Personalis Forms Research Collaboration to Better Predict Immunotherapy Response for Gastroesophageal Cancer
October 04 2022 - 09:00AM
Business Wire
Personalis, Inc. (Nasdaq: PSNL) has joined with Duke University
and Olink Proteomics AB to form a research collaboration to study
the effects of immunotherapy on advanced gastroesophageal cancer.
Specifically, the collaboration will focus on identifying composite
biomarkers—those that integrate multiple biological entities into a
single readout—to help guide therapeutic decision making.
Gastroesophageal cancer is the fourth most common cancer
worldwide, with nearly 50% of patients having developed
unresectable or metastatic disease at the time of diagnosis.
Chemotherapy is currently the standard of care for patients with
this type of advanced disease; however, its effectiveness is often
diminished as many patients develop therapeutic resistance. When
this happens, the median overall survival for patients drops to
less than 9 months.
Fortunately, pembrolizumab, an immunotherapeutic targeting
PDL1/PD1, has been approved by the FDA for use in patients with
chemorefractory gastroesophageal cancer. The effectiveness of this
biologic has inspired significant interest in applying it as a
first-line, standard of care treatment for patients with advanced
disease.
To that end, the goal of the collaborative study is to
characterize key tumor and immunological responses to pembrolizumab
and, in so doing, shine light on the potential mechanisms that lead
to either sensitivity or resistance to immunotherapeutics in
gastroesophageal cancer. By detailing how tumors respond to
treatment at the genomic, transcriptomic, and proteomic levels, the
team aims to uncover biomarkers that may help physicians predict
tumor responses to pembrolizumab and adjust treatment strategies
accordingly.
“Biomarkers that predict and characterize tumor responses to
anti-PDL1/PD1 therapy remain poorly understood, largely due to the
complex and multifaceted interactions between the tumor and immune
system. Through comprehensive plasma and tumor immune profiling, we
aim to clarify the interconnected roles of tumor genomics and
proteomics, as well as the development of composite biomarkers to
clinically predict and follow immunotherapy response,” said Andrew
Nixon, PhD, Director of the Phase I Biomarker Laboratory, Duke
University School of Medicine.
“This study has the potential to identify the mechanisms of
immune resistance in metastatic gastroesophageal cancer, which may
enable strategies to optimize response rates to existing
immunotherapies and develop novel therapeutics that overcome
resistance,” said Marijana Rucevic, PhD, Senior Scientific
Director, Olink Proteomics. “We are honored to participate in this
essential and exciting research effort with Duke and Personalis,
and to further direct the strengths of Olink’s PEA technology
against the growing challenge of cancer drug development and
personalized cancer treatment.”
“We believe the clinical management of cancer can substantially
improve with early determination of patient response and by
accurately informing changes to treatment regimens. Such
determinations offer the potential to avoid unnecessary toxicities
and increase survival,” said Dr. Richard Chen, MD, Chief Medical
Officer and Senior Vice President of R&D at Personalis. “By
collaborating with researchers at Duke and Olink, we hope to
accelerate advances in oncology practice via ultra-sensitive MRD
detection.”
Personalis’ ImmunoID NeXT Platform® will be used for
characterization of tumor genomic and transcriptomic alterations,
as well as differences between responders and non-responders.
Additionally, Personalis’ NeXT Personal™ assay will be used to
analyze circulating tumor DNA (ctDNA) collected from patients in
order to profile and accurately track molecular residual disease
(MRD) over the course of therapy. Olink® Explore panels will be
used to analyze plasma samples and tumor tissues from metastatic
gastroesophageal cancer patients being treated with anti-PD1 and
anti-PD1/chemotherapy.
About NeXT Personal
NeXT Personal is a next-generation, tumor-informed liquid biopsy
assay designed to detect and quantify MRD and recurrence in
patients previously diagnosed with cancer. The assay is designed to
deliver industry-leading MRD sensitivity down to the 1
part-per-million range, an approximately 10- to 100-fold
improvement over other available technologies. It leverages whole
genome sequencing of a patient’s tumor to identify up to 1,800
specially selected somatic variants that are subsequently used to
create a personalized liquid biopsy panel for each patient. This
may enable earlier detection across a broader variety of cancers
and stages, including typically challenging early-stage, low
mutational burden, and low-shedding cancers. NeXT Personal is also
designed to simultaneously detect and quantify clinically relevant
mutations in ctDNA that may be used in the future to help guide
therapy when cancer is detected. These include known targetable
cancer mutations, drug resistance mutations, and new variants that
can emerge and change over time, especially under therapeutic
pressure.
About Personalis
Personalis, Inc. is a leader in advanced cancer genomics,
enabling the next generation of precision cancer therapies and
diagnostics. The Personalis NeXT Platform® is designed to adapt to
the complex and evolving understanding of cancer, providing its
biopharmaceutical customers and clinicians with information on all
of the approximately 20,000 human genes, together with the immune
system, from a single sample. To enable cancer sequencing,
Personalis' Clinical Laboratory was built with a focus on clinical
accuracy, quality, big data, scale and efficiency. The laboratory
is GxP-aligned as well as Clinical Laboratory Improvement
Amendments of 1988-certified and College of American
Pathologists-accredited. For more information, visit the Personalis
website and follow Personalis on LinkedIn and Twitter.
About Olink Holding AB
Olink Holding AB (publ) (Nasdaq: OLK) is a company dedicated to
accelerating proteomics together with the scientific community,
across multiple disease areas to enable new discoveries and improve
the lives of patients. Olink provides a platform of products and
services which are deployed across major pharmaceutical companies
and leading clinical and academic institutions to deepen the
understanding of real-time human biology and drive 21st century
healthcare through actionable and impactful science. The Company
was founded in 2016 and is well established across Europe, North
America and Asia. Olink is headquartered in Uppsala, Sweden.
Forward-Looking Statements
All statements in this press release that are not historical are
“forward-looking statements” within the meaning of U.S. securities
laws, including statements relating to attributes or advantages of
NeXT Personal or the NeXT Platform, expected benefits of the
company’s collaboration with Duke University and Olink Proteomics
AB, expected performance or adoption of the NeXT Personal assay,
Personalis’ business opportunities, leadership, plans or
expectations, or other future events. Such forward-looking
statements involve risks and uncertainties that could cause actual
results to differ materially from any anticipated results or
expectations expressed or implied by such statements. Factors that
could materially affect actual results can be found in Personalis’
filings with the U.S. Securities and Exchange Commission, including
Personalis’ most recent reports on Forms 8-K, 10-K and 10-Q, and
include those listed under the caption “Risk Factors.” Personalis
disclaims any obligation to update such forward-looking
statements.
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Investor Relations Contact for Personalis: Caroline
Corner investors@personalis.com www.westwicke.com 415-202-5678
Media Contact for Personalis: Jennifer Temple
pr@personalis.com www.personalis.com 650-752-1300
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