Mesothelioma Mesomark Blood Test
TESTThe BLOOD MESOSELIOMA MESOMARK Food and Drug Administration (FDA) approved the MESOMARK test to help monitor response to treatment in patients with malignant mesothelioma. The MESOMARK test marks the beginning of a new era in monitoring mesothelioma malignancies, “said Dr. Jeffrey W. Allard, vice president and Dean of Fujirebio Diagnostics.” As the first in vitro test for patients with aggressive disease, enabling physicians to more accurately detect recurrence and monitor treatment of patients. “The test kits developed MESOMARK test to measure levels of a biomarker, mesothelin, in serum. Biomarkers substances in concentrations higher than normal blood, urine or body tissues of patients with certain types of cancer. The test can be used monitor patients confirmed as mesothelioma, for recurrence in patients after surgery, or for measuring response to treatment. “current diagnostic tests are less than ideal for quantification of changes in tumor volume, which is the key to combat the disease, “continued Allard.” As the MESOMARK results correlate with the volume * volume provides a much needed tool for monitoring the status of the patient. It is our plan to collect additional data in the future to support the use of tests to detect mesothelioma. “MESOMARK test now makes it possible – with a simple blood test to monitor response to therapy and relapse after treatment. This provides a significant advantage for patients fight against this aggressive cancer. “The Meso Foundation is the national research funding, patient support and advocacy organization dedicated to mesothelioma as a life-threatening illness. Those wishing to take part in the tests MESOMARK asked to provide one or more blood samples. Blood samples will then be sent to a national reference laboratory for testing. In combination with other clinical and laboratory data obtained from the medical decisions about treatment and care can be simplified. You can stop testing at any time. LINKS: Diagnisis Mesothelioma
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