Test Outperforms Traditional Tool in Predicting Melanoma Spread to Lymph Nodes
A prospective study shows the test more accurately identifies patients who may safely avoid biopsy compared to the Melanoma Institute Australia nomogram.
A prospective study shows the test more accurately identifies patients who may safely avoid biopsy compared to the Melanoma Institute Australia nomogram.
The whole-genome sequencing assay is now available for breast, colorectal, and renal cancers following new clinical study results.
The companion diagnostic identifies PTEN protein loss, helping clinicians determine which patients may benefit from Truqap in combination with abiraterone acetate.
Initial results from a real-world study of the ProVue Lung test demonstrate 83% sensitivity for Stage I cancer in high-risk patients.
Read MoreFindings from the OPTIMA trial show that the Prosigna test identifies patients who can safely skip chemotherapy and use hormone therapy alone.
Read MoreResearchers reported that the test reduced unnecessary biopsies by up to 64% without compromising detection of aggressive prostate cancers.
Read MoreThe updated test includes additional DPYD variants recommended by the Association for Molecular Pathology to help identify patients who may be at risk for severe chemotherapy side effects.
Read MoreNew clinical utility data showed that offering a blood-based lung cancer test increased screening participation compared with low-dose CT screening alone.
Read MoreMonitoring circulating tumor DNA dynamics outperformed standard markers for predicting survival and relapse in early-stage patients.
Read MoreThe study demonstrated that patients who test positive for ctDNA “actually benefit from chemotherapy.”
Read MoreResearch shows optical genome mapping identifies genomic changes in nearly 98% of T-cell acute lymphoblastic leukemia cases compared to 55% with traditional analysis.
Read MoreThe digital pathology platform provides patient-specific risk estimates to help clinicians tailor treatment for metastatic hormone-sensitive disease.
Read MoreResults from the NHS-Galleri study show a 26% reduction in metastatic cancer diagnoses by the third round of screening.
Read MoreThe diagnostic test identifies specific genetic mutations to help select patients for a targeted therapy combination.
Read MoreThe test uses a new approach to identify signs of cancer recurrence with faster result times for healthcare providers and patients.
Read MoreClinical results show high sensitivity for colorectal cancer relapse and ultra-low detection limits for lung cancer.
Read MoreThe tissue- and blood-based tests identify patients with specific gene mutations who may benefit from a combination therapy.
Read MoreResults from the PATHFINDER 2 trial show the Galleri test identifies 6.5 times more cancers when used with standard screenings.
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