Feb 01,2024

BD partners with Techcyte to offer AI-enhanced cervical cancer screening

BD has partnered with Techcyte to offer an artificial intelligence (AI)-enabled cervical cancer screening system. Accordingly, Techcyte has developed a system to reduce the amount of cells pathologists need to review on BD Surepath and Hologic Thinprep slides. The system, which has yet to win approval in the U.S., uses AI to present “the most diagnostically relevant images.” BD supports screening with its human papillomavirus (HPV) assay and liquid-based Pap test, Surepath. While HPV testing is, by BD’s own admission, more sensitive, the company expects Pap tests to “continue to play an important diagnostic role, as programs are transitioning to the new standard of care.” Techcyte’s system is compatible with multiple liquid-based cytology preparations, including Surepath. Traditionally, cytotechnologists and pathologists viewed glass slides under a microscope. To use Techcyte’s system, technologists prepare slides using systems such as Surepath and scan them to create digital files. The AI algorithm then identifies cells with features that suggest they may be diagnostically relevant. The system is CE marked under the old European Union directive. However, Techcyte has yet to win Food and Drug Administration approval or receive a CE mark under the new EU regulation. BD and Techcyte expect to make the system available in Europe in the first half of the year and enter the U.S. market once the FDA approves the system for clinical use.

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Feb 08,2024

Paige Expands its AppLab Marketplace with Six New Digital Pathology Providers to Deliver a More Robust and Streamlined User Experience for Diagnosing Cancer

Paige announced a significant expansion of its AppLab marketplace, with the addition of six new digital pathology and AI providers. New applications from these industry-leading companies, including Imagene, Histofy, Aiosyn, Clinsight, DoMore Diagnostics, and Stratipath, will be added to the AppLab to provide support for pathology labs worldwide in building deeply integrated and customized AI-enabled workflows. The Paige AppLab is a comprehensive marketplace where, within a few clicks, pathologists can seamlessly browse, trial, and purchase a robust set of diagnostic support tools from various providers that can be then accessed in the Paige Platform and FullFocus® viewer to support each unique step of cancer diagnosis. The newly introduced applications unlock advanced AI-powered capabilities such as biomarker detection from H&E-stained slides, assistance with the grading and assessment of cancer across tissue types, risk-stratification, and more.

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Feb 12,2024

Proscia Receives FDA Clearance for Digital Pathology Software Solution

Proscia, a provider of digital and computational pathology solutions, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Concentriq AP-Dx. The digital pathology solution was cleared for the purpose of primary diagnosis, reported the company, adding that it is cleared for clinical use with the Hamamatsu NanoZoomer S360MD Slide scanner in the United States. Proscia’s Concentriq AP-Dx is a comprehensive diagnostic software solution that immerses pathologists in an intuitive experience for viewing, interpreting, and managing whole slide images and helps to drive confidence and efficiency gains. In addition to its 510(k) clearance, Proscia was the first company to achieve CE-IVDR certification to advance primary diagnosis in the European Union. The company also has a product licensed in Canada and cleared in the United Kingdom among other countries.

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Feb 09,2024 TOP STORY

Hologic AI-powered cancer screening system wins FDA approval

Medical technology firm Hologic has been granted clearance from the FDA to market its Genius Digital Diagnostics System, powered by the company's Genius Cervical AI algorithm. The digital cytology system–a medical diagnostic tool used to examine cells under a microscope to detect abnormalities or diseases–integrates deep learning-based AI with advanced volumetric imaging technology to aid in detecting precancerous lesions and cervical cancer cells. Cervical cancer screenings typically involve a Pap test, where cervical cell samples are collected at an OB-GYN office and sent to a lab for analysis on glass slides. By digitizing glass slides for analysis through the AI algorithm, the company says the system can enhance sensitivity without compromising specificity and facilitating more timely and effective treatment decisions. Its commercial launch is expected later this year. Its technology is already available in Europe, Australia and New Zealand.

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Jan 25,2022

French Healthtech Resilience Raises €40 Million to Improve the Care Pathway for Cancer Patients

After a €5M financing in 2021, Resilience announces a €40M Series A round led by the global investment firm Cathay Innovation with strong support from the French VC Singular. Three European funds: Exor Seeds, Picus Capital and Seaya Ventures are also participating in the round as well as a consortium of healthcare players: Fondation Santé Service, MACSF, Ramsay Santé and Vivalto Ventures. This funding will allow the company to accelerate the deployment of its medical devices (CE Class IIa) in healthcare institutions and to enrich its application with new functionalities dedicated to the well-being of patients. Co-founded less than a year ago by two tech entrepreneurs, Céline Lazorthes and Jonathan Benhamou, in partnership with the Gustave Roussy Institute, the 5th largest cancer center in the world, Resilience’s mission is to reinvent the way we treat cancer through digital and remote medical monitoring.

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Jan 24,2024 TOP STORY

Sciensus acquires oncology symptom tracker app Vinehealth

UK-based pharmaceutical supply company, Sciensus, has announced that it has acquired the cancer patient support app, Vinehealth, with the aim of using data collected from the app to support what the company calls actionable insights. The Vinehealth App is an oncology platform designed to allow users to report and track symptoms of disease progression in real time, whilst allowing that same data to be shared with clinicians. The app joins Sciensus’ roster of telehealth and remote patient monitoring apps including the company’s own InTouch app. It also adds further support for oncology patients to the company’s remit, which already covers more than 50 indications digitally.

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Feb 01,2024 TOP STORY

ArteraAI Raises $20M to Personalize Cancer Therapy With Multimodal AI

ArteraAI, a pioneer in multi-modal artificial intelligence (MMAI) for cancer treatment personalization, announced today an additional $20M in funding. This latest round, backed by prominent investors like Prosperity7 Ventures, EDBI, and Wilson Sonsini Goodrich & Rosati, brings the company’s total funding to $110M since its inception less than a year ago. ArteraAI’s MMAI platform analyzes digital pathology images and clinical data to deliver accurate predictions about cancer progression and response to treatment. This information empowers clinicians to make more informed decisions about personalized treatment plans, potentially improving patient outcomes and reducing unnecessary procedures. The company also offers an AI-enabled Prostate test that is the first of its kind to provide both predictive and prognostic results for patients with localized prostate cancer/ ArteraAI’s multimodal artificial intelligence (MMAI) biomarker test leverages a unique algorithm that assesses digital images from a patient’s biopsy and learns from a patient’s clinical data. 

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Jan 22,2024

Cedars-Sinai AI tool accurately detects pancreatic cancer

Cedars-Sinai Cancer investigators have used a unique precision medicine and artificial intelligence (AI) tool called the Molecular Twin Precision Oncology Platform to identify biomarkers that outperform the standard test for predicting pancreatic cancer survival. Their study, published in the peer-reviewed journal Nature Cancer, demonstrates the viability of a tool that could one day guide and improve treatment for all cancer patients.  Investigators used the Molecular Twin platform to analyze blood and tissue samples from 74 patients with the most common and most aggressive pancreatic cancer type, pancreatic ductal adenocarcinoma. Investigators first combined 6,363 different biological data points, including genetic and molecular information, to create a model that accurately predicted disease survival in 87% of patients. The full and streamlined models, and the blood-protein test, outperformed the only Food and Drug Administration-approved pancreatic cancer test, a blood test called CA 19-9. The findings were validated in independent datasets from The Cancer Genome Atlas, Massachusetts General Hospital, and Johns Hopkins University.

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Jan 31,2024 TOP STORY

Trialbee and Massive Bio Join Forces to Improve Clinical Trial Access and Patient Recruitment for Oncology and Hematology

Trialbee announced its Omnichannel Network partnership with Massive Bio, a global leader in AI enabled patient journey mapping platform, to help better connect cancer patients and their oncologists/hematologists to clinical trials. Trialbee and Massive Bio share similar approaches to recruitment for cancer trials with an emphasis on patient-centered research coupled with total transparency to ensure sites have the information they need to follow-up with interested study candidates. Because many of these trials potentially represent the latest and most innovative methods to save lives, improving the outlook for generations to come, the companies are committed to working together to act. "This partnership with Trialbee brings another channel of identification and outreach with hyper-targeted digital recruitment so we can reach more patients together – including those at community-based practices, which was the founding reason of Massive Bio, so we can improve health equity and access for all." said Selin Kurnaz, PhD, CEO of Massive Bio. Interested participants will be tracked and managed all within the Trialbee Honey Platform™, which centralizes and standardizes recruitment and enrollment data from all sources to provide unprecedented transparency into the process while reducing burden on sites.

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Feb 05,2024

Deep Bio's DeepDx Prostate Featured in CancerX's Solutions Catalog, Pioneering Digital Innovation in Oncology

Deep Bio, a pioneer of AI-powered cancer diagnostics solutions, proudly announced the inclusion of DeepDx Prostate in CancerX's Solutions Catalog. The Solutions Catalog, launched in 2023, represents CancerX's inaugural concrete initiative, strategically designed for digital transformation to enhance access to cancer care and alleviate financial burdens on patients. It is segmented into three key areas: Screening/Diagnosis, Treatment/End-of-Life Care, and Survivorship, and acts as a reference guide showcasing commercialized digital products and solutions in medical institutions across the United States.

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