulating tumor cells will be detected by Immunomagnetic negative screening and targeted PCR method.3 years

Secondary

MeasureTime frame
Liconography using conventional CT examination results.3 years
carcinoembryonic antigen(CEA) concentration will be detected by electrochemical luminescence.3 years

Outcome results

None listed

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