We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

LabMedica

Download Mobile App
Recent News Expo Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Postsurgical Immunoassay Predicts Prostate Cancer Recurrence

By LabMedica International staff writers
Posted on 18 Oct 2010
A novel test could reliably detect early increases in prostate specific antigen levels, a biomarker commonly used to measure the recurrence of prostate cancer.

A simple blood test can measure PSA in men who have undergone prostate cancer-treating surgery with unprecedented sensitivity and at much lower levels than standard PSA tests because it can selectively capture and measure individual PSA molecules.

Single Molecule Array (SiMoA) technology is based upon the isolation of individual immunocomplexes on beads using standard enzyme linked immunosorbent assay (ELISA) reagents. The AccuPSA test uses beads with or without labeled immunocomplexes are loaded into arrays containing femtoliter-sized wells and the arrays are sealed in the presence of the enzyme substrate and fluorescently imaged. Fluorescent product molecules of the enzyme-substrate reaction are confined in a 50 fL volume, giving rise to a local high concentration of product within a matter of a few seconds that can be easily detected using a low cost imaging system.

The AccuPSA test is manufactured by Quanterix Corporation, (Cambridge, MA, USA). To demonstrate the assay's clinical potential, PSA was measured in serum from 60 men who had undergone radical prostatectomy for prostate cancer. For the majority of these patients PSA is initially reported as undetectable following surgery, but may be present at very low levels that predict the likelihood of disease recurrence. The test was so sensitive that it was able to measure residual PSA levels in all samples tested. The PSA levels had been reported to be undetectable in these samples by standard tests, highlighting the sensitivity and precision of the SiMoA technology. The findings were presented at the Fourth American Association for Cancer Research's International Conference on Molecular Diagnostics in Cancer Therapeutic Development that was held during September 23 – 27, 2010, in Denver (CO, USA).

David Wilson, Ph.D., senior director at Quanterix Corporation, said, "AccuPSA has the potential to eliminate unnecessary treatments and enable earlier detection of recurrence, which may lead to earlier treatment, better outcomes and have a positive impact on health care costs."

Related Links:

Quanterix Corporation
American Association for Cancer Research



Platinum Member
COVID-19 Rapid Test
OSOM COVID-19 Antigen Rapid Test
Verification Panels for Assay Development & QC
Seroconversion Panels
POCT Fluorescent Immunoassay Analyzer
FIA Go
Gold Member
Rheumatoid Factors (RF) Test
Rheumatoid Factors (RF)

Latest Clinical Chem. News

Mass Spectrometry-Based Monitoring Technique to Predict and Identify Early Myeloma Relapse
18 Oct 2010  |   Clinical Chem.

‘Brilliantly Luminous’ Nanoscale Chemical Tool to Improve Disease Detection
18 Oct 2010  |   Clinical Chem.

Low-Cost Portable Screening Test to Transform Kidney Disease Detection
18 Oct 2010  |   Clinical Chem.