This data warrants further testing of the long - term cardioprotective benefit of an mTORKi in
neuroendocrine tumor patients prone to carcinoid syndrome.
Not exact matches
Finding new treatments is critical because less than 5 percent of
patients with pancreatic
neuroendocrine tumors respond to everolimus, the most commonly used pharmaceutical, François said.
Patients with aggressive
neuroendocrine tumors (NETs) have limited treatment options and there are few oncologists who are specialised in this relatively rare disease.
Researchers at the 2016 Annual Meeting of the Society of Nuclear Medicine and Molecular Imaging (SNMMI) are presenting a molecular imaging technique that allows oncologists to set
patients» radiotherapy doses right at that critical limit of delivering the most powerful kill to
neuroendocrine tumors (NETs) while protecting vulnerable vital organs.
«Molecular imaging of
neuroendocrine tumors optimizes radiotherapy dose: Study shows the use of PET and SPECT tailors radionuclide treatment for
neuroendocrine cancer
patients and reduces the risk of toxicity.»
In 2011, based on initial findings from two clinical trials, the Food and Drug Administration approved sunitinib and everolimus for
patients with pancreatic
neuroendocrine tumors.
In the first set of experiments, the Johns Hopkins scientists sequenced nearly all protein - encoding genes in 10 of the 68 samples of pancreatic
neuroendocrine tumors and compared these sequences with normal DNA from each
patient to identify
tumor - specific changes or mutations.