External quality assurance of circulating tumor cell enumeration using the CellSearch® system: A feasibility study
March 2011
Article
| Related Files |
|---|
|
Redirect to publisher's version
(publisher's version.url.txt, 38 bytes) |
Background: Circulating tumor cells (CTCs) are cells that have detached from solid tumors and entered the blood. CTCs can be detected, among others, by semi-automated immunomagnetic enrichment and image cytometry using CellSearch® (Veridex, Raritan, NJ). We studied the feasibility of external quality assurance (EQA) of the entire CellSearch procedure from blood draw to interpretation of results in multiple laboratories. Methods: Blood samples from six cancer patients and controls were distributed to 14 independent laboratories to test between-laboratory, between-assay, and between-instrument variation. Additionally, between-operator variability was assessed through the interpretation of blinded images of all blood samples on a website. Results: Shipment and storage of samples had no influence on CTC values. Between-instrument (coefficient of variation (CV) < 12%) and between-assay variation was low (CV ≤ 20%), indicating high reproducibility. However, between-laboratory CV ranged from 45 to 64%. Although inter-operator agreement on image interpretation (Fleiss' I° statistics) ranged from " to "almost perfect," image interpretation, particularly of samples containing high numbers of apoptotic cells, was the main contributor to between-laboratory variation. Conclusions: This multicenter study shows the feasibility of an EQA program for CTC detection in patient samples, and the importance of continuation of such a program for the harmonization of CTC enumeration.
- article
- human
- priority journal
- controlled study
- human cell
- clinical article
- multicenter study
- feasibility study
- cancer patient
- cancer cell
- quality control
- blood sampling
- imaging
- medical instrumentation
- tumor cell
- apoptosis
- kappa statistics
- laboratory
- external quality assessment
- circulating tumor cells
- immunomagnetic enrichment
- rare events
- tumor embolism