Researchers Develop Minimally Invasive Skin Cancer Monitoring Platform
This skin cancer monitoring approach integrates a minimally invasive microneedle platform with a sensitive, single-molecule detection method.
This skin cancer monitoring approach integrates a minimally invasive microneedle platform with a sensitive, single-molecule detection method.
Unilabs and Proscia have announced that the diagnostic group has chosen Proscia's DermAI skin pathology solution.
The blood test followed by PET-CT imaging was 99.6% specific for cancer.
The TARDIS test could help avoid unnecessary surgeries and enable physicians to continuously monitor cancer.
Read MoreMonitoring cancer therapy in real time enables physicians to make smarter treatment decisions.
Read MoreStudy results support use of the blood test as a surrogate endpoint in clinical trials to assess the effectiveness of immune checkpoint inhibitors.
Read MoreNano-Signature Discovery Could Revolutionize Cancer Diagnosis A quick and easy test to...
Read MoreThe test will help patients receive a definitive diagnosis for suspicious skin lesion biopsies.
Read MoreStudy data demonstrate that about half of patients have clinically actionable mutations that are being missed.
Read MoreStudies are demonstrating the potential of the Parsortix system to enhance laboratory efficiency, reduce costs, support medical decisionmaking, and improve patient care.
Read MoreThe research panels can be performed using Qiagen’s GeneReader NGS system and other platforms, providing deep analysis of disease-related genomic mutations.
Read MoreProtagen has extended its collaboration with the National Center for Tumor Diseases, Heidelberg, to investigate the immunocompetence of urothelial cancer patients receiving immunotherapy.
Read MoreAlmost two-thirds of the patients with CDKN2A mutations responded with tumors that shrank, and for a third of the patients the tumors disappeared completely.
Read MoreThe partners will apply deep machine learning to develop biomarker models for relevant treatment-associated endpoints such as immune-related adverse events, clinical response, or survival.
Read MoreThe panel accurately and sensitively detects more than 1,600 variants of clinical significance.
Read MoreAnti-idiotypic antibodies will enable monitoring of for pembrolizumab and nivolumab levels in cancer patients undergoing treatment.
Read MoreCirculating tumor DNA is a reliable biomarker of tumor progression following immunotherapy treatment.
Read MoreProtagen and Gustave Roussy will partner to utilize Protagen’s SeroTag technology to help identify biomarkers that predict and monitor immune-related adverse events in cancer patients treated with checkpoint inhibitors.
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