The
study achievements are confirmed in a recent subject about Endocrine-Related
Cancer, a publication of the Society for Endocrinology.
"Neuroendocrine tumors are
sometimes asymptomatic and, from the time of diagnosis, have regularly
metastasized, usually towards the liver," said the study's corresponding author, Larry K.
Kvols, M.D., a senior member at Moffitt and section head of neuroendocrine
oncology. "Operations are crucial in controlling metastatic NET and might
be curative for early disorder, but a large number of affected individuals need
further therapy."
Based
on Kvols, octreotide and lanreotide, drugs that mimic genuine somatostatin, are
now "the mainstay" for symptom regulation of neuroendocrine tumors.
However, many affected individuals ultimately fail to reply to this therapy and
has poor prognoses.
The
multicenter clinical trial, performed at sites in the United States and Europe,
enrolled 89 affected individuals and evaluated 44 for performance and 45 for
tolerability. Pasireotide "effectively managed indications."
Exploration of tumor response in 23 affected individuals confirmed 13 with
stable disorder and 10 with progressive disorder. The medication was "most
effective and well-tolerated" and adverse events, most typically
gastrointestinal, were "mild or modestly severe."
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