Test Validated to Predict Recurrence Risk and Radiation Therapy Benefit in Breast Cancer
A blinded validation in more than 400 women shows the test provides clearer guidance on recurrence risk and radiation therapy decisions.
A blinded validation in more than 400 women shows the test provides clearer guidance on recurrence risk and radiation therapy decisions.
Coverage applies to stage II and III breast cancer patients across three major subtypes for up to six years of recurrence monitoring.
Research-use kit interrogates 84 genes using single-tube protocol, compatible with existing molecular laboratory equipment.
Oncoguard Liver test demonstrates seven times greater sensitivity for very early-stage hepatocellular carcinoma compared to ultrasound surveillance.
Read MoreTAPS+ chemistry preserves DNA integrity in challenging samples including FFPE tissue and circulating tumor DNA.
Read MoreThe test measures microRNA-371a-3P biomarker and can guide treatment decisions while reducing need for some CT scans during surveillance.
Read MoreA new study demonstrates the capability of a blood test in detecting ovarian cancer up to three years prior to diagnosis in prospectively collected samples.Â
Read MoreCirculating tumor DNA testing can identify stage 3 patients who may safely receive reduced treatment intensity, international study finds.
Read MoreSelf-collection for HPV and other infections offers a more convenient, private way to complete recommended screenings—helping reach women who might otherwise delay or skip care.
Read MoreThe mass spectrometry-based assay achieved 100% sensitivity in detecting patients who later progressed to cancer in a blinded cohort study.
Read MoreA study of nearly 1,800 patients shows a threefold difference in sentinel node metastasis rates between high-risk and low-risk groups.
Read MoreThe agreement focuses on clinical validation of ESR1 mutation detection assay for advanced breast cancer testing using ddPCR technology.
Read MorePATHFINDER 2 study results indicate more than half of cancers detected by Galleri test were found in early stages, with three-quarters having no current screening options.
Read MoreA study of over 10 million men reveals frequent testing of patients unlikely to benefit, raising questions about current screening practices.
Read MoreThe permit enables the company to offer its PROphetNSCLC test to physicians and patients across New York State, completing nationwide availability.
Read MoreGerman laboratory brings tumor-informed MRD testing to European market through licensing agreement with Quest Diagnostics subsidiary.
Read MoreNew automated workflow combines at-home sampling with robotic lab processing.
Read MorePartnership will bring Galleri multi-cancer early detection test to South Korea, with potential expansion to Japan and Singapore.
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