Philips incorporates Biodesix blood-based proteomic nodule risk assessment testing into Lung Cancer Orchestrator to advance early lung cancer diagnosis
June 30 2022 - 09:00AM
GlobeNewswire Inc.
Philips incorporates Biodesix blood-based proteomic nodule risk
assessment testing into Lung Cancer Orchestrator to advance early
lung cancer diagnosis
June 30, 2022Solution adds proteomic analysis of blood-based
biomarkers to Philips Lung Cancer Orchestrator to better assess the
risk of lung nodule malignancy, enhancing decision-making for
diagnosis and treatment Amsterdam, the Netherlands
– Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in
health technology, today announced it has teamed up with Biodesix,
Inc. (Colorado, U.S.) (Nasdaq: BDSX), a leading data-driven
diagnostic solutions company, to incorporate the results of
Biodesix’s Nodify Lung® blood-based lung nodule risk assessment
testing into Philips Lung Cancer Orchestrator lung cancer patient
management system. The incorporation of proteomics data – along
with the radiologic and patient history data currently used to
determine treatment decisions – can help create diagnostic
efficiency for cancer care centers in the management of a growing
number of lung nodule cases, via the contextual launch of Biodesix
Nodify Lung application within Lung Cancer Orchestrator. Philips
Lung Cancer Orchestrator solution is designed to enable health
systems to operationalize lung cancer screening and lung nodule
management programs at scale.Lung cancer remains the leading cause
of cancer deaths worldwide [1], with current 5-year survival rates
after diagnosis typically less than 20% [2]. If detected and
treated early, however, research shows 10-year survival rates could
increase to more than 90% [3]. Thanks to the adoption of low-dose
CT (computer tomography) screening and better management of
incidental lung nodule findings, early-stage diagnosis and
treatment is now possible, but has resulted in rapidly increasing
caseloads. For example, recent changes in U.S. guidelines have
nearly doubled the number of people now eligible for lung cancer
screening [4].“By incorporating Biodesix’s Nodify Lung testing, we
take another step in leveraging integrated diagnostics from
imaging, genomics, and now proteomic results from a simple blood
draw to address key moments in the lung cancer patient journey,
support care team decision-making, and help health systems learn
from their practice patterns in a dashboard view,” said Louis
Culot, General Manager Oncology Informatics and Genomics at
Philips. “We expect the inclusion of Biodesix’s ground-breaking
technology in Philips Lung Cancer Orchestrator to help drive more
confident decisions for the care team, and ultimately benefit
patients.”As a next-step after radiologic lung nodule assessment,
minimally-invasive biopsy procedures such as endobronchial biopsy
(accessing a nodule via the patient’s airways), are already helping
early-stage diagnosis. With 62% of biopsies conducted on benign
nodules [5], by detecting the presence of blood-based biomarkers
combined with clinical and radiomic factors, Biodesix’s Nodify Lung
blood-based proteomic tests help clinicians to reclassify the risk
of malignancy to better target resources to those who need them. If
a nodule is malignant, the delay in surgical care for cancer
patients by four weeks increases the mortality by 6-8% [6].“We are
delighted that our tests are being incorporated into Philips’
vision for end-to-end cancer care management using a
multi-diagnostic approach,” said Scott Hutton, Chief Executive
Officer at Biodesix. “By integrating our Nodify® tests in Philips
Lung Cancer Orchestrator we hope to make these tests more
accessible to physicians and patients and more easily utilized by
care teams with the ultimate goal of improving patient care and
outcomes.”Philips Lung Cancer Orchestrator is an integrated patient
management system for CT lung cancer screening programs and
incidental lung nodule findings that keeps track of patients,
appointments, diagnostic images, test results, and clinical
decisions for every step of a lung cancer patient’s screening and
treatment journey. Fitting seamlessly into conventional screening
and diagnostic workflows, it coordinates the end-to-end patient
journey to create a fully traceable, fully documented timeline of
scheduled actions, and aggregates data on tumor staging, radiology,
pathology, and biomarker analyses for informed decision-making. The
ability to order and receive the results expedites Biodesix’s
proteomic testing directly to and from the Lung Cancer Orchestrator
at the same time it adds new insights on nodule risk of malignancy
to further support the decision-making process.Lung Cancer
Orchestrator is part of Philips’ expanding portfolio of integrated
cancer care solutions that seamlessly connect data, technology,
operations, and clinical workflows to enable pivotal
decision-making. Visit Philips Oncology to learn how Philips
combines smart diagnostic and imaging technologies with connected
workflows that integrate patient data from disparate systems, to
provide solutions that put expert information at clinicians’
fingertips to help expand the quality and reach of personalized
cancer care.[1] International Agency for Research on Cancer, World
Health Organization. Press Release N° 263. Latest global cancer
data: Cancer burden rises to 18.1 million new cases and 9.6 million
cancer deaths in 2018. 12 September
2018[2]https://www.medicinenet.com/what_is_the_most_survivable_cancer/article.htm[3]
International Early Lung Cancer Action Program Investigators.
Survival of patients with stage 1 lung cancer detected on CT
screening. N Engl J Med. 2006;355:1763- 1771 DOI:
10.1056/NEJMoa060476.[4] Lane E, et al. Nearly twice as many people
are now eligible for lung cancer screenings—here is what you need
to know. Advisory Board publication. 2021.Washington, DC.
https://www.advisory.com/sponsored/lung-cancer[5]
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665735/[6] Mortality
due to cancer treatment delay: systematic review and meta-analysis.
BMJ 2020;371:m4087 http://dx.doi.org/10.1136/bmj.m4087For
further information, please contact:Kathy O’ReillyPhilips
Global Press OfficeTel.: +1 978-221-8919E-mail:
kathy.oreilly@philips.comTwitter: @kathyoreillyAbout Royal
PhilipsRoyal Philips (NYSE: PHG, AEX: PHIA) is a leading health
technology company focused on improving people's health and
well-being, and enabling better outcomes across the health
continuum – from healthy living and prevention, to diagnosis,
treatment and home care. Philips leverages advanced technology and
deep clinical and consumer insights to deliver integrated
solutions. Headquartered in the Netherlands, the company is a
leader in diagnostic imaging, image-guided therapy, patient
monitoring and health informatics, as well as in consumer health
and home care. Philips generated 2021 sales of EUR 17.2 billion and
employs approximately 78,000 employees with sales and services in
more than 100 countries. News about Philips can be found at
www.philips.com/newscenter.About BiodesixBiodesix is a
leading data-driven diagnostic solutions company with a focus in
lung disease. The Company develops diagnostic tests addressing
important clinical questions by combining multi-omics through the
power of artificial intelligence. Biodesix is the first company to
offer eight non-invasive tests for patients with lung diseases. The
blood based Nodify Lung® nodule risk assessment testing strategy,
consisting of the Nodify XL2® and the Nodify CDT® tests, evaluates
the risk of malignancy in incidental pulmonary nodules, enabling
physicians to better triage patients to the most appropriate course
of action. The blood based IQLung™ strategy for lung cancer
patients integrates the GeneStrat® ddPCR™ test, the GeneStrat NGS™
test and the VeriStrat® test to support treatment decisions across
all stages of lung cancer with results in an unprecedented 36-72
hours, expediting time to treatment. Biodesix also leverages the
proprietary and advanced Diagnostic Cortex® AI (Artificial
Intelligence) platform, to collaborate with many of the world’s
leading biotechnology and pharmaceutical companies to solve complex
diagnostic challenges in lung disease. Biodesix launched the
SARS-CoV-2 ddPCR™ test, the Platelia SARS-CoV-2 Total Ab, and the
cPass™ SARS-CoV-2 Neutralization Antibody test (cPass™
Neutralization Test Kit, GenScript, Inc,) in response to the global
pandemic and virus that impacts the lung and causes COVID-19. For
more information about Biodesix, visit biodesix.com.
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