Heather Wetzel-The Personalis ACE CancerPlus Test A Comprehensive DNA & RNA Sequencing Solution for
Oncologists and pathologists are increasingly utilizing information on genomic alterations in tumors to help guide patient care andΒ ...
Senior Vice President of Investor Relations, Proassurance
Search every verified Heather Wietzel interview, podcast appearance, and on-the-record quote β each transcript cross-checked by AI and human review to confirm speaker identity. Heather Wetzel, then a representative of Personalis, presented a web seminar in September 2016 on the company's ACE CancerPlus test, a DNA and RNA sequencing test for solid tumors. During the presentation, Wetzel described the test as reporting on 181 clinically relevant genes, powered by a larger panel of over 1,300 genes, and capable of detecting base substitutions, insertions, deletions, copy number alterations, and gene fusions. She stated that early testing through the Department of Veterans Affairs, primarily in non-small cell lung cancer patients, showed that the majority of patients had variants associated with FDA-approved therapies. Wetzel discussed challenges in clinical next-generation sequencing, including poorly focused gene panels, coverage gaps, and difficulties with FFPE tissue samples. She said that Personalis had developed in-house technologies to successfully sequence approximately 90% of FFPE samples received. She noted that the test's validation involved nearly 40 tumor cell lines and achieved over 99% sensitivity for base substitutions at a 5% allele fraction. Wetzel added that the test was available only in North America, ordered by physicians, with a turnaround time of approximately three weeks and pricing competitive with similar tests.
“The Ace CancerPlus test consists of reporting on 181 genes of clinical relevance, powered by a larger extended cancer panel of over 1300 genes. This test includes DNA and RNA analysis of solid tumors, enabling detection of base substitutions, insertions, deletions, copy number alterations, and gene fusions, many of whi...”
“Our early testing with the Ace CancerPlus test through the Department of Veterans Affairs has shown that the majority of patients, primarily with non-small cell lung cancer, have variants associated with FDA-approved therapies, helping to advance precision medicine and make these drugs more available to veterans nation...”
“One of the main challenges in clinical next-generation sequencing cancer testing is having a poorly focused gene test panelβeither too many or too few genes that aren't clinically relevant. Coverage gaps, limited gene fusion analysis, and difficulties with FFPE samples also pose significant challenges that we have addr...”
“Our Ace platform uses proprietary chemistries and probe designs to supplement standard sequencing technology, improving coverage especially in difficult regions like high GC content and medically important non-exonic regions, resulting in comprehensive gene coverage for clinical reporting.”
“We include full RNA analysis of all 181 genes in the panel to detect gene fusions comprehensively, allowing detection of known and novel fusion events, including those involving fusion partners not on the panel, which is critical for identifying actionable targets in solid tumors.”
“While FFPE tissue samples are challenging due to DNA degradation and often fail quality control in many labs, our in-house developed technologies have enabled us to successfully extract and sequence approximately 90% of FFPE samples received, improving access to clinical testing for many patients.”
“Validation of the Ace CancerPlus test involved nearly 40 different tumor cell lines and a range of allele fractions from 5% to 95%, achieving over 99% sensitivity for base substitutions at 5% allele fraction and similarly high sensitivity and specificity for insertions, deletions, copy number alterations, and gene fusi...”
“We have designed our clinical reports to be concise and intuitive for clinicians, summarizing relevant variants and associated FDA-approved therapies or clinical trials upfront, enabling easier interpretation and clinical decision-making compared to typical lengthy reports.”
“The Ace CancerPlus test is currently available only in North America, ordered by physicians, and billed as self-pay or institutional billing. We plan to expand globally in the future, and the turnaround time for results is approximately three weeks.”
“The cost of the Ace CancerPlus test is competitively priced in line with similar tumor profiling tests from other laboratories, though specific pricing details are provided upon inquiry to our media contact.”
Oncologists and pathologists are increasingly utilizing information on genomic alterations in tumors to help guide patient care andΒ ...
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