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

Hormone Receptor Antibody Reagents Assessed for Breast Cancer

By LabMedica International staff writers
Posted on 08 Aug 2017
Print article
Image: Breast cancer: immunohistochemical comparison of three estrogen receptor antibodies: A through C, 1D5 and 6F11 show negativity, whereas SP1 shows positivity (Photo courtesy of Stanford University Medical Center).
Image: Breast cancer: immunohistochemical comparison of three estrogen receptor antibodies: A through C, 1D5 and 6F11 show negativity, whereas SP1 shows positivity (Photo courtesy of Stanford University Medical Center).
Immunohistochemical analysis of estrogen receptor (ER) and progesterone receptor (PgR) expression in breast cancer is the current standard of care and directly determines therapy.

Estrogen receptor–expressing breast cancers tend to have better prognosis than ER-negative breast cancers and even more importantly, patients with strongly ER-positive tumors derive substantial benefit from therapies inhibiting estrogen signaling.

Scientists at the Stanford University Medical Center (Stanford, CA, USA) compared the performance of different antibody reagents for ER and PgR immunohistochemical analysis by using College of American Pathologists (CAP) proficiency testing data. The team retrospectively analyzed tissue microarrays of ten 2-mm cores per slide and analyzed survey data from 80 ER and 80 PgR cores by antibody clone from more than 1,200 laboratories. The laboratories were instructed to stain the provided slides by using their clinically validated protocols (assuming a negative control is run and is appropriately negative) and score them according to the ASCO/CAP guidelines.

The team found that laboratories used the following ER antibodies: SP1 (72%), 6F11 (17%), 1D5 (3%), and the PgR antibodies 1E2 (61%), 16 (12%), PgR-636 (13%), PgR-1294 (8%) in 2015. While 63 of 80 ER cores (79%) were scored similarly using each of the three antibodies, there were significant differences for others, with SP1 yielding more positive interpretations. Four cores were scored as ER negative by more than half of the laboratories using 1D5 or 6F11, while SP1 produced positive results in more than 70% of laboratories using that antibody. Despite the greater variety of PgR antibody reagents and greater PgR tumor heterogeneity, 61 of 80 cores (76%) were scored similarly across the four PgR antibodies.

The authors concluded that analysis of proficiency testing data provides useful comparative data regarding analytic variables in ER and PgR testing. They highlighted the striking differences in ER results by antibody clone, with SP1 yielding more positive results than either 6F11 or 1D5. Accurate ER and PgR testing in breast cancer is crucial for appropriate treatment. The study was published on July 17, 2017, in the journal Archives of Pathology & Laboratory Medicine.

Related Links:
Stanford University Medical Center

Gold Member
Antipsychotic TDM Assays
Saladax Antipsychotic Assays
Verification Panels for Assay Development & QC
Seroconversion Panels
New
Fecal DNA Extraction Kit
QIAamp PowerFecal Pro DNA Kit
New
Centromere B Assay
Centromere B Test

Print article

Channels

Molecular Diagnostics

view channel
Image: The study investigated D-dimer testing in patients who are at higher risk of pulmonary embolism (Photo courtesy of Adobe Stock)

D-Dimer Testing Can Identify Patients at Higher Risk of Pulmonary Embolism

Pulmonary embolism (PE) is a commonly suspected condition in emergency departments (EDs) and can be life-threatening if not diagnosed correctly. Achieving an accurate diagnosis is vital for providing effective... Read more

Microbiology

view channel
Image: Schematic representation illustrating the key findings of the study (Photo courtesy of UNIST)

Breakthrough Diagnostic Technology Identifies Bacterial Infections with Almost 100% Accuracy within Three Hours

Rapid and precise identification of pathogenic microbes in patient samples is essential for the effective treatment of acute infectious diseases, such as sepsis. The fluorescence in situ hybridization... Read more
Sekisui Diagnostics UK Ltd.