Liquid Biopsy Could Identify Advanced Breast Cancer Patients
By LabMedica International staff writers Posted on 09 Aug 2017 |
![Image: The Ion Ampliseq library preparation kits (Photo courtesy of Thermo Fisher Scientific). Image: The Ion Ampliseq library preparation kits (Photo courtesy of Thermo Fisher Scientific).](https://globetechcdn.com/mobile_labmedica/images/stories/articles/article_images/2017-08-09/RLJ-262.jpg)
Image: The Ion Ampliseq library preparation kits (Photo courtesy of Thermo Fisher Scientific).
A novel blood test has been developed that measures genetic changes in circulating cancer DNA that could help identify patients with metastatic breast cancer who could benefit from a change of treatment.
Somatic mutation profiling of breast tumor tissues has identified a number of distinct breast cancer molecular subtypes characterized by diverse somatic mutations, including single nucleotide variants (SNVs) and copy number alterations (CNAs).
Scientists at the University of Leicester (Leicester, UK) recruited 42 patients with radiological-confirmed metastatic breast cancer (MBC) and nine women attending for breast screening mammography as age-matched controls. Blood samples were collected and the plasma processed using the Circulating Nucleic Acids kit.
The team designed a custom 158-amplicon panel (size range 125–175 bp) across 16 genes based on previous studies and publically available databases. Library preparation and Personal Genome Machine (PGM) sequencing were performed using the Ion Ampliseq library preparation kit. Droplet digital polymerase chain reaction (ddPCR) was used to validate tumor protein p53 (TP53), phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA), and estrogen receptor 1 (ESR1) mutations.
The scientists identified no mutations in cell free DNA (cfDNA) of healthy controls, whereas exactly half the patients with metastatic breast cancer had at least one mutation or amplification in cfDNA (mean 2, range 1–6) across a total of 13 genes. Longitudinal follow up showed dynamic changes to mutations and gene amplification in cfDNA indicating clonal and subclonal response to treatment that was more dynamic than cancer antigen 15-3 (CA15-3).
At the time of blood sampling disease progression was occurring in seven patients with erb-b2 receptor tyrosine kinase 2 (ERBB2) gene amplification in their cfDNA and three of these patients were human epidermal growth factor receptor 2 (HER2) negative at diagnosis, suggesting clonal evolution to a more aggressive phenotype. Six of the women with hormone-driven cancers had mutations in the ESR1 gene, which has been linked to resistance to anti-hormone treatments.
David Guttery, PhD, a leading author of the study, said, “We have developed a novel blood test that can simultaneously detect somatic mutations and copy number alterations that are integral in driving the growth of breast cancer. By analyzing blood plasma to measure for cancer-specific changes to key breast cancer genes, including the HER2 and estrogen receptor genes, we hope this test could help doctors and patients choose the best treatment at the best time.” The study was described by Professor Jacqui A. Shaw, PhD, in an oral presentation at the Frank May Prize Lecture on June 26, 2017, at the University of Leicester.
Related Links:
University of Leicester
Somatic mutation profiling of breast tumor tissues has identified a number of distinct breast cancer molecular subtypes characterized by diverse somatic mutations, including single nucleotide variants (SNVs) and copy number alterations (CNAs).
Scientists at the University of Leicester (Leicester, UK) recruited 42 patients with radiological-confirmed metastatic breast cancer (MBC) and nine women attending for breast screening mammography as age-matched controls. Blood samples were collected and the plasma processed using the Circulating Nucleic Acids kit.
The team designed a custom 158-amplicon panel (size range 125–175 bp) across 16 genes based on previous studies and publically available databases. Library preparation and Personal Genome Machine (PGM) sequencing were performed using the Ion Ampliseq library preparation kit. Droplet digital polymerase chain reaction (ddPCR) was used to validate tumor protein p53 (TP53), phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA), and estrogen receptor 1 (ESR1) mutations.
The scientists identified no mutations in cell free DNA (cfDNA) of healthy controls, whereas exactly half the patients with metastatic breast cancer had at least one mutation or amplification in cfDNA (mean 2, range 1–6) across a total of 13 genes. Longitudinal follow up showed dynamic changes to mutations and gene amplification in cfDNA indicating clonal and subclonal response to treatment that was more dynamic than cancer antigen 15-3 (CA15-3).
At the time of blood sampling disease progression was occurring in seven patients with erb-b2 receptor tyrosine kinase 2 (ERBB2) gene amplification in their cfDNA and three of these patients were human epidermal growth factor receptor 2 (HER2) negative at diagnosis, suggesting clonal evolution to a more aggressive phenotype. Six of the women with hormone-driven cancers had mutations in the ESR1 gene, which has been linked to resistance to anti-hormone treatments.
David Guttery, PhD, a leading author of the study, said, “We have developed a novel blood test that can simultaneously detect somatic mutations and copy number alterations that are integral in driving the growth of breast cancer. By analyzing blood plasma to measure for cancer-specific changes to key breast cancer genes, including the HER2 and estrogen receptor genes, we hope this test could help doctors and patients choose the best treatment at the best time.” The study was described by Professor Jacqui A. Shaw, PhD, in an oral presentation at the Frank May Prize Lecture on June 26, 2017, at the University of Leicester.
Related Links:
University of Leicester
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