The Smoldering Multiple Myeloma Paradigm
The standard of care for SMM patients varies based on jurisdiction between “monitor and don’t treat” all SMM patients till the patient presents in the clinic with myeloma symptoms (too late), to “treating all” SMM patients regardless of their risk of progression, exposing the larger subset of these patients who have stable SMM to unnecessary treatment. Both ends of the spectrum have their negative impact on SMM patients.
Identifying high risk SMM patients is a critical unmet need in the management of these patients. High risk SMM patients may benefit from immediate treatment intervention, with a possibility to achieve cure based on the most recent advanced treatment regimens. Equally important, the larger subset of low-risk patients can be monitored overtime, without exposure to unnecessary, debilitating and costly treatment.
TeloView® Assay for Smoldering Multiple Myeloma - TeloViewSMM (LDT)
Clinical Validation of TeloViewSMM
In a landmark publication published in the American Journal of Hematology, TeloViewSMM has demonstrated a clinically unprecedented and highly actionable prognostic performance for predicting risk of SMM progression to MM.
TeloViewSMM confirms or rules out the risk of patients to progress to full stage MM within 2 years
TeloViewSMM was validated by a clinical trial in collaboration with Mayo Clinic and Dana Farber Cancer Institute including over 170 SMM patients. The results were published in the American Journal of Hematology
TeloViewSMM’s sample requirements can be met with a simple blood draw orbone marrow samples.
TeloViewSMM is a clinically validated LDT accredited by College of American Pathologists (CAP)
TeloViewSMM is currently offered under the SMART protocol, an observational study in the USA, Canada & Europe. Contact Telo Genomics to participate.