Overview
LUTATHERA Is the First FDA-Approved RLT for the Treatment of Adult Patients With SSTR-Positive GEP-NETs1
LUTATHERA |
Somatostatin Receptor Expression
GEP-NETs Overexpress SSTR Subtype 22
![94% icon](https://usim.beprod.lutathera-hcp.com/sites/lutathera_hcp_com/files/styles/single_featured_content_card_without_content_width_744/public/2023-10/up-to-94-percent.png?itok=psKDKO6a)
of GEP-NETs have been demonstrated to express SSTRs, with 86% expressing SSTR subtype 22,a,b
aBased on a study of 100 cases with clinical and pathological data selected from a prospectively built database of patients with gastroenteropancreatic endocrine tumors referred from 3 institutions.2
bThis work was supported by grants from Novartis.
Patients with GEP-NETs with a high density of SSTR expression may be considered for targeted treatment with LUTATHERA.3
Mechanism of Action for LUTATHERA
LUTATHERA is a targeted treatment that uses radiation to damage SSTR-positive cells and neighboring cells.3
PRECISION TARGETING FOR | ENTERS THE CELLS3 |
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FDA, US Food and Drug Administration; GEP-NETs, gastroenteropancreatic neuroendocrine tumors; RLT, radioligand therapy; SSA, somatostatin analog; SSTR, somatostatin receptor.